Department of Molecular Biology & Immunology, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.
Biochem Biophys Res Commun. 2012 Sep 7;425(4):836-41. doi: 10.1016/j.bbrc.2012.07.163. Epub 2012 Aug 7.
Protein kinase C (PKC) is the receptor for tumor promoting phorbol esters, which are potent activators of conventional and novel PKCs, but persistent treatment with phorbol esters leads to downregulation of these PKCs. However, PKCη, a novel PKC isozyme, resists downregulation by tumor-promoting phorbol esters, but little is known about how PKCη level is regulated. Phosphorylation and dephosphorylation play an important role in regulating activity and stability of PKCs. In the present study, we have investigated the molecular mechanism of PKCη regulation. Several PKC activators, including phorbol 12,13-dibutyrate, 12-O-tetradecanoylphorbol-13-acetate and indolactam V caused upregulation of PKCη, whereas the general PKC inhibitor Gö 6983, but not the conventional PKC inhibitor Gö 6976 led to the downregulation of PKCη. Upregulation of PKCη was associated with an increase in phosphorylation of PKCη. Silencing of phosphoinositide-dependent kinase-1, which phosphorylates PKCη at the activation loop, failed to prevent PKC activator-induced upregulation of PKCη. Knockdown of PKCε but not PKCα inhibited PKC activator-induced upregulation of PKCη. Thus, our results suggest that the regulation of PKCη is unique and PKCε is required for the PKC activator-induced upregulation of PKCη.
蛋白激酶 C(PKC)是肿瘤促进佛波酯的受体,佛波酯是经典和新型 PKC 的有效激活剂,但持续的佛波酯处理会导致这些 PKC 的下调。然而,新型 PKC 同工型 PKCη 抵抗肿瘤促进佛波酯的下调,但对于 PKCη 水平如何调节知之甚少。磷酸化和去磷酸化在调节 PKCs 的活性和稳定性方面起着重要作用。在本研究中,我们研究了 PKCη 调节的分子机制。几种 PKC 激活剂,包括佛波醇 12,13-二丁酸酯、12-O-十四烷酰佛波醇-13-乙酸酯和吲哚拉坦 V 导致 PKCη 的上调,而通用 PKC 抑制剂 Gö 6983 而不是经典 PKC 抑制剂 Gö 6976 导致 PKCη 的下调。PKCη 的上调与 PKCη 激活环磷酸化的增加有关。磷酸肌醇依赖性激酶-1 的沉默,其在激活环中磷酸化 PKCη,未能阻止 PKC 激活剂诱导的 PKCη 上调。PKCε 的敲低而不是 PKCα 的敲低抑制了 PKC 激活剂诱导的 PKCη 上调。因此,我们的结果表明 PKCη 的调节是独特的,PKCε 是 PKC 激活剂诱导的 PKCη 上调所必需的。