Navé B T, Siddle K, Shepherd P R
Department of Clinical Biochemistry, University of Cambridge, UK.
Biochem J. 1996 Aug 15;318 ( Pt 1)(Pt 1):203-5. doi: 10.1042/bj3180203.
The effects of insulin and phorbol 12-myristate 13-acetate (PMA) on the levels of cellular phosphoinositides were investigated in 3T3-L1 adipocytes. Stimulation for 4 min with PMA (1 microM) or insulin (10 nM) increased levels of PtdIns(3,4,5)P3 approx. 2-fold and 6-fold respectively. PMA also had a small effect on the cellular levels of PtdIns4P, whereas insulin had no effect on PtdIns4P levels; levels of PtdIns(4,5)P2 and PtdIns3P were not significantly affected by either agent. Insulin increased the levels of the p85 alpha subunit of phosphoinositide (PI) 3-kinase associated with membranes, whereas PMA decreased levels of membrane-associated p85 alpha. PMA did not increase PI 3-kinase activity in anti-phosphotyrosine or anti-p85 immunoprecipitates. The stimulation of glucose transport by insulin or PMA was blocked by 100 nM wortmannin or 10 ng/ml LY294002, indicating that PI 3-kinase is essential for stimulation by both agents. In summary, these results demonstrate: (1) that PMA and insulin stimulate PtdIns(3,4,5)P3 production by distinct mechanisms in 3T3-L1 adipocytes, and (2) that stimulation of PtdIns(3,4,5)P3 production by PMA is likely to be important in signalling pathways leading from PMA stimulation to end-point responses such as glucose transport.
在3T3-L1脂肪细胞中研究了胰岛素和佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)对细胞磷酸肌醇水平的影响。用PMA(1μM)或胰岛素(10 nM)刺激4分钟,分别使磷脂酰肌醇-3,4,5-三磷酸(PtdIns(3,4,5)P3)水平增加约2倍和6倍。PMA对细胞中磷脂酰肌醇-4-磷酸(PtdIns4P)水平也有轻微影响,而胰岛素对PtdIns4P水平无影响;两种试剂对磷脂酰肌醇-4,5-二磷酸(PtdIns(4,5)P2)和磷脂酰肌醇-3-磷酸(PtdIns3P)水平均无显著影响。胰岛素增加了与膜相关的磷酸肌醇(PI)3-激酶p85α亚基的水平,而PMA降低了膜相关p85α的水平。PMA在抗磷酸酪氨酸或抗p85免疫沉淀物中未增加PI 3-激酶活性。胰岛素或PMA对葡萄糖转运的刺激被100 nM渥曼青霉素或10 ng/ml LY294002阻断,表明PI 3-激酶对两种试剂的刺激至关重要。总之,这些结果表明:(1)PMA和胰岛素通过不同机制刺激3T3-L1脂肪细胞中PtdIns(3,4,5)P3的产生;(2)PMA刺激PtdIns(3,4,5)P3的产生可能在从PMA刺激到诸如葡萄糖转运等终点反应的信号通路中起重要作用。