Abstract
Placental insufficiency causes intrauterine growth restriction (IUGR), a common complication of pregnancy. In skeletal muscle, IUGR reduces fetal myofibril size, reduces myoblast proliferation, and reduces expression of genes in cell cycle regulation clusters. The myocardium is striated like skeletal muscle, and IUGR also reduces cell cycle activity and maturation in cardiomyocytes, despite cardiac output preferentially directed to the coronary circulation. We hypothesized that cardiomyocyte growth restriction would be accompanied by similar changes in cell cycle regulation genes, and would reduce cardiomyocyte cell cycle activity, number, maturity and size. Pregnant ewes were housed in elevated ambient temperatures from ~40 to ~115 days of gestation (dGA) to produce placental insufficiency and IUGR; fetal hearts were studied at ~134 dGA. Hearts were biopsied for mRNA analysis and then dissociated into individual myocytes (Control n=8; IUGR n=15), or dissected (Control n=9; IUGR n=13). IUGR fetuses had low circulating insulin and insulin-like growth factor-1 (IGF-1), and high circulating cortisol. Bodies and hearts of IUGR fetuses were lighter than Controls. Cardiomyocytes of IUGR fetuses were smaller, less mature, less active in the cell cycle, and less numerous than Controls. Further, there was a pattern of down-regulation of cell cycle genes in IUGR ventricles. IUGR growth profiles in heart and skeletal muscle suggest similar regulation despite differences in blood and nutrient delivery prioritization. IGF-1 signaling is suggested as a mechanism regulating altered growth in IUGR striated muscle and a potential therapeutic candidate.
INTRODUCTION
Intrauterine growth restriction (IUGR) results from inadequate placental function limiting fetal nutrient delivery, impairing normal growth and development (Marconi and Paolini 2008). Infants affected by placental insufficiency redirect a greater proportion of oxygenated blood flow to the upper body, which enhances nutrient delivery to vital organs, including heart and brain, at the expense of other tissues such as skeletal muscle (Baschat and Hecher 2004; Bellotti, et al. 2004; Brown and Hay 2016). These fetal adaptations have life-long health implications, a phenomenon known as the developmental origins of health and disease first articulated by Barker and colleagues (Barker and Thornburg 2013; de Boo and Harding 2006; Fernandez-Twinn and Ozanne 2010). Placental restriction is associated with obesity, reduced lean body mass, insulin resistance, and cardiovascular disease in adulthood (Alexander, et al. 2015; Camm, et al. 2015; Fall 2011; Phillips, et al. 1994). Thus, while the heart and skeletal muscle are differently prioritized to receive nutrients during placental insufficiency, there are negative consequences for both following IUGR.
Hearts of fetal humans, sheep, rodents, and other mammals, grow by myocyte proliferation, terminal differentiation (which is associated with cellular enlargement, multinucleation, and cessation of proliferation), and enlargement of both proliferative and terminally differentiated myocytes (Burrell, et al. 2003; Clubb and Bishop 1984; Huttenbach, et al. 2001; Jonker, et al. 2015; Kim, et al. 1992; Zak 1974). Despite shunting shown to maintain coronary perfusion during IUGR in humans and sheep (Baschat and Hecher 2004; Bellotti et al. 2004; Tare, et al. 2014), hearts of fetal sheep with experimental placental insufficiency are reduced in weight (Bubb, et al. 2007; Louey, et al. 2007; Morrison, et al. 2007; Tare et al. 2014). IUGR is associated with less mature cardiomyocytes and reduced proliferation in near term fetal sheep, while disagreement persists as to whether the cells are smaller in fetal sheep and humans (Botting, et al. 2014; Bubb et al. 2007; Louey et al. 2007; Mayhew, et al. 1999; Morrison et al. 2007; Murotsuki, et al. 1997; Takahashi, et al. 1995).
Cardiac and skeletal muscle are both striated muscle, characterized by the organization of contractile proteins into sarcomeres, an abundance of mitochondria, and (in many species, including humans and sheep) multinucleation in maturity (Adler, et al. 1996). Unlike fetal cardiac muscle, in which working myocytes undergo cytokinesis, skeletal muscle grows by proliferation of myoblasts, and their subsequent differentiation and fusion to form multinucleated myotubes (Brown and Hay 2016). Also unlike the heart, skeletal muscle blood flow is reduced in IUGR, leading to a substantial reduction in oxygen and amino acid delivery (Poudel, et al. 2015; Rozance, et al. 2018); total mass and cross sectional area of hindlimb muscles are consequently reduced (Rozance et al. 2018; Soto, et al. 2017). Myoblasts capable of proliferating are maintained proportional to total number of nuclei, and even enhanced relative to myofiber number (indicating immaturity), but cell cycle activity in those myoblasts is reduced (Soto et al. 2017; Yates, et al. 2014). Pathway analysis in near-term IUGR skeletal muscle found decreased expression of clusters of genes related to proliferation and differentiation (Soto et al. 2017).
We hypothesized that in near-term fetuses with severe IUGR we would find ventricular cardiomyocyte immaturity, reduced proliferation, and suppression of intracellular growth regulatory pathways similar to those suppressed in skeletal muscle (Brown and Hay 2016; Soto et al. 2017). To test this hypothesis, we used a well-established sheep model of chronic, progressive placental insufficiency that results in severe IUGR (Limesand, et al. 2007; Regnault, et al. 2007; Thureen, et al. 1992). Placental insufficiency is initiated mid-gestation to reduce placental transfer of oxygen, amino acids and glucose similar to that experienced by the human IUGR fetus (Barry, et al. 2008; Bell, et al. 1987). We examined growth characteristics of cardiomyocytes and mRNA levels of genes that regulate the cardiomyocyte cell cycle.
MATERIALS AND METHODS
Animal model
Animal use was approved by the Institutional Animal Care and Use Committee of the University of Colorado, Denver.
Columbia-Rambouillet sheep (ovis aries) with singleton pregnancies were studied at the University of Colorado Perinatal Research Center as previously described (Soto et al. 2017). The fetuses in this study were included in previously published studies (Brown, et al. 2012; Culpepper, et al. 2016; Rozance et al. 2018). In brief, pregnant ewes were housed in environmental chambers with elevated ambient temperatures (40C for 12h; 35C for 12h) and 40% humidity from ~40 days gestation (dGA, term = 147 dGA) to ~115dGA to produce placental insufficiency and IUGR, after which they were housed in ambient temperatures and humidity (IUGR, n=15). Control ewes were housed in the same facility at ambient temperatures and normal humidity (Control, n=8). All sheep had ad libitum access to water. Maternal feed intake was matched on an absolute basis between sheep in the Control and IUGR groups (maternal weight-adjusted feed intake did not differ between groups).
Animals underwent surgery for fetal and maternal catheter placement as previously described, including catheterization of the fetal abdominal aorta (Soto et al. 2017). Briefly, ewes were fasted for 24h and water deprived for 12h prior to surgery. Diazepam (0.2mg/kg) and ketamine (20mg/kg) were administered intravenously, and then ewes were maintained throughout surgery on isoflurane inhalation anesthesia (2-4%). Maternal analgesia was provided with intramuscular banamine (1.1mg/kg). Surgical recovery was at least 5 days.
On the morning of tissue collection, fetal arterial blood was assayed for measurement of pH, partial pressure of CO2 (PCO2), partial pressure of O2 (PO2), O2 saturation, O2 content, hemoglobin, insulin, insulin-like growth factor 1 (IGF-1), norepinephrine and cortisol using biochemical methods previously described (Brown et al. 2012; Limesand, et al. 2006).
Fetal heart collection
Animals were euthanized by intravenous pentobarbital sodium (Fatal Plus, Bortech Pharmaceuticals, Dearborn, MI). The fetus was weighed, and the heart immediately excised. Blood was flushed from fetal hearts with a heparin-containing Tyrodes solution (Jonker, et al. 2007). As the high-pressure pumping chambers, we focused on the ventricles. Mid-ventricular biopsies were excised and frozen, and wound edges were sealed with cyanoacrylate. Hearts were enzymatically dissociated and cells were fixed with formaldehyde as previously described (Jonker et al. 2007). As ventricular wall weight cannot be obtained from dissociated hearts, a contemporaneous groups of control and IUGR age-matched fetuses with similar physiological and physical parameters were used to obtain ventricular wall weights (Control n=9, IUGR n=13) as previously described (Jonker et al. 2007).
Cardiomyocyte measurements
Length and width measurements were obtained from random, non-repeating photomicrographs from no fewer than 90 isolated cardiomyocytes separately from each ventricular wall, as previously described (Jonker et al. 2007). A shape factor, measured from no fewer than 10 mononucleated and binucleated myocytes per fetal ventricular wall, was used to calculate myocyte volume from length and width measurements (Jonker et al. 2007).
The number of nuclei in at least 300 myocytes from each ventricular wall of each animal were tabulated to determine the fractions of mono-, bi-, and quadrinucleated cells.
Detection of anti-Ki-67 antibody binding (MIB-1, Dako, Carpinteria, CA, USA) was used to determine cell cycle activity from ~500 cells per ventricular wall per animal as previously described (Jonker et al. 2007).
Cardiac number myocyte quantification
Cardiomyocyte number was calculated as previously described (Jonker et al. 2015; Jonker et al. 2007), with minor modifications. The proportional relationship between ventricular wall weight and heart weight was derived from values measured from a subset of animals (Control, n=9; IUGR, n=13). This was used to calculate ventricular wall weights from total heart weight for each enzymatically dissociated heart. Wall weights were multiplied by the proportion of myocardium which is composed of myocytes (Smolich, et al. 1989), and divided by the specific gravity of 1.05g/ml, which was then divided by the proportionally-represented myocyte volumes (Jonker et al. 2015; Jonker et al. 2007) to yield myocyte number per wall. As there were not enough quadrinucleated cells to obtain morphometric measurements, and as they have been found previously to be twice the volume of binucleated cells (Jonker et al. 2015), they were included in calculations using twice the volume of binucleated cells.
RNA extraction and quantitative real time PCR analysis
Total RNA was isolated from myocardial biopsies, reverse transcribed and used in qPCR using the ΔΔCT method (Lightcycler 480 II; Roche Life Science, Indianapolis, IN) as previously described (Brown, et al. 2014; Soto et al. 2017). Genes for analysis were selected based on the KEGG pathway analysis for fetal sheep IUGR skeletal muscle previously published, in addition to some other key cell cycle regulators (Soto et al. 2017). Those primers for qPCR assays that were not published previously (Soto et al. 2017), are provided in Table 1. mRNA expression levels of reference genes did not vary by treatment or ventricular wall, therefore all experimental genes are expressed as a ratio with the equal-weighted average of the reference genes. mRNA levels are expressed relative to average LV control values.
Table 1.
Forward | Reverse | |
---|---|---|
Cyclin A2 (CCNA2) | CCTGCAAACTGCAAAGTTGAA | GGTGAAGGTCCAGGAGACA |
Cyclin D1 (CCND1) | ACTACCTGGACCGCTTCCT | TTGGAGAGGAAGTGCTCGAT |
Cyclin D2 (CCND2) | TCCTCTCGCCATCAATTACC | TCCTGAGGCTTGATGGAGTT |
Cyclin dependent kinase 4 (CDK4) | ATTTCCTTCATGCCAACTGCA | CCAACACTCCACATGTCCAC |
Cyclin dependent kinase 6 (CDK6) | GCATCGTGATCTAAAACCACA | GAGTCCAATCACGTCCAAGA |
Activator of S phase kinase (DBF4) | ATCTGGGAGGGCGAGTTGAAGAAT | TGAGGTGATGTGGTTTCCGCAGTA |
Myeloid ecotropic viral integration site 1 homolog (Meis1) | ATATCATGAGGGCGTGGCTG | ATAGGTCCTGGTGCCCTGAT |
Myeloid leukemia factor 2 (MLF2) | CTCAGCATCACAGATGGCAA | CATGTCGTTCATCATCCCAA |
Cyclin-dependent kinase inhibitor 1A (p21) | GAGGACCACTTGGACCTGT | TCTGCGTTTGGAGTGGTAGA |
Cyclin-dependent kinase inhibitor 1B (p27) | GCTTGCCCGAGTTCTACTAC | CATTTTCTTCTGTTCTGTTGGC |
Ribosomal protein L32 (RPL32) | AATCAAGCGGAACTGGCG | GGCATTGGGATTGGTGATT |
Ribosomal protein L37a (RPL37A) | ACCAAGAAGGTCGGAATCGT | GGCACCACCAGCTACTGTTT |
Transcription factor Dp-1 (TFDP1) | AGGTCTTCATCGACCAGAACCTCA | TACCAATCACCACTTGCTGCGAGA |
Protein Kinase C Inhibitor Protein-1 (YWHAZ) | CAAACGCTTCACAAGCAGAGAGCA | TGCTGTGACTGATCCACAATCCCT |
Statistical analysis
Comparisons of blood parameters and necropsy weights were by Student’s unpaired t-test (Prism 6, GraphPad Software, San Diego, CA). Sex distribution was assessed using Chi square test. Treatment (Control, IUGR), ventricular wall (LV, septum, RV) and sex (male, female) were initially screened as main effects by Student’s unpaired t-test; although sex differences do sometimes emerge in fetal cardiac studies (Botting, et al. 2018; Lumbers, et al. 2009), no significant sex effect was found in this dataset, thus sex was not included in the final analysis. The effect of sex was not evaluated for mRNA gene expression due to limited sample size. Two-way analysis of variance (ANOVA) was used to determine the effects of treatment and ventricular wall on cardiomyocyte and mRNA parameters. When indicated by a significant interaction term, multiple comparisons were conducted with Holm-Sidak correction. Pearson’s correlation coefficients were calculated to explore relationships between circulating hormones and cardiomyocyte parameters in IUGR fetuses; if significant, linear regression was performed to determine if relationships were similar between Control and IUGR fetuses. If not different, regression relationships were determined for all fetuses pooled. P<0.05 was considered statistically significant.
RESULTS
Fetal physiological characteristics
Gestational age (Control 134.9±0.8, IUGR 134.2±1.2) and sex distribution (Control 50% male, IUGR 53% male) were not different between groups. Placental insufficiency reduced fetal arterial PO2, hemoglobin saturation, O2 content, and plasma glucose (Table 2). No changes were observed in pH, PCO2, total hemoglobin, or plasma lactate. IUGR reduced fetal arterial plasma insulin and IGF-1 levels, and increased cortisol and norepinephrine levels.
Table 2.
Comparison of Means | |||
---|---|---|---|
Control (n=8) |
IUGR (n=15) |
P-Value | |
pH | 7.35±0.02 | 7.35±0.02 | ns |
Hemoglobin (mmol L−1) | 7.8±1.6 | 7.4±1.0 | ns |
PCO2 (mmHg) | 50.7±2.8 | 51.5±2.2 | ns |
PO2 (mmHg) | 19.8±1.6 | 14.8±2.8* | 0.0002 |
O2 saturation (%) | 47.6±5.9 | 30.7±10.9* | 0.0006 |
O2 content (mmol L−1) | 3.1±0.5 | 2.1±0.9* | 0.0063 |
Glucose (mg dL−1) | 21±5 | 14±4* | 0.0019 |
Lactate (mmol L−1) | 2.5±0.5 | 2.7±0.9 | ns |
Insulin (ng mL−1) | 0.4±0.2 | 0.2±0.1* | 0.0171 |
Cortisol (ng mL−1) | 9.2±7.0 | 23.6±18.2* | 0.0431 |
Norepinephrine (pg mL−1) | 602±404 | 1,699±1,492* | 0.0034 |
IGF-1 (ng mL−1) | 125±37 | 54±33* | 0.0001 |
Groups compared by Student’s t-test. Not significant (ns). Data are shown as mean±standard deviation.
Placental insufficiency reduced fetal body weight (Fig. 1A) and heart weight (Fig. 1B). The ratio of heart-to-body weight was not different, but tended to be lower in IUGR (P=0.0613; Fig. 1C). Because IUGR changed hormone levels, the relationship of heart weight with these factors was tested in IUGR fetuses and found to be correlated with IGF-1 (r=0.8497, P<0.0001) (Fig. 1D).
Ventricular wall weights were reduced by IUGR (main effect, P<0.0001) and affected by anatomical location (main effect, P<0.0001), but there was no significant interaction between these terms (P=0.0619; Fig. 1E). Wall weights normalized to heart weight were affected by anatomical location only (P<0.0001) (Fig. 1F).
Cardiomyocyte growth and maturation
The interaction term between treatment and anatomical location of cell origin was not significant for any myocyte measurement.
IUGR reduced cell cycle activity expressed as a percentage of mononucleated myocytes (P=0.0191; Fig. 2A). Ventricular source did not affect cell cycle activity (P=0.0905). IUGR reduced the proportion of binucleated myocytes, an index of maturation (P=0.0383; Fig. 3B). Proportion quadrinucleated was not different between groups and was less than 1% of all cells (data not shown).
Mononucleated myocyte lengths were reduced by IUGR (P=0.0012) and were different across the ventricular walls (P=0.0012) (Fig. 3A). IUGR did not affect mononucleated width (P=0.0612), but ventricular origin did (P<0.0001; Fig. 3B). Mononucleated myocyte volumes were reduced by IUGR (P=0.009) and different across the ventricular walls (P<0.0001; Fig. 3C).
Binucleated myocyte lengths were reduced by IUGR (P=0.0108) and affected by ventricular origin (P<0.0001; Fig. 3D). Binucleated widths were not changed by IUGR, but were different across the ventricular walls (P<0.0001; Fig. 3E). IUGR reduced binucleated myocyte volumes (P=0.0196), which were also affected by ventricular origin (P<0.0001; (Fig. 3F).
Cardiomyocyte number was reduced by IUGR (P=0.0361) and different across the ventricular walls (P<0.0001; Fig. 4).
Associations between circulating factors and myocyte parameters
Because IUGR changed circulating hormones, the correlation of cardiomyocyte growth parameters with these factors was tested in IUGR fetuses. IGF-1 levels in IUGR fetuses were correlated with myocyte number in the LV (r=0.6903, P=0.0044), septum (r=0.7388, P=0.0025), and RV (r=0.5682, P=0.034) (Fig. 5).
Insulin levels in IUGR fetuses were correlated with LV binucleate length (r=0.5763, P=0.0245), RV binucleate length (r=0.5472, P=0.0429), RV binucleate width (r=0.6034, P=0.0223), and RV mononucleate length (r=0.5988, P=0.0237) (Fig. 6). There was a tendency for a correlation with septum binucleate length (r=0.5067, P=0.0644). It was determined that the slopes of the regressions binucleate length against insulin levels differed significantly between Control and IUGR fetuses for LV (P=0.0181), and that the regression for Control fetuses was not significant, therefore the relationship for the IUGR fetuses alone was determined.
Log-transformed cortisol levels in IUGR fetuses were negatively correlated with LV binucleated width (r=−0.5312, P=0.0416), and RV binucleated length (r=−0.6427, P=0.132) (Fig. 7). There were tendencies for correlation with RV proportion binucleated (r=0.5291, P=0.0517), and negative correlation with RV binucleate width (r=−0.5297, P=0.0514).
Log-transformed norepinephrine levels in IUGR fetuses were correlated with RV proportion binucleated (r=0.5507, P=0.0413), and septum (r=−0.6112, P=0.0202). There was a tendency for negative correlation with RV binucleate width (r=−0.4684, P=0.0912), and binucleate length in the septum (r=−0.5193, P=0.0570). Linear regression relationships for RV proportion binucleated were not different between Control and IUGR fetuses, but the regression relationship for all fetuses together was not significant. Linear regression relationships for septum proportion binucleated had different intercepts between Control and IUGR fetuses (P=0.0103), and the slope of the regression for the Control relationship was not different from zero.
Cardiac mRNA expression levels
Reference genes RPL32, RPL37A, and MLF2 did not vary with treatment or between ventricles (Table 3).
Table 3.
Relative Expression Levels | Interaction | Main Effects | |||||
---|---|---|---|---|---|---|---|
RV | LV | Treatment | Ventricle | ||||
Control (n=3) |
IUGR (n=7) |
Control (n=7) |
IUGR (n=13) |
P-value | P-value | P-value | |
Reference genes | |||||||
RPL32 | 0.99±0.22 | 0.93±0.18 | 1.00±0.04 | 0.98±0.25 | ns | ns | ns |
RPL37A | 1.01±0.31 | 1.03±0.17 | 1.00±0.16 | 1.08±0.27 | ns | ns | ns |
MLF2 | 1.03±0.15 | 1.05±0.24 | 1.00±0.18 | 0.92±0.28 | ns | ns | ns |
Cyclins | |||||||
Cyclin A2 | 1.28±0.55 | 0.67±0.23 | 1.00±0.51 | 0.57±0.23 | ns | 0.0014 | ns |
Cyclin B1 | 1.98±1.18 | 0.74±0.23 | 1.00±0.44 | 0.67±0.33 | 0.0306 | ||
Cyclin B2 | 1.61±0.88 | 0.74±0.26 | 1.00±0.27 | 0.72±0.23 | ns | 0.0006 | 0.0381 |
Cyclin D1 | 1.15±0.16 | 1.16±0.22 | 1.00±0.23 | 1.13±0.34 | ns | ns | ns |
Cyclin D2 | 1.87±0.24 | 1.50±0.30 | 1.00±0.20 | 1.02±0.16 | 0.043 | ||
Cyclin E2 | 1.03±0.27 | 0.94±0.15 | 1.00±0.21 | 0.82±0.25 | ns | ns | ns |
Cyclin dependent kinases | |||||||
CDK1 | 1.37±0.57 | 0.86±0.29 | 1.00±0.35 | 0.62±0.37 | ns | 0.009 | ns |
CDK4 | 1.02±0.13 | 1.10±0.21 | 1.00±0.15 | 0.94±0.19 | ns | ns | ns |
CDK6 | 1.40±0.07 | 1.14±0.16 | 1.00±0.14 | 0.97±0.09 | 0.0345 | ||
Cyclin dependent kinase inhibitors | |||||||
CDKN2C (p18) | 1.12±0.19 | 1.06±0.19 | 1.00±0.18 | 0.80±0.22 | ns | ns | 0.0348 |
CDKN1A (p21) | 0.49±0.15 | 0.67±0.18 | 1.00±0.42 | 0.91±0.26 | ns | ns | 0.0041 |
CDKN1B (p27) | 0.92±0.03 | 1.23±0.35 | 1.00±0.11 | 0.99±0.25 | ns | ns | ns |
Cell cycle effectors and checkpoint genes | |||||||
MCM6 | 0.97±0.21 | 0.99±0.15 | 1.00±0.20 | 0.87±0.19 | ns | ns | ns |
PLK1 | 1.47±0.99 | 0.78±0.28 | 1.00±0.78 | 0.70±0.30 | ns | 0.0299 | ns |
CDC20 | 1.26±0.56 | 0.84±0.22 | 1.00±0.34 | 0.74±0.22 | ns | 0.0101 | ns |
MAD2 | 1.23±0.40 | 0.87±0.21 | 1.00±0.26 | 0.70±0.32 | ns | 0.0134 | ns |
BUB1 | 2.20±1.49 | 0.48±0.51 | 1.00±0.69 | 0.38±0.48 | ns | 0.0004 | 0.0303 |
ESPL1 | 1.00±0.56 | 0.70±0.30 | 1.00±0.63 | 0.54±0.18 | ns | 0.0251 | ns |
CHK1 | 1.09±0.21 | 1.10±0.31 | 1.00±0.25 | 0.83±0.38 | ns | ns | ns |
DBF4 | 1.50±0.47 | 0.79±0.14 | 1.00±0.36 | 0.83±0.29 | 0.0398 | ||
YWHAZ | 1.34±0.19 | 1.13±0.19 | 1.00±0.14 | 0.93±0.19 | ns | ns | 0.0015 |
Transcription factors | |||||||
TFDP1 | 0.96±0.10 | 0.94±0.14 | 1.00±0.09 | 0.94±0.16 | ns | ns | ns |
Meis1 | 1.21±0.11 | 1.04±0.32 | 1.00±0.19 | 1.07±0.28 | ns | ns | ns |
Groups compared by 2-way ANOVA.
Different from ipsilateral control by Holm-Sidak test (P<0.05). Data are shown as mean±standard deviation.
IUGR reduced expression of cyclin A2 and cyclin B2 (Table 3). Treatment interacted with ventricular source for cyclin B1 and cyclin D2; for both genes RV expression was lower in IUGR, while RV expression was greater than LV. RV expression was also greater than LV for cyclin B2. There was no effect of treatment or ventricle on cyclin D1 or cyclin E2 levels.
IUGR reduced ventricular CDK1 expression (Table 3). The interaction term was significant for CDK6; IUGR reduced CDK6 expression in the RV, and expression was greater in the RV than the LV. There was no effect of treatment or ventricle on CDK4 levels.
CDKN2C (p18) expression was greater in the RV than LV, while CDKN1A (p21) was lower in the RV (Table 3). There was no effect of treatment or ventricle on CDKN1B (p27) levels.
IUGR reduced expression of PLK1, CDC20, MAD2, BUB1B, and ESPL1 (Table 3). Treatment interacted with ventricular source for DBF4; IUGR reduced DBF4 expression in the RV, and RV expression was greater than LV. RV expression was also greater than LV for BUB1B, and YWHAZ. There was no effect of treatment or ventricle on CHK1.
There was no effect of treatment or ventricle on transcription factors TFDP1 or Meis1 (Table 3).
DISCUSSION
We found that near-term fetuses affected by chronic placental insufficiency and IUGR had smaller cardiomyocytes with reduced terminal differentiation and proliferation, and consequently a diminished myocyte complement in the heart. Impaired growth and maturation was found across all ventricular walls, and these differences all contribute to the smaller hearts found in IUGR fetuses. These changes were supported by reduced mRNA expression of cyclins and cell cycle effectors and checkpoint genes in IUGR hearts.
Comparison of the heart and skeletal muscle in IUGR
Although the work demanded of fetal skeletal muscle is less than that of cardiac muscle, both are types of striated muscle and cellular complements of both are mostly set by the time of birth (Bergmann, et al. 2015; Burrell et al. 2003; Jonker et al. 2015; Rowe and Goldspink 1969; Widdowson, et al. 1972). We found previously that skeletal muscle is lighter in IUGR fetuses, the cross-sectional area of the myofibers is smaller, and that there is less myoblast proliferation, yet the skeletal muscle maintains the pool of Pax7+ myoblasts with proliferative potential (Rozance et al. 2018; Soto et al. 2017; Yates et al. 2014). Our findings in this study are comparable, with lighter hearts in IUGR fetuses, smaller myocytes, lower indices of proliferation, and decreased maturation.
Life-long reduction in lean mass (Fall 2011) and cardiomyocyte number (Vranas, et al. 2017) suggests that no adaptive mechanism helps the IUGR newborn undergo adequate physiological “catch-up” of muscle growth. Nevertheless, in near-term IUGR skeletal muscle the pool of Pax7+ myoblasts with proliferative potential is not reduced, and in the heart the mononucleated population of cardiomyocytes capable of proliferating is increased, suggesting opportunity for therapeutic intervention. Indeed, cultured Pax7+ skeletal myoblasts from IUGR fetuses responded much more aggressively to proliferative signals than Control cells in vitro (Soto et al. 2017). As circulating insulin and IGF-1 concentrations are reduced, this suggests that an IGF-1 rescue strategy in IUGR could yield a rapid increase in myocyte endowment at term (Eremia, et al. 2007; Harding, et al. 1994; Soto et al. 2017; Sundgren, et al. 2003).
Pathway analysis in near-term IUGR skeletal muscle found decreased expression of clusters of genes related to cell cycle regulation (Soto et al. 2017). The most profoundly affected genes include G1 progression regulators cyclin E2 and p18, initiator of DNA replication MCM6, G2/M progression regulator PLK1, regulators of commitment to mitosis cyclin B1, cyclin B2 and CDK1, regulator of nuclear movement and chromosome separation CDC20, spindle assembly quality control molecule MAD2, spindle checkpoint regulator BUB1B, initiator of separation of sister chromatids in mitosis ESPL1, and DNA damage cell cycle arrestor CHK1. We found that many of those genes with reduced expression in skeletal muscle are also reduced in cardiac muscle, including PLK1, cyclin B1, cyclin B2, CDK1, CDC20, MAD2, BUB1B and ESPL1, supporting the parallels in response to in utero challenge between these two types of striated muscle despite differences in preferential nutrient delivery during IUGR.
Hormonal regulation of cardiac growth in IUGR
Hormonal regulation of growth might help explain similar growth and gene expression patterns in IUGR skeletal muscle and heart despite preservation of nutrient delivery to the myocardium. In order to reduce the rate of spurious findings, we screened cardiac growth parameters against circulating hormone concentrations by performing correlations only within IUGR fetuses, followed up by testing whether regressions between Control and IUGR fetuses were different and, if they were not, performing regression on pooled fetal parameters. These results do not show causality, but indicated potential mechanisms regulating specific aspects of myocyte growth in the near-term fetal heart.
In IUGR fetuses, IGF-1 and insulin levels are half those in Control fetuses. IGF-1 is the main endocrine driver of fetal growth (Hellstrom, et al. 2016; Murray and Clayton 2013), is critical to skeletal muscle growth in development (Liu, et al. 1993; Mavalli, et al. 2010), and is a profound stimulus of cardiomyocyte proliferation in the fetal heart (Sundgren et al. 2003). Fetal heart weight and cardiomyocyte numbers were predicted by circulating IGF-1 levels. Circulating insulin levels predicted most myocyte length dimensions as well as one width dimension. Consequently, IGF-1 and/or insulin receptors might be therapeutic targets for treatment to increase fetal myocyte replication.
In contrast to IGF-1 and insulin, cortisol and norepinephrine levels are more than doubled in near-term IUGR fetuses. In fetal cardiomyocytes, cortisol has been linked to proliferation (Feng, et al. 2013; Giraud, et al. 2006; Reini, et al. 2008) and enlargement (Lumbers, et al. 2005), but also to apoptosis (Feng et al. 2013; Reini et al. 2008). However, cortisol reduced myoblast proliferation and causes myotube atrophy through decreased protein synthesis and increased protein degradation (Morgan, et al. 2016). Cortisol in fetal skeletal muscle suppresses IGF-1 expression (Li, et al. 2002), but not IGF-1 receptor 1 expression (Jellyman, et al. 2012), and IGF-1 opposes the effects of cortisol on skeletal muscle (Glass 2010; Morgan et al. 2016). Circulating cortisol levels negatively predicted two binucleated myocyte dimension parameters, supporting a role of growth repression in the heart. How cortisol interacts with low levels of IGF-1 to suppress growth or induce apoptosis in IUGR skeletal and cardiac muscle remains to be determined.
Norepinephrine is a non-selective adrenergic agonist linked to hypertrophy in adult cardiomyocytes. Phenylephrine, a selective α-adrenergic agonist, strongly stimulates hypertrophy in fetal sheep cardiomyocytes. It is notable that we found a reduction in cardiomyocyte size in IUGR fetuses concurrent with elevated norepinephrine, which suggests that cardiac adrenergic signaling is altered in IUGR or that there is a mechanism actively repressing fetal cardiomyocyte growth during placental restriction. Indeed, high circulating fetal norepinephrine inhibits overall fetal growth (Bassett and Hanson 1998; Milley 1997).
Interpretation of cardiac effects of IUGR
Body and heart weight were reduced in this study, as is common in models of placental restriction (Louey et al. 2007; Morrison et al. 2007; Tare et al. 2014). Reduction in heart weight relative to body weight, towards which there was a tendency in this study, has been found in carunclectomy-induced IUGR (Bubb et al. 2007). The carunculectomy model is created by surgical excision of placental implantation sites in ewes prior to breeding, which induces a progressive phenotype from early in gestation similar to the environmental model used in this study. This contrasts with fetoplacental embolization, induced in the last third of gestation, in which heart weight relative to body weight is unchanged (Louey et al. 2007) or increased (Murotsuki et al. 1997).
The relative contributions of small myocyte size, inhibited proliferation, and less terminal differentiation to overall cardiac undergrowth in IUGR can be estimated by calculating the loss in mass attributable to each difference. Reduced heart weight is due to smaller myocyte size (~30-55%), reduced myocyte number (~20-40%), changes in non-myocyte components (~20%), and reduced terminal differentiation (~5-10%; because binucleated cells are larger than mononucleated cells). Reduced proliferation and maturation is common to humans affected by placental insufficiency and animal models of IUGR (Botting et al. 2014; Bubb et al. 2007; Louey et al. 2007; Mayhew et al. 1999; Morrison et al. 2007; Murotsuki et al. 1997; Takahashi et al. 1995).
Although diminished cellular volume due shorter myocytes in IUGR was the largest contributor to reduced heart weight in this study, there is disagreement among other studies about the role of retarded myocyte enlargement in IUGR hearts. One study in carunclectomized ewes indicates that IUGR reduces mononucleated myocyte length and width, but only binucleated width near term (Morrison et al. 2007), however, these results are confounded by the finding that control binucleated myocytes shrink in length and width over the period of 132-141 dGA. In contrast, no differences in myocyte dimensions have been found in fetoplacental embolization models, which are initiated in the last third of gestation (Bubb et al. 2007; Louey et al. 2007). It may be that the effect of IUGR on cardiomyocyte size occurs over a long period and is only detectable when placental insufficiency is initiated early in gestation.
Differences between LV and RV myocytes
Due to hemodynamic shunts, both fetal ventricles pump against similar pressure into the systemic circulation and are more alike in mass and geometry in the fetus than at any later age. Despite these similarities, fetal myocyte appear to have a ventricular “identity”: RV cardiomyocytes are larger and less numerous than LV myocytes (Burrell et al. 2003; Jonker et al. 2007). Although these differences were found in this study, the changes induced by IUGR did not vary by ventricular wall, consistent with other studies (Bubb et al. 2007; Jonker, et al. 2011; Segar, et al. 2013). Relationships shown between circulating hormones and myocyte parameters that are significant only in one ventricle should not be taken as proof of a ventricular “identity”, as causative effects of hormones has not been established in this study. The basis of the apparent ventricular “identity” remains unknown.
Strengths and limitations of the study
The ovine model of chronic and progressive placental insufficiency used in this study shares many phenotypic characteristics with human placental insufficiency, including similar patterns of heart and brain sparing, lower rates of amino acid, glucose, and oxygen transfer from mother to the fetus, reduced circulating growth factors, and elevated catecholamines (Barry et al. 2008). This model also allowed for chronic catheterization of the fetal circulation for fetal blood sampling concurrent with cardiac tissue collection, to correlate in vivo physiological measures with comprehensive morphometric data. Further, cardiomyocytes from left, right and septal ventricular walls were isolated after heart dissociation, which allowed for ventricular-specific comparisons of cardiomyocyte number, maturity, and size. However, we were not adequately powered to assess sex differences for all measurements in this study, despite reports of sexual dimorphism in cardiomyocyte number related to IUGR (Botting et al. 2018). Further, tissue availability limited further evaluation of downstream signaling activation by insulin and IGF-1.
Conclusions
IUGR fetuses had low circulating insulin and IGF-1 levels, high circulating cortisol levels, and light bodies and hearts. IUGR cardiomyocytes were smaller, less mature, less active in the cell cycle, and less numerous than Control cells, and there was down-regulation of cell cycle genes in IUGR hearts. We did not find differences in heart size and cardiomyocyte indices attributable to fetal sex, therefore sex as a main effect was not included in the final model. Interactions between sex and treatment could not be fully evaluated due to small sample size and should be pursued in future studies. Similarities between heart and skeletal muscle in IUGR leading to reductions in myocyte cell cycle activity, number, size and maturation suggest similarities in regulation of growth, perhaps through IGF-1 and insulin signaling, despite differences in nutrient delivery prioritization. Further studies are required to understand the potential of fetal anabolic hormones such as insulin and IGF-1 as therapeutic agents to increase myocyte number in hearts of IUGR fetuses.
ACKNOWLEDGEMENTS
We thank Samantha Louey for critical review of the manuscript.
FUNDING
This work was supported by NIH Grants K12 HD057022, R01 HD079404, and The Center for Women’s Health Research, University of Colorado School of Medicine (LDB), and R01 HD071068 (SSJ).
Footnotes
DECLARATION OF INTEREST
The authors have nothing to declare.
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