Klonisch Thomas, Steger Klaus, Kehlen Astrid, Allen William R, Froehlich Christine, Kauffold Johannes, Bergmann Martin, Hombach-Klonisch Sabine
Departments of Anatomy and Cell Biology, Martin Luther University Halle-Wittenberg, Faculty of Medicine, Halle, Germany.
Biol Reprod. 2003 Jun;68(6):1975-81. doi: 10.1095/biolreprod.102.008466. Epub 2003 Jan 8.
We employed molecular and immunological techniques to investigate the expression of INSL3, a member of the insulin-like superfamily, in prepubertal testis, postpubertal testes exhibiting normal and disturbed spermatogenesis, and cryptorchid testes of male horses. In addition, the partial cDNA coding sequences of the equine homologue of the human relaxin/INSL3-receptor Lgr8 were determined. Nonradioactive in-situ hybridization with a cRNA probe for equine Insl3 and immunohistochemistry with a specific rabbit INSL3 antiserum localized Insl3 transcripts and immunoreactive INSL3 ligand to Leydig cells in all types of testes investigated. Quantitative polymerase chain reaction analysis revealed a down-regulation of Insl3 and an up-regulation of the relaxin/INSL3-receptor expression in unilateral cryptorchid versus descended testes. Western blot analysis of protein extracts from adult normal and cryptorchid testes and prepubertal testes showed a single immunoreactive band at 14.5 kDa, which correlates with the predicted size of equine proINSL3. Densitometric analysis of Western blot data of adult normal testes revealed significantly stronger expression of immunoreactive proINSL3 as compared to extracts derived from cryptorchid or prepubertal testes. Thus, decreased expression of immunoreactive INSL3 in cryptorchid and prepubertal equine testis is transcriptionally regulated. The detection of transcripts for equine Lgr8 in the testis has identified the testis as a potential target of INSL3.
我们采用分子和免疫技术,研究胰岛素样超家族成员INSL3在雄性马驹青春期前睾丸、青春期后精子发生正常和紊乱的睾丸以及隐睾中的表达。此外,还测定了人松弛素/INSL3受体Lgr8的马同源物的部分cDNA编码序列。用马Insl3的cRNA探针进行非放射性原位杂交,并用特异性兔INSL3抗血清进行免疫组织化学分析,结果显示,在所有研究类型的睾丸中,Insl3转录本和免疫反应性INSL3配体均定位于睾丸间质细胞。定量聚合酶链反应分析显示,单侧隐睾与下降睾丸相比,Insl3表达下调,松弛素/INSL3受体表达上调。对成年正常睾丸、隐睾和青春期前睾丸的蛋白质提取物进行的蛋白质印迹分析显示,在14.5 kDa处有一条单一的免疫反应带,这与马proINSL3的预测大小相关。对成年正常睾丸蛋白质印迹数据的光密度分析显示,与隐睾或青春期前睾丸提取物相比,免疫反应性proINSL3的表达明显更强。因此,隐睾和青春期前马睾丸中免疫反应性INSL3表达的降低是受转录调控的。在睾丸中检测到马Lgr8的转录本,表明睾丸是INSL3的潜在靶点。