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参与胰岛细胞形成的细胞外基质蛋白。

Extracellular matrix proteins involved in pseudoislets formation.

机构信息

Centre Européen d'Etude du Diabète, Strasbourg, France.

出版信息

Islets. 2009 Nov-Dec;1(3):232-41. doi: 10.4161/isl.1.3.9754.

DOI:10.4161/isl.1.3.9754
PMID:21099277
Abstract

Extracellular matrix proteins are known to mediate, through integrins, cell adhesion and are involved in a number of cellular processes, including insulin expression and secretion in pancreatic islets. We investigated whether expression of some extracellular matrix proteins were implied in islets-like structure formation, named pseudoislets. For this purpose, we cultured the β-cell line, RINm5F, during 1, 3, 5 and 7 days of culture on treated or untreated culture plate to form adherent cells or pseudoislets and analysed insulin, collagen IV, fibronectin, laminin 5 and β1-integrin expression. We observed that insulin expression and secretion were increased during pseudoislets formation. Moreover, we showed by immunohistochemistry an aggregation of insulin secreting cells in the centre of the pseudoislets. Peripheral β-cells of pseudoislets did not express insulin after 7 days of culture. RT-PCR and immunohistochemistry studies showed a transient expression of type IV collagen in pseudoislets for the first 3 days of culture. Study of fibronectin expression indicated that adherent cells expressed more fibronectin than pseudoislets. In contrast, laminin 5 was more expressed in pseudoislets than in adherent cells. Finally, expression of β1-integrin was increased in pseudoislets as compared to adherent cells. In conclusion, laminin 5 and collagen IV might be implicated in pseudoislets formation whereas fibronectin might be involved in cell adhesion. These data suggested that extracellular matrix proteins may enhance the function of pseudoislets.

摘要

细胞外基质蛋白通过整合素介导细胞黏附,并参与许多细胞过程,包括胰岛中胰岛素的表达和分泌。我们研究了一些细胞外基质蛋白的表达是否与胰岛样结构的形成有关,这些结构被称为拟胰岛。为此,我们将β细胞系 RINm5F 在经过处理或未经处理的培养板上培养 1、3、5 和 7 天,以形成贴壁细胞或拟胰岛,并分析胰岛素、IV 型胶原、纤连蛋白、层粘连蛋白 5 和β1-整合素的表达。我们观察到在拟胰岛形成过程中胰岛素的表达和分泌增加。此外,我们通过免疫组织化学显示胰岛素分泌细胞在拟胰岛的中心聚集。在培养 7 天后,拟胰岛的外周β细胞不再表达胰岛素。RT-PCR 和免疫组织化学研究表明,在培养的前 3 天,IV 型胶原在拟胰岛中呈瞬时表达。纤连蛋白表达的研究表明,贴壁细胞比拟胰岛表达更多的纤连蛋白。相反,层粘连蛋白 5 在拟胰岛中的表达多于贴壁细胞。最后,β1-整合素的表达在拟胰岛中比在贴壁细胞中增加。总之,层粘连蛋白 5 和 IV 型胶原可能参与拟胰岛的形成,而纤连蛋白可能参与细胞黏附。这些数据表明细胞外基质蛋白可能增强拟胰岛的功能。

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