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糖尿病中产生胰岛素原的骨髓来源细胞与肝细胞的融合。

Fusion of proinsulin-producing bone marrow-derived cells with hepatocytes in diabetes.

作者信息

Fujimiya Mineko, Kojima Hideto, Ichinose Masumi, Arai Ryohachi, Kimura Hiroshi, Kashiwagi Atsunori, Chan Lawrence

机构信息

Department of Anatomy, Section of Endocrinology and Metabolism, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.

出版信息

Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):4030-5. doi: 10.1073/pnas.0700220104. Epub 2007 Feb 27.

Abstract

We previously reported that diabetes in mice is associated with the appearance of proinsulin-producing (Proins-P) cells in the liver. It was unclear, however, whether these Proins-P bone marrow-derived cells (BMDC) merely transit through the liver or undergo fusion with hepatocytes, normally an extremely rare event. In this study, we found that, in diabetes, BMDC in the liver produce not only Proins but also TNF-alpha, suggesting that diabetes reprograms gene expression in BMDC, turning on "inappropriate" genes. Bone marrow transplantation using genetically marked donor and recipient mice showed that fusion occurs between Proins-P BMDC and hepatocytes. Cell fusion is further supported by the presence of the Y chromosome in Proins-P cells in female mice that received male bone marrow transplantation cells. Morphologically, Proins-P fusion cells are albumin-producing hepatocytes that constitute approximately 2.5% of the liver section area 5 months after diabetes induction. An extensive search failed to reveal any fusion cells in nondiabetic mice. Thus, diabetes causes fusion between Proins-P BMDC and hepatocytes in vivo, an observation that has implications for the pathophysiology of diabetes as well as the fundamental biology of heterotypic cell fusion.

摘要

我们之前报道过,小鼠中的糖尿病与肝脏中产生胰岛素原的(Proins-P)细胞的出现有关。然而,尚不清楚这些源自骨髓的Proins-P细胞(BMDC)是仅仅通过肝脏,还是与肝细胞发生融合,而肝细胞融合通常是极其罕见的事件。在本研究中,我们发现,在糖尿病状态下,肝脏中的BMDC不仅产生胰岛素原,还产生肿瘤坏死因子-α(TNF-α),这表明糖尿病会重新编程BMDC中的基因表达,开启“不适当”的基因。使用基因标记的供体和受体小鼠进行骨髓移植显示,Proins-P BMDC与肝细胞之间发生了融合。在接受雄性骨髓移植细胞的雌性小鼠的Proins-P细胞中存在Y染色体,这进一步支持了细胞融合的发生。从形态学上看,Proins-P融合细胞是产生白蛋白的肝细胞,在糖尿病诱导5个月后,它们约占肝脏切片面积的2.5%。广泛搜索未在非糖尿病小鼠中发现任何融合细胞。因此,糖尿病会导致Proins-P BMDC与肝细胞在体内发生融合,这一观察结果对糖尿病的病理生理学以及异型细胞融合的基础生物学具有重要意义。

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