McIlroy J, Chen D, Wjasow C, Michaeli T, Backer J M
Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Mol Cell Biol. 1997 Jan;17(1):248-55. doi: 10.1128/MCB.17.1.248.
We have developed a polyclonal antibody that activates the heterodimeric p85-p110 phosphatidylinositol (PI) 3'-kinase in vitro and in microinjected cells. Affinity purification revealed that the activating antibody recognized the N-terminal SH2 (NSH2) domain of p85, and the antibody increased the catalytic activity of recombinant p85-p110 dimers threefold in vitro. To study the role of endogenous PI 3'-kinase in intact cells, the activating anti-NSH2 antibody was microinjected into GRC + LR73 cells, a CHO cell derivative selected for tight quiescence during serum withdrawal. Microinjection of anti-NSH2 antibodies increased bromodeoxyuridine (BrdU) incorporation fivefold in quiescent cells and enhanced the response to serum. These data reflect a specific activation of PI 3'-kinase, as the effect was blocked by coinjection of the appropriate antigen (glutathione S-transferase-NSH2 domains from p85 alpha), coinjection of inhibitory anti-p110 antibodies, or treatment of cells with wortmannin. We used the activating antibodies to study signals downstream from PI 3'-kinase. Although treatment of cells with 50 nM rapamycin only partially decreased anti-NSH2-stimulated BrdU incorporation, coinjection with an anti-p70 S6 kinase antibody effectively blocked anti-NSH2-stimulated DNA synthesis. We also found that coinjection of inhibitory anti-ras antibodies blocked both serum- and anti-NSH2-stimulated BrdU incorporation by approximately 60%, and treatment of cells with a specific inhibitor of MEK abolished antibody-stimulated BrdU incorporation. We conclude that selective activation of physiological levels of PI 3'-kinase is sufficient to stimulate DNA synthesis in quiescent cells. PI 3'-kinase-mediated DNA synthesis requires both p70 S6 kinase and the P21ras/MEK pathway.
我们已研发出一种多克隆抗体,该抗体在体外及显微注射入细胞后能激活异源二聚体p85-p110磷脂酰肌醇(PI)3'-激酶。亲和纯化显示,激活抗体识别p85的N端SH2(NSH2)结构域,且该抗体在体外使重组p85-p110二聚体的催化活性提高了三倍。为研究内源性PI 3'-激酶在完整细胞中的作用,将激活抗NSH2抗体显微注射入GRC + LR73细胞,这是一种在血清撤除期间选择用于严格静止的CHO细胞衍生物。抗NSH2抗体的显微注射使静止细胞中的溴脱氧尿苷(BrdU)掺入增加了五倍,并增强了对血清的反应。这些数据反映了PI 3'-激酶的特异性激活,因为通过共注射适当的抗原(来自p85α的谷胱甘肽S-转移酶-NSH2结构域)、共注射抑制性抗p110抗体或用渥曼青霉素处理细胞,该效应被阻断。我们使用激活抗体来研究PI 3'-激酶下游的信号。尽管用50 nM雷帕霉素处理细胞仅部分降低了抗NSH2刺激的BrdU掺入,但与抗p70 S6激酶抗体共注射有效地阻断了抗NSH2刺激的DNA合成。我们还发现,共注射抑制性抗ras抗体可使血清和抗NSH2刺激的BrdU掺入均减少约60%,并且用MEK的特异性抑制剂处理细胞可消除抗体刺激的BrdU掺入。我们得出结论,PI 3'-激酶生理水平的选择性激活足以刺激静止细胞中的DNA合成。PI 3'-激酶介导的DNA合成需要p70 S6激酶和P21ras/MEK途径。