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小鼠Reg2、Reg3α和Reg3β基因的年龄依赖性和胰腺特异性协调表达。

Coordinated age-dependent and pancreatic-specific expression of mouse Reg2Reg3α, and Reg3β genes.

作者信息

Wang Ying, Jacovetti Cecile, Li Bing, Siddique Tehmina, Xiong Xiaoquan, Yin Hongping, Wang Min, Zhao Hong, Liu Jun-Li

机构信息

School of Life Science and Technology, China Pharmaceutical University, Nanjing, P.R. China.

出版信息

Growth Factors. 2011 Apr;29(2-3):72-81. doi: 10.3109/08977194.2011.562866. Epub 2011 Mar 16.

Abstract

Reg family proteins such as Reg1 and islet neogenesis-associated protein (INGAP) have long been implicated in the growth and/or neogenesis of pancreatic islet cells. Recent reports further suggest similar roles to be played by new members such as Reg2, Reg3α, and Reg3β. We have studied their age-, isoform-, and tissue-specific expressions. RNA and protein were isolated from C57BL/6 mice aged 7, 30, and 90 days. Using real-time polymerase chain reaction, the levels of Reg gene expression in the pancreas were 20-600-fold higher than that in other tissues (≫duodenum>stomach>liver); gene expression of Reg2, Reg3α, and Reg3β was age dependent as it was hardly detectable at day 7, increased drastically at day 30, and significantly decreased at day 90; the levels of pancreatic proteins displayed similar age-dependent variations. Using dual-labeled immunofluorescence, Reg2, Reg3α, and Reg3β were abundantly expressed in most acinar cells of the pancreas, in contrast to INGAP which exhibited stepwise increases from day 7 to day 90 and colocalized with the α-cells. These new Reg genes were mainly expressed in the pancreas, with clear age-dependent and isoform-specific patterns.

摘要

Reg家族蛋白,如Reg1和胰岛新生相关蛋白(INGAP),长期以来一直被认为与胰岛细胞的生长和/或新生有关。最近的报道进一步表明,Reg2、Reg3α和Reg3β等新成员也发挥着类似作用。我们研究了它们在年龄、异构体和组织特异性方面的表达情况。从7日龄、30日龄和90日龄的C57BL/6小鼠中分离RNA和蛋白质。使用实时聚合酶链反应,胰腺中Reg基因的表达水平比其他组织(≫十二指肠>胃>肝脏)高20 - 600倍;Reg2、Reg3α和Reg3β的基因表达具有年龄依赖性,在7日龄时几乎检测不到,在30日龄时急剧增加,在90日龄时显著下降;胰腺蛋白质水平也呈现出类似的年龄依赖性变化。使用双标记免疫荧光法,Reg2、Reg3α和Reg3β在胰腺的大多数腺泡细胞中大量表达,而INGAP从7日龄到90日龄呈逐步增加,并与α细胞共定位。这些新的Reg基因主要在胰腺中表达,具有明显的年龄依赖性和异构体特异性模式。

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