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多磷酸肌醇合成与血小板形状改变。

Polyphosphoinositide synthesis and platelet shape change.

作者信息

Hartwig J H, Barkalow K

机构信息

Experimental Medicine Division, Brigham & Women's Hospital, Boston, MA 02115, USA.

出版信息

Curr Opin Hematol. 1997 Sep;4(5):351-6. doi: 10.1097/00062752-199704050-00009.

Abstract

Polyphosphoinositides both integrate signaling pathways at the cytoplasmic surface of the plasma membrane and serve as the final messenger of signaling pathways. They have a well-defined role in the release of calcium through the degradative pathway. Recent work, however, has highlighted the role of the polyphosphoinositide synthetic pathways in activated cells. This review emphasizes the role of polyphosphoinositides in recruiting signaling proteins that have pleckstrin homology domains and in directly regulating actin assembly in the human blood platelet.

摘要

多磷酸肌醇既在质膜的细胞质表面整合信号通路,又作为信号通路的最终信使。它们在通过降解途径释放钙方面具有明确的作用。然而,最近的研究突出了多磷酸肌醇合成途径在活化细胞中的作用。本综述强调了多磷酸肌醇在募集具有普列克底物蛋白同源结构域的信号蛋白以及直接调节人血小板中的肌动蛋白组装方面的作用。

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