Research ArticlePANCREATITIS

Pancreatitis is an FGF21-deficient state that is corrected by replacement therapy

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Science Translational Medicine  08 Jan 2020:
Vol. 12, Issue 525, eaay5186
DOI: 10.1126/scitranslmed.aay5186

Pancreatic stress management

Pancreatitis results from the premature activation of digestive enzymes in the pancreas and can be potentially life threatening. Hernandez et al. found pancreatic fibroblast growth factor 21 (FGF21) deficiency in three mouse models and patient biopsies of acute and chronic pancreatitis. The authors showed that this deficiency resulted from the activation of the integrated stress response, and accordingly, both FGF21 administration and pharmacologic stress response inhibition restored FGF21 and alleviated symptoms in acute and chronic models of the disease. FGF21 treatment also prevented pancreatitis onset in a model of endoscopic retrograde cholangiopancreatography, a therapeutic procedure that carries pancreatitis risk. This study could have implications for the clinical management of pancreatitis.


The exocrine pancreas expresses the highest concentrations of fibroblast growth factor 21 (FGF21) in the body, where it maintains acinar cell proteostasis. Here, we showed in both mice and humans that acute and chronic pancreatitis is associated with a loss of FGF21 expression due to activation of the integrated stress response (ISR) pathway. Mechanistically, we found that activation of the ISR in cultured acinar cells and mouse pancreata induced the expression of ATF3, a transcriptional repressor that directly bound to specific sites on the Fgf21 promoter and resulted in loss of FGF21 expression. These ATF3 binding sites are conserved in the human FGF21 promoter. Consistent with the mouse studies, we also observed the reciprocal expression of ATF3 and FGF21 in the pancreata of human patients with pancreatitis. Using three different mouse models of pancreatitis, we showed that pharmacologic replacement of FGF21 mitigated the ISR and resolved pancreatitis. Likewise, inhibition of the ISR with an inhibitor of the PKR-like endoplasmic reticulum kinase (PERK) also restored FGF21 expression and alleviated pancreatitis. These findings highlight the importance of FGF21 in preserving exocrine pancreas function and suggest its therapeutic use for prevention and treatment of pancreatitis.


Pancreatitis is one of the most common and debilitating diseases of the gastrointestinal tract, leading to substantial morbidity and mortality (1). Pancreatitis results from the premature activation of digestive enzymes in the pancreas itself, which causes tissue damage and inflammation. Common causes of pancreatitis include alcohol abuse and gallstones (2). About a third of pancreatitis cases in humans are caused by alcohol, which has the highest rates of morbidity (2, 3). Pancreatitis also occurs in 5 to 10% of patients undergoing endoscopic retrograde cholangiopancreatography (ERCP), a procedure used to examine the pancreatic and biliary ducts as well as the gallbladder (2). Treatments for pancreatitis are limited and generally supportive in nature (2, 46). Thus, there is a pressing need for new therapies.

Fibroblast growth factor 21 (FGF21) is a hormone secreted by the liver in response to diverse metabolic stresses including starvation and the consumption of alcohol or simple sugars (79). FGF21 acts on a heteromeric cell surface receptor complex composed of a conventional FGF receptor, FGFR1c, together with an obligate co-receptor, β-klotho (79). FGF21 is also highly expressed in the exocrine pancreas, where it acts directly on acinar cells in an autocrine/paracrine manner to stimulate digestive enzyme secretion (10, 11). This prevents protein overload and relieves endoplasmic reticulum (ER) stress. Mice lacking FGF21 are particularly susceptible to pancreatitis induced by the cholecystokinin (CCK) analog cerulein (10, 12). Conversely, genetic overexpression of FGF21 confers protection in this model. Likewise, prophylactic FGF21 administration reduces fibrogenesis in a mouse model of l-arginine–induced chronic pancreatitis (13).

Here, we tested the hypothesis that loss of FGF21 is a principal driving factor of pancreatitis. On the basis of this concept, we further investigated using FGF21 therapeutically to reverse preexisting pancreatitis in cerulein- and alcohol-induced mouse models and to prevent pancreatitis in a murine model of ERCP.


FGF21 is down-regulated in pancreatitis

Pharmacologic FGF21 protects against cerulein-induced acute pancreatitis (CIP) (10, 12). To test whether endogenous FGF21 expression changes during CIP, we treated mice with seven hourly injections of cerulein and collected pancreas and blood samples at 4, 8, 12, and 18 hours after the first injection (fig. S1A). CIP was confirmed by histology (fig. S1B) and increased expression of genetic markers of inflammation (Tnfa and Il6) and oxidative (Hmox1) and ER stress (Chop) (fig. S1C). Consistent with previous observations (12), Fgf21 mRNA was increased by CIP at the 4-hour time point but unchanged compared to vehicle at 8 hours (Fig. 1A). Unexpectedly, however, Fgf21 expression markedly decreased at 12 hours and was virtually undetectable by 18 hours. Similarly, pancreatic FGF21 protein concentrations were elevated by CIP at 4 hours and then gradually decreased to undetectable by 18 hours (Fig. 1B). Plasma FGF21 concentrations remained low (<1.5 ng/ml) and were not affected by CIP (Fig. 1C). Fgf21 expression was also suppressed in a chronic model of CIP (fig. S1, D and E), in which cerulein was injected on 6 days over the course of 2 weeks (14, 15). Induction of CIP in this chronic model was confirmed by an increase in pancreatic myeloperoxidase (MPO) activity (fig. S1F) and genetic markers of inflammation (Tnfa and Il6) as well as oxidative stress (Hmox1) and ER stress (Chop) (fig. S1G).

Fig. 1 FGF21 replacement ameliorates pancreatitis.

(A to C) Pancreatic FGF21 mRNA (A) and protein (B), and plasma FGF21 (C) at 4, 8, 12, or 18 hours after the first cerulein injection in CIP. (D) Pancreatic Fgf21 mRNA after 24 hours of AIP and EIP. (E and F) Pancreatic FGF21 mRNA and protein and plasma FGF21 protein in CIP (E) or AIP (F) after a 24-hour treatment regimen of FGF21 (1 mg/kg) (four intraperitoneal injections). (G and H) Plasma amylase activity in CIP (G) and AIP (H). (I and J). Pancreatic MPO activity in CIP (I) and AIP (J). (K and L) Histological grading of mouse pancreata in CIP (K) and AIP (L). (M) FGF21 in plasma (at 6 and 24 hours), and pancreatic FGF21 mRNA and protein (at 24 hours) after inducing EIP with intraductal infusion of contrast agent in the absence or presence of FGF21 (100 μg/ml). (N) Serum amylase activity at 6 and 24 hours from mice in (M). (O and P) Pancreatic MPO activity (O) and histological grading of pancreata (P) of mice in (M). Results are expressed as means ± SEM. n = number of mice per group for all experiments. n = 3 to 4 in (A) to (C); n = 3 for AIP and n = 5 for EIP in (D); n = 6 in (E), (G), (I), and (K); n = 8 in (F), (H), (J), and (L); n = 5 in (M) to (P). *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001. Asterisks indicate statistically different values relative to vehicle. Statistical differences (P > 0.05) are indicated between all values that have different letters.

To determine whether the loss of Fgf21 is a general feature of pancreatitis, we investigated two other clinically relevant mouse models: alcohol-induced pancreatitis (AIP) and ERCP-induced pancreatitis (EIP) (1419). AIP occurs within 24 hours after two injections of ethanol and its non-oxidative metabolite palmitoleic acid (POA) (fig. S1, H and I). Likewise, infusion of ERCP radiocontrast dye at high pressure into the pancreatic ducts of mice (fig. S1J) resulted in EIP (fig. S1K), similar to that observed in humans (2). As in CIP, AIP and EIP caused a marked decrease in pancreatic Fgf21 (Fig. 1D). Thus, a hallmark feature of pancreatitis is the loss of pancreatic Fgf21 expression.

Therapeutic administration of FGF21 reverses pancreatitis

To test whether therapeutic administration of FGF21 reverses pancreatitis, recombinant FGF21 was injected four times over a 12- to 16-hour period after induction of CIP (fig. S2A) and AIP (fig. S2B), and the mice were sacrificed 2 hours after the last FGF21 dose (fig. S2, A and B). FGF21 treatment increased plasma FGF21 concentrations to 10 to 15 ng/ml and restored pancreatic FGF21 protein (but not mRNA) expression in both CIP (Fig. 1E) and AIP (Fig. 1F). FGF21 treatment reversed all of the sequelae of pancreatitis in both the CIP and AIP models, which included restoring plasma amylase (Fig. 1, G and H) and pancreatic MPO (Fig. 1, I and J) activities to normal and markedly reducing pancreatic edema, inflammatory infiltrate, necrosis, and the combined overall severity score of these parameters (Fig. 1, K and L, and fig. S2, C and D). FGF21 treatment also reduced pancreatic gene expression markers of inflammation and oxidative and ER stress (fig. S2, E and F). Thus, therapeutic administration of FGF21 rescues the loss of endogenous FGF21 in the pancreas and thereby decreases injury due to pancreatitis. Although plasma FGF21 concentrations were induced in the AIP model (Fig. 1F), which was expected on the basis of ethanol’s ability to induce hepatic Fgf21 expression (20), this did not restore FGF21 concentrations in the pancreas and was insufficient to reverse pancreatitis.

We also explored FGF21’s potential to prevent EIP by mixing FGF21 in with the radiocontrast agent and thereby locally administering FGF21 directly into the exocrine pancreas during the ductal infusion procedure (fig. S2G). Intraductal administration of FGF21, which restricts the recombinant FGF21 to the pancreas and its duct, maintained normal endogenous pancreatic FGF21 mRNA and protein expression without increasing plasma FGF21 concentrations (Fig. 1M). FGF21 treatment by this method also strongly protected against EIP-induced changes in serum amylase (Fig. 1N) and pancreatic MPO activity (Fig. 1O) as well as pancreatic histology and gene expression (Fig. 1P and fig. S2, H and I). These results indicate that FGF21 is efficacious therapeutically to both treat and prevent various causes of pancreatitis.

FGF21 reverses pancreatitis by acting directly on the exocrine pancreas

Endogenous FGF21 acts in an autocrine/paracrine manner on pancreatic acinar cells to induce digestive enzyme secretion and maintain proteostasis (10). To test whether recombinant FGF21 acts directly on pancreatic acinar cells to elicit its therapeutic effects, we used KlbCela1 mice, in which Klb expression was selectively disrupted in acinar cells using a tamoxifen-inducible elastase-Cre driver (10). We confirmed the reduction in Klb expression after tamoxifen administration by quantitative polymerase chain reaction (qPCR) (Fig. 2A). Basal pancreatic FGF21 mRNA (Fig. 2B), but not protein (Fig. 2C), was lower in KlbCela1 than in control Klbfl/fl mice. CIP repressed FGF21 mRNA (Fig. 2B) and protein (Fig. 2C) expression in both KlbCela1 and Klbfl/fl mice. Administration of exogenous FGF21 increased plasma FGF21 markedly (Fig. 2D), restored FGF21 protein concentrations to normal in pancreas (Fig. 2C), lowered plasma amylase activity (Fig. 2E), and reduced pancreatic edema, inflammatory infiltrate, and necrosis caused by CIP in Klbfl/fl, but not in KlbCela1, mice (Fig. 2, F and G). FGF21 administration also reversed CIP-mediated induction of gene markers of inflammation and ER and oxidative stress in Klbfl/fl, but not in KlbCela1, mice (Fig. 2H). We conclude that FGF21 acts directly on the acinar cells of the exocrine pancreas to mediate its therapeutic effects.

Fig. 2 β-Klotho in acinar cells is required for the therapeutic effects of FGF21 in pancreatitis.

(A) Pancreatic Klb mRNA in wild-type (Klbfl/fl) and acinar cell–specific β-klotho KO (KlbCela1) mice (n = 3). (B and C) Pancreatic FGF21 mRNA (B) and protein (C) in CIP after a 24-hour treatment regimen of FGF21 (1 mg/kg) (four intraperitoneal injections) in Klbfl/fl and KlbCela1 mice. (D and E) Plasma FGF21 (D) and amylase activity (E) of mice in (B). (F and G) Representative H&E images of stained pancreata (F) and histological grading (G) of mice in (B). Scale bar indicates 50 μm for all images. (H) Pancreatic inflammation (Tnfα and Il6), oxidative stress (Hmox1), and ER stress (Chop) markers of mice in (B). Results are expressed as means ± SEM. n, number of mice per group. n = 3 (vehicle), 4 (CIP), and 5 (CIP + FGF21) in (B) to (G). ****P < 0.0001. Asterisks indicate statistically different values relative to vehicle. Statistical differences (P > 0.05) are indicated between all values that have different letters.

ATF3 represses FGF21 expression in pancreatitis

The transcription factor ATF4, which is induced by the PKR-like endoplasmic reticulum kinase (PERK) arm of the integrated stress response (ISR), is a strong inducer of FGF21 expression in the liver and muscle (2124). Mice lacking the related transcription factor ATF3 have elevated pancreatic Fgf21 mRNA in response to cerulein treatment (25). Because ATF3 is induced by ATF4 and can repress its activity, we examined the roles of these two transcription factors in regulating pancreatic FGF21 in the context of CIP. Pancreatic ATF4 mRNA (fig. S3A) and protein (Fig. 3, A and B) concentrations were induced 4 hours into CIP but returned to basal between 8 and 18 hours (Fig. 3, A and B, and fig. S3A). In contrast, ATF3 mRNA (fig. S3B) and protein (Fig. 3, A and C) expression, which are absent under normal physiological conditions, were markedly elevated at all time points after cerulein treatment. We also examined pancreatic Atf3 and Atf4 expression in the chronic CIP (fig. S3C), AIP (fig. S3D), and EIP (fig. S3E) models. Atf3 mRNA was elevated in all models, whereas Atf4 was decreased in chronic CIP and unchanged in AIP and EIP (fig. S3, C to E). Thus, ATF3 and ATF4 were differentially regulated in all four models of pancreatitis.

Fig. 3 ATF3 is induced in pancreatitis and binds to the Fgf21 promoter.

(A) Immunoblot of pancreatic ATF4 and ATF3 at 4, 8, 12, or 18 hours after the first cerulein injection in CIP with β-actin as loading control. (B and C) Quantification of ATF4 (B) and ATF3 (C) in (A). (D) Schematic of the mouse −1497/+5 bp region of the Fgf21 promoter with the sequences and positions of the wild-type (WT) and mutant amino acid response elements (AARE). (E to H) ChIP assays quantified by qPCR for ATF4 (E and G) and ATF3 (F and H) binding to the AARE1 + 3 or AARE2 response elements from mouse pancreas in the CIP time-course experiment. IgG, immunoglobulin G. Results are expressed as means ± SEM. n = 3 to 4 mice per group for all experiments. *P < 0.05; **P < 0.01; ****P < 0.0001. Asterisks indicate statistically different values relative to vehicle.

As part of these time course studies, we also analyzed ATF3 and ATF4 occupancy on the Fgf21 promoter by chromatin immunoprecipitation (ChIP)–qPCR. The Fgf21 promoter contains three ATF4 response elements (AAREs) (Fig. 3D). All three AAREs are conserved in the mouse and human FGF21 promoter (21, 26). We analyzed the AARE1 and AARE3 sites together (AARE1 + 3), because they are only 10 base pairs (bp) apart (Fig. 3D). ATF4 binding to the AARE1 + 3 sites increased at 4 hours after induction of CIP but decreased at 12 and 18 hours compared to the saline-treated control mice (Fig. 3E). ATF3 binding to the AARE1 + 3 site also increased at 4 hours of CIP but, unlike ATF4, was maintained throughout the experiment (Fig. 3F). We detected little or no ATF4 (Fig. 3G and fig. S3F) or ATF3 (Fig. 3H and fig. S3G) on the AARE2 or control sites. These data suggest that CIP-mediated induction of ATF3 suppresses Fgf21 transcription by competing with ATF4 for binding to the Fgf21 promoter.

We further examined the contribution of ATF3 to CIP-mediated repression of Fgf21 using the 266-6 mouse acinar cell line. Treatment of cells with cerulein recapitulated the repression of Fgf21 mRNA observed in vivo (Fig. 4A). In cell-based reporter assays, an Fgf21 promoter construct that included all three amino acid response elements was repressed by cerulein (Fig. 4B). Knockdown of ATF3 by small interfering RNA (siRNA) (fig. S4A) increased basal Fgf21 promoter activity and blocked its repression by cerulein (Fig. 4B). Conversely, ATF3 overexpression repressed the Fgf21 promoter (Fig. 4C). Overexpressing ATF4 increased reporter activity, whereas overexpressing ATF3 reduced it (Fig. 4D). Titrating ATF3 against a fixed amount of ATF4 (fig. S4, B to D) caused a dose-dependent repression of Fgf21 promoter activity, reaching full repression at an ATF3-to-ATF4 ratio of about 100:1 (Fig. 4E). This ratio is consistent with that observed in vivo due to pancreatitis (Fig. 3, A to C). Together, these data show that ATF3 represses Fgf21 gene expression. Promoter loss-of-function mutations in each of the individual AAREs (Fig. 4D) and promoter truncation mutants (Fig. 4F) revealed that AARE1 is the principal site for induction and repression by ATF4 and ATF3, respectively. Accordingly, cerulein failed to repress Fgf21 promoter activity in the AARE1 mutant (Fig. 4G). Thus, ATF3 and ATF4 control Fgf21 expression primarily by competing for the AARE1 element.

Fig. 4 ATF3 competes with ATF4 to repress Fgf21 promoter activity.

(A) Fgf21 mRNA in 266-6 mouse acinar cells treated with vehicle (black bar) or 100 nM cerulein (white bar) for 12 hours (N = 3). (B and C) Repression of the Fgf21 promoter using a luciferase reporter gene evaluated after Atf3 siRNA knockdown (N = 4) (B) or ATF3 overexpression (N = 4) (C) in 266-6 cells treated as in (A). (D) Wild-type and AARE mutant Fgf21 promoter luciferase (Luc) activity in 266-6 cells overexpressing ATF3 and ATF4 (N = 4). (E) Fgf21 promoter luciferase activity in 266-6 cells expressing increasing amounts (0.01 to 100 ng) of ATF3 expression plasmid and a fixed amount (1 ng) of ATF4 expression plasmid (N = 8). (F) Truncated Fgf21 promoter luciferase assays in 266-6 cells overexpressing ATF3 and ATF4 (N = 6). (G) Wild-type and AARE mutant Fgf21 promoter luciferase activity in 266-6 cells treated as in (A) (N = 4). Results are expressed as means ± SEM. N, number of replicates. ***P < 0.001; ****P < 0.0001. Asterisks indicate statistically different values relative to vehicle. Statistical differences (P > 0.05) are indicated between all values that have different letters.

Dysregulation of the ATF4/ATF3/FGF21 axis is conserved in human pancreatitis

We explored the translational relevance of our findings by analyzing pancreata from chronic and acute pancreatitis patients (data file S1). As expected, there was a high degree of fibrosis, edema, and inflammation in sections from patients with pancreatitis (Fig. 5A). Consistent with our mouse studies, ATF3 expression was increased (Fig. 5, B and C), and FGF21 (Fig. 5, D and E) and ATF4 (Fig. 5, F and G) expression was decreased in patients with chronic and acute pancreatitis. These findings indicate that human pancreatitis is associated with a loss of FGF21 that correlates with an increased ATF3:ATF4 ratio.

Fig. 5 Pancreatic FGF21, ATF3, and ATF4 concentrations in human patients with pancreatitis.

(A) H&E staining of pancreata from a representative normal and pancreatitis patient. (B to G) Pancreatic concentrations of FGF21 (B and C), ATF3 (D and E), and ATF4 (F and G) in normal individuals and patients with chronic (CP) and acute (AP) pancreatitis. Representative immunofluorescence images are shown in (B), (D), and (F), and quantification of samples (normal, n = 14; chronic, n = 49; and acute pancreatitis, n = 3) is shown in (C), (E), and (G). In the immunofluorescence images, DAPI staining is blue and FGF21, ATF3, and ATF4 stainings are gray. Scale bar indicates 50 μm for all images. Results in (C), (E), and (G) are expressed as means ± SEM. Statistical differences (P > 0.05) are indicated between all values that have different letters. R.F.U., relative fluorescence units.

PERK inhibition reverses pancreatitis in an FGF21-dependent manner

A prediction of our findings is that PERK inhibition would block pancreatitis-mediated induction of ATF3 in the pancreas, thereby providing another tractable target for therapeutic intervention. Accordingly, mice administered the PERK inhibitor GSK2656157 were refractory to CIP-mediated repression of FGF21 mRNA and protein (Fig. 6, A and B). Therapeutic administration of GSK2656157 also lowered plasma amylase activity to near normal (Fig. 6C) and improved pancreatic histology (Fig. 6, D and E) and mRNA markers of inflammation and oxidative and ER stress (Fig. 6F). The protective effects of GSK2656157 were completely absent in FGF21-KO (knockout) mice (Fig. 6, C to F), further supporting the idea that the loss of FGF21 is a major contributor to pancreatitis. Moreover, the finding that PERK inhibition reverses pancreatitis by restoring endogenous FGF21 expression reinforces the notion that FGF21 replacement therapy may be an effective way to treat pancreatitis.

Fig. 6 Inhibition of PERK ameliorates pancreatitis in an FGF21-dependent manner.

(A to F) Wild-type (WT) or FGF21 KO mice (FGF21-KO) were treated with FGF21 (1 mg/kg) or GSK2656157 (25 mg/kg) (four intraperitoneal injections) after CIP. (A and B) Pancreatic FGF21 mRNA (A) and protein (B). (C to F) Plasma amylase activity (C), representative H&E images (D), histological grading (E), and pancreatic mRNA markers of inflammation (Tnfα and Il6), oxidative stress (Hmox1), and ER stress (Chop) (F) in mice treated with therapeutic or vehicle control. Scale bar indicates 50 μm for all images. Results are expressed as means ± SEM; n = 6 mice per group. Statistical differences (P > 0.05) are indicated between all values that have different letters.


Here, we have examined the utility of using FGF21 therapeutically to treat pancreatitis. We show that FGF21 in the pancreas is markedly reduced in human pancreatitis as well as murine models of the disease elicited by a range of different insults, including cerulein, alcohol, and the ERCP procedure. We note that FGF21 expression is also reduced in mice lacking the bHLH (basic helix-loop-helix) transcription factor MIST1, which exhibit acinar cell disorganization and are particularly sensitive to CIP (27). Thus, FGF21 deficiency is a general feature of pancreatitis. We further show that restoring FGF21 pharmacologically reverses pancreatitis in CIP and AIP and inhibits pancreatitis in EIP. In CIP, FGF21’s beneficial effects require β-klotho in the acinar cells, demonstrating that FGF21 acts directly on the exocrine pancreas. These findings highlight the clinical potential of FGF21 for treating different forms of pancreatitis.

In this study, we also addressed how different inducers of pancreatitis suppress FGF21 expression. Our data support a common mechanism involving ISR-mediated induction of ATF3 (fig. S5). Consistent with previous literature, the onset of pancreatitis leads initially to an induction of ATF4 with a corresponding increase in FGF21, which may be an initial attempt to overcome damage to the pancreatic tissue (12). However, as pancreatitis persists, the subsequent induction of ATF3 efficiently represses Fgf21 transcription. We show that ATF3 represses the Fgf21 promoter by competing with ATF4 for binding to a conserved AARE response element. Thus, whereas previous studies have suggested that ISR is an adaptive pathway in acute pancreatitis (12, 27, 28), we suggest that it becomes maladaptive over time. We show that ATF3 is also increased in human pancreatitis, suggesting that this mechanism translates to human disease.

The ISR pathway represents an additional new target for treating pancreatitis. We show that inhibiting ISR with GSK2656157 restored endogenous FGF21 concentrations and ameliorated pancreatitis. The restorative effect required FGF21, further highlighting the importance of FGF21 in maintaining pancreatic function.

There are several limitations to this study. Regarding the mouse models, although cerulein mimics the sequelae of pancreatitis in humans, excessive CCK receptor activation is not a clinically relevant cause of the disease. Moreover, it is necessary to co-administer POA to elicit ethanol-induced pancreatitis in mice. Although FGF21 stimulates digestive enzyme secretion to maintain pancreatic proteostasis (10) and mitigates the ISR, it remains to be determined precisely how FGF21 mediates its anti-inflammatory actions and protects against pancreatitis. Last, a definitive conclusion about FGF21 expression in the acute form of pancreatitis in humans will require analysis of a greater number of patient samples. Nevertheless, we show that pancreatitis is broadly characterized as an FGF21-deficient state of the pancreas in mice and humans and that restoring FGF21 has notable therapeutic effects in a range of different mouse models of the disease. Given that several FGF21 analogs and mimetics have already progressed to clinical trials for other indications related to metabolic disease (9), it may be possible to test FGF21 for treating human pancreatitis in the near future.


Study design

This study was designed to characterize the effect of pancreatitis on the FGF21 pathway by analyzing the samples of pancreata from mice and humans with acute and chronic forms of the disease. On the basis of the finding that pancreatitis was universally associated with a loss of FGF21, we then investigated the efficacy of FGF21 replacement therapy in three murine models of pancreatitis that mimic the acute and chronic disease observed in humans. Accordingly, the endpoints for the in vivo experiments assessed FGF21 concentrations in pancreas and plasma and pancreatitis severity. Cell culture experiments were designed to characterize the molecular mechanism underlying FGF21 down-regulation by pancreatitis. Measurements of plasma/serum amylase and pancreatic MPO activities, histological grading, and gene expression markers were used to assess the degree of pancreatitis. All histological grading was performed in a blinded fashion with the samples de-identified before submission for grading. For all in vivo experiments, mice were age- and weight-matched across experimental groups. Sample size (n) is defined as biological replicates for in vivo experiments and technical replicates (N) for cell culture experiments. Sample size for human pancreatitis tissue was determined by availability. For all in vivo experiments, sample sizes of n = 3 to 8 mice per group were used, and for cell culture experiments, n = 4 to 8 were used to achieve 20% differences between treatment groups or genotype-dependent effects at 80% power with a 95% confidence interval (α = 0.05). In vivo experiments were performed twice (n = 2) and cell culture experiments were performed three times (n = 3) to verify their reproducibility. Outliers were identified using the ROUT method (GraphPad Prism).

Recombinant FGF21

Recombinant human FGF21 used in all the experiments was a gift from Novo Nordisk.

Quantitative real-time PCR

RNA from pancreas or cells was extracted using RNA Stat-60 (Iso-Tex Diagnostics). Complementary DNA (cDNA) was generated from RNA (2 μg) using the High-Capacity cDNA Reverse Transcription Kit (Life Technologies). qPCR was performed by the SYBR Green method (29). Primer sequences for the genes analyzed can be found in table S1. U36B4 (NM_007475) was used as the reference mRNA.


The Institutional Animal Care and Research Advisory Committee of the University of Texas Southwestern Medical Center and the University of Pittsburgh School of Medicine approved all experiments. Mice were housed in a pathogen-free facility and fed a standard chow diet (Harlan Teklad). C57BL/6J mice were purchased through the University of Texas Southwestern Mouse Breeding Core. Swiss Webster mice were purchased from Charles River Laboratories. FGF21-KO (Fgf21tm1.2Djm) (30) inducible acinar cell–specific β-klotho KO mice (KlbCela1) (10) and wild-type littermates were maintained on a C57BL/6J background. Male mice were used for all experiments, except for the EIP studies, where female Swiss Webster mice were used. In KlbCela1 mice, Cre expression was induced via intraperitoneal injection of tamoxifen (50 μg/g) (Sigma) for three consecutive days, followed by Klb KO validation by qPCR for experiments 2 weeks later.

CIP and FGF21 treatment

Acute pancreatitis was induced by administration of seven hourly intraperitoneal injections of cerulein (50 μg/kg) (Tocris Bioscience), whereas mice in the control group were injected with saline. For the therapeutic treatments, FGF21 (1 mg/kg) and GSK2656157 (25 mg/kg) (Cayman Chemical) were administered intraperitoneally four times after CIP. In studies where GSK2656157 was used, the vehicle injected was 5% dimethyl sulfoxide (DMSO) diluted in saline to facilitate the solubilization of GSK2656157.

Chronic pancreatitis

To induce chronic CIP, C57BL/6J mice were given six hourly intraperitoneal injections of cerulein (50 μg/kg; Tocris Bioscience) per day for 6 days during the course of 2 weeks.

AIP and FGF21 treatment

Male Swiss Webster mice were given ethanol (1.3 g/kg) in combination with POA (150 mg/kg) twice intraperitoneally over 1 hour to induce AIP. FGF21 was administered four times intraperitoneally at 1 mg/kg before collecting tissue and plasma, 24 hours after the induction of AIP.

EIP and FGF21 treatment

ERCP was performed as previously described (1719). Female Swiss Webster mice were used for these experiments, which were performed at the University of Pittsburgh. Iohexol (300 mg/ml) (Omnipaque 300, GE Healthcare) was the radiocontrast agent infused intraductally. Where indicated, FGF21 was combined with the radiocontrast agent at a final concentration of 1 μg/ml. Plasma was collected at 6 and 24 hours. Tissues were harvested 24 hours after ERCP.

Amylase and pancreatic MPO activity

Amylase activity in mouse plasma/serum was measured using an amylase assay kit (Abcam). MPO activity was measured from pancreas homogenized in MPO assay buffer using an MPO activity assay kit (Sigma).


Mouse pancreas was harvested and fixed in 10% neutral buffered formalin overnight at 4°C. Paraffin sections were embedded, sectioned, and hematoxylin and eosin (H&E)–stained by the UT Southwestern (UTSW) Molecular Pathology Core. Paraffin-embedded pancreas sections were deparaffinized in xylene and rehydrated through an ethanol gradient (100, 95, 70, and 50%). Antigen retrieval was performed for 30 min in citric acid–based antigen unmasking solution (Vector Laboratories) before immunofluorescence. H&E-stained pancreas was graded on an equal weight score (from 0 to 3) for edema (0 = absent; 1 = focally increased between lobules; 2 = diffusely increased; 3 = acini disrupted and separated), inflammatory infiltration (0 = absent; 1 = in ducts, around ductal margins; 2 = in the parenchyma, <50% of the lobules; 3 = in the parenchyma, >50% of the lobules), necrosis (0 = absent; 1 = periductal necrosis, <5% of cells; 2 = focal necrosis, 5 to 20% of cells; 3 = diffuse parenchymal necrosis, 20 to 50% of cells), and total severity score (sum of edema, inflammatory infiltrate, and necrosis scores) as previously described (31). Five different fields per mouse pancreas were analyzed in a blinded fashion. Images were acquired with a Zeiss Axio Scan.Z1 slide scanner.


Sections were incubated for 1 hour in blocking buffer [1% bovine serum albumin (BSA), 5% normal donkey serum, and 0.3% Triton X-100 in 1× phosphate-buffered saline (PBS)], followed by overnight incubation at 4°C with primary antibodies in blocking buffer (table S2). Sections were washed in 1× PBS three times for 5 min each time, followed by incubation for 1 hour with Alexa Fluor–conjugated secondary antibodies against the primary antibody’s host species in blocking buffer. Sections were washed in 1× PBS three times for 5 min each time, stained with 4′,6-diamidino-2-phenylindole (DAPI) (Life Technologies), and mounted with Aqua-Poly/Mount (Polysciences).


Pancreas was homogenized using FastPrep-24 lysing matrix bead tubes (MP Biomedicals), and cells were homogenized by passaging through an insulin syringe in 1× radioimmunoprecipitation assay buffer (Cell Signaling Technology) supplemented with a cocktail of protease and phosphatase inhibitors (Roche). Protein lysate concentrations were measured using the DC Protein Assay (Bio-Rad). Equal protein amounts were loaded and electrophoresed in a 4 to 20% SDS–polyacrylamide gel electrophoresis gel (Bio-Rad) and transferred to nitrocellulose membranes (Bio-Rad). Membranes were blocked with 5% BSA in tris-buffered saline with 0.5% Tween 20 for 1 hour. Probing of membranes with primary antibodies was performed overnight at 4°C (table S2). Membranes were then incubated with horseradish peroxidase–conjugated secondary antibodies (Cell Signaling Technology) against the primary antibody’s host species for 1 hour. Membranes were developed using the Clarity ECL substrate solution (Bio-Rad), and the signal was detected with an ImageQuant LAS 4000 luminescent imager (General Electric). Quantification was done using ImageJ.

Chromatin immunoprecipitation

ChIP assays were performed using the SimpleChIP Plus Enzymatic Chromatin IP Kit with magnetic beads (Cell Signaling Technology). Twenty-five milligrams from each mouse pancreas was used for each immunoprecipitation, and 4% of the total isolated digested chromatin was used as input. Primer sequences for the sites analyzed by qPCR are in table S3.

Enzyme-linked immunosorbent assay

Mouse FGF21 in either plasma or pancreatic tissue was measured using a mouse FGF21 enzyme-linked immunosorbent assay (ELISA) kit (BioVendor).


The full-length mouse Fgf21 promoter (−1497/+5) firefly luciferase reporter construct and its truncated versions were generated as previously described (32). For AARE mutagenesis experiments, the full-length Fgf21 promoter reporter construct was mutated, as shown in Fig. 3D. Mouse ATF3 and ATF4 expression plasmids were purchased from GenScript. Empty expression vector [pcDNA3.1+/C-(K)DYK] was used as a control. The Renilla luciferase pRL-CMV reporter vector was used as the normalizing control in the dual-luciferase reporter assays (Promega). Mouse ATF3 siRNA was purchased as a pool of three to four targeting siRNAs (Santa Cruz Biotechnology).

Cell culture and transfection assays

266-6 cells were cultured in 10% fetal bovine serum in Dulbecco’s modified Eagle’s medium (DMEM) (Life Technologies) with antibiotics. Cells were transfected by incubating either plasmids or siRNA with Lipofectamine 2000 (Life Technologies) for 6 hours in serum and antibiotic-free DMEM in a 96-well plate. At 6 hours, the transfection medium was replaced with complete medium and the cells were incubated for another 18 hours. Cells were treated with vehicle, 100 nM cerulein, or 100 nM GSK2656157 for another 12 hours before measuring luciferase activity. Where indicated, 100 ng of Fgf21 promoter-luciferase or truncated versions was transfected per well. One nanogram of Atf3 or Atf4 expression plasmid and pRL-CMV (Renilla luciferase control) were cotransfected per well. The pcDNA3.1+/C-(K)DYK empty vector was used to bring the final amount of DNA to 200 ng per well. In the ATF3 dose response experiment, the ATF3 and pcDNA3.1+/C-(K)DYK amounts were modulated to reach the appropriate ATF3 dosing. Where indicated, 5 pmol of ATF3 siRNA was transfected. Cells were washed once in 1× PBS and lysed in 1× passive lysis buffer (Promega) and incubated for 15 min on an orbital shaker for 15 min before measuring luciferase activities with a dual-luciferase assay kit (Promega).

Human pancreatic tissue samples

Pancreas samples from 14 healthy individuals and 52 individuals with pancreatitis were procured via the University of Texas Southwestern Tissue Resource, a shared resource at the Simmons Comprehensive Cancer Center (UTSW CC), the National Disease Research Interchange (NDRI), and US Biomax (tissue arrays PA804a and BBS14011). The pancreas biopsies from patients were paraffin-embedded, sectioned, and H&E-stained by the UTSW CC. Pancreatitis was confirmed from the histological samples by the pathologist at the University of Texas Southwestern Tissue Resource. Tissue immunofluorescence for FGF21, ATF3, and ATF4 was performed as described above for paraffin-embedded sections. Clinical data corresponding to the samples analyzed and obtained either through the UTSW CC, NDRI, or US Biomax were de-identified and are available in data file S1. The samples from NDRI were procured and processed under protocol DKAM14 to M.A.K.

Statistical analyses

Nonparametric, two-tailed Student’s t test was used for two-group analyses. One-way and two-way analyses of variance (ANOVAs) with Newman-Keuls post hoc correction (GraphPad Prism) were used for multiple group analyses. Data are presented as the mean ± SEM; P < 0.05 was considered significant. Raw data from this study are available in data file S2.


Fig. S1. Experimental design and characterization of acute and chronic pancreatitis mouse models.

Fig. S2. Experimental design, histology, and gene expression data for FGF21 therapy experiments in three different models of pancreatitis.

Fig. S3. Atf3 and Atf4 expression in pancreatitis mouse models and ATF3 and ATF4 ChIP experimental controls.

Fig. S4. ATF3 and ATF4 expression in 266-6 cells.

Fig. S5. Model of FGF21’s protective role in pancreatitis.

Table S1. qPCR primer sequences.

Table S2. Primary antibody list.

Table S3. ChIP-qPCR primer sequences.

Data file S1. Human pancreas tissue donor information.

Data file S2. Raw numbers for each data point in each graph from the study.


Acknowledgments: We thank B. Andersen (Novo Nordisk) for providing recombinant FGF21 and Y. Zhang and M. Grzemska for their support with the mouse experiments. Funding: This work was supported by the NIH (grants R01DK067158 and P01AG051459 to S.A.K. and D.J.M.; grants R01DK093491 and R01DK103002 to S.Z.H.), the Robert A. Welch Foundation (grants I-1558 to S.A.K. and I-1275 to D.J.M.), a Ford Foundation Fellowship (to G.H.), the Juvenile Diabetes Research Foundation (SRA-2019-702-Q-R to M.A.K.), the UTSW NCI Cancer Center (grant 5P30CA142543 to S.A.K. and D.J.M.), and the Howard Hughes Medical Institute (to D.J.M.). Author contributions: G.H., S.Z.H., S.A.K., and D.J.M. designed the experiments and wrote the paper. G.H., T.L., T.A.J., L.W., M.A.K., F.A., and K.V. performed and analyzed experiments. S.Z.H., S.A.K., and D.J.M. supervised the project. All authors commented on and approved the paper. Competing interests: The FGF21 protein was provided by Novo Nordisk. G.H., S.A.K., and D.J.M. collaborate with and have received travel reimbursement from Novo Nordisk and are authors on a patent related to this work (“Methods and compositions for the treatment of secretory disorders”; US20190201490A1 and WO2017205517A1). Data and materials availability: All data related to this study can be found in the paper or Supplementary Materials. Mouse strains and plasmid DNA can be provided under a materials transfer agreement from UTSW.
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