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Gap junction mediated miRNA intercellular transfer and gene regulation: A novel mechanism for intercellular genetic communication

机译:间隙连接介导的miRNA细胞间转移和基因调控:细胞间遗传通讯的新机制。

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摘要

Intercellular genetic communication is an essential requirement for coordination of cell proliferation and differentiation and has an important role in many cellular processes. Gap junction channels possess large pore allowing passage of ions and small molecules between cells. MicroRNAs (miRNAs) are small regulatory RNAs that can regulate gene expression broadly. Here, we report that miRNAs can pass through gap junction channels in a connexin-dependent manner. Connexin43 (Cx43) had higher permeability, whereas Cx30 showed little permeability to miRNAs. In the tested connexin cell lines, the permeability to miRNAs demonstrated: Cx43 > Cx26/30 > Cx26 > Cx31 > Cx30 = Cx-null. However, consistent with a uniform structure of miRNAs, there was no significant difference in permeability to different miRNAs. The passage is efficient; the miRNA level in the recipient cells could be up to 30% of the donor level. Moreover, the transferred miRNA is functional and could regulate gene expression in neighboring cells. Connexin mutation and gap junctional blockers could eliminate this miRNA intercellular transfer and gene regulation. These data reveal a novel mechanism for intercellular genetic communication. Given that connexin expression is cell-specific, this connexin-dependent, miRNA intercellular genetic communication may play an important role in synchronizing and coordinating proliferation and differentiation of specific cell types during multicellular organ development.
机译:细胞间遗传通讯是协调细胞增殖和分化的基本要求,并在许多细胞过程中发挥重要作用。间隙连接通道具有大孔,允许离子和小分子在细胞之间通过。微小RNA(miRNA)是小的调控RNA,可以广泛调控基因表达。在这里,我们报告miRNA可以通过连接蛋白依赖的方式通过间隙连接通道。连接蛋白43(Cx43)具有较高的通透性,而Cx30对miRNA的通透性很小。在测试的连接蛋白细胞系中,证明对miRNA的渗透性:Cx43→Cx26 / 30→Cx26→Cx31→Cx30→Cx-null。但是,与miRNA的均匀结构一致,不同miRNA的通透性没有显着差异。通道是有效的;受体细胞中的miRNA水平可能高达供体水平的30%。而且,转移的miRNA是有功能的,可以调节邻近细胞中的基因表达。连接蛋白突变和间隙连接阻滞剂可以消除这种miRNA细胞间转移和基因调控。这些数据揭示了细胞间遗传通讯的新机制。鉴于连接蛋白的表达是细胞特异性的,这种连接蛋白依赖性的miRNA细胞间遗传通讯可能在多细胞器官发育过程中在同步和协调特定细胞类型的增殖和分化中起重要作用。

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