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蛋白激酶 D1 的抑制作用会干扰有丝分裂的进程。

Protein kinase D1 inhibition interferes with mitosis progression.

机构信息

Consejo Nacional de Investigaciones Científicas y Técnicas, Instituto de Inmunología, Genética y Metabolismo, Facultad de Farmacia y Bioquímica, Hospital de Clínicas "José de San Martín," Universidad de Buenos Aires, Ciudad Autónoma de Buenos Aires (CABA), Buenos Aires, Argentina.

Section of Molecular Hematology and Therapy, Department of Stem Cell Transplantation and Cellular Therapy, M.D. Anderson Cancer Center, University of Texas, Houston, TX.

出版信息

J Cell Physiol. 2019 Nov;234(11):20510-20519. doi: 10.1002/jcp.28651. Epub 2019 Apr 17.

Abstract

Protein kinase D1 (PKD1) plays a vital role in signal transduction, cell proliferation, membrane trafficking, and cancer; however, the majority of the studies up to date had centered primarily on PKD1 functions in interphase, very little is known about its role during cell division. We previously demonstrated that during mitosis PKD1 is activated and associated with centrosomes, spindles, and midbodies. However, these observations did not address whether PKD1 was associated with mitosis regulation. Accordingly, we used rapidly acting PKD-specific inhibitors to examine the contribution of PKD1 the sequence of events in mitosis. We found that although PKD1 overexpression did not affect mitosis progression, suppression of its catalytic activity by two structurally unrelated inhibitors (kb NB 142-70 and CRT 0066101) induced a significant delay in metaphase to anaphase transition time. PKD1 inhibition during mitosis also produced the appearance of abnormal spindles, defects in chromosome alignment, and segregation as well as apoptosis. Thus, these observations indicate that PKD1 activity is associated with mitosis regulation.

摘要

蛋白激酶 D1(PKD1)在信号转导、细胞增殖、膜运输和癌症中发挥着重要作用;然而,迄今为止的大多数研究主要集中在 PKD1 在间期中的功能,其在细胞分裂过程中的作用知之甚少。我们之前的研究表明,在有丝分裂过程中,PKD1 被激活并与中心体、纺锤体和中间体相关联。然而,这些观察结果并没有解决 PKD1 是否与有丝分裂调控有关。因此,我们使用快速作用的 PKD 特异性抑制剂来检查 PKD1 对有丝分裂过程中一系列事件的贡献。我们发现,尽管 PKD1 的过表达不会影响有丝分裂的进展,但两种结构上不相关的抑制剂(kb NB 142-70 和 CRT 0066101)抑制其催化活性会导致中期到后期的过渡时间显著延迟。有丝分裂过程中 PKD1 的抑制也会产生异常纺锤体、染色体排列和分离缺陷以及细胞凋亡。因此,这些观察结果表明,PKD1 的活性与有丝分裂调控有关。

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