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肥胖的瘦素缺乏(ob/ob)小鼠下丘脑弓状核中信号转导和转录激活因子3(STAT3)信使核糖核酸及STAT3蛋白表达下调。

Down-regulated STAT3 messenger ribonucleic acid and STAT3 protein in the hypothalamic arcuate nucleus of the obese leptin-deficient (ob/ob) mouse.

作者信息

Håkansson-Ovesjö M L, Collin M, Meister B

机构信息

Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.

出版信息

Endocrinology. 2000 Nov;141(11):3946-55. doi: 10.1210/endo.141.11.7779.

Abstract

Leptin is a weight-reducing hormone produced by adipose tissue, which reduces food intake via hypothalamic leptin receptors and the JAK-STAT signaling pathway. In vivo studies have shown that leptin activates specifically STAT3 in the hypothalamus. We have studied the cellular localization of STAT3 messenger RNA (mRNA) and STAT3 protein in the mouse mediobasal hypothalamus using, respectively, in situ hybridization and immunohistochemistry. Strong STAT3 mRNA and STAT3 immunoreactivity was demonstrated in neurons located in the ventral part of the mouse arcuate nucleus. Comparison of STAT3 mRNA levels in the arcuate nucleus of lean control mice and obese leptin-deficient ob/ob mice showed that the levels of STAT3 mRNA in the arcuate nucleus were significantly lower (31% less in ob/ob mice), compared with control mice. Hybridization with a probe specific for STAT3alpha mRNA showed that the down-regulated STAT3 expression in the arcuate nucleus of ob/ob mice is represented by STAT3alpha. There was a marked difference in numbers and intensity of STAT3-immunoreactive cell bodies, with virtually no STAT3-immunoreactive cell bodies in the mediobasal hypothalamus of ob/ob mice, compared with control mice. Direct double-labeling immunofluorescence histochemistry of sections from control mice, combining a goat antiserum raised against a peptide sequence present in all leptin receptor isoforms (Ob-R) or a guinea pig anti-serum generated to a peptide sequence specific for Ob-Rb with rabbit STAT3 antiserum, demonstrated colocalization of STAT3 and Ob-R as well as colocalization of STAT3 and Ob-Rb, in many cell bodies of the arcuate nucleus. The results suggest that circulating leptin acts via leptin receptor-/STAT3-containing neurons in the ventral arcuate nucleus and that congenital leptin deficiency, as seen in obese ob/ob mice, results in a down-regulation of STAT3 mRNA and protein levels.

摘要

瘦素是一种由脂肪组织产生的减肥激素,它通过下丘脑瘦素受体和JAK-STAT信号通路减少食物摄入。体内研究表明,瘦素在下丘脑中特异性激活STAT3。我们分别使用原位杂交和免疫组织化学研究了小鼠中基底部下丘脑STAT3信使核糖核酸(mRNA)和STAT3蛋白的细胞定位。在位于小鼠弓状核腹侧的神经元中显示出强烈的STAT3 mRNA和STAT3免疫反应性。比较瘦素对照小鼠和肥胖瘦素缺乏的ob/ob小鼠弓状核中STAT3 mRNA水平,发现与对照小鼠相比,ob/ob小鼠弓状核中STAT3 mRNA水平显著降低(减少31%)。用针对STAT3α mRNA的特异性探针杂交表明,ob/ob小鼠弓状核中下调的STAT3表达由STAT3α代表。与对照小鼠相比,ob/ob小鼠中基底部下丘脑STAT3免疫反应性细胞体的数量和强度存在明显差异,几乎没有STAT3免疫反应性细胞体。对对照小鼠切片进行直接双标记免疫荧光组织化学,将针对所有瘦素受体异构体(Ob-R)中存在的肽序列产生的山羊抗血清或针对Ob-Rb特异性肽序列产生的豚鼠抗血清与兔STAT3抗血清结合,在弓状核的许多细胞体中证明了STAT3与Ob-R以及STAT3与Ob-Rb的共定位。结果表明,循环瘦素通过腹侧弓状核中含瘦素受体/STAT3的神经元起作用,并表明肥胖ob/ob小鼠中所见的先天性瘦素缺乏导致STAT3 mRNA和蛋白水平下调。

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