Growth hormone regulation of SOCS-2, SOCS-3, and CIS messenger ribonucleic acid expression in the rat

被引:95
作者
Tollet-Egnell, P
Flores-Morales, A
Stavréus-Evers, A
Sahlin, L
Norstedt, G
机构
[1] Karolinska Hosp, Karolinska Inst, Dept Mol Med, S-17176 Stockholm, Sweden
[2] Karolinska Hosp, Karolinska Inst, Div Reprod Endocrinol, S-17176 Stockholm, Sweden
关键词
D O I
10.1210/en.140.8.3693
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The SOCS (suppressors of cytokine signaling) proteins have been suggested to function as inhibitors of cytokine receptor signaling. We have analyzed SOCS-2, SOCS-3, and CIS expression in relation to GH actions in the rat. SOCS-2, SOCS-3, and CIS transcripts were detected in various GH responsive tissues, including liver, muscle, and fat. In addition to the finding that different tissues express different levels of SOCS-2, SOCS-3, and CIS messenger RNA (mRNA), the steady-state levels of these SOCS transcripts were dependent on the endocrine status of the animal. SOCS-3 expression was 5-fold higher in fat from old compared with younger rats. Hypophysectomy reduced the levels of SOCS-2 and CIS mRNA in liver, muscle, and fat, whereas SOCS-3 expression was unchanged. Using primary cultures of rat hepatocytes, GH was shown to increase SOCS-2, SOCS-3, and CIS mRNA levels with different kinetics. SOCS-3 was rapidly and transiently induced, whereas SOCS-2 and CIS were increased in a slower fashion. Glucocorticoids blocked GH-induced SOCS-3 expression in cultured hepatocytes, whereas SOCS-2 and CIS expression was potentiated. Our data fit well with a concept of SOCS proteins acting as modulators of GH signal transduction.
引用
收藏
页码:3693 / 3704
页数:12
相关论文
共 59 条
[1]   Growth hormone preferentially induces the rapid, transient expression of SOCS-3, a novel inhibitor of cytokine receptor signaling [J].
Adams, TE ;
Hansen, JA ;
Starr, R ;
Nicola, NA ;
Hilton, DJ ;
Billestrup, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (03) :1285-1287
[2]   Growth suppression by glucocorticoid therapy [J].
Allen, DB .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1996, 25 (03) :699-&
[3]  
Angelin Bo, 1994, Current Opinion in Lipidology, V5, P160, DOI 10.1097/00041433-199405030-00002
[4]   IDENTIFICATION OF JAK2 AS A GROWTH-HORMONE RECEPTOR-ASSOCIATED TYROSINE KINASE [J].
ARGETSINGER, LS ;
CAMPBELL, GS ;
YANG, XN ;
WITTHUHN, BA ;
SILVENNOINEN, O ;
IHLE, JN ;
CARTERSU, C .
CELL, 1993, 74 (02) :237-244
[5]   Mechanism of signaling by growth hormone receptor [J].
Argetsinger, LS ;
CarterSu, C .
PHYSIOLOGICAL REVIEWS, 1996, 76 (04) :1089-1107
[6]   GROWTH-HORMONE INDUCTION OF HEPATIC SERINE-PROTEASE INHIBITOR-2.1 TRANSCRIPTION IS MEDIATED BY A STAT5-RELATED FACTOR-BINDING SYNERGISTICALLY TO 2 GAMMA-ACTIVATED SITES [J].
BERGAD, PL ;
SHIH, HM ;
TOWLE, HC ;
SCHWARZENBERG, SJ ;
BERRY, SA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :24903-24910
[7]   Identification of SOCS-3 as a potential mediator of central leptin resistance [J].
Bjorbaek, C ;
Elmquist, JK ;
Frantz, JD ;
Shoelson, SE ;
Flier, JS .
MOLECULAR CELL, 1998, 1 (04) :619-625
[8]   Characterization of Stat5a and Stat5b homodimers and heterodimers and their association with the glucocortiocoid receptor in mammary cells [J].
Cella, N ;
Groner, B ;
Hynes, NE .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (04) :1783-1792
[9]   THE HEMATOPOIETIN RECEPTOR SUPERFAMILY [J].
COSMAN, D .
CYTOKINE, 1993, 5 (02) :95-106
[10]   DIMERIZATION OF THE EXTRACELLULAR DOMAIN OF THE HUMAN GROWTH-HORMONE RECEPTOR BY A SINGLE HORMONE MOLECULE [J].
CUNNINGHAM, BC ;
ULTSCH, M ;
DEVOS, AM ;
MULKERRIN, MG ;
CLAUSER, KR ;
WELLS, JA .
SCIENCE, 1991, 254 (5033) :821-825