Tsumanuma I, Jin L, Zhang S, Bayliss J M, Scheithauer B W, Lloyd R V
Department of Laboratory Medicine and Pathology, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.
Pituitary. 2000 Dec;3(4):211-20. doi: 10.1023/a:1012994712851.
Leptin is an adipocyte-derived cytokine with many functions including signaling the status of body energy stores through activation of the leptin receptor (OBR). Activation of the long form of OB-R (OB-Rb) results in JAK2 phosphorylation, activation of STATs, and subsequent gene expression. Activated STAT3 induces SOCS-3 expression in some cell types, which in turn down-regulates the JAK/STAT pathway. Although both leptin and OB-R are expressed in pituitary cells, the mechanism of signal transduction and its regulation in this organ has not been studied extensively. In these experiments we show that leptin reduces proliferation in a human pituitary cell line (HP75) and also increased apoptosis in these cells. Leptin also increased SOCS-3 mRNA and protein expression and tyrosine-phosphorylation in the HP75 human pituitary cell line. These findings suggest that SOCS-3 plays an important role in the inhibition of proximal leptin signal transduction in the anterior pituitary.
瘦素是一种由脂肪细胞产生的细胞因子,具有多种功能,包括通过激活瘦素受体(OBR)来传递身体能量储备状态的信号。长型OB-R(OB-Rb)的激活会导致JAK2磷酸化、STATs激活以及随后的基因表达。激活的STAT3在某些细胞类型中诱导SOCS-3表达,进而下调JAK/STAT途径。尽管瘦素和OB-R在垂体细胞中均有表达,但该器官中信号转导及其调节机制尚未得到广泛研究。在这些实验中,我们表明瘦素可降低人垂体细胞系(HP75)的增殖,并增加这些细胞的凋亡。瘦素还可增加HP75人垂体细胞系中SOCS-3 mRNA和蛋白表达以及酪氨酸磷酸化。这些发现表明,SOCS-3在抑制垂体前叶近端瘦素信号转导中起重要作用。