Liu Ping, Scharenberg Andrew M, Cantrell Doreen A, Matthews Sharon A
Division of Cell Biology and Immunology, College of Life Sciences, University of Dundee, Dow Street, Dundee, DD1 5EH, Scotland, UK.
FEBS Lett. 2007 Apr 3;581(7):1377-82. doi: 10.1016/j.febslet.2007.02.055. Epub 2007 Mar 2.
To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569-1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFkappaB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology.
为了研究蛋白激酶D(PKD)酶的重要性,我们构建了一个PKD基因缺失的DT40 B淋巴细胞系。此前我们已经表明,PKD在调节DT40 B细胞中的II类组蛋白去乙酰化酶方面具有重要作用[马修斯,S.A.,刘,P.,斯皮塔勒,M.,奥尔森,E.N.,麦肯锡,T.A.,坎特雷尔,D.A.和沙伦伯格,A.M.(2006年)蛋白激酶D家族激酶在B淋巴细胞中II类组蛋白去乙酰化酶调节中的重要作用。《分子细胞生物学》26卷,第1569 - 1577页]。我们现在表明,PKD在调节DT40 B细胞中的HSP27磷酸化方面也是必需的。然而,与之前在其他细胞类型中的观察结果相反,PKD酶并不调节诸如增殖或存活反应等基本细胞过程,也不调节B细胞抗原受体下游的NFκB转录活性。因此,PKD在DT40 B细胞生物学中具有选择性作用。