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Calpain 8/nCL-2 and Calpain 9/nCL-4 Constitute an Active Protease Complex, G-Calpain, Involved in Gastric Mucosal Defense

机译:钙蛋白酶8 / nCL-2和钙蛋白酶9 / nCL-4组成一种活性蛋白酶复合物G-钙蛋白酶,参与胃粘膜防御。

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摘要

Calpains constitute a superfamily of Ca2+-dependent cysteine proteases, indispensable for various cellular processes. Among the 15 mammalian calpains, calpain 8/nCL-2 and calpain 9/nCL-4 are predominantly expressed in the gastrointestinal tract and are restricted to the gastric surface mucus (pit) cells in the stomach. Possible functions reported for calpain 8 are in vesicle trafficking between ER and Golgi, and calpain 9 are implicated in suppressing tumorigenesis. These highlight that calpains 8 and 9 are regulated differently from each other and from conventional calpains and, thus, have potentially important, specific functions in the gastrointestinal tract. However, there is no direct evidence implicating calpain 8 or 9 in human disease, and their properties and physiological functions are currently unknown. To address their physiological roles, we analyzed mice with mutations in the genes for these calpains, Capn8 and Capn9. Capn8−/− and Capn9−/− mice were fertile, and their gastric mucosae appeared normal. However, both mice were susceptible to gastric mucosal injury induced by ethanol administration. Moreover, the Capn8−/− stomach showed significant decreases in both calpains 9 and 8, and the same was true for Capn9−/−. Consistent with this finding, in the wild-type stomach, calpains 8 and 9 formed a complex we termed “G-calpain,” in which both were essential for activity. This is the first example of a “hybrid” calpain complex. To address the physiological relevance of the calpain 8 proteolytic activity, we generated calpain 8:C105S “knock-in” (Capn8CS/CS) mice, which expressed a proteolytically inactive, but structurally intact, calpain 8. Although, unlike the Capn8−/− stomach, that of the Capn8CS/CS mice expressed a stable and active calpain 9, the mice were susceptible to ethanol-induced gastric injury. These results provide the first evidence that both of the gastrointestinal-tract-specific calpains are essential for gastric mucosal defense, and they point to G-calpain as a potential target for gastropathies caused by external stresses.
机译:钙蛋白酶构成了Ca2 +依赖的半胱氨酸蛋白酶的超家族,对于各种细胞过程都是必不可少的。在15种哺乳动物钙蛋白酶中,钙蛋白酶8 / nCL-2和钙蛋白酶9 / nCL-4主要在胃肠道中表达,并局限于胃中的胃表面粘液(凹坑)细胞。关于钙蛋白酶8的可能功能是在内质网与高尔基体之间的囊泡运输中,而钙蛋白酶9与抑制肿瘤发生有关。这些突显了钙蛋白酶8和9彼此之间的调节和与常规钙蛋白酶的调节不同,因此在胃肠道中具有潜在重要的特定功能。但是,尚无直接证据表明钙蛋白酶8或9与人类疾病有关,并且它们的性质和生理功能目前尚不清楚。为了解决它们的生理作用,我们分析了这些钙蛋白酶Capn8和Capn9基因突变的小鼠。 Capn8-/-和Capn9-/-小鼠可育,胃粘膜正常。但是,两只小鼠都容易受到乙醇给药引起的胃粘膜损伤。此外,Capn8-/-胃在钙蛋白酶9和8中均显示出显着降低,而对于Capn9-/-而言同样如此。与此发现一致的是,在野生型胃中,钙蛋白酶8和9形成了我们称为“ G-钙蛋白酶”的复合物,其中两者都是必需的。这是“混合”钙蛋白酶复合物的第一个例子。为了解决钙蛋白酶8蛋白水解活性的生理相关性,我们生成了钙蛋白酶8:C105S“敲入”(Capn8CS / CS)小鼠,该小鼠表达了蛋白酶水解但结构完整的钙蛋白酶8。尽管与Capn8- / −胃,Capn8CS / CS小鼠的胃中表达稳定且活跃的钙蛋白酶9,这些小鼠易受乙醇诱导的胃损伤。这些结果提供了第一个证据,即两种胃肠道特异的钙蛋白酶对于胃粘膜防御都是必不可少的,并且它们都指出G-钙蛋白酶是外在压力引起的胃病的潜在靶标。

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