McLaren T T, Foster P M, Sharpe R M
MRC Reproductive Biology Unit, Centre for Reproductive Biology, Edinburgh, UK.
J Reprod Fertil. 1994 Nov;102(2):293-300. doi: 10.1530/jrf.0.1020293.
The objective of this study was to identify the early (after 4 and 24 h) effects of short-term local testicular heating (43 degrees C for 30 min) on the secretion of proteins by seminiferous tubules isolated from adult rats at stages II-V, VI-VIII or IX-XII of the spermatogenic cycle, and cultured in vitro for 24 h with [35S]methionine. Incorporation of [35S]methionine into secreted and intracellular proteins was assessed and the pattern of protein secretion was evaluated using two-dimensional SDS-PAGE. Seminiferous tubules isolated from control rats exhibited the characteristic, androgen-dependent increase in protein secretion at stages VI-VIII. At 4 h after exposure to local testicular heating, seminiferous tubules at these stages showed a significant increase (P < 0.001) in the overall incorporation of [35S]methionine into secreted proteins, whereas seminiferous tubules at stages II-V and IX-XII showed no significant change. In marked contrast, seminiferous tubules isolated from rats 24 h after local testicular heating showed a significant decrease in the incorporation of [35S]methionine into secreted proteins at stages VI-VIII (P < 0.001) and to a lesser extent at IX-XII (P < 0.05), whereas seminiferous tubules at stages II-V showed no change in incorporation. Prior treatment to maintain normal intratesticular concentrations of testosterone in heat-exposed rats failed to prevent these changes. Similar results were obtained when incorporation of [35S]methionine into intracellular proteins was evaluated 4 and 24 h after exposure to local testicular heating.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究的目的是确定短期局部睾丸加热(43摄氏度,持续30分钟)对从成年大鼠生精周期II - V、VI - VIII或IX - XII阶段分离出的曲细精管蛋白质分泌的早期(4小时和24小时后)影响。这些曲细精管在体外与[35S]甲硫氨酸一起培养24小时。评估[35S]甲硫氨酸掺入分泌蛋白和细胞内蛋白的情况,并使用二维SDS - PAGE评估蛋白质分泌模式。从对照大鼠分离出的曲细精管在VI - VIII阶段呈现出雄激素依赖性的蛋白质分泌特征性增加。在局部睾丸加热4小时后,这些阶段的曲细精管中[35S]甲硫氨酸掺入分泌蛋白的总量显著增加(P < 0.001),而II - V阶段和IX - XII阶段的曲细精管则无显著变化。与之形成鲜明对比的是,局部睾丸加热24小时后从大鼠分离出的曲细精管在VI - VIII阶段(P < 0.001)以及在较小程度上在IX - XII阶段(P < 0.05),[35S]甲硫氨酸掺入分泌蛋白的量显著减少,而II - V阶段的曲细精管掺入量没有变化。预先处理以维持热暴露大鼠睾丸内正常的睾酮浓度未能阻止这些变化。在评估局部睾丸加热4小时和24小时后[35S]甲硫氨酸掺入细胞内蛋白的情况时也得到了类似结果。(摘要截断于250字)