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有证据表明,α5β1整合素介导睾丸间质细胞与纤连蛋白的结合,并增强体外培养时由支持细胞分泌的促有丝分裂因子所刺激的睾丸间质细胞增殖。

Evidence that α5β1 integrins mediate Leydig cell binding to fibronectin and enhance Leydig cell proliferation stimulated by a Sertoli cell-secreted mitogenic factor in vitro.

作者信息

Wu N, Murono E P, Carver W E, Terracio L, Bacro T

机构信息

Research Service, Dorn Veterans' Hospital and Department of Physiology, University of South Carolina School of Medicine, Columbia, SC.

出版信息

Endocrine. 1996 Aug;5(1):75-83. doi: 10.1007/BF02738659.

Abstract

We reported previously that coculture of immature rat Sertoli cells with Leydig cells or the addition of a concentrate from Sertoli cell-conditioned medium (SCCM) stimulated Leydig cell [(3)H]-thymidine incorporation, increased cell number, and altered Leydig cell morphology (Wu and Murono, 1994). In the present studies, the effect of various extracellular matrix proteins on immature Leydig cell binding, proliferation and response to SCCM concentrate was investigated. Pretreatment of culture wells with 50 μg/mL collagen I or 10 μg/mL laminin inhibited Leydig cell binding to culture wells about 95 and 89%, respectively; however, 5 μg/mL fibronectin did not change the level of attachment. The binding of Leydig cells to fibronectin was reduced by antifibronectin or-β1 integrin antibodies (66 and 91%, respectively). Treatment of culture wells with five or 50 μg/mL fibronectin alone increased [(3)H]thymidine incorporation about twofold. When Leydig cells were cultured in wells precoated with increasing concentrations of fibronectin and then treated with SCCM concentrate for 2 d, [(3)H]-thymidine incorporation increased progressively with the concentration of fibronectin, beyond the levels observed with SCCM concentrate alone. This response was associated with increases in both Leydig cell number and labeling indices. When Leydig cells were cultured on fibronectin, their numbers increased by 3.7-and 5.1-fold following treatment with SCCM concentrates or coculture for 6 d, respectively; whereas, they increased 2.6- and 3.9-fold, respectively, when cultured on plastic. Labeling indices of Leydig cells cultured on plastic for 2 d and treated with SCCM or cocultured were 6.9 and 11.9%, respectively, while labeling indices of Leydig cells grown on fibronectin increased further to 17.6 and 26.3%, respectively. α5β1 integrin complexes and α5 integrin mRNA were expressed in Leydig cells, suggesting that binding to fibronectin may be mediated by α5β1 integrins, a fibronectin receptor. These results suggest that Leydig cell proliferation stimulated by a Sertoli cell-secreted mitogenic factor(s) is enhanced by Leydig cell binding fibronectin, and that this binding may be mediated by α5β1 integrins.

摘要

我们之前报道过,未成熟大鼠支持细胞与睾丸间质细胞共培养,或添加支持细胞条件培养基(SCCM)浓缩物,可刺激睾丸间质细胞的[³H]胸腺嘧啶核苷掺入,增加细胞数量,并改变睾丸间质细胞形态(Wu和Murono,1994年)。在本研究中,研究了各种细胞外基质蛋白对未成熟睾丸间质细胞黏附、增殖及对SCCM浓缩物反应的影响。用50μg/mLⅠ型胶原或10μg/mL层粘连蛋白预处理培养孔,分别使睾丸间质细胞与培养孔的黏附减少约95%和89%;然而,5μg/mL纤连蛋白并未改变黏附水平。抗纤连蛋白或β1整合素抗体可使睾丸间质细胞与纤连蛋白的黏附减少(分别为66%和91%)。单独用5或50μg/mL纤连蛋白处理培养孔,可使[³H]胸腺嘧啶核苷掺入增加约两倍。当睾丸间质细胞在预包被有浓度递增的纤连蛋白的孔中培养,然后用SCCM浓缩物处理2天时,[³H]胸腺嘧啶核苷掺入随纤连蛋白浓度逐渐增加,超过单独使用SCCM浓缩物时观察到的水平。这种反应与睾丸间质细胞数量和标记指数的增加相关。当睾丸间质细胞在纤连蛋白上培养时,用SCCM浓缩物处理或共培养6天后,其数量分别增加3.7倍和5.1倍;而在塑料上培养时,分别增加2.6倍和3.9倍。在塑料上培养2天并用SCCM处理或共培养的睾丸间质细胞的标记指数分别为6.9%和11.9%,而在纤连蛋白上生长的睾丸间质细胞的标记指数进一步分别增加到17.6%和26.3%。α5β1整合素复合物和α5整合素mRNA在睾丸间质细胞中表达,表明与纤连蛋白的结合可能由纤连蛋白受体α5β1整合素介导。这些结果表明,支持细胞分泌的促有丝分裂因子刺激的睾丸间质细胞增殖,因睾丸间质细胞与纤连蛋白的结合而增强,且这种结合可能由α5β1整合素介导。

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