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. 2018 Oct 23;9:1494. doi: 10.3389/fphys.2018.01494

Fibroblast Growth Factor 23 Expression Is Increased in Multiple Organs in Mice With Folic Acid-Induced Acute Kidney Injury

Daniela Egli-Spichtig 1, Martin Y H Zhang 1, Farzana Perwad 1,*
PMCID: PMC6206018  PMID: 30405444

Abstract

Fibroblast growth factor 23 (FGF23) regulates phosphate homeostasis and vitamin D metabolism. In patients with acute kidney injury (AKI), FGF23 levels rise rapidly after onset of AKI and are associated with AKI progression and increased mortality. In mouse models of AKI, excessive rise in FGF23 levels is accompanied by a moderate increase in FGF23 expression in bone. We examined the folic acid-induced AKI (FA-AKI) mouse model to determine whether other organs contribute to the increase in plasma FGF23 and assessed the vitamin D axis as a possible trigger for increased Fgf23 gene expression. Twenty-four hours after initiation of FA-AKI, plasma intact FGF23 and 1,25(OH)2D were increased and kidney function declined. FA-treated mice developed renal inflammation as shown by increased Tnf and Tgfb mRNA expression. Fgf23 mRNA expression was 5- to 15-fold upregulated in thymus, spleen and heart of FA-treated mice, respectively, but only 2-fold in bone. Ectopic renal Fgf23 mRNA expression was also detected in FA-AKI mice. Plasma FGF23 and Fgf23 mRNA expression in thymus, spleen, heart, and bone strongly correlated with renal Tnf mRNA expression. Furthermore, Vdr mRNA expression was upregulated in spleen, thymus and heart and strongly correlated with Fgf23 mRNA expression in the same organ. In conclusion, the rapid rise in plasma FGF23 in FA-AKI mice is accompanied by increased Fgf23 mRNA expression in multiple organs and increased Vdr expression in extra osseous tissues together with increased plasma 1,25(OH)2D and inflammation may trigger the rise in FGF23 in FA-AKI.

Keywords: fibroblast growth factor 23, acute kidney injury, 1, 25(OH)2D, inflammation, vitamin D receptor, tumor necrosis factor

Introduction

Fibroblast growth factor 23 (FGF23) is a potent regulator of phosphate homeostasis and vitamin D metabolism (Shimada et al., 2004). FGF23 binds to its co-receptor αKlotho and FGFR receptors 1c, 3 and 4 to activate mitogen activated protein kinase (MAPK) signaling pathway (Kurosu et al., 2006; Ranch et al., 2011; Chen et al., 2018). In the kidney, FGF23 inhibits phosphate reabsorption and suppresses 1,25-dihydroxyvitamin D (1,25(OH)2D) production by downregulation of Cyp27b1 and upregulation of Cyp24a1 gene expression (Shimada et al., 2004; Perwad et al., 2007). Cyp27b1 and Cyp24a1 encode the enzymes 1α-hydroxylase and 24-hydroxylase, respectively, which are responsible for 1,25(OH)2D synthesis (Takeyama et al., 1997) and degradation (Ohyama et al., 1991). FGF23 is mainly expressed in bone but low levels of expression are detected in thymus, spleen and heart (Fon Tacer et al., 2010).

In patients with acute kidney injury (AKI), plasma and urinary C-term FGF23 (cFGF23) levels rise rapidly after onset of AKI and are independently associated with AKI progression and adverse outcomes (Leaf et al., 2013, 2016, 2017). Increase in cFGF23 levels is independent of changes in plasma PTH, phosphate and vitamin D metabolites (Leaf et al., 2016). In pediatric and adult patients with AKI following cardiac surgery, there is a transient increase in plasma intact FGF23 (iFGF23) levels which subsequently normalize (Hanudel et al., 2016; Leaf et al., 2016). Preoperative plasma cFGF23 levels in pediatric and adult patients undergoing cardiac surgery are associated with increased risk of AKI and post-operative mortality (Speer et al., 2015; Hanudel et al., 2016). Although, pre- and post-operative cFGF23 levels serve as prognostic tools to predict post-operative AKI severity and complications (Speer et al., 2015; Leaf et al., 2016), the mechanisms by which FGF23 levels increase in AKI are poorly understood.

In the folic acid-induced AKI (FA-AKI) mouse model, plasma FGF23 levels rise rapidly after onset of AKI and are partially independent of phosphate and 1,25(OH)2D suggesting that there are other contributing mechanisms (Christov et al., 2013). FGF23 production is elevated in bone of FA-AKI mice (Christov et al., 2013) and systemic FGF receptor blockade reduces bone Fgf23 mRNA expression and normalizes FGF23 levels (Hassan et al., 2016). Considering that FGF23 production in bone is only modestly increased in FA-AKI, other organs may contribute to the massive increase in FGF23 levels (Christov et al., 2013; Hassan et al., 2016). In hemorrhagic shock and sepsis-induced AKI rat model, Fgf23 gene expression is increased in bone marrow and is erythropoietin (EPO)-dependent (Toro et al., 2018).

In this study, we determined whether other organs contribute to the increase in plasma FGF23 levels in the FA-AKI mouse model and assessed the vitamin D axis as possible mechanism for stimulation of FGF23 production in multiple organs.

Methods

Animals

Eight-week-old male and female C57Bl/6J mice from in house breeding were used for all experiments. Animals were allowed ad libitum access to water and food (PicoLab Mouse Diet 20 5058). AKI was induced by intraperitoneal injection of folic acid (250 mg/kg; F7876, Sigma-Aldrich) or vehicle (0.15 M NaHCO3) as previously described (Christov et al., 2013). After 24 h, mice were anesthetized with Ketamine/Xylazine before blood and organs were collected. All animal studies were performed according to approved protocols (Institutional animal care and use committee, San Francisco).

Plasma Analysis

Blood was drawn from the heart and collected in BD MicrotainerTM Tubes containing Lithium Heparin (Becton, Dickinson and Company) for plasma separation. Plasma was aliquoted, rapidly frozen and stored at −80°C. Plasma phosphate, creatinine and BUN were measured with Phosphorus Liqui-UV® test, Creatinine LiquiColor® test, or Urea Nitrogen (BUN) Liqui-UV® (Rate), respectively (EKF Stanbio, United States). The plasma concentration of iFGF23 (Immutopics International, United States) and 1,25(OH)2D (Immunodiagnostic Systems Inc, United Kingdom) were measured by enzyme-linked immunosorbent assays according to manufacturers’ protocols.

RNA Extraction, Reverse Transcription, and qPCR

Organs were harvested and rapidly frozen in liquid nitrogen. Tissues were homogenized using either a BeadBugTM microtube homogenizer or a liquid nitrogen cooled mortar and pestle. Total RNA from bone (one femur and tibia each), bone marrow (spin down from femur and tibia), heart, spleen, and thymus was extracted with TRIzol (Life Technologies Europe B.V., Switzerland) and total RNA from kidney with NucleoSpin® RNA lysis buffer followed by purification with NucleoSpin® RNA Miniprep (Clontech, United States) according to the manufacturers’ protocol including Dnase1 digestion. Total RNA extractions were analyzed for purity and concentration using the NanoDrop ND-1000 spectrophotometer. RNA samples were diluted to a final concentration of 100 ng/μl and cDNA was prepared with reagents from Invitrogen (United States) if not stated otherwise. In brief, in a reaction volume of 40 μl, 300 ng of RNA was used as template and mixed with the following final concentrations of RT buffer (1×): MgCl2 (5.5 mmol/l), random hexamers (2.5 μmol/l), dNTP mix (500 μmol/l each; Bioline Ltd., United States), RNase inhibitor (0.4 U/μl), multiscribe reverse transcriptase (1.25 U/μl), and RNAse-free water. Reverse transcription was performed with temperature conditions set at 25°C for 10 min, 48°C for 30 min, and 95°C for 5 min on a thermocycler (Eppendorf). Quantitative PCR (qPCR) was performed using the ABI PRISM 7900HT Detection System (Applied Biosystems). Primers were designed using Primer 3 software (Untergasser et al., 2012). Mouse primer/probe sequences: Tnf Fwd 5′-CAGACCCTCACACTCAGATCATCT-3′, Rev 5′-CCTCCACTTGGTGGTTTGCT-3′, Probe 5′-ATTCGAGTGACAAGCCTGTAGCCCACGT-3′; Tgfb1 Fwd 5′-CCGCAACAAGCCATCTATG-3′, Rev 5′-TGCTTCCCGAATGTCTGACG-3′; Klotho Fwd 5′-CAGCTCCAGGCTCGGGTA-3′, Rev 5′-AGGTGTTGTAGAGATGCCAGACTTT-3′, Probe 5′-TTGCCCACAACCTACTTTGGCTCATG-3′; Vdr Fwd 5′-CACAAGACCTACGACCCCAC-3′, Rev 5′-CCGGTTCCATCATGTCCAGT-3′; Gus Fwd 5′-CTCATCTGGAATTTCGCCGA-3′, Rev 5′-GGCGAGTGAAGATCCCCTTC-3′, Probe 5′-CGAACCAGTCACCGCTGAGAGTAATCG-3′; Fgf23 Fwd 5′-GACCAGCTATCACCTACAGATCCA-3′, Rev 5′-CGGCGTCCTCTGATGTAATCA-3′, Probe 5′-CCCATCAGACCATCTACAGTGCCCTGA-3′; Cyp27b1 Fwd 5′-CCTCTGCCGAGACTGGGA-3′, Rev 5′-TCCCGAAAAAGGAAGTGGGT-3′, Probe 5′-TGTTTGCCTTTGCCCAGAGGCAC-3′; Cyp24a1 Fwd 5′-TACGCTGCTGTCACGGAGC-3′, Rev 5′-TCTGGATTTCCCGGAGAAGTC-3′, Probe 5′-CAGTGGAGACGACCGCAAACAGCTT-3′;. Primers and probes were purchased either from Elim Biopharma (United States), IDT (United States), or Applied Biosystems (Eukaryotic 18S rRNA Endogenous Control primer probe set). Probes were labeled with the reporter dye FAM at the 5′-end and the quencher dye TAMRA or BHQ1 at the 3′-end. qPCR reactions were performed using the TaqMan Fast Advanced Master Mix or PowerUp SYBR Green Master Mix (Applied Biosystems, United States).

Statistical Analysis

Statistics were performed using unpaired Student‘s t-test and linear regression with Pearson correlation (GraphPad Prism version 7, GraphPad, San Diego, CA, United States). P < 0.05 was considered significant.

Results

iFGF23, Vitamin D and Inflammation in FA-AKI

We administered wild type mice with FA or vehicle by intraperitoneal injections to determine the effect of FA-AKI on Fgf23 gene expression. Twenty-four hours after AKI induction, plasma iFGF23 and phosphate increased significantly while kidney function declined in FA-treated mice (Figures 1A–D). Further, plasma 1,25(OH)2D increased by 3-fold in FA-treated mice which was accompanied by 6-fold increase in renal Cyp27b1 and 17-fold reduction in Cyp24a1 mRNA expression (Figures 1E–G). FA-AKI reduced Klotho mRNA expression and triggered renal inflammation as demonstrated by increased Tnf and Tgfb mRNA expression (Figures 1H–J). We performed linear regression analyses to determine the relationships between plasma iFGF23, 1,25(OH)2D, and inflammation in FA-AKI. Plasma iFGF23 significantly correlated with plasma 1,25(OH)2D and both plasma iFGF23 and 1,25(OH)2D significantly correlated with renal mRNA expression of the inflammatory cytokine Tnf (Figures 1K–M).

FIGURE 1.

FIGURE 1

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Mineral homeostasis, renal function and inflammation parameters in mice with FA-AKI. (A) Plasma iFGF23, (B) phosphate, (C) BUN, (D) creatinine and (E) 1,25(OH)2D levels, as well as relative renal (F) Cyp27b1, (G) Cyp24a1, (H) Klotho, (I) Tnf and (J) Tgfb mRNA expression in vehicle (open triangle) and FA (black squares) treated mice after 24 h. Gus was used as housekeeping gene and values were normalized to vehicle group. Five to eight mice per group. Student’s t-test ∗ p < 0.05. Pearson correlation, R2- and p-values of linear regression analysis with 95% confidence interval for (K) plasma 1,25(OH)2D and iFGF23, (L) plasma iFGF23 and renal Tnf mRNA expression, (M) plasma 1,25(OH)2D and renal Tnf mRNA expression. Ten to eleven mice. ∗p < 0.05.

Multiple Organs Contribute to Rapidly Increased iFGF23 in FA-AKI Mice

As previously shown, Fgf23 mRNA expression was upregulated by 2-fold in bone in FA-treated mice compared to the control group (Figure 2A). Furthermore, Fgf23 mRNA expression increased significantly in spleen, heart and thymus, by 5-, 8-, and 14-fold, respectively. Ectopic renal Fgf23 mRNA expression was detected in FA-treated mice while it was absent in the control group (not shown). There was no change in Fgf23 mRNA expression in whole bone marrow with FA treatment (not shown). Previous studies have shown that activation of vitamin D receptor (VDR) by 1,25(OH)2D upregulates Fgf23 expression in bone (Liu et al., 2006). We determined the effect of increased plasma 1,25(OH)2D on Vdr mRNA expression in the organs we analyzed Fgf23 mRNA expression. We observed a 1.5- to 4-fold upregulation of Vdr mRNA expression in FA-treated mice in spleen, heart and thymus but there was no change in gene expression levels in bone (Figure 2B). Fgf23 mRNA expression in thymus, spleen, heart, and bone significantly correlated with Vdr mRNA expression within the same organ as well as with renal Tnf mRNA expression (Figure 2C).

FIGURE 2.

FIGURE 2

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Fgf23 and Vdr mRNA expression in different organs in mice with FA-AKI and correlation between tissue specific Fgf23, Vdr and renal Tnf expression. Relative (A) Fgf23 and (B) Vdr mRNA expression in bone, spleen, thymus and heart in vehicle (triangle) and FA-treated (squares) mice after 24 h. 18SrRNA (bone, spleen, thymus) or Gus (heart) were used as housekeeping genes and values were normalized to vehicle group. Five to eight mice per group. Student’s t-test ∗p < 0.05. (C) Pearson correlation, R2- and p-values of linear regression analysis for Fgf23 and Vdr mRNA expression within the same organ as well as between organ specific Fgf23 mRNA and renal Tnf mRNA expression. Ten to eleven mice. ∗p < 0.05.

Discussion

In patients with AKI, higher FGF23 levels are associated with AKI progression and increased mortality but mechanisms by which circulating FGF23 increase with kidney injury are unknown (Leaf et al., 2013, 2016, 2017). In the FA-AKI mouse model, increased Fgf23 mRNA in bone was shown to contribute to the increase in plasma FGF23 (Christov et al., 2013). In this study, we demonstrate that increased Fgf23 mRNA expression in multiple organs including bone accompanies the rapid increase in plasma iFGF23 in FA-AKI mice. Furthermore the rise in plasma iFGF23 is paralleled by increased plasma 1,25(OH)2D. Interestingly, the two lymphoid organs, thymus and spleen, show a very high induction of Fgf23 mRNA expression in mice with FA-AKI. The pattern of Fgf23 expression in lymphoid organs and its rapid increase following AKI suggest that FGF23 plays an important role in the inflammatory response triggered by FA-AKI including increased Tnf expression and elevated plasma IL-6 (Moreno et al., 2011; Wen et al., 2012). We confirmed that FA-AKI increases renal mRNA expression of inflammatory cytokines, Tnf and Tgfb. Moreover, we demonstrate that plasma iFGF23, 1,25(OH)2D and Fgf23 mRNA expression significantly correlated with renal Tnf mRNA expression. Inflammatory stimuli such as LPS, IL-1β, and TNF have been shown to increase Fgf23 mRNA expression in vivo and in vitro (Ito et al., 2015; Masuda et al., 2015; David et al., 2016). In mice with LPS-induced intermittent chronic inflammation, Fgf23 mRNA expression in spleen is increased and splenectomy reduces plasma FGF23 levels (Bansal et al., 2017). Whether these cytokines upregulate Fgf23 mRNA expression in spleen and thymus in FA-AKI need further evaluation.

Ectopic renal FGF23 expression has been reported in animal models of chronic kidney disease and in mice with unilateral ureter obstruction (Zanchi et al., 2013; Spichtig et al., 2014; Smith et al., 2017). Renal FGF23 expression in uremic rats does not contribute to increased circulatory FGF23 levels but local production may further trigger renal fibrosis in these animals (Mace et al., 2017; Smith et al., 2017). Our findings of renal Fgf23 mRNA expression in FA-treated mice expands the pathological conditions where ectopic renal FGF23 expression is present. Hemorrhagic shock and sepsis-induced AKI in rats result in EPO-EPO receptor-dependent upregulation of Fgf23 mRNA levels in the bone marrow (Toro et al., 2018). In our study, we did not detect any changes in Fgf23 mRNA expression in whole bone marrow of FA-AKI mice. AKI disrupts the crosstalk between kidney and heart and contributes to acute reno-cardiac syndrome (Kingma et al., 2015). The resulting cardiac dysfunction is attributed to changes in kidney function, hemodynamics and inflammatory mediators (Kingma et al., 2015). Further studies are needed to determine whether the inflammatory response caused by FA-AKI is responsible for the increase in Fgf23 mRNA expression in the heart of FA-AKI mice.

In bone, 1,25(OH)2D activates VDR and allows VDR binding to VDR response elements in the Fgf23 promoter region to upregulate Fgf23 mRNA expression (Liu et al., 2006). Therefore, increase in local VDR expression together with high plasma 1,25(OH)2D may be responsible for increased Fgf23 mRNA expression seen in different organs in FA-treated mice. Indeed, we found elevated plasma 1,25(OH)2D in FA-AKI mice and increased Vdr mRNA expression in spleen, thymus and heart but not in bone. Moreover, Vdr mRNA expression strongly correlated with Fgf23 mRNA expression in the same organ. Therefore, activation of 1,25(OH)2D-VDR signaling pathway may contribute to increase in plasma iFGF23 in FA-AKI mice.

Increased plasma 1,25(OH)2D in FA-AKI mice was accompanied by increased renal Cyp27b1 and decreased Cyp24a1 mRNA expression. These results suggest that FGF23 is unable to regulate renal vitamin D metabolism in FA-AKI mice which could be partially explained by interrupted FGF23 signaling due to a decrease in renal Klotho expression with AKI (Hu et al., 2010). Similar to our study, 3/4 nephrectomized rats also demonstrate increased renal Cyp27b1 and decreased Cyp24a1 and Vdr mRNA expression (Takemoto et al., 2003). However, in patients with CKD and acute renal inflammation plasma 1,25(OH)2D is low with increased CYP27b1, CYP24a1, and VDR expression (Zehnder et al., 2008). Renal CYP27b1 expression in these patients was localized to activated macrophages and epithelial cells (Zehnder et al., 2008). Therefore, humans and rodents differ in the renal expression patterns for genes in the vitamin D metabolic pathway.

In summary, we demonstrate that the rapid rise in plasma iFGF23 in mice with FA-AKI is accompanied by increased Fgf23 mRNA expression in multiple organs including bone, thymus, spleen, heart and kidney. Furthermore, increased plasma iFGF23 levels are paralleled by increased plasma 1,25(OH)2D and increased Vdr mRNA expression in thymus, spleen, and heart.

Author Contributions

DE-S and FP conceived the study, provided the methodology, and wrote, reviewed, and edited the manuscript. DE-S performed the formal analysis and visualization process and wrote the original draft of the manuscript. DE-S and MZ contributed to the investigation process. FP gathered resources and supervised the study and acquired funding. All authors read, edited, and approved the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Footnotes

Funding. This study was supported by grants from CTSI-SOS award to FP and the Novartis Foundation for medical-biological research to DE-S (#17B060).

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