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在缺乏连接蛋白43的培养星形胶质细胞中,缝隙连接通讯、细胞间信号传导及生长发生改变。

Altered gap junctional communication, intercellular signaling, and growth in cultured astrocytes deficient in connexin43.

作者信息

Naus C C, Bechberger J F, Zhang Y, Venance L, Yamasaki H, Juneja S C, Kidder G M, Giaume C

机构信息

Department of Anatomy and Cell Biology, University of Western Ontario, London, Canada.

出版信息

J Neurosci Res. 1997 Sep 1;49(5):528-40. doi: 10.1002/(SICI)1097-4547(19970901)49:5<528::AID-JNR3>3.0.CO;2-D.

Abstract

Astrocytes are characterized by extensive intercellular communication mediated primarily by gap junction channels composed of connexin43. To examine this junctional protein in astrocytic functions, astrocytes were cultured from embryonic mice with a null mutation in the connexin43 gene (Reaume et al.: Science 267:1831-1834, 1995). Using anti-Cx43 antibodies, immunoblotting and immunostaining indicated that homozygous null astrocytes were devoid of Cx43. They are also deficient in intercellular dye transfer. Astrocytes cultured from heterozygous embryos express significantly lower Cx43 compared to wild type, and their dye coupling is reduced. Markers of glial differentiation, such as glial fibrillary acidic protein and S100, appeared similar in all genotypes. Measurement of intercellular calcium concentration following mechanical stimulation of confluent astrocytes revealed that the number of cells affected by a rise in intracellular calcium was reduced in homozygous cultures compared to wild type. In fact, the calcium response in homozygous astrocytes was similar to that observed in wild-type astrocytes in the presence of a gap junction blocker. The growth rate of astrocytes lacking Cx43 was reduced compared to wild-type astrocytes. These results suggest that gap junctional intercellular communication mediated by Cx43 is not critical for astrocyte differentiation but is likely involved in the regulation of intercellular calcium signaling and cell growth.

摘要

星形胶质细胞的特征是通过主要由连接蛋白43组成的缝隙连接通道进行广泛的细胞间通讯。为了研究这种连接蛋白在星形胶质细胞功能中的作用,从连接蛋白43基因发生无效突变的胚胎小鼠中培养星形胶质细胞(雷姆等人:《科学》267:1831 - 1834,1995)。使用抗Cx43抗体,免疫印迹和免疫染色表明纯合无效星形胶质细胞缺乏Cx43。它们在细胞间染料转移方面也存在缺陷。与野生型相比,从杂合胚胎培养的星形胶质细胞表达的Cx43明显较低,并且它们的染料偶联减少。胶质细胞分化标志物,如胶质纤维酸性蛋白和S100,在所有基因型中看起来相似。对汇合的星形胶质细胞进行机械刺激后测量细胞间钙浓度发现,与野生型相比,纯合培养物中受细胞内钙升高影响的细胞数量减少。实际上,纯合星形胶质细胞中的钙反应与在存在缝隙连接阻滞剂的情况下野生型星形胶质细胞中观察到的反应相似。与野生型星形胶质细胞相比,缺乏Cx43的星形胶质细胞的生长速率降低。这些结果表明,由Cx43介导的缝隙连接细胞间通讯对星形胶质细胞分化并不关键,但可能参与细胞间钙信号传导和细胞生长的调节。

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