母体蛋白限制影响绵羊胎儿卵巢发育。

Reproduction & Fertility Pub Date : 2021-06-17 eCollection Date: 2021-04-01 DOI:10.1530/RAF-20-0073
Chinwe U Nwachukwu, Kathryn J Woad, Nicole Barnes, David S Gardner, Robert S Robinson
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引用次数: 6

摘要

产妇营养不良对胎儿的发育有重要影响。事实上,胎儿卵巢发育不良可能会产生终身影响,可能会降低卵巢储备和后代的生育能力。本研究探讨了母体蛋白限制对胎羊卵巢生殖细胞和血管发育的影响。母羊从受孕至妊娠第65天(gd65),分别饲喂对照(n = 7)或低蛋白(n = 8)饲粮(17.0 g vs 8.7 g粗蛋白质/MJ代谢能)。在gd65上,对胎儿卵巢进行组织学和免疫组织化学分析,以量化生殖细胞(OCT4, VASA, DAZL),增殖(Ki67),凋亡(caspase 3)和血管化(CD31)。蛋白质限制降低了胎儿卵巢重量(P < 0.05),但对胎儿体重没有影响(P > 0.05)。生殖细胞密度不受母体饲料的影响(P > 0.05)。卵巢皮层OCT4+ve细胞数量明显高于DAZL+ve细胞(P < 0.001)和VASA+ve细胞(P < 0.001)。两组鱼卵索内OCT4、DAZL和VASA+ve细胞的数量、密度和估计总重相似(P > 0.05)。同样,母体蛋白限制对生殖细胞增殖和凋亡指标(P > 0.05)以及皮层髓质血管的数量、面积、周长和微血管化程度没有影响(P > 0.05)。总之,母体蛋白限制降低卵巢重量,但不影响生殖细胞发育进程、增殖、凋亡或卵巢血管。这表明母体蛋白的减少有可能调节后代卵巢的发育。总结:母亲在怀孕期间饮食的变化会影响后代的生长,并可能导致后代在以后的生活中出现生育问题。我们研究了在怀孕早期减少喂给绵羊的蛋白质是否会影响它们女儿的卵巢。然后,我们将我们的发现与完全饮食的绵羊的后代进行了比较。我们测量了卵巢的大小,并估计了其中包含的生殖细胞(成为卵子的细胞)的数量。我们使用细胞标记来评估生殖细胞生长、分裂和死亡模式的潜在变化,以及卵巢血液供应的发展情况。我们发现蛋白质限制减少了卵巢的大小。然而,生殖细胞发育、生长或死亡的模式并未因饮食不良而改变,血管也未受影响。这表明母亲的饮食可以通过一种未知的机制改变卵巢发育,并可能降低后代的生育能力。
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Maternal protein restriction affects fetal ovary development in sheep.

Maternal malnutrition has important developmental consequences for the foetus. Indeed, adverse fetal ovarian development could have lifelong impact, with potentially reduced ovarian reserve and fertility of the offspring. This study investigated the effect of maternal protein restriction on germ cell and blood vessel development in the fetal sheep ovary. Ewes were fed control (n = 7) or low protein (n = 8) diets (17.0 g vs 8.7 g crude protein/MJ metabolizable energy) from conception to day 65 of gestation (gd65). On gd65, fetal ovaries were subjected to histological and immunohistochemical analysis to quantify germ cells (OCT4, VASA, DAZL), proliferation (Ki67), apoptosis (caspase 3) and vascularisation (CD31). Protein restriction reduced the fetal ovary weight (P < 0.05) but had no effect on fetal weight (P > 0.05). The density of germ cells was unaffected by maternal diet (P > 0.05). In the ovarian cortex, OCT4+ve cells were more abundant than DAZL+ve (P < 0.001) and VASA+ve cells (P < 0.001). The numbers, density and estimated total weight of OCT4, DAZL, and VASA+ve cells within the ovigerous cords were similar in both dietary groups (P > 0.05). Similarly, maternal protein restriction had no effect on germ cell proliferation or apoptotic indices (P > 0.05) and the number, area and perimeter of medullary blood vessels and degree of microvascularisation in the cortex (P > 0.05). In conclusion, maternal protein restriction decreased ovarian weight despite not affecting germ cell developmental progress, proliferation, apoptosis, or ovarian vascularity. This suggests that reduced maternal protein has the potential to regulate ovarian development in the offspring.

Lay summary: Variations in a mother's diet during pregnancy can influence her offspring's growth and might cause fertility problems in the offspring in later life. We investigated whether reducing the protein fed to sheep during early pregnancy affects their daughters' ovaries. We then compared our findings to the offspring of sheep on a complete diet. We measured ovary size and estimated the number of germ cells (cells that become eggs) they contained. We used cell markers to assess potential changes in the pattern of germ cell growth, division, and death, and how the ovarian blood supply had developed. We found that protein restriction reduced ovary size. However, the pattern of germ cell development, growth, or death was not altered by poor diet and blood vessels were also unaffected. This suggests that maternal diet can change ovarian development by an unknown mechanism and might reduce future fertility in their offspring.

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