Stepanyan Z, Kocharyan A, Pyrski M, Hübschle T, Watson A M D, Schulz S, Meyerhof W
Department of Molecular Genetics, German Institute of Human Nutrition, Potsdam-Rehbrücke, Germany.
J Neuroendocrinol. 2003 Sep;15(9):822-30. doi: 10.1046/j.1365-2826.2003.01077.x.
Hypothalamic leptinoceptive neurones can be visualized by histochemical demonstration of leptin-induced nuclear translocation of the signalling molecule STAT3. We investigated the relationship of the leptinoceptive neurones to the somatostatin signalling system. With double-labelling immunohistochemistry, we studied the colocalization of leptin-activated transcription factor, STAT3, with somatostatin receptor subtypes, sst1, sst2A, sst2B, sst3 and sst4, or the neuropeptide itself, in the rat hypothalamus. Immunoreactivity for all the entities was widely distributed throughout the entire hypothalamus. Despite the wide distribution, only few cases of colocalization of somatostatin with leptin-activated STAT3 were detected in the paraventricular, arcuate and dorsomedial nuclei. A moderate to high degree of colocalization of nuclear STAT3 and all investigated subtypes of somatostatin receptors was found in the lateral and dorsal hypothalamic areas and in the dorsomedial hypothalamic nucleus. Immunoreactivity for sst1, sst2B and sst4 was present in STAT3-containing nuclei of the paraventricular, periventricular, arcuate and ventromedial hypothalamic neurones, as well as in the retrochiasmatic and posterior hypothalamic areas. Despite the wide distribution of sst2A in the rat hypothalamus, few events of colocalization with leptin-activated STAT3 were observed in the dorsomedial nucleus and in the lateral and dorsal hypothalamic areas only. Many leptin-responsive neurones of the dorsal, lateral, periarcuate, perifornical and posterior hypothalamic areas, as well as in the ventromedial and dorsomedial hypothalamic nuclei, displayed sst3 immunoreactivity at their neuronal cilia. These results provide strong anatomical evidence for the direct interaction of leptin and the somatostatin systems in neuroendocrine control loops such as the energy homeostasis, growth or stress response.
通过对瘦素诱导的信号分子信号转导和转录激活因子3(STAT3)核转位进行组织化学示踪,可观察到下丘脑的瘦素感受神经元。我们研究了瘦素感受神经元与生长抑素信号系统之间的关系。利用双标免疫组织化学技术,我们研究了瘦素激活的转录因子STAT3与生长抑素受体亚型sst1、sst2A、sst2B、sst3和sst4或神经肽本身在大鼠下丘脑的共定位情况。所有这些物质的免疫反应性广泛分布于整个下丘脑。尽管分布广泛,但仅在室旁核、弓状核和背内侧核中检测到少数生长抑素与瘦素激活的STAT3共定位的情况。在外侧和背侧下丘脑区域以及背内侧下丘脑核中发现核STAT3与所有研究的生长抑素受体亚型存在中度至高程度的共定位。sst1、sst2B和sst4的免疫反应性存在于室旁核、室周核、弓状核和腹内侧下丘脑神经元含STAT3的细胞核中,以及视交叉后和下丘脑后部区域。尽管sst2A在大鼠下丘脑中分布广泛,但仅在背内侧核以及外侧和背侧下丘脑区域观察到少数与瘦素激活的STAT3共定位的情况。背侧、外侧、弓状核周围、穹窿周和下丘脑后部区域以及腹内侧和背内侧下丘脑核中的许多瘦素反应性神经元在其神经元纤毛处显示sst3免疫反应性。这些结果为瘦素与生长抑素系统在神经内分泌控制回路(如能量稳态、生长或应激反应)中的直接相互作用提供了有力的解剖学证据。