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层粘连蛋白通过与整合素α6β1相互作用抑制人黄素化颗粒细胞的孕酮生成。

Laminin suppresses progesterone production by human luteinizing granulosa cells via interaction with integrin alpha 6 beta 1.

作者信息

Fujiwara H, Honda T, Ueda M, Nakamura K, Yamada S, 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. 1997 Jul;82(7):2122-8. doi: 10.1210/jcem.82.7.4095.

Abstract

We previously raised a murine monoclonal antibody (mAb), OG-1, against human granulosa cells (GC) and reported that human GC express the OG-1 antigen with the highest immunoreactivity during the periovulatory phase. Later, we showed that the OG-1 antigen is identical to human integrin alpha 6, and that human GC express integrin alpha 6 beta 1, but not alpha 6 beta 4. In the present study, we examined the expression of laminin (LN), the ligand for integrin alpha 6 beta 1. Flow cytometry showed that LN was bound to the cell surface of some GC obtained from preovulatory follicles of patients undergoing in vitro fertilization. Immunohistochemistry showed that LN was detected between luteinizing GC in the early corpora lutea. To examine the effect of LN on steroidogenesis by human luteinizing GC, GC obtained from patients undergoing in vitro fertilization were cultured on mouse LN-coated or noncoated plastic dishes in medium containing 5% FCS for 24 h. In the absence or presence in hCG (1 IU/mL), GC cultured on LN-coated dishes produced 0.70- and 0.67-fold less progesterone than those on noncoated dishes, respectively (P < 0.05). We examined the effect of the interaction of integrin alpha 6 beta 1 and LN on steroidogenesis by human luteinizing GC. We cultured GC with 5 micrograms/mL of the anti-alpha 6 mAb GoH3, which inhibits the interaction between human integrin alpha 6 beta 1 and mouse LN, or with a control rat mAb (TER199) on mouse LN-coated dishes in serum-free medium for 24 h. In the absence or presence of hCG (1 IU/mL), GC cultured with GoH3 produced 1.97- and 1.94-fold more progesterone than the control cells (P < 0.01 and P < 0.05, respectively). In contrast, when GC were cultured on dishes coated with type IV collagen, progesterone production was not enhanced by GoH3. Furthermore, the anti-alpha 6 mAb OG-1, which does not inhibit the interaction between integrin alpha 6 beta 1 and LN, had no effect on the progesterone production by GC cultured on LN. These results indicate that LN suppresses the luteinization of human luteinizing GC via integrin alpha 6 beta 1 and that integrin alpha 6 beta 1 regulates the luteinization of human GC during the periovulatory phase.

摘要

我们之前制备了一种针对人颗粒细胞(GC)的鼠单克隆抗体(mAb)OG-1,并报道人GC在排卵前期表达OG-1抗原,免疫反应性最高。后来,我们发现OG-1抗原与人整合素α6相同,且人GC表达整合素α6β1,但不表达α6β4。在本研究中,我们检测了整合素α6β1的配体层粘连蛋白(LN)的表达。流式细胞术显示,LN与从接受体外受精患者的排卵前卵泡中获取的部分GC的细胞表面结合。免疫组织化学显示,在早期黄体的黄体化GC之间可检测到LN。为了检测LN对人黄体化GC类固醇生成的影响,将从接受体外受精患者获取的GC在含5%胎牛血清的培养基中,于包被有小鼠LN或未包被的塑料培养皿中培养24小时。在不存在或存在人绒毛膜促性腺激素(hCG,1 IU/mL)的情况下,在包被有LN的培养皿中培养的GC产生的孕酮分别比在未包被培养皿中的少0.70倍和0.67倍(P<0.05)。我们检测了整合素α6β1与LN的相互作用对人黄体化GC类固醇生成的影响。我们在无血清培养基中,将GC与5微克/毫升抑制人整合素α6β1与小鼠LN相互作用的抗α6单克隆抗体GoH3或对照大鼠单克隆抗体(TER199)一起在包被有小鼠LN的培养皿中培养24小时。在不存在或存在hCG(1 IU/mL)的情况下,与GoH3一起培养的GC产生的孕酮分别比对照细胞多1.97倍和1.94倍(分别为P<0.01和P<0.05)。相反,当GC在包被有IV型胶原的培养皿中培养时,GoH3不会增强孕酮的产生。此外,不抑制整合素α6β1与LN相互作用的抗α6单克隆抗体OG-1对在LN上培养的GC的孕酮产生没有影响。这些结果表明,LN通过整合素α6β1抑制人黄体化GC的黄体化,且整合素α6β1在排卵前期调节人GC的黄体化。

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