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胰岛样细胞簇接触胰岛(ATLANTIS)的 Reg I 在 EMC 病毒诱导的糖尿病小鼠β细胞有丝分裂中的关键作用。

Crucial role of Reg I from acinar-like cell cluster touching with islets (ATLANTIS) on mitogenesis of beta cells in EMC virus-induced diabetic mice.

机构信息

Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Yamanashi, Japan.

Division of Immunology and Molecular Medicine, Okinaka Memorial Institute for Medical Research, Tokyo, Japan; Department of Endocrinology and Metabolism, Toranomon Hospital, Tokyo, Japan.

出版信息

Biochem Biophys Res Commun. 2018 Sep 5;503(2):963-969. doi: 10.1016/j.bbrc.2018.06.103. Epub 2018 Jun 28.

Abstract

Recently, we reported the presence of distinct cell clusters named acinar-like cell clusters touching Langerhans islets with thin interstitial surrounding (ATLANTIS) in human pancreas. A morphological study in humans demonstrated that ATLANTIS and islet cell clusters are found together in the microenvironment enclosed by a common basement membrane, and ATLANTIS releases vesicles containing Regenerating gene protein (REG Iα) to islet cell clusters. We examined 1) the presence or absence of ATLANTIS in homozygous Reg I (mouse homologue of human REG Iα) deficient (Reg I) and wild-type mice, and 2) the possible role of ATLANTIS in the regeneration of beta cell clusters after encephalomyocarditis (EMC) virus (D-variant) infection in Reg I and wild-type mice. ATLANTIS was found in both wild-type and Reg I mice. In both groups, mean blood glucose increased transiently to greater than 14.0 mmol/L at 5 days after EMC virus infection and recovered to baseline at 12 days. At 12 days after EMC virus infection, lower BrdU labeling indices were observed in islet beta cells of Reg I mice compared to wild-type mice. Beta cell volume 12 days after EMC virus infection in Reg I mice did not differ from that of wild-type mice. These results suggest that Reg I, which is released from ATLANTIS to islet beta cell clusters, has a crucial role in beta cell regeneration in EMC virus-induced diabetes. The presence of mechanism(s) other than that mediated by Reg I in beta cell restoration after destruction by EMC virus was also suggested.

摘要

最近,我们报道了在人类胰腺中存在着一种名为腺泡样细胞簇的独特细胞簇,这些细胞簇与胰岛接触,周围有薄的间质(ATLANTIS)。在人类中的形态学研究表明,ATLANTIS 和胰岛细胞簇一起存在于由共同基底膜包围的微环境中,ATLANTIS 释放含有再生基因蛋白 (REG Iα) 的囊泡到胰岛细胞簇。我们检查了 1)在同源性 Reg I(人类 REG Iα 的小鼠同源物)缺陷(Reg I)和野生型小鼠中 ATLANTIS 的存在或缺失,以及 2)ATLANTIS 在 EMC 病毒(D-变体)感染后胰岛细胞簇再生中的可能作用在 Reg I 和野生型小鼠中。在野生型和 Reg I 小鼠中均发现了 ATLANTIS。在两组中,平均血糖在 EMC 病毒感染后 5 天短暂升高至 14.0mmol/L 以上,并在 12 天恢复至基线。在 EMC 病毒感染后 12 天,Reg I 小鼠的胰岛β细胞中 BrdU 标记指数低于野生型小鼠。Reg I 小鼠在 EMC 病毒感染后 12 天的β细胞体积与野生型小鼠无差异。这些结果表明,从 ATLANTIS 释放到胰岛β细胞簇的 REG I 在 EMC 病毒诱导的糖尿病中β细胞再生中起着至关重要的作用。还提示了在 EMC 病毒破坏后,除了由 REG I 介导的机制之外,还存在其他机制来恢复β细胞。

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