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细胞因子刺激人黄体化颗粒细胞上二肽基肽酶-IV的表达。

Cytokines stimulate dipeptidyl peptidase-IV expression on human luteinizing granulosa cells.

作者信息

Fujiwara H, Fukuoka M, Yasuda K, Ueda M, Imai K, Goto Y, Suginami H, Kanzaki H, Maeda M, Mori T

机构信息

Department of Gynecology and Obstetrics, Faculty of Medicine, Kyoto University, Japan.

出版信息

J Clin Endocrinol Metab. 1994 Oct;79(4):1007-11. doi: 10.1210/jcem.79.4.7962267.

Abstract

We have previously reported that dipeptidyl peptidase-IV (DPPIV) is a differentiation antigen for human granulosa cells that is initially expressed during corpus luteum formation. To investigate the involvement of cytokines in luteal cell differentiation, we examined the expression and activity of DPPIV in human luteinizing granulosa cells cultured in vitro. Human granulosa cells obtained from patients who had undergone in vitro fertilization were cultured for 7 days in the absence (controls) or presence of hCG (1 U/mL), tumor necrosis factor-alpha (TNF alpha; 10 ng/mL), or interleukin 1-alpha (IL-1 alpha; 10 ng/mL). Flow cytometry showed that the percentage of cultured granulosa cells treated with TNF alpha and IL-1 alpha that was positive for DPPIV expression was significantly higher than that in controls (43.7 +/- 5.4% and 43.4 +/- 5.6%, respectively, vs. 21.7 +/- 3.5%; P < 0.01), whereas hCG treatment produced no remarkable difference in DPPIV expression (24.0 +/- 5.2%). The DPPIV activity of cells treated with TNF alpha and IL-1 alpha was also significantly higher than that of controls, whereas hCG treatment produced no significant difference from control values. These findings indicate that TNF alpha and IL-1 alpha stimulate DPPIV expression and activity in human luteinizing granulosa cells in vitro and suggest the involvement of cytokines in the differentiation of granulosa cells during corpus luteum formation.

摘要

我们之前曾报道,二肽基肽酶-IV(DPPIV)是人类颗粒细胞的一种分化抗原,在黄体形成过程中开始表达。为了研究细胞因子在黄体细胞分化中的作用,我们检测了体外培养的人黄素化颗粒细胞中DPPIV的表达和活性。从接受体外受精的患者中获取的人颗粒细胞,在无(对照组)或有hCG(1 U/mL)、肿瘤坏死因子-α(TNFα;10 ng/mL)或白细胞介素1-α(IL-1α;10 ng/mL)的情况下培养7天。流式细胞术显示,用TNFα和IL-1α处理的培养颗粒细胞中DPPIV表达阳性的百分比显著高于对照组(分别为43.7±5.4%和43.4±5.6%,而对照组为21.7±3.5%;P<0.01),而hCG处理在DPPIV表达上没有显著差异(24.0±5.2%)。用TNFα和IL-1α处理的细胞的DPPIV活性也显著高于对照组,而hCG处理与对照值相比没有显著差异。这些发现表明,TNFα和IL-1α在体外刺激人黄素化颗粒细胞中DPPIV的表达和活性,并提示细胞因子参与黄体形成过程中颗粒细胞的分化。

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