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EMC3对小鼠肠道上皮细胞中CFTR功能和钙动员至关重要。

EMC3 is critical for CFTR function and calcium mobilization in the mouse intestinal epithelium.

作者信息

Penrod Sarah, Tang Xiaofang, Moon Changsuk, Whitsett Jeffrey A, Naren Anjaparavanda P, Huang Yunjie

机构信息

Division of Pediatric Pulmonology, Allergy, and Sleep Medicine, Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana, United States.

Division of Neonatology, Perinatal and Pulmonary Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2025 Jan 1;328(1):G72-G82. doi: 10.1152/ajpgi.00066.2024. Epub 2024 Dec 6.

Abstract

Membrane proteins, such as the cystic fibrosis transmembrane-conductance regulator (CFTR), play a crucial role in gastrointestinal functions and health. Endoplasmic reticulum (ER) membrane protein complex (EMC), a multi-subunit insertase, mediates the incorporation of membrane segments into lipid bilayers during protein synthesis. Whether EMC regulates membrane proteins' processing and function in intestinal epithelial cells remains unclear. To investigate the role of EMC in the intestinal epithelium, we generated mice in which EMC subunit 3 (EMC3) was deleted in intestinal epithelial cells (EMC3). EMC3 mice were viable but notably smaller compared with their wild-type littermates. Although the intestinal structure was generally maintained, EMC3 crypts exhibited altered morphology, particularly at the base of the crypts with decreased goblet cells and paneth cells. Levels of multiple polytopic membrane proteins, including CFTR, were decreased in EMC3-deficient epithelial cells. Several calcium ATPase pumps were downregulated, and calcium mobilization was impaired in EMC3 enteroids. CFTR-mediated organoid swelling in EMC3 mice was impaired in response to both cAMP-dependent signaling and calcium-secretagogue stimulation. Our study demonstrated that EMC plays a critical role in maintaining intestinal epithelium homeostasis by regulating membrane protein biogenesis and intracellular calcium homeostasis. Maintaining intracellular calcium homeostasis may be a universal cellular function regulated by EMC. We generated mice in which endoplasmic reticulum membrane protein complex (EMC) subunit 3 was deleted from intestinal epithelium cells and studied the molecular functions of EMC in vivo. Our findings demonstrate the importance of intestinal EMC in the biogenesis of membrane proteins in vivo, including CFTR, and highlight its critical role in maintaining intracellular calcium homeostasis and, consequently, in calcium-dependent functions in the intestine and beyond.

摘要

膜蛋白,如囊性纤维化跨膜传导调节因子(CFTR),在胃肠道功能和健康中起着至关重要的作用。内质网(ER)膜蛋白复合物(EMC)是一种多亚基插入酶,在蛋白质合成过程中介导膜片段插入脂质双层。EMC是否调节肠上皮细胞中膜蛋白的加工和功能仍不清楚。为了研究EMC在肠上皮中的作用,我们构建了在肠上皮细胞中缺失EMC亚基3(EMC3)的小鼠(EMC3小鼠)。EMC3小鼠能够存活,但与野生型同窝小鼠相比明显更小。尽管肠道结构总体上得以维持,但EMC3隐窝表现出形态改变,特别是在隐窝底部,杯状细胞和潘氏细胞减少。在EMC3缺陷的上皮细胞中,包括CFTR在内的多种多聚体膜蛋白水平降低。几种钙ATP酶泵下调,并且EMC3肠类器官中的钙动员受损。在EMC3小鼠中,CFTR介导的类器官肿胀在对cAMP依赖性信号和钙分泌刺激的反应中受损。我们的研究表明,EMC通过调节膜蛋白生物合成和细胞内钙稳态在维持肠上皮稳态中起关键作用。维持细胞内钙稳态可能是由EMC调节的一种普遍细胞功能。我们构建了从肠上皮细胞中缺失内质网膜蛋白复合物(EMC)亚基3的小鼠,并在体内研究了EMC的分子功能。我们的研究结果证明了肠道EMC在体内膜蛋白生物合成(包括CFTR)中的重要性,并突出了其在维持细胞内钙稳态以及因此在肠道及其他部位的钙依赖性功能中的关键作用。

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