Pancreatic Crosstalk in the Disease Setting: Understanding the Impact of Exocrine Disease on Endocrine Function

被引:0
|
作者
Villaca, Catharina B. P. [1 ]
Mastracci, Teresa L. [1 ,2 ,3 ]
机构
[1] Indiana Univ Indianapolis, Dept Biol, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Dept Biochem & Mol Biol, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Ctr Diabet & Metab Dis, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
BODY-MASS INDEX; DIABETES-MELLITUS SECONDARY; BETA-CELL DYSFUNCTION; CYSTIC-FIBROSIS GENE; NF-KAPPA-B; HEREDITARY PANCREATITIS; INSULIN-SECRETION; ISLET-CELL; BICARBONATE SECRETION; ZYMOGEN ACTIVATION;
D O I
10.1002/cphy.c230008
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The exocrine and endocrine are functionally distinct compartments of the pancreas that have traditionally been studied as separate entities. However, studies of embryonic development, adult physiology, and disease pathogenesis suggest there may be critical communication between exocrine and endocrine cells. In fact, the incidence of the endocrine disease diabetes secondary to exocrine disease/dysfunction ranges from 25% to 80%, depending on the type and severity of the exocrine pathology. Therefore, it is necessary to investigate how exocrine-endocrine "crosstalk" may impact pancreatic function. In this article, we discuss common exocrine diseases, including cystic fibrosis, acute, hereditary, and chronic pancreatitis, and the impact of these exocrine diseases on endocrine function. Additionally, we review how obesity and fatty pancreas influence exocrine function and the impact on cellular communication between the exocrine and endocrine compartments. Interestingly, in all pathologies, there is evidence that signals from the exocrine disease contribute to endocrine dysfunction and the progression to diabetes. Continued research efforts to identify the mechanisms that underlie the crosstalk between various cell types in the pancreas are critical to understanding normal pancreatic physiology as well as disease states. (c) 2024 American Physiological Society. Compr Physiol 14:5371-5387, 2024.
引用
收藏
页码:5371 / 5387
页数:17
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