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一种细胞计数因子通过差异性调节环磷酸腺苷(cAMP)诱导的cAMP和环磷酸鸟苷(cGMP)脉冲大小来调节盘基网柄菌中的群体大小。

A cell number-counting factor regulates group size in Dictyostelium by differentially modulating cAMP-induced cAMP and cGMP pulse sizes.

作者信息

Tang L, Ammann R, Gao T, Gomer R H

机构信息

Howard Hughes Medical Institute and the Department of Biochemistry and Cell Biology, Rice University, Houston, Texas 77005-1892, USA.

出版信息

J Biol Chem. 2001 Jul 20;276(29):27663-9. doi: 10.1074/jbc.M102205200. Epub 2001 May 22.

Abstract

A secreted counting factor (CF), regulates the size of Dictyostelium discoideum fruiting bodies in part by regulating cell-cell adhesion. Aggregation and the expression of adhesion molecules are mediated by relayed pulses of cAMP. Cells also respond to cAMP with a short cGMP pulse. We find that CF slowly down-regulates the cAMP-induced cGMP pulse by inhibiting guanylyl cyclase activity. A 1-min exposure of cells to purified CF increases the cAMP-induced cAMP pulse. CF does not affect the cAMP receptor or its interaction with its associated G proteins or the translocation of the cytosolic regulator of adenylyl cyclase to the membrane in response to cAMP. Pulsing streaming wild-type cells with a high concentration of cAMP results in the formation of small groups, whereas reducing cAMP pulse size with exogenous cAMP phosphodiesterase during stream formation causes cells to form large groups. Altering the extracellular cAMP pulse size does not phenocopy the effects of CF on the cAMP-induced cGMP pulse size or cell-cell adhesion, indicating that CF does not regulate cGMP pulses and adhesion via CF's effects on cAMP pulses. The results suggest that regulating cell-cell adhesion, the cGMP pulse size, or the cAMP pulse size can control group size and that CF regulates all three of these independently.

摘要

一种分泌性计数因子(CF),部分通过调节细胞间黏附来调控盘基网柄菌子实体的大小。聚集和黏附分子的表达由cAMP的中继脉冲介导。细胞也会以短暂的cGMP脉冲对cAMP作出反应。我们发现CF通过抑制鸟苷酸环化酶活性,缓慢下调cAMP诱导的cGMP脉冲。将细胞暴露于纯化的CF 1分钟会增加cAMP诱导的cAMP脉冲。CF不影响cAMP受体或其与相关G蛋白的相互作用,也不影响腺苷酸环化酶的胞质调节因子响应cAMP向膜的转运。用高浓度cAMP脉冲刺激野生型流动细胞会导致小群体的形成,而在流动形成过程中用外源性cAMP磷酸二酯酶减小cAMP脉冲大小会使细胞形成大群体。改变细胞外cAMP脉冲大小并不会模拟CF对cAMP诱导的cGMP脉冲大小或细胞间黏附的影响,这表明CF并非通过对cAMP脉冲的作用来调节cGMP脉冲和黏附。结果表明,调节细胞间黏附、cGMP脉冲大小或cAMP脉冲大小可以控制群体大小,且CF独立调节这三者。

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