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前血小板形成的机制。

Mechanics of proplatelet elaboration.

作者信息

Italiano J E, Patel-Hett S, Hartwig J H

机构信息

Translational Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

J Thromb Haemost. 2007 Jul;5 Suppl 1:18-23. doi: 10.1111/j.1538-7836.2007.02487.x.

Abstract

The cellular and molecular basis of the intricate process by which megakaryocytes (MKs) form and release platelets remains poorly understood. Work has shown that proplatelets, long cytoplasmic extensions made by mature MKs, are essential intermediates in platelet biogenesis. Microtubules are the main structural component of proplatelets and it is microtubule sliding, driven by dynein motors within cortical bundles, which elongates and thins proplatelets. Kinesin motors carry their cargo of platelet-specific granules and organelles into the proplatelets using the microtubule bundles as tracks. Extension of proplatelets is associated with repeated actin-dependent bending and bifurcation, which results in considerable amplification of free proplatelet ends. Large proplatelets, dissociated from the residual MK cell body, have the capacity to mature platelets. Only the ends of proplatelets form marginal microtubule coils similar to that observed in mature platelets, demonstrating that platelet formation completes primarily at proplatelet ends. Understanding the molecular basis of platelet formation requires detailed knowledge of how the MK microtubule machinery interacts to generate proplatelets and release platelets.

摘要

巨核细胞(MKs)形成并释放血小板这一复杂过程的细胞和分子基础仍知之甚少。研究表明,前血小板是成熟巨核细胞产生的长细胞质延伸物,是血小板生物发生过程中的关键中间体。微管是前血小板的主要结构成分,由皮质束中的动力蛋白驱动的微管滑动使前血小板伸长并变细。驱动蛋白利用微管束作为轨道,将其携带的血小板特异性颗粒和细胞器运入前血小板。前血小板的延伸与肌动蛋白依赖性的反复弯曲和分叉有关,这导致游离前血小板末端大量增加。与残留的巨核细胞体分离的大型前血小板具有成熟为血小板的能力。只有前血小板的末端形成类似于成熟血小板中观察到的边缘微管盘绕,这表明血小板形成主要在前血小板末端完成。了解血小板形成的分子基础需要详细了解巨核细胞微管机制如何相互作用以产生前血小板并释放血小板。

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