Thongkittidilok C, Wildt D E, Songsasen N
Center for Species Survival, Smithsonian Conservation Biology Institute, National Zoological Park, Front Royal, VA, USA.
Reprod Domest Anim. 2017 Apr;52 Suppl 2:114-122. doi: 10.1111/rda.12852. Epub 2016 Nov 7.
We investigated the influence of epidermal growth factor (EGF) and vascular endothelial growth factor (VEGF) on in vitro follicle development within ovarian cortices recovered from pre-pubertal (≤6 months) versus peri-pubertal dogs (≥10 months). Ovarian cortices were cultured for 3 or 7 days in EGF (0 or 10 ng/ml) and VEGF (0, 0.1 or 1 ng/ml) and subjected to histological and apoptosis analyses. Fresh cortices from the same dogs served as "non-cultured controls" (NCC) and were evaluated similarly. The response of ovarian follicles to growth factors differed between pre-pubertal versus peri-pubertal tissues. For pre-pubertal dogs, percentage of structurally normal follicles in cortices cultured for 3 days in low VEGF (0.1 ng/ml) and EGF alone was comparable to that of the NCC. Follicle density declined in all cultured groups even after 3 days. Primary follicle diameter in all cortices cultured for 7 days, except in low VEGF, was smaller than that of the NCC, and percentage apoptotic follicles sharply increased in all treatment groups compared to the NCC. For peri-pubertal donors, percentages of structurally normal follicles decreased in all culture treatments at 3 and 7 days of incubation compared to the NCC. However, more normal follicles were found in cortices cultured in low VEGF and the two VEGF and EGF combinations than in the absence of growth factors or with EGF alone. Culture reduced the density of developing follicles, but follicle diameter was similar to that of the NCC. TUNEL analysis revealed that high-VEGF (1 ng/ml) treatment protected follicles against apoptosis, with the proportion of apoptotic follicles at Day 7 being comparable to that of the NCC. The findings demonstrate that the response of ovarian cortices to growth factor supplementation varied between pre-pubertal versus peri-pubertal donors.
我们研究了表皮生长因子(EGF)和血管内皮生长因子(VEGF)对从青春期前(≤6个月)与青春期前后(≥10个月)犬只回收的卵巢皮质内体外卵泡发育的影响。将卵巢皮质在EGF(0或10 ng/ml)和VEGF(0、0.1或1 ng/ml)中培养3天或7天,然后进行组织学和凋亡分析。来自同一只犬只的新鲜皮质用作“未培养对照”(NCC),并进行类似评估。青春期前与青春期前后组织中卵巢卵泡对生长因子的反应有所不同。对于青春期前的犬只,在低VEGF(0.1 ng/ml)和单独EGF中培养3天的皮质中结构正常卵泡的百分比与NCC相当。即使在3天后,所有培养组中的卵泡密度也都下降了。除低VEGF组外,所有培养7天的皮质中的初级卵泡直径均小于NCC,并且与NCC相比,所有治疗组中凋亡卵泡的百分比急剧增加。对于青春期前后的供体,与NCC相比,在培养3天和7天时,所有培养处理中结构正常卵泡的百分比均下降。然而,在低VEGF以及两种VEGF和EGF组合培养的皮质中发现的正常卵泡比在无生长因子或仅含EGF的情况下更多。培养降低了发育中卵泡的密度,但卵泡直径与NCC相似。TUNEL分析显示,高VEGF(1 ng/ml)处理可保护卵泡免于凋亡,第7天凋亡卵泡的比例与NCC相当。研究结果表明,青春期前与青春期前后供体的卵巢皮质对生长因子补充的反应有所不同。