Phillipson-Weiner Lindsey, Mirek Emily T, Wang Yongping, McAuliffe W Geoffrey, Wek Ronald C, Anthony Tracy G
Department of Nutritional Sciences, Rutgers, The State University of New Jersey, New Brunswick, New Jersey;
Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, New Brunswick, New Jersey; and.
Am J Physiol Gastrointest Liver Physiol. 2016 Jun 1;310(11):G1061-70. doi: 10.1152/ajpgi.00052.2016. Epub 2016 Mar 11.
Treatment with the antileukemic agent asparaginase can induce acute pancreatitis, but the pathophysiology remains obscure. In the liver of mice, eukaryotic initiation factor 2 (eIF2) kinase general control nonderepressible 2 (GCN2) is essential for mitigating metabolic stress caused by asparaginase. We determined the consequences of asparaginase treatment on the pancreata of wild-type (WT, GCN2-intact) and GCN2-deleted (ΔGcn2) mice. Mean pancreas weights in ΔGcn2 mice treated with asparaginase for 8 days were increased (P < 0.05) above all other groups. Histological examination revealed acinar cell swelling and altered staining of zymogen granules in ΔGcn2, but not WT, mice. Oil Red O staining and measurement of pancreas triglycerides excluded lipid accumulation as a contributor to acini appearance. Instead, transmission electron microscopy revealed dilatation of the endoplasmic reticulum (ER) and accumulation of autophagic vacuoles in the pancreas of ΔGcn2 mice treated with asparaginase. Consistent with the idea that loss of GCN2 in a pancreas exposed to asparaginase induced ER stress, phosphorylation of protein kinase R-like ER kinase (PERK) and its substrate eIF2 was increased in the pancreas of asparaginase-treated ΔGcn2 mice. In addition, mRNA expression of PERK target genes, activating transcription factors 4, 3, and 6 (Atf4, Atf3, and Atf6), fibroblast growth factor 21 (Fgf21), heat shock 70-kDa protein 5 (Hspa5), and spliced Xbp1 (sXbp1), as well as pancreas mass, was elevated in the pancreas of asparaginase-treated ΔGcn2 mice. Furthermore, genetic markers of oxidative stress [sirtuin (Sirt1)], inflammation [tumor necrosis factor-α (Tnfα)], and pancreatic injury [pancreatitis-associated protein (Pap)] were elevated in asparaginase-treated ΔGcn2, but not WT, mice. These data indicate that loss of GCN2 predisposes the exocrine pancreas to a maladaptive ER stress response and autophagy during asparaginase treatment and represent a genetic basis for development of asparaginase-associated pancreatitis.
使用抗白血病药物天冬酰胺酶进行治疗可诱发急性胰腺炎,但其病理生理学机制仍不清楚。在小鼠肝脏中,真核起始因子2(eIF2)激酶一般控制非抑制性2(GCN2)对于减轻由天冬酰胺酶引起的代谢应激至关重要。我们确定了天冬酰胺酶治疗对野生型(WT,GCN2完整)和GCN2缺失(ΔGcn2)小鼠胰腺的影响。用天冬酰胺酶治疗8天的ΔGcn2小鼠的平均胰腺重量比所有其他组都增加了(P<0.05)。组织学检查显示,ΔGcn2小鼠而非WT小鼠出现腺泡细胞肿胀和酶原颗粒染色改变。油红O染色和胰腺甘油三酯测量排除了脂质积累是腺泡外观改变的原因。相反,透射电子显微镜显示,用天冬酰胺酶治疗的ΔGcn2小鼠胰腺中内质网扩张和自噬泡积累。与暴露于天冬酰胺酶的胰腺中GCN2缺失诱导内质网应激的观点一致,在经天冬酰胺酶治疗的ΔGcn2小鼠胰腺中,蛋白激酶R样内质网激酶(PERK)及其底物eIF2的磷酸化增加。此外,在经天冬酰胺酶治疗的ΔGcn2小鼠胰腺中,PERK靶基因、激活转录因子4、3和6(Atf4、Atf3和Atf6)、成纤维细胞生长因子21(Fgf21)、热休克70 kDa蛋白5(Hspa5)和剪接的Xbp1(sXbp1)的mRNA表达以及胰腺质量均升高。此外,在经天冬酰胺酶治疗的ΔGcn2小鼠而非WT小鼠中,氧化应激的遗传标记[沉默调节蛋白(Sirt1)]、炎症[肿瘤坏死因子-α(Tnfα)]和胰腺损伤[胰腺炎相关蛋白(Pap)]升高。这些数据表明,在天冬酰胺酶治疗期间,GCN2缺失使外分泌胰腺易发生适应性内质网应激反应和自噬,这代表了天冬酰胺酶相关性胰腺炎发生的遗传基础。