The effect of suppressor of cytokine signaling 3 on GH signaling in β-cells

被引:26
作者
Ronn, SG
Hansen, JA
Lindberg, K
Karlsen, AE
Billestrup, N
机构
[1] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[2] Novo Nordisk AS, Signal Transduct, DK-2880 Bagsvaerd, Denmark
关键词
D O I
10.1210/me.2002-0082
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
GH is an important regulator of cell growth and metabolism. In the pancreas, GH stimulates mitogenesis as well as insulin production in beta-cells. The cellular effects of GH are exerted mainly through activation of the Janus kinase-signal transducer and activator of transcription (STAT) pathway. Recently it has been found that suppressors of cytokine signaling (SOCS) proteins are able to inhibit GH-induced signal transduction. In the present study, the role of SOCS-3 in GH signaling was investigated in the pancreatic beta-cell lines RIN-5AH and INS-1 by means of inducible expression systems. Via stable transfection of the beta-cell lines with plasmids expressing SOCS-3 under the control of an inducible promoter, a time- and dose-dependent expression of SOCS-3 in the cells was obtained. EMSA showed that SOCS-3 is able to inhibit GH-induced DNA binding of both STAT3 and STAT5 in RIN-5AH cells. Furthermore, using Northern blot analysis it was shown that SOCS-3 can completely inhibit GH-Induced insulin production in these cells. Finally, 5-bromodeoxyuridine incorporation followed by fluorescence-activated cell sorting analysis showed that SOCS-3 inhibits GH-induced proliferation of INS-1 cells. These findings support the hypothesis that SOCS-3 is a major regulator of GH signaling in insulin-producing cells.
引用
收藏
页码:2124 / 2134
页数:11
相关论文
共 60 条
[11]   Role of the suppressor of cytokine signaling-3 in mediating the inhibitory effects of interleukin-1β on the growth hormone-dependent transcription of the acid-labile subunit gene in liver cells [J].
Boisclair, YR ;
Wang, JR ;
Shi, JR ;
Hurst, KR ;
Ooi, GT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (06) :3841-3847
[12]   EFFECT OF HOMOLOGOUS PLACENTAL LACTOGENS, PROLACTINS, AND GROWTH-HORMONES ON ISLET B-CELL DIVISION AND INSULIN-SECRETION IN RAT, MOUSE, AND HUMAN ISLETS - IMPLICATION FOR PLACENTAL-LACTOGEN REGULATION OF ISLET FUNCTION DURING PREGNANCY [J].
BRELJE, TC ;
SCHARP, DW ;
LACY, PE ;
OGREN, L ;
TALAMANTES, F ;
ROBERTSON, M ;
FRIESEN, HG ;
SORENSON, RL .
ENDOCRINOLOGY, 1993, 132 (02) :879-887
[13]   Stat3 as an oncogene [J].
Bromberg, JF ;
Wrzeszczynska, MH ;
Devgan, G ;
Zhao, YX ;
Pestell, RG ;
Albanese, C ;
Darnell, JE .
CELL, 1999, 98 (03) :295-303
[14]   ACTIVATION OF ACUTE-PHASE RESPONSE FACTOR (APRF)/STAT3 TRANSCRIPTION FACTOR BY GROWTH-HORMONE [J].
CAMPBELL, GS ;
MEYER, DJ ;
RAZ, R ;
LEVY, DE ;
SCHWARTZ, J ;
CARTERSU, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (08) :3974-3979
[15]  
Cohney SJ, 1999, MOL CELL BIOL, V19, P4980
[16]   Potentiation of growth hormone-induced liver suppressors of cytokine signaling messenger ribonucleic acid by cytokines [J].
Colson, A ;
Le Cam, A ;
Maiter, D ;
Edery, M ;
Thissen, JP .
ENDOCRINOLOGY, 2000, 141 (10) :3687-3695
[17]   STAT5b mediates the GH-induced expression of SOCS-2 and SOCS-3 mRNA in the liver [J].
Davey, HW ;
McLachlan, MJ ;
Wilkins, RJ ;
Hilton, DJ ;
Adams, TE .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1999, 158 (1-2) :111-116
[18]  
De Sepulveda P, 1999, EMBO J, V18, P904
[19]   SOCS-3 is an insulin-induced negative regulator of insulin signaling [J].
Emanuelli, B ;
Peraldi, P ;
Filloux, C ;
Sawka-Verhelle, D ;
Hilton, D ;
Van Obberghen, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (21) :15985-15991
[20]   A new protein containing an SH2 domain that inhibits JAK kinases [J].
Endo, TA ;
Masuhara, M ;
Yokouchi, M ;
Suzuki, R ;
Sakamoto, H ;
Mitsui, K ;
Matsumoto, A ;
Tanimura, S ;
Ohtsubo, M ;
Misawa, H ;
Miyazaki, T ;
Leonor, N ;
Taniguchi, T ;
Fujita, T ;
Kanakura, Y ;
Komiya, S ;
Yoshimura, A .
NATURE, 1997, 387 (6636) :921-924