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Aquaporin 7 Is a β-Cell Protein and Regulator of Intraislet Glycerol Content and Glycerol Kinase Activity, β-Cell Mass, and Insulin Production and Secretion▿ †

机译:Aquaporin 7是一种β细胞蛋白,是胰岛内甘油含量和甘油激酶活性,β细胞质量以及胰岛素产生和分泌的调节剂。

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摘要

To investigate if intracellular glycerol content plays a role in the regulation of insulin secretion in pancreatic β cells, we studied the expression of the glycerol channels, or aquaglyceroporins, encoded by the aquaporin 3 (Aqp3), Aqp7, and Aqp9 genes in mouse islets. We found expression of Aqp7 only, not that of Aqp3 or Aqp9, in the endocrine pancreas at both the mRNA (by reverse transcription-PCR) and protein (by immunohistochemistry) levels. Immunohistochemistry revealed a complete overlap between insulin and Aqp7 immunostaining in the pancreatic islet. Inactivation of Aqp7 by gene targeting produced viable and healthy mice. Aqp7−/− mice harbored an increased intraislet glycerol concentration with a concomitant increase of the glycerol kinase transcript level and enzyme activity. The islet triglyceride content in the Aqp7−/− mice was also increased compared to that in the Aqp7+/+ mice. Interestingly, Aqp7−/− mice displayed reduced β-cell mass and insulin content but increased insulin-1 and insulin-2 mRNAs. The reduction of β-cell mass in Aqp7−/− mice can be explained at least in part by a reduction in cell proliferation through protein kinase C and the c-myc cascade, with a reduction in the transcript levels of these two genes. Concomitantly, there was a decreased rate of apoptosis, as reflected by terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling and caspase 3 and Bax expression in Aqp7−/− mice. Compared with Aqp7+/+ islets, islets isolated from Aqp7−/− mice secreted insulin at a higher rate under basal low-glucose conditions and on exposure to a high (450 mg/dl) glucose concentration. Aqp7−/− mice exhibited normal fasting blood glucose levels but elevated blood insulin levels. Their plasma glucose response to an intraperitoneal (i.p.) glucose tolerance test was normal, but their plasma insulin concentrations were higher than those of wild-type mice during the 2-h test. An i.p. insulin tolerance test showed similar plasma glucose lowering in Aqp7−/− and Aqp7+/+ mice, with no evidence of insulin resistance. In conclusion, we found that pancreatic β cells express AQP7, which appears to be a key regulator of intraislet glycerol content as well as insulin production and secretion.
机译:为了研究细胞内甘油含量是否在胰腺β细胞中胰岛素分泌的调节中发挥作用,我们研究了小鼠胰岛中水通道3(Aqp3),Aqp7和Aqp9基因编码的甘油通道或水甘油孔蛋白的表达。我们发现内分泌胰腺仅在mRNA(通过逆转录PCR)和蛋白(通过免疫组织化学)水平表达Aqp7,而不是Aqp3或Aqp9。免疫组化显示胰岛中胰岛素和Aqp7免疫染色之间完全重叠。通过基因靶向使Aqp7失活可产生健康的小鼠。 Aqp7 //-小鼠的胰岛内甘油浓度升高,甘油激酶转录水平和酶活性也随之升高。与Aqp7 + / +小鼠相比,Aqp7-/-小鼠的胰岛甘油三酯含量也增加了。有趣的是,Aqp7-/-小鼠的β细胞量和胰岛素含量降低,但胰岛素1和胰岛素2 mRNA升高。 Aqp7-/-小鼠中β细胞质量的降低至少可以部分解释为通过蛋白激酶C和c-myc级联的细胞增殖减少,以及这两个基因的转录水平降低。同时,凋亡减少的速率降低了,这是由末端脱氧核苷酸转移酶介导的dUTP-生物素缺口末端标记以及caspase 3和Bax在Aqp7-/-小鼠中的表达所反映的。与Aqp7 + / +胰岛相比,从Aqp7-/-小鼠分离的胰岛在基础低葡萄糖条件下以及暴露于高(450 mg / dl)葡萄糖浓度时分泌胰岛素的速率更高。 Aqp7-/-小鼠表现出正常的空腹血糖水平,但血液胰岛素水平升高。他们对腹膜内(i.p.)葡萄糖耐量试验的血浆葡萄糖反应正常,但在2小时试验中其血浆胰岛素浓度高于野生型小鼠。一个IP胰岛素耐受性测试显示,Aqp7-/-和Aqp7 + / +小鼠血浆葡萄糖降低相似,没有胰岛素抵抗的迹象。总之,我们发现胰腺β细胞表达AQP7,它似乎是胰岛内甘油含量以及胰岛素产生和分泌的关键调节剂。

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