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蛋白激酶C介导的ZYG1磷酸化诱导成肌细胞以及盘基网柄菌细胞的融合。

PKC-Mediated ZYG1 Phosphorylation Induces Fusion of Myoblasts as well as of Dictyostelium Cells.

作者信息

Amagai Aiko, Macwilliams Harry, Isono Takahiro, Omatsu-Kanbe Mariko, Urano Shinya, Yamamoto Kazuo, Maeda Yasuo

机构信息

Graduate School of Life Sciences, Tohoku University, Sendai 980-8577, Japan.

出版信息

Int J Cell Biol. 2012;2012:657423. doi: 10.1155/2012/657423. Epub 2012 Feb 6.

Abstract

We have previously demonstrated that a novel protein ZYG1 induces sexual cell fusion (zygote formation) of Dictyostelium cells. In the process of cell fusion, involvements of signal transduction pathways via Ca(2+) and PKC (protein kinase C) have been suggested because zygote formation is greatly enhanced by PKC activators. In fact, there are several deduced sites phosphorylated by PKC in ZYG1 protein. Thereupon, we designed the present work to examine whether or not ZYG1 is actually phosphorylated by PKC and localized at the regions of cell-cell contacts where cell fusion occurs. These were ascertained, suggesting that ZYG1 might be the target protein for PKC. A humanized version of zyg1 cDNA (mzyg1) was introduced into myoblasts to know if ZYG1 is also effective in cell fusion of myoblasts. Quite interestingly, enforced expression of ZYG1 in myoblasts was found to induce markedly their cell fusion, thus strongly suggesting the existence of a common signaling pathway for cell fusion beyond the difference of species.

摘要

我们之前已经证明,一种新型蛋白质ZYG1可诱导盘基网柄菌细胞的有性细胞融合(合子形成)。在细胞融合过程中,由于PKC(蛋白激酶C)激活剂可大大增强合子形成,因此有人提出了通过Ca(2+)和PKC的信号转导途径的参与。事实上,ZYG1蛋白中有几个被PKC磷酸化的推导位点。于是,我们设计了本研究来检测ZYG1是否真的被PKC磷酸化,并定位在发生细胞融合的细胞间接触区域。这些都得到了证实,表明ZYG1可能是PKC的靶蛋白。将人源化的zyg1 cDNA(mzyg1)导入成肌细胞,以了解ZYG1在成肌细胞的细胞融合中是否也有效。非常有趣的是,发现在成肌细胞中强制表达ZYG1可显著诱导它们的细胞融合,因此强烈表明存在一种超越物种差异的细胞融合共同信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b164/3296296/4f3dc09221e2/IJCB2012-657423.001.jpg

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