To assess whether cell to cell communications via connexins (Cx) participate to insulin secretion in vivo, we studied insulinoma cells (INS1) implanted in rats after stable transfection with connexin 43 (Cx43). We found that compared to wild-type and transfected cells, which in vivo express modest levels of Cx43 and junctional communication, cells overexpressing Cx43 communicated extensively, featured decreased growth, and induced a much higher hyperinsulinemia. As a result, rats with insulinomas made of these cells became more severely hypoglycemic than rats implanted with either wild-type, neomycin-transfected cells or cells transfected with a Cx43 antisense complementary DNA. Rats implanted with transfected cells that expressed modest level of Cx43 showed levels of circulating insulin similar to those in rats implanted with wild-type INS1 cells. The data show that overexpression of Cx43 influences the growth and secretion of the implanted insulinoma cells, providing evidence for a contribution of Cx-mediated cell to cell communication in the functioning of insulin-producing cells in vivo.

译文

为了评估通过连接蛋白(Cx)进行的细胞间通信是否参与体内胰岛素分泌,我们研究了用连接蛋白43(Cx43)稳定转染后在大鼠体内植入的胰岛素瘤细胞(INS1)。我们发现,与野生型和转染细胞相比,在体内表达适度水平的Cx43和交界处的通讯,过表达Cx43的细胞广泛地通讯,其特征是生长减少,并诱导更高的高胰岛素血症。结果,与植入野生型新霉素转染的细胞或转染了Cx43反义互补DNA的细胞的大鼠相比,由这些细胞制成的胰岛素瘤大鼠的降血糖作用更为严重。植入表达Cx43水平适度的转染细胞的大鼠,其循环胰岛素水平与植入野生型INS1细胞的大鼠相似。数据表明,Cx43的过表达影响植入的胰岛素瘤细胞的生长和分泌,为Cx介导的细胞在体内胰岛素产生细胞的功能中对细胞通讯的贡献提供了证据。

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