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血小板生成的体液调节。

Humoral control of thrombopoiesis.

作者信息

Levin J, Evatt B L

出版信息

Blood Cells. 1979 Mar 23;5(1):105-21.

PMID:555683
Abstract

There is increasing evidence that an important mechanism by which platelet production is regulated depends upon a humoral substance (thrombopoietin) that affects the production of platelets by megakaryocytes. Plasma from thrombocytopenic donors increases the rate of appearance or concentrations of subsequently administered Na235SO4 or selenomethionine-75Se in platelets. Both isotopes are initially incorporated into the cytoplasm of megakaryocytes, and labeled platelets appear in the circulation after their production and release from megakaryocytes. Thrombopoiesis-stimulating activity also can be detected in the plasma of normal donors when endogenous thrombopoiesis has been suppressed in recipient assay animals by the hypertransfusion of platelets. Recent studies have indicated that certain fractions of plasma from throbocytopenic donors are also capable of stimulating thrombopoiesis in recipient animals. The nature of thrombopoietin(s) and its mechanism of action remain unknown. However, currently available data indicate that thrombopoiesis-stimulating factors may act both on diploid precursors and immature megakaryocytes and upon maturing megakaryocytes. The site of production of thrombopoietin also is unknown. Although the sensor that regulates thrombopoietin or other humoral mediators of thrombopoiesis has not been identified, it appears that platelet numbers, per se, are not the sole variable to which megakaryocytopoiesis eventually responds.

摘要

越来越多的证据表明,血小板生成的一种重要调节机制依赖于一种影响巨核细胞血小板生成的体液物质(血小板生成素)。血小板减少供体的血浆会提高随后注入的Na235SO4或硒代蛋氨酸-75Se在血小板中的出现率或浓度。这两种同位素最初都被整合到巨核细胞的细胞质中,标记的血小板在从巨核细胞产生并释放后出现在循环中。当通过血小板过度输注在受体检测动物中抑制内源性血小板生成时,也可以在正常供体的血浆中检测到血小板生成刺激活性。最近的研究表明,血小板减少供体血浆的某些部分也能够刺激受体动物的血小板生成。血小板生成素的性质及其作用机制仍然未知。然而,目前可得的数据表明,血小板生成刺激因子可能对二倍体前体和未成熟巨核细胞以及成熟巨核细胞都起作用。血小板生成素的产生部位也未知。虽然尚未确定调节血小板生成素或其他血小板生成体液介质的传感器,但似乎血小板数量本身并不是巨核细胞生成最终响应的唯一变量。

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