Rocha David R, Martins Jorge André M, van Tilburg Mauricio F, Oliveira Rodrigo V, Moreno Frederico B, Monteiro-Moreira Ana Cristina O, Moreira Renato A, Araújo Airton A, Moura Arlindo A
Department of Animal Science, Federal University of Ceará, Fortaleza, Brazil.
School of Pharmacy, University of Fortaleza, Fortaleza, Brazil.
Theriogenology. 2015 Nov;84(8):1291-305. doi: 10.1016/j.theriogenology.2015.07.008. Epub 2015 Jul 17.
The present study evaluated the effects of heat stress on the ram seminal plasma proteome. Six Morada Nova rams were scrotal insulated for 8 days. Scrotal circumference, sperm parameters, and seminal fluid proteins were evaluated before (Day 0) and twice during scrotal insulation (Days 4 and 8), and weekly until semen parameters returned to preinsulation values (normal). Seminal proteins were analyzed by two-dimensional SDS-PAGE and mass spectrometry. Scrotal circumference decreased from 30 ± 0.4 cm on Day 0 to 22.6 ± 0.6 cm on Day 36 (P < 0.05) and became equivalent to preinsulation values on Day 71. Motile sperm became nearly absent from Day 8 to Day 64 but returned to normal on Day 113. Percentage of normal sperm changed similarly and returned to normal on Day 106. Rams were azoospermic between Days 29 and 64, and sperm concentration came back to normal on Day 92. The number of spots/two-dimensional gel reduced from 256 ± 31 on Day 0 to 104 ± 14 on Day 29 (when rams were azoospermic) and then increased to 183 ± 9 on Day 113 (P < 0.05), similar to spot counts before insulation. The intensities of 24 spots, referring to 17 seminal plasma proteins, were affected by treatment (P < 0.05). After insulation, seminal plasma had greater expression of actin (two isoforms), albumin, heat shock protein 70 kDa, protein DJ-1, HRPE773-like, C-reactive protein precursor, bodhesin-2 (one isoform), spermadhesins. Most protein spots had the greatest intensity between Days 8 and 29, returning to preinsulation values on Day 113 (when many sperm criteria returned to normal). Proteins downregulated after scrotal insulation included dipeptidyl peptidase 3, isoforms of heat shock protein 90 kDa, RSVP22, MMP2 and of Bdh2. In this case, RSVP22 was reduced on Day 113 and all others, on Day 134. Expression of MMP2 and HSP90.1 was reduced throughout the study. Integrin β5, V-type H(+)-ATPase subunit A, ZBTB 42-like protein, isoforms of Bdh2, PSP-I, and RSVP22 were upregulated after testis insulation. Intensities of these spots were maximum (P < 0.05) 8 days after insulation started or on Day 29. Expression of most of such proteins returned to normal on Day 113. In conclusion, scrotal insulation affected testis and sperm parameters of rams, indicating alterations in both spermatogenesis and sperm maturation. Changes of seminal plasma proteome were coincidental with variations in semen parameters. Proteins affected by heat challenge are potentially involved in sperm protection, maturation, and fertilization.
本研究评估了热应激对公羊精浆蛋白质组的影响。选用6只莫拉达诺瓦公羊,对其阴囊进行8天的隔热处理。在隔热处理前(第0天)以及隔热处理期间(第4天和第8天)进行两次评估,之后每周评估一次,直至精液参数恢复到隔热处理前的正常水平。通过二维SDS - PAGE和质谱分析法对精浆蛋白质进行分析。阴囊周长从第0天的30±0.4厘米降至第36天的22.6±0.6厘米(P<0.05),并在第71天恢复到隔热处理前的水平。从第8天到第64天,活动精子几乎消失,但在第113天恢复正常。正常精子百分比变化情况类似,在第106天恢复正常。公羊在第29天至第64天无精子,精子浓度在第92天恢复正常。二维凝胶上的蛋白斑点数量从第0天的256±31个减少到第29天(公羊无精子时)的104±14个,然后在第113天增加到183±9个(P<0.05),与隔热处理前的斑点计数相似。24个斑点(涉及17种精浆蛋白)的强度受处理影响(P<0.05)。隔热处理后,精浆中肌动蛋白(两种异构体)、白蛋白、70 kDa热休克蛋白、DJ - 1蛋白、HRPE773样蛋白、C反应蛋白前体、博德辛 - 2(一种异构体)、精子黏附素的表达增加。大多数蛋白斑点在第8天至第29天强度最大,在第113天(许多精子指标恢复正常时)恢复到隔热处理前的水平。阴囊隔热处理后下调的蛋白包括二肽基肽酶3、90 kDa热休克蛋白异构体、RSVP22、基质金属蛋白酶2和博德辛2。在这种情况下,RSVP22在第113天减少,其他所有蛋白在第134天减少。在整个研究过程中,基质金属蛋白酶2和热休克蛋白90.1的表达均降低。睾丸隔热处理后,整合素β5、V型H(+) - ATP酶亚基A、ZBTB 42样蛋白、博德辛2异构体、PSP - I和RSVP22上调。这些斑点的强度在隔热处理开始8天后或第29天最大(P<0.05)。大多数此类蛋白的表达在第113天恢复正常。总之,阴囊隔热处理影响了公羊的睾丸和精子参数,表明精子发生和精子成熟均发生了改变。精浆蛋白质组的变化与精液参数变化一致。受热应激影响的蛋白质可能参与精子保护、成熟和受精过程。