期刊文献+

受激活调节正常T细胞表达和分泌因子及其受体CCR1、CCR5在大鼠附睾的表达与定位

Expression of regulated upon activation normal T-cell expressed and secreted and its receptors CCR1 and CCR5 in rat epididymis~
下载PDF
导出
摘要 目的:观察受激活调节正常T细胞表达和分泌因子(RANTEs)与其受体CCR1、CCR5在大鼠附睾中的表达和定位。方法:采用免疫组织化学法检测成年大鼠附睾上皮RANTES及其受体的细胞定位,免疫荧光双标染色分别显示RANTES与CCR1、CCR5的细胞共定位情况。RT-PCR检测RANTES及其受体mRNA表达水平,免疫印迹检测RAN—TES及其受体的蛋白量。结果:RANTES与其受体CCR1、CCR5在大鼠附睾各段呈特异性表达。免疫印迹在大鼠附睾各段检测到RANTES及其受体CCR1、CCR5特异性蛋白条带。RANTES与其受体CCR1、CCR5在大鼠附睾上皮主要表达于基细胞。双重免疫荧光显示RANTES与CCR1、CCR5在附睾管基细胞共存。结论:RANTES可能通过自分泌或(和)旁分泌方式在大鼠附睾基细胞功能活动方面起重要作用。 Objective: To observe the expression and the cellular localization of regulated upon activation normal T-cell expressed and secreted (RANTES) as well as its receptors CCR1 and CCR5 in the rat epididymis. Methods: Reverse transcription-polymerase chain reaction (RT-PCR) was used to examine the expression of RANTES and its receptors mRNA in rat epididymis. The presence of RANTES and its receptors protein was assayed by Western blotting. Paraffin-embedded sections were prepared from rat epididymis, and immunohistochemical staining was carried out to detect cellular location of RANTES and its receptors. Colocalization of RANTES, CCR1, and CCR5 in rat epididymis was detected by immunofluorescence. Results: RT-PCR analysis showed the specific expression of RANTES and its receptors in the segments of adult rat epididymis. The distinctive single band of RANTES protein and its receptors protein was identified in the segments of rat epididymis with Western blotting. The positive staining of RANTES and its receptors were mainly observed in the basal cells of the epididymal epithelium. The immunofluorescence of RANTES coincided with CCR1 and CCR5 in the basal cells of epididymis. Conclusion : The expressions of RANTES and its receptors CCR1 and CCR5 were found restricted in the basal cells of the rat epididymis. These results revealed that RANTES may play a role in the physiological function of the basal cells of rat epididymis through autocrine or/and paracrine way.
出处 《解剖学杂志》 CAS CSCD 北大核心 2013年第3期269-273,共5页 Chinese Journal of Anatomy
基金 国家自然科学基金(81170614) 陕西省自然科学基金(2010JM4001)
关键词 受激活调节正常T细胞表达和分泌因子 CCR1 CCR5 附睾 基细胞 大鼠 regulated upon activation normal T-cell expressed and secreted CCR1 CCR5 epididymis basal cell rat
  • 相关文献

参考文献12

  • 1Cornwall G A. New insights into epididymal biology and function[J]. Hum Reprod Update,2009,15(2): 213-227.
  • 2LevyJ A. The unexpected pleiotropic activities of RANTES[J].J Immuno] , 2009,182(7) :3945-3946.
  • 3李臻,张远强.β-趋化性细胞因子RANTES的研究进展[J].生理科学进展,2006,37(1):79-82. 被引量:18
  • 4Naz R K, Leslie M H. Immunobiologic implication of RANTES in seminal plasma of fertile, infertile and immunoinfertile men[J]. AmJ Reprod Immunol , 2000,44(4): 197-204.
  • 5PolitchJ A, Tucker L, Bowman F P, et al. Concentrations and significance of cytokines and other immunologic factors in semen of healthy fertile men[n Hum Reprod, 2007,22(11) :2928-2935.
  • 6孙质健,李臻,赵洁,张远强.β-趋化性细胞因子RANTES在人睾丸和附睾中的表达[J].生殖与避孕,2006,26(10):593-597. 被引量:3
  • 7Hinton B T, Dott H M. Setchell B P. Measurement of the motili?ty of rat spermatozoa collected by micropuncture from the testis and from different regions along the epididymis[]}J Reprod Fer- til, 1979, 55 (1): 167-172.
  • 8Li Z, Sun ZJ, Liao C G, er al. Regulated upon activation normal Tvcell expressed and secreted originating from the epididymis dif?ferentially associates with viable and defective spermatozoa[J} Fertil Steril,2010,93(S):2 661-2 667.
  • 9Olson G E, NagDas S K, Winfrey V P. Structural differentiation of spermatozoa during post-testicular maturation. / /Robaire B, Hinton B T Ceds ). The epididymis: from molecules to clinical practicet M). New York: Kluwer Academic/Plenum Publishers, 2002:371-387.
  • 10Shum W W, Ruan Y C, Da Silva N, et at. Establishment of cell?cell cross talk in the epididymis: control of luminal acidification[nJ Androl,2011,32(6):576-586.

二级参考文献23

  • 1康振华,王为忠,陈冬利,王春艳,朱参胜,杜俊峰,金伯泉.抗人RANTES分子单克隆抗体的制备及特性鉴定[J].细胞与分子免疫学杂志,2005,21(3):322-324. 被引量:10
  • 2李臻,张远强.β-趋化性细胞因子RANTES的研究进展[J].生理科学进展,2006,37(1):79-82. 被引量:18
  • 3Proudfoot AE, Handel TM, Johnson Z, et al. Glycosaminoglycan binding and oligomerization are essential for the in vivo activity of certain chemokines. Proc Natl Acad Sci USA, 2003, 100 : 1885 - 1890.
  • 4Marino AP, Silva AA, Santos PV, et al. CC-chemokine receptors : a potential therapeutic target for Trypanosoma cruzielicited myocarditis. Mem Inst Oswaldo Cruz, 2005, 100( Suppl 1 ) : 93 - 96.
  • 5Sigrist S, Oberholzer J, Bohbot A, et al. Activation of human macrophages by allogeneic islets preparations: inhibition by AOP-RANTES and heparinoids. Immunology, 2004,111 : 416- 421.
  • 6Vielhauer V, Berning E, Eis V, et al. CCR1 blockade reduces interstitial inflammation and fibrosis in mice with glomerulosclerosis and nephrotic syndrome. Kidney Int, 2004,66 : 2264 - 2278.
  • 7Schols D. HIV co-receptors as targets for antiviral therapy.Curr Top Med Chem, 2004, 4 : 883 - 893.
  • 8Ferreira MA. Cytokine expression in allergic inflammation:systematic review of in vivo challenge studies. Mediators Inflamm, 2003, 12 : 259 -267.
  • 9Johnson Z, Kosco-Vilbois MH, Herren S, et al. Interference with heparin binding and oligomerization creates a novel anti-inflammatory strategy targeting the chemokine system. J Immunol, 2004, 173 : 5776 - 5785.
  • 10Jennes W, Sawadogo S, Koblavi-Deme S, et al. Cellular human immunodeficicncy virus (HIV)-protective factors: a comparison of HIV-exposed seronegative female sex workers and female blood donors in Abidjan, Cote dlvoire. J Infect Dis, 2003, 187 : 206-214.

共引文献19

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部