Leptin-induced nuclear translocation of STAT3 immunoreactivity in hypothalamic nuclei involved in body weight regulation

被引:165
作者
Hübschle, T
Thom, E
Watson, A
Roth, J
Klaus, S
Meyerhof, W
机构
[1] Univ Giessen, Inst Vet Physiol, D-35392 Giessen, Germany
[2] German Inst Human Nutr, Dept Biochem, D-14558 Potsdam, Germany
[3] German Inst Human Nutr, Dept Physiol Nutr & Mol Genet, D-14558 Potsdam, Germany
关键词
hypothalamus; food intake; appetite control; leptin; interleukin-6; cytokines; transcription factors; signal transducers and activator of transcription; STAT3; c-Fos; immunohistochemistry; confocal microscopy;
D O I
10.1523/JNEUROSCI.21-07-02413.2001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Leptin is involved in the hypothalamic control of food intake and body weight. Fos immunohistochemistry has been used to functionally map leptin target neurons involved in these regulatory processes. However, only a subset of hypothalamic neurons expressing the long form of the leptin receptor (Ob-Rb) also coexpress the neuronal activation marker Fos after leptin stimulation. To functionally map all leptin target neurons, regardless of whether leptin-mediated neuronal activation or inhibition occurs, we immunohistochemically investigated the leptin-induced nuclear translocation of the signal transducer and activator of transcription molecule STAT3, which represents a crucial step in the regulation of leptin-dependent gene expression. As proven by colocalization studies with the nuclear 4',6-diamidino-2-phenylindole dilactate stain, intracerebroventricular leptin treatment, but not intracerebroventricular application of pyrogen-free saline, induced a time-dependent nuclear translocation of STAT3 immunoreactivity in hypothalamic nuclei, with strong nuclear STAT3 signals detectable in the arcuate nucleus, the lateral hypothalamus, and the ventro-medial and dorsomedial hypothalamic nuclei. This leptin-induced STAT3 translocation pattern proved to be distinct from that induced by interleukin-6, another cytokine using STAT3 in its signaling pathway. Combined immunohistochemical STAT3 and Fos detection after leptin treatment revealed a higher number of STAT3-positive than Fos-positive cell nuclei in the aforementioned hypothalamic structures and showed that Fos immunoreactivity colocalized only in a subset of all leptin-responsive STAT3 nuclei. These results suggest that the detection of nuclear STAT3 immunoreactivity represents a new neuroanatomical tool to functionally map central leptin actions. They further support the importance of ventrally located caudal hypothalamic structures representing the main leptin targets involved in body weight regulation.
引用
收藏
页码:2413 / 2424
页数:12
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[1]   Activation of downstream signals by the long form of the leptin receptor [J].
Banks, AS ;
Davis, SM ;
Bates, SH ;
Myers, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (19) :14563-14572
[2]   Leptin receptor long-form splice-variant protein expression in neuron cell bodies of the brain and co-localization with neuropeptide Y mRNA in the arcuate nucleus [J].
Baskin, DG ;
Schwartz, MW ;
Seeley, RJ ;
Woods, SC ;
Porte, D ;
Breininger, JF ;
Jonak, Z ;
Schaefer, J ;
Krouse, M ;
Burghardt, C ;
Campfield, LA ;
Burn, P ;
Kochan, JP .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1999, 47 (03) :353-362
[3]   Divergent signaling capacities of the long and short isoforms of the leptin receptor [J].
Bjorbaek, C ;
Uotani, S ;
da Silva, B ;
Flier, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (51) :32686-32695
[4]   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
[5]   A COMPARISON OF 2 IMMEDIATE-EARLY GENES, C-FOS AND NGFI-B, AS MARKERS FOR FUNCTIONAL ACTIVATION IN STRESS-RELATED NEUROENDOCRINE CIRCUITRY [J].
CHAN, RKW ;
BROWN, ER ;
ERICSSON, A ;
KOVACS, KJ ;
SAWCHENKO, PE .
JOURNAL OF NEUROSCIENCE, 1993, 13 (12) :5126-5138
[6]   Evidence that the diabetes gene encodes the leptin receptor: Identification of a mutation in the leptin receptor gene in db/db mice [J].
Chen, H ;
Charlat, O ;
Tartaglia, LA ;
Woolf, EA ;
Weng, X ;
Ellis, SJ ;
Lakey, ND ;
Culpepper, J ;
Moore, KJ ;
Breitbart, RE ;
Duyk, GM ;
Tepper, RI ;
Morgenstern, JP .
CELL, 1996, 84 (03) :491-495
[7]   Proopiomelanocortin neurons are direct targets for leptin in the hypothalamus [J].
Cheung, CC ;
Clifton, DK ;
Steiner, RA .
ENDOCRINOLOGY, 1997, 138 (10) :4489-4492
[8]   The weight-reducing effect of an intracerebroventricular bolus injection of leptin in genetically Obese falfa rats - Reduced sensitivity compared with lean animals [J].
Cusin, I ;
RohnerJeanrenaud, F ;
StrickerKrongrad, A ;
Jeanrenaud, B .
DIABETES, 1996, 45 (10) :1446-1451
[9]   STATs and gene regulation [J].
Darnell, JE .
SCIENCE, 1997, 277 (5332) :1630-1635
[10]   Leptin activates hypothalamic CART neurons projecting to the spinal cord [J].
Elias, CF ;
Lee, C ;
Kelly, J ;
Aschkenasi, C ;
Ahima, RS ;
Couceyro, PR ;
Kuhar, MJ ;
Saper, CB ;
Elmquist, JK .
NEURON, 1998, 21 (06) :1375-1385