Maguire S M, Millar M R, Sharpe R M, Saunders P T
MRC Reproductive Biology Unit, Edinburgh, UK.
Mol Cell Endocrinol. 1993 Jul;94(1):79-88. doi: 10.1016/0303-7207(93)90054-n.
Cyclic protein 2 (CP-2) is a product of the Sertoli cell which is secreted in a cyclical manner according to the stage of the spermatogenic cycle. This study has assessed the influence of the germ cell complement on expression of CP-2 mRNA. Adult rats were treated with 650 mg/kg methoxyacetic acid (MAA) to induce the specific depletion of > 80% of pachytene and later spermatocytes from most tubules, and expression of CP-2 mRNA was then assessed at various times after treatment when particular germ cell types were depleted selectively. CP-2 mRNA was specifically localised to the Sertoli cells of the seminiferous tubules by non-radioactive in situ hybridisation using a digoxigenin-labelled riboprobe. A stage specific variation in CP-2 mRNA levels was observed, with the mRNA being most abundant at stages IV-VII of the spermatogenic cycle. Northern analysis revealed that treatment with MAA led to an apparent increase in the amount of the major 1.7 kb CP-2 transcript when either pachytene spermatocytes or round spermatids were depleted. In contrast, the level of CP-2 mRNA was decreased by more than half at 21 days after MAA treatment. This decrease was confirmed by in situ hybridisation at 21 days after MAA treatment, when CP-2 mRNA expression was found to be decreased or absent from tubules at stages at which CP-2 mRNA is normally expressed (stages IV-VII) when elongate spermatids were depleted selectively from these tubules. These observations lead us to hypothesise that elongate spermatids positively modulate CP-2 mRNA expression in the Sertoli cell.
循环蛋白2(CP-2)是支持细胞的产物,它根据生精周期的阶段以周期性方式分泌。本研究评估了生殖细胞组成对CP-2 mRNA表达的影响。成年大鼠用650 mg/kg甲氧基乙酸(MAA)处理,以诱导大多数曲细精管中>80%的粗线期及更晚期的精母细胞特异性缺失,然后在处理后的不同时间点评估CP-2 mRNA的表达,此时特定类型的生殖细胞被选择性地耗尽。使用地高辛标记的核糖探针通过非放射性原位杂交将CP-2 mRNA特异性定位到曲细精管的支持细胞中。观察到CP-2 mRNA水平存在阶段特异性变化,在生精周期的IV-VII阶段mRNA最为丰富。Northern分析显示,当粗线期精母细胞或圆形精子细胞被耗尽时,用MAA处理导致主要的1.7 kb CP-2转录本的量明显增加。相反,MAA处理后21天CP-2 mRNA水平下降了一半以上。MAA处理后21天的原位杂交证实了这种下降,此时当从这些曲细精管中选择性耗尽伸长型精子细胞时,在正常表达CP-2 mRNA的阶段(IV-VII阶段),曲细精管中CP-2 mRNA表达降低或缺失。这些观察结果使我们推测伸长型精子细胞对支持细胞中CP-2 mRNA的表达具有正向调节作用。