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Interactions of connexin 43 and aquaporin-4 in the formation of glioma-induced brain edema

机译:连接蛋白43和水通道蛋白4在胶质瘤诱导的脑水肿形成中的相互作用

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摘要

Connexin 43 (Cx43) and aquaporin-4 (AQP4) have important roles in the formation of glioma-induced brain edema; however, the association between these two factors in the development of edema has remained to be elucidated. In the present study, immunofluorescence and western blot analysis revealed that in a rat model of intracranial C6 glioma, Cx43 expression levels were low to undetectable and AQP4 expression levels were low in glioma cells. Significantly higher Cx43 and AQP4 levels were detected in the tissue surrounding the glioma. To further investigate the potential interaction between Cx43 and AQP4, normal glial cells and C6 glioma cells were cultured in hypotonic medium. Reverse transcription quantitative polymerase chain reaction indicated that AQP4 and Cx43 mRNA expression levels increased as a function of time in normal glial cells and C6 glioma cells in a hypotonic environment. However, the increase observed in normal glial cells was significantly lower than that observed in C6 glioma cells. Furthermore, AQP4 expression levels changed prior to alterations in Cx43 expression. Following AQP4 silencing in C6 cells, the increase in Cx43 expression was significantly attenuated (P<0.05). In normal cells, Cx43 silencing did not influence AQP4 expression (P>0.05). Therefore, it was hypothesized that AQP4 and Cx43 had two distinct mechanisms underlying brain edema formation within and surrounding the glioma. Cx43 may be a downstream effector of AQP4. The elucidation of this pathway may aid in the development of drugs targeting the interaction between AQP4 and Cx43, providing novel therapeutic possibilities for glioma-induced brain edema.
机译:连接蛋白43(Cx43)和水通道蛋白4(AQP4)在神经胶质瘤诱导的脑水肿的形成中起重要作用。然而,这两个因素在水肿发展中的关系仍有待阐明。在本研究中,免疫荧光和蛋白质印迹分析表明,在颅内C6胶质瘤大鼠模型中,胶质瘤细胞中Cx43表达水平低至无法检测,而AQP4表达水平低。在神经胶质瘤周围的组织中检测到明显更高的Cx43和AQP4水平。为了进一步研究Cx43和AQP4之间的潜在相互作用,在低渗培养基中培养正常的神经胶质细胞和C6胶质瘤细胞。逆转录定量聚合酶链反应表明,在低渗环境中,正常神经胶质细胞和C6胶质瘤细胞中,AQP4和Cx43 mRNA表达水平随时间而增加。然而,在正常神经胶质细胞中观察到的增加明显低于在C6神经胶质瘤细胞中观察到的增加。此外,AQP4表达水平先于Cx43表达改变。在C6细胞中AQP4沉默后,Cx43表达的增加显着减弱(P <0.05)。在正常细胞中,Cx43沉默不影响AQP4表达(P> 0.05)。因此,假设AQP4和Cx43具有两种不同的机制,它们是胶质瘤内部和周围脑水肿形成的基础。 Cx43可能是AQP4的下游效应子。该途径的阐明可能有助于开发针对AQP4与Cx43之间相互作用的药物,为神经胶质瘤诱发的脑水肿提供了新的治疗可能性。

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