The Pathogenic Role of Persistent Milk Signaling in mTORC1- and Milk-MicroRNA-Driven Type 2 Diabetes Mellitus

Abstract

Milk, the secretory product of the lactation genome, promotes growth of the newborn mammal. Milk delivers insulinotropic amino acids, thus maintains a molecular crosstalk with the pancreatic β-cell of the milk recipient. Homeostasis of β-cells and insulin production depend on the appropriate magnitude of mTORC1 signaling. mTORC1 is activated by branched-chain amino acids (BCAAs), glutamine, and palmitic acid, abundant nutrient signals of cow´s milk. Furthermore, milk delivers bioactive exosomal microRNAs. After milk consumption, bovine microRNA-29b, a member of the diabetogenic microRNA-29-family, reaches the systemic circulation and the cells of the milk consumer. MicroRNA-29b downregulates branched-chain α-ketoacid dehydrogenase, a potential explanation for increased BCAA serum levels, the metabolic signature of insulin resistance and type 2 diabetes mellitus (T2DM). In non-obese diabetic mice, microRNA-29b downregulates the anti-apoptotic protein Mcl-1, which leads to early β-cell death. In all mammals except Neolithic humans, milk-driven mTORC1 signaling is physiologically restricted to the postnatal period. In contrast, chronic hyperactivated mTORC1 sig-naling has been associated with the development of age-related diseases of civilization including T2DM. Notably, chronic hyperactivation of mTORC1 enhances endoplasmic reticulum stress that promotes apoptosis. In fact, hyperactivated β-cell mTORC1 signaling induced early β-cell apoptosis in a mouse model. The EPIC-InterAct Study demonstrated an association between milk consumption and T2DM in France, Italy, United Kingdom, Germany, and Sweden. In contrast, fermented milk products and cheese exhibit an inverse correlation. Since the early 1950´s, refrigeration technology allowed widespread consumption of fresh pasteurized milk, which facilitates daily intake of bioactive bovine microRNAs. Persistent uptake of cow´s milk-derived microRNAs apparently transfers an overlooked epigenetic diabetogenic program that should not reach the human food chain.

INTRODUCTION

The worldwide rising prevalence of type 2 diabetes mellitus (T2DM) has been attributed to rising rates of obesity and poor lifestyles, genetic and developmental susceptibility to disease [1]. According to the US National Diabetes Statisitics Report 2014 [2] 29.1 million people or 9.3% of the U.S. population have diabetes mellitus.

T2DM is characterized by progressive β-cell dysfunctioning, early β-cell apoptosis resulting from low-grade local and systemic inflammation, increased oxidative stress and insulin resistance, recently extensively reviewed elsewhere [3-6].

Notably, since the 1960´s there is a steady increase in the prevalence rate of T2DM in industrialized countries [7]. Shortly prior to the 1960’s, the refrigerator and widespread cooling technology was introduced into most households and food stores of developed countries. Cooling technology allows daily access to fresh pasteurized cow´s milk, whereas in former times and less developed countries primarily fermented milk and milk products have been consumed due to the unavailability of cooling facilities.

The pathogenesis of age-related diseases of civilization such as obesity, T2DM, metabolic syndrome, cancer, neurodegenerative diseases and early aging have all been related to persistently increased activation of the nutrient-sensitive kinase mechanistic target of rapamycin complex 1 (mTORC1) [8-14]. Remarkably, milk is the only and sufficient nutrient system of all mammals that allows appropriate postnatal growth. It has recently been recognized that milk is not “just food” but represents a sophisticated signaling system of mammalian evolution that adequately activates mTORC1 of the cells of the milk recipient to drive controlled species-specific growth [15]. Milk contains abundant essential branched-chain amino acids (BCAAs: leucine, isoleucine, and valine) and glutamine that are important nutrient signals that communicate with pancreatic β-cells of the milk recipient to promote mTORC1-mediated insulin synthesis and secretion. Insulin itself is an important growth hormone that activates mTORC1 of insulin-dependent cells facilitating anabolism and growth of the newborn organism. Notably, it is not the carbohydrate content of milk and skim milk that exerts strong insulinotropic effects, but the insulinotropic amino acids that operate as nutrient signals stimulating insulin secretion. In all mammals, except humans since the Neolithic revolution, this insulinotropic signaling system is restricted to the postnatal growth phase and has not been designed by evolution for lifelong use. Downregulation of intestinal lactase expression resulting in lactose intolerance after the weaning period is thus the original genetic makeup of humans and all other mammals.

It is the intention of this review to provide evidence that persistent abuse of mTORC1-activating and microRNA-transmitting bovine milk is a major overlooked pathogenic and epigenetic factor promoting the epidemic of T2DM.

1. MILK´S HARDWARE DRIVING MTORC1 SIGNALING

mTORC1 of β-cells plays a pivotal role in β-cell homeostasis, insulin synthesis and insulin secretion [16-19]. mTORC1 orchestrates cell growth and proliferation [20]. mTORC1 is the central hub of metabolism that activates nucleotide, protein and lipid synthesis and promotes cell cycle progression under conditions of nutrient and growth factor availability [20-30]. Moreover, mTORC1 plays a fundamental role in lipid accumulation and adipogenesis [31-35]. Thus, persistently overactivated mTORC1 signaling stimulates weight gain, increases body mass, and fat mass [31-36], known risk factors promoting the development of T2DM.

Basically, there are five major pathways that activate mTORC1: 1) growth factors such as insulin and IGF-1 [20, 23, 24,28], 2) sufficient cellular energy (glucose, ATP) [36-38], 3) the availability of amino acids, predominantly essential BCAAs such as leucine [21-29, 39], 4) the presence of glutamine for cellular leucine uptake and glutaminolysis-mediated activation of mTORC1 [40-42], and 5) the availability of saturated fatty acids, especially palmitic acid [43] (Fig.1).

Fig. (1).

Schematic working model representing the potential crosstalk bewteen milk signaling and persistent β-cell mTORC1 hyperactivation promoting endoplasmic reticulum (ER)-stress and early β-cell apoptosis. Milk is a rich source of branched-chain amino acids (BCAAs). Leucine (Leu) and glutamine (Gln) synergistically activate β-cell mTORC1. mTORC1 activation is important for insulin synthesis. Insulin synthesis is further promoted by whey-stimulated secretion of glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide 1(GLP-1). Milk-derived exosomal microRNA-29b (miR29b) may represent a shutoff mechanism of mitochondrial BCAA catabolism that increases BCAA plasma levels enhancing BCAA-driven β-cell mTORC1 activation. Persistent milk-mediated β-cell mTORC1 activation promotes ER-stress leading to early β-cell apoptosis. ER-clearance is impaired by mTORC1-mediated inhibition of autophagy further promoting β-cell apoptosis. ER-stress in a vicious cycle via activating transcription factor 4 (ATF4)-mediated upregulation of L-type amino acid transporter (LAT) aug-ments leucine-mTORC1 signaling. Further enhancement of β-cell apoptosis may result from milk miR29b-mediated inhibition of anti-apoptotic Mcl-1. Milk miR-21-mediated inhibition of FoxO1 may increase β-cell proliferation and may increase oxidative stress further promoting β-cell apoptosis. See list of abbreviations.

It will be demonstrated that persistent and excessive cow´s milk consumption provides and mediates abundant nutrient and growth factor signals that overactivate β-cell mTORC1 signaling of the human milk recipient promoting endoplasmic reticulum (ER)-stress and early β-cell apoptosis.

1.1. Milk Provides BCAAs Activating mTORC1

Milk proteins provide highest amounts of essential BCAAs, especially leucine [44]. Leucine plays a pivotal role for activating mTORC1 [39]. Of all animal proteins, whey proteins contain the highest amount of leucine (14%) [44], and in comparison to meat (8% leucine), whey proteins undergo fast intestinal hydrolysis, thus operate like an i.v.-amino acid infusion [45-49].

1.2. Milk Provides Glutamine Activating mTORC1

Milk protein (8.09 g glutamine/100 g) in comparison to beef protein (4.75 g glutamine/100 g) provides 70% more glutamine [49]. In the β-cell, glutamine is an important activator of mTORC1. Glutamine functions as a gatekeeper for cellular leucine uptake via the L-type amino acid transporter (LAT) and is a precursor of the glutaminolysis pathway that activates mTORC1 [16, 50-52]. Leucine is an allosteric activator of glutamate dehydrogenase (GDH), the key-regulating enzyme of the glutaminolysis pathway [50-52]. This intimate interplay of glutamine and leucine maximizes the flux through GDH in pancreatic β-cells, which is important for mTORC1-S6K1-dependent insulin secretion [52]. Thus, leucine and glutamine should be regarded as milk´s amino acid messengers that activate β-cell mTORC1 signaling during the postnatal period of mammalian life.

1.3. Milk Stimulates Incretin and Insulin Secretion

The insulinemic index of whole cow´s milk (148±14) and skim milk (140±13) is much higher than the glycemic indices of whole milk (42±5) and skim milk (37±9), repectively [53,54]. Fast hydrolysis and immediate intestinal absorption of insulinotropic amino acids of the whey protein fraction of cow´s milk raise insulin levels to much higher magnitudes than intestinal digestion of structural proteins such as beef (insulinemic index: 51) [53,54]. The major insulinotropic protein fraction of cow´s milk is the whey protein fraction [55]. Whey-derived leucine and other whey-derived amino acids stimulate glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide (GLP-1) secretion of enteroendocrine K- and L-cells, respectively [56-60]. Dipeptidyl peptidase-IV (DPP-IV) activity is of critical importance for the biological activity and half-life of these incretins. Remarkably, milk protein-derived peptides have been shown to inhibit DPP-IV activity and thus increase incretin activity enhancing incretin-mediated insulin synthesis and secretion [61,62].

Additionally, whey-derived amino acids directly exert inulinotropic effects on pancreatic β-cells [16,18,19]. Milk protein consumption in comparison to meat protein intake thus results in significant hyperinsulinemia [63]. Furthermore, i.v.-infusion of bovine β-casomorphin 4, a bovine milk protein peptide that is generated in the intestinal tract, has been shown to stimulate μ-receptors of β-cells and substantially increases insulin secretion in dogs [64]. Thus, milk intake may also stimulate neuroendocrine regulatory networks of the β-cell that augment insulin secretion.

1.4. Milk Stimulates IGF-1 Secretion Activating mTORC1

A meta-analysis confirmed that continued milk consumption increases serum levels of insulin-like growth factor-1 (IGF-1) [65]. The European Prospective Investigation into Cancer and Nutrition (EPIC) confirmed a relationship between milk intake in 2,109 European women with increased IGF-1 serum levels [66]. A 20% increase in serum IGF-1 levels has been observed in prepubertal children previously not used to milk consumption after a daily intake of 710 mL of ultra-heat treated (UHT) milk for 4 weeks [67]. A recent study including 193 overweight adolescents aged 12-15 years drank either 1L/day of skim milk, whey, casein or water for 12 weeks. All milk-based-drinks contained 35 g milk protein/L. IGF-1 significantly increased with skim milk and tended to increase with casein compared to the pre-test control group [68].Casein in comparison to whey protein has been shown to differentially enhance hepatic IGF-1 synthesis [55]. Notably, per capita cheese comsumption, the major dairy source of casein, increased in Germany from 5 kg in 1950 to 24.4 kg in 2013 [69].

1.5. Milk Provides Palmitic Acid Activating mTORC1

Bovine milk contains about 3.5 to 5% total lipid. About 98% of the lipid is composed of triacylglycerols, transported in milk fat globules [70]. The major fatty acid of total fatty acids of milk lipids is palmitate (C16:0) with 32.3 wt% [70,71]. Palmitate like BCAAs activates mTORC1 at the lysosomal compartment [43].

Thus milk, the promoter of postnatal growth of mammals, activates mTORC1 of the milk recipient either by transfer or induction of pivotal mTORC1 activating signaling pathways.

2. MILK´S SOFTWARE: EXOSOMAL MICRORNAS

In 2013, Melnik and colleagues [15] hypothesized that milk functions as a genetic transfection system of the milk recipient by transfer of exosomal bioactive bovine milk microRNAs to modulate early metabolic programming. The microRNA regulatory network appears to represent milk´s epigenetic software that augments mTORC1 signaling and cell cycle progression to optimize growth conditions of the newborn mammal. Valadi et al. [72] were the first who demonstrated that exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells. Thus, secreted exosomal microRNAs have been appreciated as important players of gene regulation and intercellular communication [73-75]. MicroRNAs bind through partial sequence homology to the 3´-untranslated region (UTR) of target mRNAs and cause either translational block or mRNA degradation [76].

Recently, Witwer and Hirschi [77] challenged the hypothesis that diet-derived foreign microRNAs, especially plant-derived xenomirs, might be absorbed and could regulate vertebrate metabolism and function. The caveat of Witwer and Hirschi [77] is primarily based on repeated negative results evaluating the intestinal uptake of plant-derived microRNAs [78-80], which could not confirm the reported intestinal absorption of rice-derived MIR168a [81].

In mammals however, microRNAs enclosed by membranous microvesicles (exosomes) play a pivotal role for horizontal microRNA transfer [82]. Milk is apparently mammal´s longest distance interindividual exosomal signaling system that allows maternal-neonatal communication for metabolic regulation of the newborn. In fact, breast milk in comparison to all other human body fluids contains the highest amounts of total RNAs [83]. It has been suggested that bovine and human milk exosomal microRNAs may be transferred to the infant to promote immune regulatory functions [84-86]. MicroRNA-containing exosomes of 30-100 nm diameter have been identified in human breast milk, cow´s milk, bovine whey and colostrum [87-89]. Exosomes from bovine colostrum and mature milk are able to deliver microRNAs into cultured cells thereby increasing cytoplasmic microRNA levels [89]. Recently, Baier et al. [90] provided evidence that microRNAs of commercial pasteurized cow´s milk are absorbed by adult human subjects in biologically meaningful amounts from nutritionally relevant doses of cow´s milk and affected gene expression of human peripheral blood mononuclear cells, HEK-293 kidney cell cultures and mouse liver cells. The authors estimated that the 245 microRNAs of bovine milk may modulate the transcription of more than 11,000 human genes [90]. The lipid bilayer of milk exosomes protects their microRNA cargo against harsh degrading conditions like low acidic pH of 1-2 and RNase-mediated degradation [86, 91]. Boiling of milk, however, results in complete microRNA degradation [92]. Recently, Howard et al. [93] studied the influence of homogenization, pasteurization, microwave treatment and storage at 4°C of commercial whole milk, fat reduced (2%) milk and skim cow´s milk on microRNA recovery. Notably, more than 50% of microRNA-29b was still detectable after pasteurization and homogenization of whole and 2% fat milk in comparioson to raw milk [93]. Nearly one third of microRNA-29b was recovered in skim milk after these procedures [93]. Storage of 2% fat milk for 15 days did not affect microRNA-29b concentrations [93]. Thus, raw cow´s milk contains the highest amounts of bioactive microRNAs, whereas pasteurized refrigerated commercial milk still contains substantial amounts of bioactive microRNAs [90, 93].

2.1. MicroRNA-21 Activates mTORC1 and Inactivates FOXO1

A major microRNA type in cow´s milk is bovine microRNA-21 [85], which is identical with the humun microRNA-21 (www.mirbase.org). Notably, microRNA-21 is involved in phosphoinositol-3-kinase (PI3K)-AKT and mTORC1 signaling pathways [94]. Critical targets of microRNA-21 are mRNAs of important tumor suppressor proteins involved in upstream and downstream suppression of mTORC1 signaling such as phosphatase and tensin homolog (PTEN) [95-97], Sprouty1 and Sprouty2 [98-100], and programmed cell death 4 (PDCD4) [101-103]. Moreover, microRNA-21 has been shown to induce the cell cycle promoter cyclin D1 in an mTORC1-dependent manner [104]. MicroRNA-21-mediated inhibition of Sprouty1 and Sprouty2 amplifies RAS-RAF-MEK-ERK signaling, which suppresses TSC2 (tuberin) and thus raises mTORC1 activity. Furthermore, microRNA-21 stimulates the initiation of translation by repression of PDCD4, which is a suppressor of translation initiation that inhibits the RNA helicase eIF4A [105]. Both, 4E-binding protein-1 (4E-BP-1) and PDCD4 are thus crucial regulatory inhibitors of translation initiation that control protein synthesis. Activation of the mTORC1 pathway and its substrate kinase S6K1 results in subsequent phosphorylation of 4E-BP-1 and PDCD4 that promotes eIF4E-eIF4G complex assembly stimulating mRNA translation [104].

Furthermore, microRNA-21 induces adipogenic differentiation and proliferation of human adipose tissue-derived mesenchymal stem cells [106, 107], thus promotes fat mass accretion. MicroRNA-21 orchestrates high glucose-induced signals to TORC1, resulting in renal cell pathology in T2DM [108]. Moreover, microRNA-21 has been demonstrated to promote renal injury in a mouse model of T2DM [109]. Thus, excess intake of bovine milk microRNA-21 may overstimulate β-cell mTORC1 activation and may contribute to renal mTORC1-driven pathology in T2DM.

Recently, the mRNA of forkhead box class O1A transcription factor (FoxO1) has been indentified as a direct target of microRNA-21 [110]. FoxO1 is a key transcription factor that plays a central role in the regulation of glucose metabolism, insulin signaling, and β-cell homeostasis [6, 110-115]. FoxO1 controls β-cell replication via the insulin/IGF-1 signaling pathway [6]. Moreover, FoxO1 regulates the expression of antioxidant enzymes such as catalase and superoxide dismutase 2 [116]. FoxO1 apparently protects β-cells against oxidative stress [6, 117] and oxidative stress-induced apoptosis [6, 117, 118] (Fig. 1). Milk is physiologically provided during the postnatal growth phase, a period with enhanced insulin demands. From a mechanistical point of view, it is conceivable that milk promotes β-cell replication and β-cell mass expansion by epigenetic transfer of exosomal microRNA-21 that downregulates FoxO1.

2.2. microRNA-29b: Milk´s Inhibitor of BCAA Catabolism?

Serum levels of circulating BCAAs are increased in obese individuals and are associated with future insulin resistance and T2DM [119-140]. Thus, increased serum BCAA levels are believed to represent a critical metabolic signature of insulin resistance and T2DM [128,132, 134-142].

The rate-controlling step of BCAA catabolism is catalyzed by the multienzyme mitochondrial branched-chain α-ketoacid dehydrogenase (BCKD) [143]. About half of the BCKD catalytic activity resides in skeletal muscle, whereas a considerable portion of activity also resides in adipose tissue [143]. The BCKD complex is composed of the branched-chain keto acid dehydrogenase (BCKDHA), the dihydrolipoamide branched-chain transacylase (DBT), and the dihydrolipoamide dehydrogenase (DLD) [143, 144]. Notably, the DBT forms the core of the BCKD complex [145]. Mersey and coworkers [146] provided evidence that human microRNA-29b controls the expression of the BCKD complex at the level of mRNA translation. Human microRNA-29b recognizes the mRNA of DBT, which forms the core of the BCKD complex and provides the binding site for all other proteins in the BCKD complex including the branched-chain α-keto acid dehydrogenase kinase (BCKDK) [146, 147]. Thus, microRNA-29b, a major microRNA of bovine milk [86, 92], suppresses BCAA catabolism. Intriguingly, Baier and coworkers [90] demonstrated that bovine microRNA-29b, which is identical to their human ortholog (www.mirbase.org), increased in substantial amounts and in a dose-dependent manner in healthy milk consumers. Furthermore, microRNA-29b increased in peripheral blood mononuclear cells (PBMCs) associated with a doubling of cellular microRNA-29b levels six hours after oral exposure to commercial cow´s milk [90]. Remarkably, milk consumption evoked 30% changes in microRNA-29b target gene expression in human PBMCs [90]. From these data, it is conceivable to suggest that bovine microRNA-29b may modify mRNA levels of its target DBT mRNA, which translates the functionally most important core component of the BCKD complex (Fig.1).

Why should milk inhibit BCAA catabolism? There is good reason to believe that milk provides a regulatory epigenetic microRNA program that rescues valuable essential BCAAs from mitochondrial oxidation in order to favor their incorporation into important functional and structural proteins required for growth and development. Leucine, isoleucine and valine are among the most hydrophobic amino acids, which are crucial determinants for hydrophobic clefts of enzymes and are important for the insertion of proteins such as receptors into cell membranes [143]. Hydrophobic residues are crucial for oxygen binding in hemoglobin and myoglobin and substrate binding of various enzymes [148]. Remarkably, surfactant protein B contains 37% of BCAAs (17.7% leucine) [149]. Leucine-rich transcription factors such as leucine zippers are most important for adequate regulation of transcription and cell signaling [150]. It is thus conceivable, that BCAA catabolism should be attenuated during the process of postnatal growth and development. From this perspective, it makes sense that milk provides a signal to switch off BCAA catabolism in order to increase BCAA levels for the formation of vitally important BCAA-dependent proteins. Notably, in stored and refrigerated whole milk and 2% fat milk more than 50% of microRNA-29b is preserved compared to unprocessed raw milk [93].

There is accumulating evidence that commercial milk consumption is associated with increased body mass index and obesity in humans and in a recently reported mouse model, which demonstrated increased mTORC1-S6K1 activation during bovine milk consumption [33,151-155]. In addition, milk-mediated transfer of microRNA-21, which induces adipogenesis [106,107], may function as a further mechanism that promotes the development of obesity, the most common comorbidity of T2DM. It has recently been demonstrated in db/db mice that long-term inhibition of microRNA-21 reduced obesity [156].

Remarkably, BCKD component transcripts were significantly lower in subcutaneous adipocytes from obese versus lean Pima Indians [139]. Moreover, mRNA abundances for BCAA catabolic enzymes were markedly reduced in omental white adipose tissue of obese persons with metabolic syndrome compared with weight-matched healthy obese subjects [139]. Lynch and Adams [157] recently concluded that attenuated mitochondrial BCAA metabolism, which appears to be a critical metabolic deviation in T2DM, is either caused by altered gene expression, mutations, or epigenetic factors that affect gene expression. Notbably, BCKDHA (branched-chain α-keto acid dehydrogenase), the gene encoding the regulated unit of BCKDC is one of the primary susceptibility genes identified that affected the risk of both T2DM and obesity [158].

Nevertheless, genetic mutations cannot explain the worldwide and steady rise in diabetes prevalence. Thus, an epigenetic modifier such as a very common dietary factor may promote BCAA dysregulation of human beings. Bovine milk microRNA-29b-attenuated BCAA catabolism may be the missing overlooked epigenetic factor that is responsible for the epidemic of T2DM.

2.3. Milk-microRNA-Mediated Insulin Resistance

Milk contains substantial amounts of the microRNA let-7 family (let-7a, let-7b, let-7c and let-7f) [85, 89]. There is accumulating evidence that the Lin28/let-7 axis regulates glucose metabolism [159]. Muscle specific loss of Lin28a, a developmentally regulated RNA-binding protein, and overexpression of let-7 resulted in insulin resistance and impaired glucose tolerance in mice [159]. Intriguingly, let-7 targets are enriched for genes that contain SNPs associated with T2DM and fasting glucose in human genome-wide association studies [159]. Lin28 selectively blocks the processing of pri-let-7 micoRNAs [160]. Notably, the restoration of the Lin28 protein blocked let-7 expression and restored glucose metabolism in adipose-derived stem cells derived from obese tissues [161]. The most interesting microRNAs in inflammatory microvesicles in association with metabolic and cardiovascular diseases recently reported are the let-7 family, microRNA17/92 family, microRNA-21, microRNA-29, microRNA-126, microRNA-133, microRNA-146 and microRNA-155 [162], which exhibit a substantial overlap with the spectrum of bovine milk microRNAs [84-89].

Palmitate, the major fatty acid of milk fat, significantly increases the expression of microRNA-29a in myocytes [163]. MicroRNA-29a targets and suppresses mRNA of insulin receptor substrate-1 (IRS-1) and attenuates IRS-1 expression. Ectopic expression of microRNA-29a thus impairs insulin signaling and glucose uptake in myocytes through a substantial decrease in IRS-1. Intriguingly, bovine milk contains microRNA-29a [89], thus presents a putative exogeneous source of microRNA-29a-mediated suppression of insulin signaling. The suppression of skeletal muscle insulin signaling via milk-derived microRNA-29a transfer may spare insulin for more important anabolic purposes as skeletal muscle activity is rather low during the nursing period. Increased circulating blood levels of palmitate in obesity may induce palmitate-mediated microRNA-29a expression in skeletal muscle, which may be fortified by milk-derived palmitate as well as direct transfer of bovine milk microRNA-29a into the systemic circulation of the milk consumer. MicroRNA-29a and let-7-family of bovine milk may thus promote microRNA-driven insulin resistance [159,164].

3. BCAA-MTORC1-S6K1-MEDIATED INSULIN RESISTANCE

Fatty acids and their metabolites have been implicated in the development of insulin resistance and T2DM. However, metabolomics technologies revealed that BCAAs and related metabolites are more strongly associated with insulin resistance than many common lipid species. Nevertheless, in animal feeding studies, BCAA supplementation required the background of a high-fat diet to promote insulin resistance [136].

Palmitate-driven microRNA-29a-mediated suppression of IRS-1 in combination with increased BCAA levels may synergize in the induction of insulin resistance. Excessive amounts of circulating BCAAs activate mTORC1 and its downstream substrate, the kinase S6K1 [23,33,165,166],which reduces insulin signaling by inhibitory phosphorylation of IRS-1 [165-174]. BCAA-mediated insulin resistance is explained by enhanced mTORC1/S6K1-mediated inhibitory phosphorylation of IRS-1 [142].

4. MILK ACCOMPANIES THE LIFELONG MARCH TO DIABETES

Accelerated fetal growth and increased birth weight are well-known risk constellations increasing the risk of T2DM and obesity later in life [175-177]. As medicine and nutritional sciences still regard milk as a source of valuable proteins, vitamins, and calcium, an increase (4 servings per day) of either milk or dairy products is recommended by most societies of gynecology and obstetrics during pregnancy [178]. Data from 50,117 mother-infant pairs of the Danish National Birth Cohort collected from 1996-2002 showed an increase of placental weight and birth weight across the whole range of milk intake [179]. The Generation R Study, a population-based prospective cohort study from fetal life until young adulthood in Rotterdam, investigated 3,405 mothers during pregnancy [180]. Maternal milk consumption of >3 glasses (450 mL of milk) per day was associated with greater fetal weight gain in the third trimester of pregnancy, which led to an 88 g higher birth weight than that with milk consumption of 0 to 1 glass per day [180]. Notably, this association was limited only to milk, whereas protein intake from nondairy food or cheese was not associated with increased birth weight. A possible explanation for this finding is the presence of biologically active microRNAs in milk and their potential absence in processed and fermented milk products such as cheese [93]. Jiang et al. [94] recently detected increased levels of microRNA-21 in placental tissue of mothers with macrosomal infants. Bovine microRNA-21 transfer to the pregnant mother by milk consumption may overstimulate trophoblast mTORC1, which controls nutrient and BCAA transfer to the fetus [181-186]. A recent literature review provided translational evidence that milk consumption during pregnancy but not fermented dairy products increased placental and birth weight [187].

After birth, high protein infant formula feeding maintains exaggerated BCAA-mTORC1 signaling associated with rapid weight gain [188-191]. Infant formula with higher protein versus formula with lower protein content has been linked to increased mTORC1 signaling [188,189], which is associated with higher weight gain velocity [190,191]. Importantly, rapid weight gain in infancy has been related to an increased risk of T2DM [192]. Data derived from the National Health and Nutrition Examination Survey (NHANES) 1999-2004 confirmed that milk consumption in children increased body mass index (BMI) [151] and induced earlier onset of menarche [193]. Increased BMI and early onset of menarche are both explained by milk-mTORC1-mediated anabolism, which obviously accelerates human growth trajectories. Remarkably, early onset of menarche is a well-known risk factor for the development of T2DM recently confirmed in a systematic review and meta-analysis [194]. Thus, there is good reason to assume that persistent bovine milk signaling deviates the physiological human axis of mTORC1 signaling during intrauterine and extrauterine life.

5. MTORC1 INDUCES ENDOPLASMIC RETICULUM-STRESS-MEDIATED Β-CELL APOPTOSIS

To maintain appropriate β-cell mass and β-cell homeostasis, a physiological level of mTORC1 signaling is required [195]. In order to adapt to the increased metabolic burden of obesity and insulin resistance, β-cells increase mass by proliferation, neogenesis and hypertrophy to enhance β-cell function [195]. There is substantial evidence that ER-stress of chronically overacticated β-cells results in early β-cell apoptosis, the hallmark of T2DM [196-198]. Studies in humans indicate that glucose intolerance appears after 20% reduction in β-cell mass, while overt diabetes develops with 65% reduction [199]. Pancreatic β-cells have a heavy engagement in insulin synthesis (> 50% of total protein synthesis) and express high levels of the ER-stress transducers eukaryotic translation initiation factor 2-alpha kinase 3 (EIF2AK3) and endoplasmic reticulum-to-nucleus signaling 1 (ERN1), which induce the unfolded protein response (UPR) [197]. Recent evidence supports the concept that hyperactivation of the UPR is closely related to β-cell dysfunction and apoptosis [196,197].

ER-stress and β-cell dysfunction have been related to increased lipotoxicity [198]. The saturated fatty acid palmitate, the most abundant fatty acid of milk lipids, has been implicated to play a major role in β-cell apoptosis [199]. Glucose amplifies fatty acid-induced ER-stress in pancreatic β-cells via activation of mTORC1 [200]. Notworthy, palmitate and BCAAs are both able to activate mTORC1 on lysosomal compartments [43].

Importantly, increased mTORC1 singaling upregulates the ER-stress response [201]. mTORC1-driven ER-stress has been associated with the induction of apoptosis [202-204]. Ozcan et al. [203] convincingly demonstrated that increased mTORC1 activity (due to loss of TSC suppressors) triggered UPR-driven apoptosis. Upon prolonged ER-stress, mTORC1 contributes to apoptotic signaling by suppressing the survival kinase AKT through feedback inhibition [205].

Apparently, in a vicious cycle, ER-stress via induction of eIF2α-P/activating transcription factor-4 (ATF4) signaling stimulates the expression of LAT thereby enhancing intra-β-cell leucine levels that further stimulate mTORC1 signaling during ER-stress [204,206] (Fig.1). Han et al. [207] demonstrated that ER-stress via ATF4 and DNA damage-inducible transcript 3 (DDIT3) upregulation increased protein synthesis leading to cell death.

ER-stress stimulates autophagy as an adaptive response to clean up terminally misfolded proteins from the ER [198] (Fig.1). It is well established that mTORC1 is a negative regulator of autophagy [208,209]. Remarkablly, it has been shown that stimulation of autophagy improved ER-stress-induced diabetes in a mouse model [210]. Furthermore, inhibition of mTORC1 during ER-stress increased autophagy and attenuated apoptosis [211].

Thus, persistent milk-mediated overstimulation of β-cell mTORC1 may promote chronic ER-stress promoting β-cell apoptosis, the hallmark of T2DM. In fact, persistent mTORC1 activation of β-cells in β-cell TSC2^-/- mice resulted in a biphasic response with hyperinsulinemia and hypoglycemia at young ages (4-28 weeks) and hypoinsulinemia and hyperglycemia due to enhanced β-cell apoptosis in adult mice [212]. These findings are in accordance with the observations of Ozcan et al. [203], who found enhanced UPR signaling in cells lacking TSC2. This experimental constellation thus resembles chronic milk-mediated mTORC1 hyperactivation, which apparently provides a most critical mechanism promoting early death of β-cells in milk consuming societies (Fig.1).

6. ARE MILK-DERIVED MICRORNAS DIABETOGENIC?

It is predicted that more than 30% of human genes are regulated by microRNAs. There is most recent scientific interest in the influence of microRNAs in the regulation of insulin signaling pathways and insulin resistance in type 1 and type 2 diabetes [213-217]. As milk promotes insulin secretion and mTORC1-driven growth, it is most conceivable that milk-derived exosomal microRNAs that reach the systemic circulation [90] may be taken up by the pancreatic β-cell to modify translation during the period of lactation and milk feeding.

The β-cell must respond immediately to changes of blood glucose levels and thus has an intimate connection to the systemic blood circulation. To facilitate this connection, the β-cells of the islets of Langerhans are embedded in a dense capillary network. Notably, islet capillaries show about ten times more fenestration than those within the exocrine tissue and are highly permeable [218-220]. Endothelial cell fenestrae produce a pore of about 100 nm in diameter and allow rapid passage of macromolecules [220].

There is recent evidence that β-cells release microRNA-containing exosomes [221, 222]. It is thus conceivable, that milk exosomes, which have a size of 50-100 nm, may reach the β-cells from the systemic circulation. The purpose of milk-mediated exosomal microRNA signaling may be the stimulation of β-cell growth and insulin secretion during the postnatal growth period, which requires an adaptation of the infant´s β-cell mass to fulfill increased insulin demands. However, persistent milk-driven microRNA signaling may deteriorate β-cell homeostasis.

Notably, the microRNA-29 family, which consists of microRNA-29a, b, and c, has been identified as diabetic microRNA markers [223]. MicroRNA-29a has been identified as one of the microRNAs that was upregulated in the serum of children with type 1 diabetes [224]. microRNA-29 has pro-apoptotic functions and is involved in renal and cardiovascular injury [225], common complications of T2DM.

MicroRNA-29b downregulates the expression of the anti-apoptotic protein myeloid cell leukemia 1 (Mcl-1) [226]. In non-obese diabetic (NOD) mice, upregulation of microRNA-29a, b, and c caused pancreatic β-cell death via suppression of Mcl-1, an essential member of the pro-survival Bcl-2 family genes [227]. Thus, the microRNA-29-Mcl-1 axis may thus play a role in the pathogenesis of diabetes and may contribute to β-cell dysfunction in prediabetic NOD mice [227]. Furthermore, studies on microRNA expression in skeletal muscles of Goto-Kakizaki (GK) rats, a non-obese model of T2DM, identified upregulated microRNA-29a and microRNA-29b in these diabetes animals compared to control animals [228]. Intriguingly, increased urinary levels of microRNA-29a, b, and c have been detected in patients with T2DM [229]. Thus, upregulation of the microRNA-29 family may be involved in the pathogenesis of type 1 and type 2 diabetes.

The systemic uptake of microRNA-29 by consumption of “fresh” commercial milk may augment diabetogenic microRNA-29 signaling. Bovine milk microRNA-29a by targeting the mRNA of insulin receptor substrate-1 (IRS-1) enhances insulin resistance [163]. Milk microRNA-29b by targeting the mRNA of DBT, the critical core component that assembles the BCKD complex [146], may explain increased BCAA-mTORC1-S6K1-mediated insulin resistance. Furthermore, by targeting Mcl-1 of β-cells, milk-derived microRNA-29b may promote early β-cell apoptosis (Fig. 1). Persistent activation of mTORC1 may impair β-cell autophagy, augmenting ER-stress-induced β-cell apoptosis. However, as a feedback mechanism, mTORC1 has been shown to promote cell survival through translation of Mcl-1 [230].

7. EPIDEMIOLOGY OVERLOOKS THE IMPACT OF MILK´S MICRORNAS

The majority of epidemiological studies show that “dairy consumption“ in general is inversely related to the risk of T2DM [231-235]. Rice and coworkers recommend the intake of more than three servings of dairy per day to reduce the risk of T2DM [236]. It is of most critical concern that most cohort studies do not accurately differentiate milk from other fermented dairy products. There are only few studies that selectively analyse the association between milk consumption and T2DM [237-242]. Surprisingly, milk, the starting material of all other processed dairy products does not convincingly exhit diabetes-protective effects as observed with fermented or processed milk products such as yoghurt. Liu et al. [237] prospectively examined the incidence of T2DM in 37,183 women in relation to the number of skim milk and whole milk servings and found no significant decrease in diabetes risk. Elwood et al. [238] studied 2,375 men of the Caerphilly cohort. Milk intake showed no significant trend with incident diabetes. Villegas et al. [239] investigated 64,191 women of the Shanghai women cohort and reported a significant decrease in diabetes risk in women consuming > 200 g milk/day versus none. Kirii et al. [240] analysed 59,796 men and women of a Japanese cohort and found no significant risk for diabetes for milk consumption in men, whereas women exposed to > 200 g milk/day showed a trend to lower diabetes risk, although not reaching statisitical significance. The Physicians´ Health Study [241] (21,660 men) exhibited a significant increase in diabetes risk. Less than 1 serving of whole milk/week was associated with a diabetes prevalence of 1.7% and > 2 servings/week with 2.6% (p<0.001), respectively. For skim/low fat milk the diabetes percentages were 1.6 and 2.3 (p<0.001) respectively [241].

The worldwide largest prospective study investigating the type of dairy product intake and incident T2DM is the European Prospective Investigation into Cancer and Nutrition (EPIC)-InterAct study [242], a nested case cohort within 8 European countries (n=340,234). Although, the pooled hazard ratios (HRs) demonstrated only a slight but not significiant increase of diabetes risk in relation to increased milk intake, HRs of individual countries showed substantial variations. Higher diabetes risks (HR > 1) were observed in the French, Italian, UK, German and Swedish cohorts, whereas the Netherlands and Denmark exhibited HR=1 (Fig. 2). Only Spain (UHT milk consumption > 96% of total milk consumption [243]) exhibitied a HR < 1 [242]. Sluijs et al. [242] convincingly concluded that the findings for milk and diabetes risk remain inconclusive and require further research of the associations with various types of milk.

Fig. (2).

Hazard ratios (HRs) (and 95% CIs) for the association of milk consumption with diabetes risk (highest compared with lowest quintile) per Eu-ropean country of the EPIC-InterAct Study (n=340,234) according to the Sluijs et al. [242] with permission the American Society of Nutrition. Notably, 80.3% of the EU population (France, Italy, UK, Germany, Sweden) exhibited an increased diabetes risk in relation to milk consump-tion, whereas 6.4% (Netherlands, Denmark) showed no correlation and 13.3% (Spain) exhibited an inverse association

Differences in heat exposure and time during milk processing may modify the biological activity of bovine microRNAs. High temperature short time (HTST) pasteurization (72°C, 15 sec), and UHT processing (140°C, 14 sec) may have different effects on the bioactivity of milk´s exosomal microRNAs. Furthermore, milk processing by the consumer prior to use (boiling or microwave treatment) is also of critical importance to evaluate milk microRNA-mediated effects on human health [93].

DISCUSSION

“Milk and sugar” are the inseparable and most common food items on everyman´s table in Western societies. It is known for a long time, that the addition of milk to a low glycemic carbohydrate meal exaggerates the insulinemic response comparable to that of a hyperglycemic carbohydrate meal [244]. Thus, milk intake is an overlooked metabolic burden of the β-cell that increases ER-stress. However, in comparison to glucose, milk´s origin and function differ. Milk is the secretory product of the lactation genome of a mammalian species that executes a sophisticated growth program designed to upregulate anabolic mTORC1 signaling of the milk recipient, the species-specific newborn mammal. Milk maintains an intimate molecular crosstalk with the pancreatic β-cell via stimulation of incretin signaling and transfer of abundant insulinotropic BCAAs that increase insulin synthesis and secretion by upregulation of β-cell mTORC1 activity. Furthermore, milk provides a microRNA signaling software. By transfer of the bovine exosomal microRNA-29 family, milk apparently attenuates BCAA catabolism, a meaningful metabolic deviation that favors BCAA incorporation into functionally important proteins during postnatal development. However, this metabolic deviation increases BCAA-mTORC1-driven β-cell ER-stress as well as BCAA-mTORC1-S6K1-driven insulin resistance of peripheral tissues.

In mammals, milk signaling generally is limited to the physiological nursing period, except the Neolithic Homo sapiens, who introduced milk consumption 8000-10,000 years ago into his food chain [245,246]. Noteworthy, humans of the early Neolithic period consumed preferentially fermented milk and milk prodcuts [245,246]. Whereas lactase persistence in most Europeans resulted from LCT mutations during the early Neolithic period [247], most Asian populations are still lactose intolerant. However, the dairy industry is able to bypass physiological lactose intolerance in humans by treating milk with exogeneous microbial lactase (β-galactosidase) [248].

The Chinese transition to the Western dietary lifestyle is reflected by the Hong Kong Dietary Survey [249]. In this cohort, a dietary pattern with “more meat and milk products” was associated with a 39 % greater risk of diabetes [249]. In Europe as well, higher animal protein (milk protein plus meat protein) consumption has been associated with a higher prevalence of T2DM compared to plant-derived protein intake [250].

Most recent evidence has been provided that fermentation such as in yoghurt or cheese production destroys or attenuates the exosomal microRNA signaling of milk [93]. Populations that gained mutations of the lactase gene resulting in lactase persistance have lifelong access to fresh milk containing both the amino acid hardware and microRNA software of milk. Modern populations experienced a further boost of “milk doping” and growth acceleration by the widespread distribution of refrigeration technology since the early 1950´s. With the intention to preserve valuable bioactive ingredients of milk such as vitamins, pasteurized fresh milk prodcuts reached the daily food chain of the modern consumer. This unnoticed change exposed people of technologically developed societies to daily microRNA signaling of milk [15,90,93]. Indeed, since the introduction of the refrigerator into our households the prevalence of diseases of civilization increased progressively. Persistent “abuse” of an mTORC1 sigaling system designed by mammalian evolution to operate only during the early postnatal growth phase of life may be a key mTORC1-dependent mechanism promoting age-related diseases of cilvilization such as obesity, T2DM, cancer, and neurodegenerative diseases [8-15]. The presented concern about the association of milk consumption and diseases of civilization is in accordance with recent results of Michaëlsson et al. [251], who reported a higher mortality in two large Swedish cohorts of men and women with high intake of milk but not fermented or processed dairy products. Furthermore, the authors observed a correlation between milk intake and serum levels of the inflammatory cytokine interleukin 6 (IL-6) [251], which is also increased in patients with T2DM [252]. Experimental evidence underlines that exposure of β-cells to IL-6 induces early β-cell death [253]. Milk-mediated IL-6 signaling may be the connecting piece that links milk consumption with low grade inflammation that promotes β-cell failure and early β-cell apotosis [3-5]. Remarkably, β-cells express IL-6 receptors, which after ligand binding induce phosphorylation of signal transducer and activator of transcription-3 (STAT3) [254]. Notably, activated STAT3 promotes the expression of microRNA-21 [255-257]. Furthermore, IL-6-mediated activation of mTORC1 [258] may further increase ER-stress-mediated β-cell apoptosis.

Milk´s biological function as a BCAA- and microRNA-donating system for mTORC1-driven growth may explain accelerated ageing and increased mortality with persistent milk consumption [251]. As early as 1934, McCay and Crowell [259] provided translational evidence that slower growth favours longevity of various animal species.

Remarkably, comorbidities of T2DM such as ischemic heart disease have been associated with milk consumption [260], whereas populations with a high prevalence of lactose malabsorption, whose milk intake is low, have a reduced risk of ischemic heart disease than populations with low (<30%) lactose malabsorption [261]. In another large recent Swedish cohort study, subjects with lactose intolerance had decreased risks of lung, breast, and ovarian cancer [262]. Increased whole milk intake has also been associated with prostate cancer-specific mortality among U.S. male physicians [241]. Activated mTORC1 signaling plays a pivotal role in the initiation and progression of prostate cancer [263,264].Thus, persistently over-activated mTORC1, milk´s crucial biological function, accelerates aging and the onset of age-related diseases of civilization [8-5].

Evidence accumulates that the widely prescribed anti-diabetic drug metformin functions as an inhibitor of mTORC1 signaling [265]. Intriguingly, the mTORC1 inhibitor metformin not only controls T2DM, but also reduces the risk of cancer [266], and apparently prolongs life span in humans [267]. Metformin thus counteracts milk-mediated activation of mTORC1.

From the perspective of evolutionary biology, milk consumption represents a novel human behavior that could exert adverse long-term health effects [151]. Continued overstimulation of mTORC1 signaling in humans due to persistent consumption of milk may accelerate aging of the β-cell associated with β-cell apoptosis. Half a century ago, the antagonistic pleiotropy theory solved the mystery of aging by postulating genes beneficial early in life at the cost of aging [268]. Early in life, milk via mTORC1 activation drives a developmental program, which persists later in life as an aimless quasi-program of aging and age-related diseases [268]. In this regard mTORC1 signaling works as pacemaker of aging [269]. In order to prevent age-related diseases such as T2DM Kapahi et al. [269] suggested to reduce mTORC1 signaling: “with TOR less is more” (Fig.3).

Fig. (3).

Schematic representation of milk-mediated disturbances of β-cell homeostasis. Persistent milk signaling overactivates β-cell mTORC1 promot-ing endoplasmic reticulum (ER)-stress resulting in early β-cell apoptosis leading to type 2 diabetes. Metformin treatment attenuates nutrient (milk)-driven overstimulation of mTORC1. Rapamycin treatment inhibits mTORC1 resulting in β-cell suppression and diabetes. Long-term β-cell survial and optimized β-cell homeostasis requires an appropriate well balanced magnitude of β-cell mTORC1 signaling

Refrigeration technology has been implemented into Western households since the 1950´s. This technological achievement allows daily and widespread access to bioactive bovine microRNAs that may affect more than 11,000 human genes [90]. This unnoticed change in human nutrition apparently plays a major role in the pathogenesis of mTORC1-driven T2DM and its mTORC1-driven comorbidities. It is of critical concern that in Western societies milk-driven mTORC1 signaling starts already during fetal life (maternal milk consumption during pregnancy), is further promoted by high protein infant formula feeding, maintained by school milk intake during adolescence, and continued into adulthood and senescence.

Despite the lack of sound evidence powered by randomized controlled trials [270], industry-associated authors still proclaim milk as a “source of healthy nutrition” preventing diseases of civilization such as T2DM [271,272]. Future randomized controlled trials have to differentiate the health effects of pasteurized, HTST versus UHT milk and fermented dairy products in relation to their microRNA bioactivity, especially of the diabetogenic microRNA-29 family.

At present, no epidemiological study has considered the impact of biologically active milk microRNAs in relation to obesity and T2DM. The adipogenic and diabetogenic risk of fresh pasteurized milk has to be differentiated from UHT milk and fermented milk products such as yoghurt. Notably, Howard et al. [93] detected only trace amounts of microRNA-29b in yoghurt. The inactivation of diabetogenic microRNAs during the fermentation process may explain the reduced risk of T2DM in association with yoghurt intake [273, 274]. Hyperactivated β-cell mTORC1 signaling in combination with milk-derived diabetogenic microRNAs superimposed by high glucose and palmitate-driven mTORC1 signaling may in a synergistic fashion accelerate ER-stress and early β-cell apoptosis resulting in its final clinical outcome: type 2 diabetes mellitus (Table 1).

Table 1.

Potential diabetogenic mediators of cow´s milk consumption

Component of Milk	Potential Diabetogenic Mechanism	References
Leucine, other BCAAs, and whey peptides	β-cell mTORC1 activation, whey-driven incretin secretion, whey peptide-mediated inhibition of dipeptidyl peptidase IV increasing incretion activity leading to exaggerated insulin production, ER-stress, early β-cell apoptosis	[16-19, 39, 52, 58, 59, 61, 62, 195, 203]
Glutamine	Activation of β-cell mTORC1 via the glutaminolysis pathway, glutamine-mediated leucine uptake, leucine-driven mTORC1 activation	[16, 41, 42]
Palmitate	β-cell mTORC1 activation, ER-stress driven by lipotoxicity and hyperactivated mTORC1, ER-stress	[43, 200]
MicroRNA-21	Inhibition of translation of tumor suppressor proteins (PTEN, Sprouty, PDCD4), increased mTORC1 signaling; inhibition of FOXO1 promoting β-cell proliferation and enhanced oxidative stress leading to β-cell apoptosis	[15, 108, 110, 116, 117]
MicroRNA-29a	Suppression of IRS-1 translation enhancing insulin resistance	[163]
MicroRNA-29b	Suppression of BCAA catabolism enhanching BCAA-driven mTORC1 signaling; suppression of anti-apototic Mcl-1 translation, early β-cell apoptosis	[90, 93, 146, 226, 227]
Let-7b	Impairment of glucose homeostasis	[159]
Casomorphin 4	Neurogenic stimulation of insulin secretion enhancing ER-stress	[64]

CONFLICT OF INTEREST

The author confirms that this article content has no conflict of interest.

ABBREVIATIONS

ATF4 =

Activating Transcription Factor 4

BCAA =

Branched-Chain Amino Acid

BCAA =

Branched-Chain Amino Acid

BCKDHA =

Branched-chain Keto Acid Dehydrogenase

HCR =

Hypoxic cytotoxicity ratio

BCKDK =

Branched-chain α-Keto Acid Dehydrogenase Kinase

Bcl2 =

B-cell CLL/lymphoma 2

Bcl2 =

B-cell CLL/lymphoma 2

DBT =

Dihydrolipoamide Branched-Chain Transacylase

DDIT3 =

DNA Damage-Inducible Transcript 3

DLD =

Dihydrolipoamide Dehydrogenase

DPP-IV =

Dipeptidyl Peptidase IV

EIF2AK3 =

Eukaryotic Translation Initiation Factor 2-alpha Kinase 3

EPIC =

European Prospective Investigation into Cancer and Nutrition

ER =

Endoplasmic Reticulum

ERN1 =

Endoplasmic Reticulum-to-Nucleus Signaling 1

FOXO1 =

Forkhead Box Class O1

GDH =

Glutamate Dehydrogenase

GIP =

Glucose-Dependent Insulinotropic Polypeptide

GLP-1 =

Glucagon-like Peptide-1

HTST =

High Temperature Short Time

IGF1R =

Insulin-Like Growth Factor-1 Receptor

IL-6 =

Interleukin 6

IR =

Insulin Receptor

IRS =

Insulin Receptor Substrate

PI3K =

Phosphoinositol-3 Kinase

LCT =

Lactase Gene

LAT =

L-type Amino Acid Transporter

Let-7 =

microRNA let-7

Leu =

Leucine

MicroRNA =

Micro-ribonucleic Acid

Mcl-1 =

Myeloid Cell Leukemia Sequence 1

mTORC1 =

Mechanistic Target Of Rapamycin Complex 1

NHANES =

National Health and Nutrition Examination Survey

NOD =

Non-obese Diabetic

PDCD4 =

Programmed Cell Death 4

PTEN =

Phosphatase And Tensin Homolog

S6K1 =

Ribosomal Protein S6 Kinase, 70-kD Kinase 1

STAT3 =

Signal Transducer and Activator of Transcription 3

T2DM =

Type 2 Diabetes Mellitus

PTEN =

Phosphatase And Tensin Homolog

TSC2 =

Tuberin

UHT =

Ultra-heat Treated

UPR =

Unfolded Protein Response

UTR =

3´-Untranslated Region