S6 PHOSPHORYLATION RESULTS FROM PROTHORACICOTROPIC HORMONE STIMULATION OF INSECT PROTHORACIC GLANDS - A ROLE FOR S6 KINASE

被引:50
作者
SONG, QS [1 ]
GILBERT, LI [1 ]
机构
[1] UNIV N CAROLINA,DEPT BIOL,CHAPEL HILL,NC 27599
来源
DEVELOPMENTAL GENETICS | 1994年 / 15卷 / 04期
关键词
INSECT MOLTING; ECDYSTEROID; S6; KINASE; RAPAMYCIN; IMMUNOSUPPRESSANT;
D O I
10.1002/dvg.1020150404
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The insect prothoracic glands are the source of steroidal molting hormone precursors and the glands are stimulated by a brain neuropeptide, prothoracicotropic hormone (PTTH). Previous work from this laboratory revealed that PTTH acts via a cascade including Ca2+/calmodulin activation of adenylate cyclase, protein kinase A, and the subsequent phosphorylation of a 34 kDa protein (p34) hypothesized, but not proven, to be the S6 protein of the 40S ribosomal subunit. The immunosuppressive macrolide, rapamycin, is a potent inhibitor of cell proliferation, a signal transduction blocker, and also prevents ribosomal S6 phosphorylation in mammalian systems. We demonstrate here that rapamycin inhibited PTTH-stimulated ecdysteroidogenesis in vitro by the prothoracic glands of the tobacco hornworm, Manduca sexta, with half-maximal inhibition at a concentration of about 5 nM. At concentrations above 5 nM, there was a 75% inhibition of ecdysteroid biosynthesis. Similar results were observed with the calcium ionophore (A23187), a known stimulator of ecdysteroidogenesis. Most importantly, the inhibition of ecdysteroid biosynthesis was accompanied by the specific inhibition of the phosphorylation of p34, indicating that p34 indeed is ribosomal protein S6. In vivo assays revealed that injection of rapamycin into day 6 fifth instar larvae resulted in a decreased hemolymph ecdysteroid titer and a dose-dependent delay in molting and metamorphosis. When S6 kin ase (S6 K) activity was examined using rapamycin-treated prothoracic glands as the enzyme source and a synthetic peptide (S6-21) ora 40S ribosomal subunit traction from Manduca tissues as substrate, the date revealed that rapamycin inhibited S6K activity. The composite data suggest that rapamycin inhibits a signal transduction element leading to p34 phosphorylation that is necessary for PTTH-stimulated ecdysteroidogenesis in this insect endocrine gland, and lend further support to the concept that p34 is S6. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:332 / 338
页数:7
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