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与 connexin43 共同诱导表达 connexin37 或 connexin40 可选择性影响细胞间分子转移。

Inducible coexpression of connexin37 or connexin40 with connexin43 selectively affects intercellular molecular transfer.

机构信息

Department of Pediatrics, University of Chicago, Chicago, IL 60637, USA.

出版信息

J Membr Biol. 2012 Jun;245(5-6):231-41. doi: 10.1007/s00232-012-9444-4. Epub 2012 Jun 23.

DOI:10.1007/s00232-012-9444-4
PMID:22729648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3501935/
Abstract

Many tissues express multiple gap junction proteins, or connexins (Cx); for example, Cx43, Cx40, and Cx37 are coexpressed in vascular cells. This study was undertaken to elucidate the consequences of coexpression of Cx40 or Cx37 with Cx43 at different ratios. EcR-293 cells (which endogenously produce Cx43) were transfected with ecdysone-inducible plasmids encoding Cx37 or Cx40. Immmunoblotting showed a ponasterone dose-dependent induction of Cx37 or Cx40 while constant levels of Cx43 were maintained. The coexpressed connexins colocalized at appositional membranes. Double whole-cell patch clamp recordings showed no significant change in total junctional conductances in cells treated with 0, 0.5, or 4 μM ponasterone; however, they did show a diversity of unitary channel sizes consistent with the induced connexin expression. In cells with induced expression of either Cx40 or Cx37, intercellular transfer of microinjected Lucifer yellow was reduced, but transfer of NBD-TMA (2-(4-nitro-2,1,3-benzoxadiol-7-yl)[aminoethyl]trimethylammonium) was not affected. In cocultures containing uninduced EcR cells together with cells induced to coexpress Cx37 or Cx40, Lucifer yellow transfer was observed only between the cells expressing Cx43 alone. These data show that induced expression of either Cx37 or Cx40 in Cx43-expressing cells can selectively alter the intercellular exchange of some molecules without affecting the transfer of others.

摘要

许多组织表达多种间隙连接蛋白或连接蛋白 (Cx);例如,Cx43、Cx40 和 Cx37 在血管细胞中共表达。本研究旨在阐明 Cx40 或 Cx37 与 Cx43 以不同比例共表达的后果。用蜕皮激素诱导的质粒转染 EcR-293 细胞(内源性产生 Cx43)。免疫印迹显示,ponasterone 剂量依赖性诱导 Cx37 或 Cx40,同时维持 Cx43 的恒定水平。共表达的连接蛋白在贴壁膜处共定位。双全细胞膜片钳记录显示,用 0、0.5 或 4 μM ponasterone 处理的细胞中总连接电导没有明显变化;然而,它们确实显示出与诱导的连接蛋白表达一致的多种单位通道大小。在用 Cx40 或 Cx37 诱导表达的细胞中,用 Lucifer yellow 微注射的细胞间转移减少,但 NBD-TMA(2-(4-硝基-2,1,3-苯并恶二唑-7-基)[氨基乙基]三甲基氯化铵)的转移不受影响。在含有未诱导的 EcR 细胞的共培养物中,与共同表达 Cx37 或 Cx40 的细胞一起,仅在单独表达 Cx43 的细胞之间观察到 Lucifer yellow 转移。这些数据表明,在表达 Cx43 的细胞中诱导表达 Cx37 或 Cx40 可以选择性地改变某些分子的细胞间交换,而不影响其他分子的转移。

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本文引用的文献

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