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细胞运动性介导了盘基网柄菌中的组织大小调控。

Cell motility mediates tissue size regulation in Dictyostelium.

作者信息

Gomer Richard, Gao Tong, Tang Yitai, Knecht David, Titus Margaret A

机构信息

Howard Hughes Medical Institute, Department of Biochemistry and Cell Biology, MS-140, Rice University, 6100 S. Main Street, Houston, TX 77005-1892, USA.

出版信息

J Muscle Res Cell Motil. 2002;23(7-8):809-15. doi: 10.1023/a:1024487930787.

Abstract

Little is known about how organisms regulate the size of multicellular structures. This review condenses some of the observations about how Dictyostelium regulates the size of fruiting bodies. Very large fruiting bodies tend to fall over, and one of the ways Dictyostelium cells prevent this is by breaking up the aggregation streams when there is an excessive number of cells in the stream. Developing cells simultaneously secrete and sense counting factor (CF), a 450 kDa complex of proteins. Diffusion calculations showed that as the number of cells in a stream or group increases, the local concentration of CF will increase, allowing the cells to sense the number of cells in the stream or group. Computer simulations predicted that a high level of CF could trigger stream breakup by decreasing cell-cell adhesion and/or increasing cell motility, effectively causing the stream to dissipate and begin to fall apart. The prediction that adhesion and motility affect group size is supported by observations that decreasing adhesion by adding antibodies that bind to adhesion protein causes the formation of smaller groups, while increasing adhesion by overexpressing adhesion proteins, or decreasing motility with drugs that disrupt actin function both cause the formation of larger groups. CF both decreases adhesion and increases motility. CF increases motility in part by increasing actin polymerization and myosin phosphorylation, and decreasing myosin polymerization. New observations using a fusion of a green fluorescent protein to a protein fragment that binds polymerized actin show that in live cells CF does not affect the distribution of polymerized actin. CF increases the levels of ABP-120, an actin-bundling protein, and new observations indicate that very low levels of CF cause an increase in levels of myoB, an unconventional myosin. Our current understanding of group size regulation in Dictyostelium is thus that motility plays a key role, and that to regulate group size cells regulate the expression of at least two proteins, as well as regulating the polymerization of both actin and myosin.

摘要

关于生物体如何调节多细胞结构的大小,我们所知甚少。本综述总结了一些关于盘基网柄菌如何调节子实体大小的观察结果。非常大的子实体往往会倒下,盘基网柄菌细胞防止这种情况发生的一种方式是,当聚集流中的细胞数量过多时,将聚集流打散。正在发育的细胞同时分泌并感知计数因子(CF),这是一种由蛋白质组成的450 kDa复合物。扩散计算表明,随着流或群体中细胞数量的增加,CF的局部浓度会升高,使细胞能够感知流或群体中的细胞数量。计算机模拟预测,高水平的CF可通过降低细胞间黏附力和/或增加细胞运动性来触发流的解体,有效地使流消散并开始瓦解。通过添加与黏附蛋白结合的抗体来降低黏附力会导致形成较小的群体,而通过过表达黏附蛋白来增加黏附力,或用破坏肌动蛋白功能的药物来降低运动性,都会导致形成较大的群体,这些观察结果支持了黏附力和运动性影响群体大小的预测。CF既能降低黏附力又能增加运动性。CF部分通过增加肌动蛋白聚合和肌球蛋白磷酸化以及减少肌球蛋白聚合来增加运动性。使用绿色荧光蛋白与结合聚合肌动蛋白的蛋白质片段融合进行的新观察表明,在活细胞中CF不影响聚合肌动蛋白的分布。CF会增加肌动蛋白成束蛋白ABP - 120的水平,新的观察结果表明,极低水平的CF会导致非常规肌球蛋白myoB的水平升高。因此,我们目前对盘基网柄菌群体大小调节的理解是,运动性起着关键作用,并且为了调节群体大小,细胞会调节至少两种蛋白质的表达,以及调节肌动蛋白和肌球蛋白的聚合。

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