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雄激素对小鼠睾丸支持细胞Akt和MEK/Erk磷酸化水平的影响

The Effect of Androgens on Akt and MEK/Erk Phosphorylation in Mouse Testicular Sertoli Cells
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摘要 磷酸化信号通路在精子发生过程中有重要作用,本文研究小鼠睾丸支持细胞中雄激素诱导的蛋白磷酸化。研究中分离培养小鼠睾丸支持细胞,建立了稳定的培养体系。蛋白磷酸化抗体芯片结果显示,睾酮快速激活Akt及MEK/Erk的磷酸化,蛋白免疫印迹验证了芯片分析结果,且激酶磷酸化的激活是由AR介导。结果表明睾酮诱导小鼠睾丸支持细胞中Akt和MEK/Erk磷酸化。 Phosphorylation signaling pathway is critical for spermatogenesis, and the paper studied the proteinphosphorylation induced by androgen in mouse Sertoli cells. Sertoli cells were isolated from mouse testes,and we built astable culture system for the primary cultured cells. Protein phosphorylation signaling pathway antibody arrays datashowed that testosterone induced fast phosphorylation of Akt and MEK/ Erk. Western blot analysis agreed with the arraydata,and it also showed that the activation of the signaling pathways was mediated by AR. We concluded that theactivation of Akt and MEK/ Erk phosphorylation in mouse Sertoli cells was induced by testosterone.
作者 毛登启 邓琼 张建文 植凡 王瑞 张颖 方维 王宏亮 梁辉 MAO Deng-qi;DENG Qiong;ZHANG Jian-wen;ZHI Fan;WANG Rui;ZHANG Ying;Fang Wei;WANG Hong-liang;LIANG Hui(Department of Urology,The People’s Hospital of Longhua,Shenzhen 518109,China)
出处 《安徽师范大学学报(自然科学版)》 CAS 2018年第2期152-156,共5页 Journal of Anhui Normal University(Natural Science)
基金 深圳市科技计划项目(JCYJ20150402144905865 JCYJ20170307141840188) 深圳市龙华区科技创新项目(20150925A0410013)
关键词 支持细胞 雄激素 磷酸化 sertoli cell androgen phosphorylation
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  • 1[1]Fujimoto K, Yamamoto T, Kitano T, et al. Promotion of cathepsin L activity in newt spermatogonial apoptosis induced by prolactin. FEBS Lett, 2002, 521:43~46.
  • 2[2]Yan W, Suominen J, Toppari J. Stem cell factor protects germ cells from apoptosis in vitro. J Cell Sci, 2000, 113:161~168.
  • 3[3]Clifton RJ, O Donnell L, Robertson DM. Pachytene spermatocytes in co-cultre inhibit rat Sertoli cell synthesis of inhibin beta B-subunit and inhibin B but not the inhibin alpha-subunit. J Endocrinol, 2002, 172:565~574.
  • 4[4]Jeong D. Long-term culture and transplantation of murine testicular germ cells. J Androl, 2003,24:661~669.
  • 5[5]Tanaka A, Nagayoshi M, Awata S, et al. Completion of meiosis in human primary spermatocytes through in vitro coculture with Vero cells. Fertil Steril, 2003, 79:795~801.
  • 6[6]Lee DR, Kaproth MT, Parks HE. In vitro production of haploid germ cells from fresh or frozen-thawed testicular cells of neonatal bulls. Biol Reprod, 2001, 65:873~878.
  • 7[7]Pellegrini M, Grimaldi P, Rossi P, et al. Developmental expression of BMP4/ALK3/SMAD5 signaling pathway in the mouse testis: a potential role of BMP4 in spermatogonia differentiation. J Cell Sci, 2003, 116:3363~3372.
  • 8[8]Tesarik J, Mendoza C, Greco E. In vitro culture facilitates the selection of healthy spermatids for assisted reproduction. Fertil Steril, 1999,72:809~813.
  • 9[9]Kanatsu-Shinohara M, Ogonuki N, Inoue K, et al. Long-term proliferation in culture and germline transmission of mouse male germline stem cells. Biol Reprod, 2003,69:612~616.
  • 10[10]Feng LX, Chen Y, Dettin L, et al. Generation and in vitro differentiation of a spermatogonial cell line. Science, 2002, 297:392~395.

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