Hübschle T, Thom E, Watson A, Roth J, Klaus S, Meyerhof W
German Institute of Human Nutrition, Departments of Biochemistry and Physiology of Nutrition and Molecular Genetics, D-14558 Potsdam-Rehbrücke, Germany.
J Neurosci. 2001 Apr 1;21(7):2413-24. doi: 10.1523/JNEUROSCI.21-07-02413.2001.
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 ventromedial 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.
瘦素参与下丘脑对食物摄入和体重的控制。Fos免疫组化已被用于对参与这些调节过程的瘦素靶神经元进行功能定位。然而,在瘦素刺激后,只有一部分表达瘦素受体长形式(Ob-Rb)的下丘脑神经元也共表达神经元激活标记Fos。为了对所有瘦素靶神经元进行功能定位,无论瘦素介导的神经元激活还是抑制是否发生,我们通过免疫组化研究了瘦素诱导的信号转导和转录激活分子STAT3的核转位,这是瘦素依赖性基因表达调节中的关键步骤。通过与核4',6-二脒基-2-苯基吲哚二乳酸染色的共定位研究证明,脑室内注射瘦素,而非注射无热原盐水,可诱导下丘脑核中STAT3免疫反应性随时间的核转位,在弓状核、下丘脑外侧区以及下丘脑腹内侧核和背内侧核中可检测到强烈的核STAT3信号。这种瘦素诱导的STAT3转位模式被证明与白细胞介素-6诱导的模式不同,白细胞介素-6是另一种在其信号通路中使用STAT3的细胞因子。瘦素处理后联合免疫组化检测STAT3和Fos发现,在上述下丘脑结构中,STAT3阳性细胞核的数量多于Fos阳性细胞核,并且表明Fos免疫反应性仅在所有对瘦素反应的STAT3核的一个子集中共定位。这些结果表明,检测核STAT3免疫反应性代表了一种用于对中枢瘦素作用进行功能定位的新神经解剖学工具。它们进一步支持了位于腹侧的下丘脑尾部结构作为参与体重调节的主要瘦素靶标的重要性。