Distinctive roles for prolactin and, growth hormone in the activation of signal transducer and activator of transcription 5 in pancreatic islets of Langerhans

被引:102
作者
Brelje, TC [1 ]
Stout, LE [1 ]
Bhagroo, NV [1 ]
Sorenson, RL [1 ]
机构
[1] Univ Minnesota, Sch Med, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
关键词
D O I
10.1210/en.2004-0201
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although the beta-cells of the pancreatic islets of Langerhans express both prolactin (PRL) and GH receptors, we have observed that PRL is considerably more effective than GH in the up-regulation of islet function in vitro. This study examined whether differences in the activation of the Janus kinase 2/signal transducer and activator of transcription (STAT) 5 signaling pathway by these closely related receptors may be involved in this disparity. The activation of STAT5B by PRL was biphasic, with an initial peak within 30 min, a nadir between 1 and 3 h, and prolonged activation after 4 h. In contrast, the response to GH was transient for 1 h. The importance of the long-term activation of STAT5B by PRL was supported by the similar dose response curves for STAT5B activation and the PRL-induced increases in insulin secretion and islet cell proliferation. Because the pulsatile secretion of GH affects its actions in other target tissues, the ability of pretreatment with either hormone to affect subsequent stimulation was also examined. Surprisingly, the response to PRL was inhibited by prior exposure for less than 3 h to either PRL or GH and disappeared with a longer pretreatment with either hormone. Similar to other tissues, the response to GH was inhibited by any length of prior exposure to GH. However, pretreatment with PRL had no effect. These experiments are the first demonstration of the transient desensitization of the PRL receptor by either PRL or GH pretreatment in any tissue and the desensitization of GH stimulation in islet cells. These observations provide insight into the mechanisms that regulate the desensitization of these receptors and, more importantly, allow the long-term activation of STAT5B by the PRL receptor. These results may apply to other members of the cytokine superfamily of receptors. We also demonstrate that the increase in islet cell proliferation required continuous stimulation with PRL, whereas the smaller effect with GH occurred with either continuous or pulsatile stimulation. In summary, this study demonstrates that islets are sensitive to the temporal pattern of stimulation by these hormones and provides a new basis for understanding their physiological roles in the regulation of islet function.
引用
收藏
页码:4162 / 4175
页数:14
相关论文
共 70 条
[51]   EFFECT OF MTTW15 MAMMOSOMATOTROPIC TUMORS ON PANCREATIC-ISLET HORMONES [J].
PARSONS, JA ;
HARTFEL, MA ;
HEGRE, OD ;
MCEVOY, RC .
DIABETES, 1983, 32 (01) :67-74
[52]   Prolactin induction of insulin gene expression: the roles of glucose and glucose transporter-2 [J].
Petryk, A ;
Fleenor, D ;
Driscoll, P ;
Freemark, M .
JOURNAL OF ENDOCRINOLOGY, 2000, 164 (03) :277-286
[53]   Inhibition and restoration of prolactin signal transduction by suppressors of cytokine signaling [J].
Pezet, A ;
Favre, H ;
Kelly, PA ;
Edery, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (35) :24497-24502
[54]   SOCS/CIS protein inhibition of growth hormone-stimulated STAT5 signaling by multiple mechanisms [J].
Ram, PA ;
Waxman, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (50) :35553-35561
[55]   Interaction of growth hormone-activated STATs with SH2-containing phosphotyrosine phosphatase SHP-1 and nuclear JAK2 tyrosine kinase [J].
Ram, PA ;
Waxman, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (28) :17694-17702
[56]   Role of the cytokine-inducible SH2 protein CIS in desensitization of STAT5b signaling by continuous growth hormone [J].
Ram, PK ;
Waxman, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (50) :39487-39496
[57]   The effect of suppressor of cytokine signaling 3 on GH signaling in β-cells [J].
Ronn, SG ;
Hansen, JA ;
Lindberg, K ;
Karlsen, AE ;
Billestrup, N .
MOLECULAR ENDOCRINOLOGY, 2002, 16 (09) :2124-2134
[58]   INTRACELLULAR PROCESSING OF GROWTH-HORMONE RECEPTORS BY ADIPOCYTES IN PRIMARY CULTURE [J].
ROUPAS, P ;
HERINGTON, AC .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1988, 57 (1-2) :93-99
[59]   GH inhibits interferon-γ-induced signal transducer and activator of transcription-1 activation and expression of the inducible isoform of nitric oxide synthase in INS-1 cells [J].
Sekine, N ;
Fukumoto, S ;
Ishikawa, T ;
Okazaki, T ;
Fujita, T .
ENDOCRINOLOGY, 2001, 142 (09) :3909-3916
[60]  
SILVA CM, 1994, J BIOL CHEM, V269, P27532