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体外巨核细胞生成中的信号转导事件。

Signal transduction events in in vitro megakaryocytopoiesis.

作者信息

Long M W

机构信息

Department of Pediatrics, University of Michigan, Ann Arbor 48109.

出版信息

Blood Cells. 1989;15(1):205-29.

PMID:2784701
Abstract

Understanding of the events following factor-mediated megakaryocyte development is hindered by a lack of adequate quantities of purified progenitor cells or progenitor cell lines. In order to study the intracellular processes activated during development, probes of various signal transduction systems are used to perturb megakaryocyte colony formation. Studies utilizing tumor promoting phorbol diesters and calcium ionophores show that protein kinase C and calcium mobilization (and/or influx) are activated during megakaryocyte development. Examination of the adenylate cyclase complex, with agonists such as cholera toxin etc., implicate cyclic AMP as another mediator of growth-factor responsiveness. Finally, synergistic interactions occur between the calcium-protein kinase C system and the adenylate cyclase complex. These observations corroborate the multifactorial regulation of megakaryocytopoiesis postulated by Williams and coworkers. The data further provide an intracellular mechanism(s) by which megakaryocytic growth factors regulate cellular development.

摘要

由于缺乏足够数量的纯化祖细胞或祖细胞系,对因子介导的巨核细胞发育后续事件的理解受到阻碍。为了研究发育过程中激活的细胞内过程,各种信号转导系统的探针被用于干扰巨核细胞集落形成。利用促肿瘤佛波酯和钙离子载体的研究表明,蛋白激酶C和钙动员(和/或内流)在巨核细胞发育过程中被激活。用霍乱毒素等激动剂对腺苷酸环化酶复合物进行检测,表明环磷酸腺苷是生长因子反应性的另一种介质。最后,钙-蛋白激酶C系统与腺苷酸环化酶复合物之间存在协同相互作用。这些观察结果证实了Williams及其同事所假设的巨核细胞生成的多因素调节。这些数据进一步提供了一种细胞内机制,通过该机制巨核细胞生长因子调节细胞发育。

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