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过氧化物酶体增殖物激活受体γ(PPARγ)在正常人胰岛细胞中的表达。

Expression of peroxisome proliferator-activated receptor gamma (PPARgamma) in normal human pancreatic islet cells.

作者信息

Dubois M, Pattou F, Kerr-Conte J, Gmyr V, Vandewalle B, Desreumaux P, Auwerx J, Schoonjans K, Lefebvre J

机构信息

UPRES 1048, University Hospital Centre of Lille, France.

出版信息

Diabetologia. 2000 Sep;43(9):1165-9. doi: 10.1007/s001250051508.

Abstract

AIMS/HYPOTHESIS: Thiazolidinediones are reported to improve pancreatic islet morphology and beta-cell function in rodents, supporting the hypothesis of a direct action of thiazolidinediones on endocrine islet cells. In this study we examined the expression of the peroxisome proliferator-activated receptor gamma, a nuclear receptor that is activated by naturally occurring fatty acids and synthetic thiazolidinediones, in normal human endocrine pancreatic cells.

METHODS

Human islets were isolated from pancreata harvested in ten brain-dead lean non-diabetic adult donors. We analysed the gene and protein expression of the human peroxisome proliferator-activated receptor gamma and evaluated the effects of peroxisome proliferator-activated receptor gamma agonist on insulin secretion in human islet preparations.

RESULTS

The RT-PCR carried out on total RNA from four distinct human islet preparations demonstrated the presence of peroxisome proliferator-activated receptor gamma mRNA. Western blot analysis showed the consistent expression of peroxisome proliferator-activated receptor gamma protein. Peroxisome proliferator-activated receptor gamma was shown to be present in all three endocrine cell types studied (alpha, beta and delta cells) by immunohistochemistry.

CONCLUSION/INTERPRETATION: We found that peroxisome proliferator-activated receptor gamma is highly expressed in human islet endocrine cells, both at the mRNA and protein levels. These results support the hypothesis of a direct influence of peroxisome proliferator-activated receptor gamma agonist on human pancreatic endocrine cells.

摘要

目的/假设:据报道,噻唑烷二酮类药物可改善啮齿动物的胰岛形态和β细胞功能,支持噻唑烷二酮类药物对胰岛内分泌细胞有直接作用的假设。在本研究中,我们检测了过氧化物酶体增殖物激活受体γ(一种由天然脂肪酸和合成噻唑烷二酮类药物激活的核受体)在正常人类胰腺内分泌细胞中的表达。

方法

从10名脑死亡的瘦型非糖尿病成年供体的胰腺中分离出人类胰岛。我们分析了人类过氧化物酶体增殖物激活受体γ的基因和蛋白表达,并评估了过氧化物酶体增殖物激活受体γ激动剂对人类胰岛制剂中胰岛素分泌的影响。

结果

对来自四种不同人类胰岛制剂的总RNA进行的逆转录聚合酶链反应(RT-PCR)证明了过氧化物酶体增殖物激活受体γ信使核糖核酸(mRNA)的存在。蛋白质印迹分析显示过氧化物酶体增殖物激活受体γ蛋白的一致表达。通过免疫组织化学显示,过氧化物酶体增殖物激活受体γ存在于所研究的所有三种内分泌细胞类型(α细胞、β细胞和δ细胞)中。

结论/解读:我们发现过氧化物酶体增殖物激活受体γ在人类胰岛内分泌细胞中在mRNA和蛋白水平均高度表达。这些结果支持过氧化物酶体增殖物激活受体γ激动剂对人类胰腺内分泌细胞有直接影响的假设。

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