Spinaci Marcella, Volpe Sara, Bernardini Chiara, de Ambrogi Marco, Tamanini Carlo, Seren Eraldo, Galeati Giovanna
Dipartimento di Morfofisiologia Veterinaria e Produzioni Animali, Facoltà di Medicina Veterinaria, Università di Bologna, via Tolara di Sopra 50, 40064 Ozzano Emilia, Italia.
J Androl. 2006 Nov-Dec;27(6):899-907. doi: 10.2164/jandrol.106.001008. Epub 2006 Jul 26.
Heat shock proteins, besides their protective function against stresses, have been recently indicated as key factors for sperm fertilizing ability. Since sexing sperm by high-speed flow-cytometry subjects them to different physical, mechanical, and chemical stresses, the present study was designed to verify, by immunofluorescence and Western blot, whether the sorting procedure induces any modification in the amount and cellular distribution of heat shock proteins 60, 70, and 90 (Hsp60, Hsp70, Hsp90). Immunolocalization and Western blot quantification of both Hsp60 and Hsp90 did not reveal differences between unsorted and sorted semen. On the contrary, a redistribution of Hsp70 immunoreactivity from the equatorial subsegment toward the equator of sperm cells was recorded after sorting; this relocation suggests capacitation-like changes of sperm membrane. This modification seems to be caused mainly by incubation with Hoechst 33342, while both passage of sperm through flow cytometer and laser beam represent only minor stimuli. A further Hsp70 redistribution seems to be due to the final steps of sperm sorting, charging, and deflection of drops, and to the dilution during collection. On the other hand, staining procedure and mechanical stress seem to be the factors most injurious to sperm viability. Moreover, Hsp70 relocation was deeply influenced by the storage method. In fact, storing sexed spermatozoa, after centrifugation, in a small volume in presence of seminal plasma induced a reversion of Hsp70 redistribution, while storage in the diluted catch fluid of collection tubes caused Hsp70 relocation in most sorted spermatozoa.
热休克蛋白除了具有抵抗应激的保护功能外,最近还被认为是精子受精能力的关键因素。由于通过高速流式细胞术对精子进行性别分选会使其受到不同的物理、机械和化学应激,因此本研究旨在通过免疫荧光和蛋白质印迹法,验证分选过程是否会引起热休克蛋白60、70和90(Hsp60、Hsp70、Hsp90)的含量及细胞分布发生任何改变。Hsp60和Hsp90的免疫定位及蛋白质印迹定量分析均未显示未分选精液和分选精液之间存在差异。相反,分选后记录到Hsp70免疫反应性从精子赤道亚段向赤道重新分布;这种重新定位表明精子膜发生了类似获能的变化。这种改变似乎主要是由与Hoechst 33342孵育引起的,而精子通过流式细胞仪及激光束照射仅为次要刺激因素。进一步的Hsp70重新分布似乎归因于精子分选、液滴充电和偏转的最后步骤以及收集过程中的稀释。另一方面,染色过程和机械应激似乎是对精子活力损害最大的因素。此外,Hsp70的重新定位受储存方法的影响很大。事实上,离心后将分选的精子在少量精浆中储存会导致Hsp70重新分布逆转,而在收集管的稀释捕获液中储存则会使大多数分选精子中的Hsp70发生重新定位。