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Autophagy and pancreatitis.自噬与胰腺炎。
Am J Physiol Gastrointest Liver Physiol. 2012 Nov 1;303(9):G993-G1003. doi: 10.1152/ajpgi.00122.2012. Epub 2012 Sep 6.
2
Impaired autophagy and organellar dysfunction in pancreatitis.胰腺炎中的自噬受损和细胞器功能障碍。
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VMP1 Constitutive Expression in Mice Dampens Pancreatic and Systemic Histopathological Damage in an Experimental Model of Severe Acute Pancreatitis.VMP1在小鼠中的组成性表达减轻了重症急性胰腺炎实验模型中的胰腺和全身组织病理学损伤。
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Ubiquitin-specific protease 7 exacerbates acute pancreatitis progression by enhancing ATF4-mediated autophagy.泛素特异性蛋白酶7通过增强ATF4介导的自噬加重急性胰腺炎的进展。
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Recent insights about autophagy in pancreatitis.胰腺炎中自噬的最新见解。
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本文引用的文献

1
Guidelines for the use and interpretation of assays for monitoring autophagy.自噬监测分析方法的使用和解读指南
Autophagy. 2012 Apr;8(4):445-544. doi: 10.4161/auto.19496.
2
Impaired autophagy and organellar dysfunction in pancreatitis.胰腺炎中的自噬受损和细胞器功能障碍。
J Gastroenterol Hepatol. 2012 Mar;27 Suppl 2(Suppl 2):27-32. doi: 10.1111/j.1440-1746.2011.07004.x.
3
Interleukin-22 ameliorates cerulein-induced pancreatitis in mice by inhibiting the autophagic pathway.白细胞介素-22 通过抑制自噬通路减轻小鼠雨蛙肽诱导的胰腺炎。
Int J Biol Sci. 2012;8(2):249-57. doi: 10.7150/ijbs.3967. Epub 2012 Jan 6.
4
p62 at the interface of autophagy, oxidative stress signaling, and cancer.p62 在自噬、氧化应激信号和癌症的界面。
Antioxid Redox Signal. 2012 Sep 1;17(5):786-93. doi: 10.1089/ars.2011.4394. Epub 2012 Jan 11.
5
Digesting new information about the role of trypsin in pancreatitis.消化有关胰蛋白酶在胰腺炎中作用的新信息。
Gastroenterology. 2011 Dec;141(6):1972-5. doi: 10.1053/j.gastro.2011.10.021. Epub 2011 Oct 25.
6
Intra-acinar trypsinogen activation mediates early stages of pancreatic injury but not inflammation in mice with acute pancreatitis.腺泡内胰蛋白酶原激活介导急性胰腺炎小鼠胰腺损伤的早期阶段,但不介导炎症反应。
Gastroenterology. 2011 Dec;141(6):2210-2217.e2. doi: 10.1053/j.gastro.2011.08.033. Epub 2011 Aug 27.
7
Mitochondria and the autophagy-inflammation-cell death axis in organismal aging.线粒体与衰老过程中自噬-炎症-细胞死亡轴
Science. 2011 Aug 26;333(6046):1109-12. doi: 10.1126/science.1201940.
8
Organellar dysfunction in the pathogenesis of pancreatitis.细胞器功能障碍在胰腺炎发病机制中的作用。
Antioxid Redox Signal. 2011 Nov 15;15(10):2699-710. doi: 10.1089/ars.2011.4068. Epub 2011 Aug 11.
9
The role of Atg proteins in autophagosome formation.自噬体形成中 Atg 蛋白的作用。
Annu Rev Cell Dev Biol. 2011;27:107-32. doi: 10.1146/annurev-cellbio-092910-154005. Epub 2011 Jul 18.
10
Pathophysiological role of autophagy: lesson from autophagy-deficient mouse models.自噬的病理生理学作用:自噬缺陷小鼠模型的启示。
Exp Anim. 2011;60(4):329-45. doi: 10.1538/expanim.60.329.

自噬与胰腺炎。

Autophagy and pancreatitis.

机构信息

Veterans Affairs Greater Los Angeles Healthcare System and University of California at Los Angeles, Los Angeles, CA 90073, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2012 Nov 1;303(9):G993-G1003. doi: 10.1152/ajpgi.00122.2012. Epub 2012 Sep 6.

DOI:10.1152/ajpgi.00122.2012
PMID:22961802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3517664/
Abstract

Acute pancreatitis is an inflammatory disease of the exocrine pancreas that carries considerable morbidity and mortality; its pathophysiology remains poorly understood. Recent findings from experimental models and genetically altered mice summarized in this review reveal that autophagy, the principal cellular degradative pathway, is impaired in pancreatitis and that one cause of autophagy impairment is defective function of lysosomes. We propose that the lysosomal/autophagic dysfunction is a key initiating event in pancreatitis and a converging point of multiple deranged pathways. There is strong evidence supporting this hypothesis. Investigation of autophagy in pancreatitis has just started, and many questions about the "upstream" mechanisms mediating the lysosomal/autophagic dysfunction and the "downstream" links to pancreatitis pathologies need to be explored. Answers to these questions should provide insight into novel molecular targets and therapeutic strategies for treatment of pancreatitis.

摘要

急性胰腺炎是一种胰腺外分泌的炎症性疾病,具有相当高的发病率和死亡率;其病理生理学仍未被很好地理解。本综述总结了实验模型和基因改变小鼠的最新发现,揭示了自噬,即主要的细胞降解途径,在胰腺炎中受损,自噬受损的一个原因是溶酶体功能缺陷。我们提出,溶酶体/自噬功能障碍是胰腺炎的一个关键起始事件,也是多种紊乱途径的汇聚点。有强有力的证据支持这一假设。对胰腺炎中自噬的研究才刚刚开始,许多关于介导溶酶体/自噬功能障碍的“上游”机制以及与胰腺炎病理的“下游”联系的问题需要探索。这些问题的答案应该为治疗胰腺炎的新的分子靶点和治疗策略提供深入了解。