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蛋白激酶C亚型在人巨核细胞系中的表达与激活

Expression and activation of protein kinase C isoforms in a human megakaryocytic cell line.

作者信息

Ballen K K, Ritchie A J, Murphy C, Handin R I, Ewenstein B M

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.

出版信息

Exp Hematol. 1996 Nov;24(13):1501-8.

PMID:8950233
Abstract

Megakaryocytes undergo a unique differentiation program, becoming polyploid through repeated cycles of DNA synthesis without concomitant cell division. We have shown previously that phorbol 12-myristate 13-acetate (PMA) induces the Dami human megakaryocytic cell line to become polyploid and to express platelet-specific proteins, including von Willebrand factor (vWF) and glycoprotein Ib (GpIb). Phorbol esters are thought to regulate gene expression principally through the activation of protein kinase C (PKC), a family of structurally related kinases with potentially unique activation requirements and substrate specificities. A survey of PKC isoforms in Dami cells revealed that, by both Western and Northern analyses, PKC isoforms alpha, beta, delta, epsilon, eta, theta, and zeta were reproducibly detected. PKC-gamma was not detected. In order to define the role of individual PKC isoforms in megakaryocytic maturation, PMA and 2-deoxyphorbol 13-phenylacetate 20-acetate (dPPA), a putative selective activator of the PKC-beta 1 isotype, were compared for their effects on Dami cell maturation. Treatment with either dPPA or PMA caused Dami cells to cease proliferating, to become polyploid, and to express vWF. We also examined dPPA and PMA for their ability to activate and to downregulate expression of different PKC isoforms. Fifteen-minute treatment with PMA resulted in the translocation of PKC isoforms alpha, epsilon, and theta from the cytosolic to the membrane fraction; twenty-four hour treatment resulted in the downregulation of these isoforms. In contrast, dPPA was found to be a potent activator of PKC-epsilon alone and exhibited weaker effects on alpha and theta. These data suggest that PKC isoforms beta, delta, eta, and zeta, which appear not to be activated by either phorbol ester, are unlikely to be primarily involved in megakaryocytic maturation in response to these agents. The isoforms that are translocated by both phorbol esters-PKC isoforms alpha and theta, and particularly epsilon-are more likely to transduce the signals that stimulate Dami cell differentiation.

摘要

巨核细胞经历独特的分化程序,通过DNA合成的重复循环而不伴随细胞分裂,从而变成多倍体。我们之前已经表明,佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)诱导人巨核细胞系Dami细胞变成多倍体,并表达血小板特异性蛋白,包括血管性血友病因子(vWF)和糖蛋白Ib(GpIb)。佛波酯被认为主要通过激活蛋白激酶C(PKC)来调节基因表达,PKC是一类结构相关的激酶,具有潜在独特的激活要求和底物特异性。对Dami细胞中PKC同工型的一项调查显示,通过蛋白质免疫印迹法(Western)和Northern印迹法分析,可重复性地检测到PKC同工型α、β、δ、ε、η、θ和ζ。未检测到PKC - γ。为了确定单个PKC同工型在巨核细胞成熟中的作用,比较了PMA和2 - 脱氧佛波醇13 - 苯乙酸酯20 - 乙酸酯(dPPA),一种假定的PKC - β1同工型的选择性激活剂,对Dami细胞成熟的影响。用dPPA或PMA处理导致Dami细胞停止增殖,变成多倍体,并表达vWF。我们还检测了dPPA和PMA激活和下调不同PKC同工型表达的能力。用PMA处理15分钟导致PKC同工型α、ε和θ从胞质溶胶转运到膜部分;处理24小时导致这些同工型下调。相比之下,发现dPPA仅是PKC - ε的有效激活剂,对α和θ的作用较弱。这些数据表明,似乎未被任何一种佛波酯激活的PKC同工型β、δ、η和ζ不太可能主要参与对这些试剂作出反应的巨核细胞成熟过程。被两种佛波酯转运的同工型——PKC同工型α和θ,特别是ε——更有可能转导刺激Dami细胞分化的信号。

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