Armstrong J L, Bonavaud S M, Toole B J, Yeaman S J
School of Biochemistry and Genetics, Medical School, University of Newcastle, Newcastle Upon Tyne NE2 4HH, United Kingdom.
J Biol Chem. 2001 Jan 12;276(2):952-6. doi: 10.1074/jbc.M004812200.
Insulin and a number of metabolic factors stimulate glycogen synthesis and the enzyme glycogen synthase. Using human muscle cells we find that glycogen synthesis is stimulated by treatment of the cells with lithium ions, which inhibit glycogen synthase kinase 3. Insulin further stimulates glycogen synthesis in the presence of lithium ions, an effect abolished by wortmannin and rapamycin. We report also that amino acids stimulate glycogen synthesis and glycogen synthase, these effects also being blocked by rapamycin and wortmannin. Amino acids stimulate p70(s6k) and transiently inhibit glycogen synthase kinase 3 without effects on the activity of protein kinase B or the mitogen-activated protein kinase pathway. Thus, the work reported here demonstrates that amino acid availability can regulate glycogen synthesis. Furthermore, it demonstrates that glycogen synthase kinase 3 can be inactivated within cells independent of activation of protein kinase B and p90(rsk).
胰岛素和一些代谢因子可刺激糖原合成及糖原合酶。利用人类肌肉细胞,我们发现用锂离子处理细胞可刺激糖原合成,锂离子能抑制糖原合酶激酶3。在存在锂离子的情况下,胰岛素可进一步刺激糖原合成,渥曼青霉素和雷帕霉素可消除这一效应。我们还报告称,氨基酸可刺激糖原合成及糖原合酶,这些效应同样会被雷帕霉素和渥曼青霉素阻断。氨基酸可刺激p70(s6k)并短暂抑制糖原合酶激酶3,而对蛋白激酶B或丝裂原活化蛋白激酶途径的活性无影响。因此,本文报道的研究表明氨基酸可用性可调节糖原合成。此外,还表明糖原合酶激酶3可在细胞内失活,且不依赖于蛋白激酶B和p90(rsk)的激活。