cdk5rap3介导的溶酶体和ER膜蛋白的调控对胰腺腺泡细胞的存活和功能至关重要。

IF 4.7 2区 生物学 Q2 CELL BIOLOGY
Yonghong Huang, Feng Zhou, Xin Xu, Yaqun Wang, Michaela Quintero, Siyang Liu, Cong Liu, Guangxun Zhu, Yafei Cai, Zheng Dong, Roni Bollag, Guangyu Wu, Maria Eugenia Sabbatini, Honglin Li
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引用次数: 0

摘要

腺泡是外分泌胰腺的功能单位,产生和分泌大量的消化酶。胰腺腺泡细胞(PACs)的损伤和功能障碍可能导致营养不良、胰腺炎和其他病理状况。Cdk5rap3是一种多功能蛋白,对动物发育和多器官组织的正常生理至关重要。有趣的是,最近的研究表明它参与内质网吞噬,内质网亚结构域的溶酶体降解。在此,我们试图研究其在胰腺腺泡细胞中的生理功能。我们发现Cdk5rap3缺陷的PACs含有较少的酶原颗粒,并发生腺泡到导管化生(ADM)和细胞凋亡,从而导致腺泡间室的显著丧失。有趣的是,Cdk5rap3消融导致溶酶体水解酶组织蛋白酶B和溶酶体蛋白LAMP1的增加,表明其在调节溶酶体稳态和活性中的新功能。组织蛋白酶B活性升高可导致胰蛋白酶原异常活化,导致Cdk5rap3缺陷的腺泡细胞凋亡,而溶酶体蛋白的增加可增强溶酶体活性,进而促进adm的发生。此外,敲除Cdk5rap3可导致内质网粗结构发生显著变化,包括CLIMP63在内的选择性内质网膜蛋白显著增加。我们对小鼠组织和组织培养细胞的研究结果强烈表明,Cdk5rap3在调节溶酶体和内质网的稳态中起关键作用,这对胰腺腺泡细胞的存活和生理功能至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cdk5rap3-mediated regulation of lysosomal and ER membrane proteins is pivotal for the survival and function of pancreatic acinar cells.

The acinus is the functional unit of the exocrine pancreas that produces and secretes a large quantity of digestive enzymes. Damage and dysfunction of pancreatic acinar cells (PACs) may lead to malnutrition, pancreatitis, and other pathological conditions. CDK5 regulatory subunit-associated protein 3 (Cdk5rap3), a multifunctional protein, is essential for animal development and normal physiology of multiple organs and tissues. Interestingly, the recent studies suggest its involvement in endoplasmic reticulum (ER)-phagy, a lysosomal degradation of the subdomains of the endoplasmic reticulum (ER). Herein, we attempted to investigate its physiological function in pancreatic acinar cells. We found that Cdk5rap3-deficient PACs contained fewer zymogen granules and underwent acinar-to-ductal metaplasia (ADM) and apoptosis, thereby resulting in a significant loss of acinar compartment. Interestingly, Cdk5rap3 ablation led to the increase of lysosomal hydrolase cathepsin B and lysosome-associated membrane protein 1 (LAMP1), indicating its novel function in the regulation of lysosomal homeostasis and activity. Elevated cathepsin B activity may lead to aberrant activation of trypsinogen and apoptosis of Cdk5rap3-deficient acinar cells, whereas the increase of lysosomal proteins may enhance lysosomal activity that in turn promotes ADM. Furthermore, Cdk5rap3 knockout led to substantial changes in the rough ER structure and a significant increase in selective ER membrane proteins, including cytoskeleton-linking membrane protein 63 (CLIMP63). Our results from both mouse tissues and tissue culture cells strongly suggest that Cdk5rap3 plays a pivotal role in regulating homeostasis of the lysosome and the ER that is essential for the survival and physiological function of pancreatic acinar cells.NEW & NOTEWORTHY Our current study has demonstrated a critical role of Cdk5rap3 protein in the maintenance and function of pancreatic acinar cells. Cdk5rap3 functions as a key regulator of the homeostasis of subcellular organelles, such as the lysosome and the ER, and its deficiency leads to loss of pancreatic mass and may contribute to the pathogenesis of pancreatic diseases.

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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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