The Center for Reproductive Medicine and Infertility, Weill Cornell Medical College, New York, NY, 10021, USA.
Ansary Stem Cell Center for Regenerative Medicine at Weill Medical College of Cornell University, New York, USA.
J Ovarian Res. 2017 Sep 19;10(1):64. doi: 10.1186/s13048-017-0354-z.
New data suggests that endothelial cells (ECs) elaborate essential "angiocrine factors". The aim of this study is to investigate the role of activated ovarian endothelial cells in early in-vitro follicular development.
Mouse ovarian ECs were isolated using magnetic cell sorting or by FACS and cultured in serum free media. After a constitutive activation of the Akt pathway was initiated, early follicles (50-150 um) were mechanically isolated from 8-day-old mice and co-cultured with these activated ovarian endothelial cells (AOEC) (n = 32), gel (n = 24) or within matrigel (n = 27) in serum free media for 14 days. Follicular growth, survival and function were assessed.
After 6 passages, flow cytometry showed 93% of cells grown in serum-free culture were VE-cadherin positive, CD-31 positive and CD 45 negative, matching the known EC profile. Beginning on day 4 of culture, we observed significantly higher follicular and oocyte growth rates in follicles co-cultured with AOECs compared with follicles on gel or matrigel. After 14 days of culture, 73% of primary follicles and 83% of secondary follicles co-cultured with AOEC survived, whereas the majority of follicles cultured on gel or matrigel underwent atresia.
This is the first report of successful isolation and culture of ovarian ECs. We suggest that co-culture with activated ovarian ECs promotes early follicular development and survival. This model is a novel platform for the in vitro maturation of early follicles and for the future exploration of endothelial-follicular communication.
In vitro development of early follicles necessitates a complex interplay of growth factors and signals required for development. Endothelial cells (ECs) may elaborate essential "angiocrine factors" involved in organ regeneration. We demonstrate that co-culture with ovarian ECs enables culture of primary and early secondary mouse ovarian follicles.
新数据表明内皮细胞 (ECs) 可分泌重要的“旁分泌因子”。本研究旨在探讨激活的卵巢内皮细胞在早期体外卵泡发育中的作用。
采用磁珠细胞分选或流式细胞术分离小鼠卵巢 ECs,在无血清培养基中培养。激活 Akt 通路后,从 8 日龄小鼠中机械分离出 50-150 μm 的早期卵泡,并与这些激活的卵巢内皮细胞 (AOEC)(n=32)、凝胶(n=24)或在无血清培养基中的 Matrigel 中(n=27)共同培养 14 天。评估卵泡的生长、存活和功能。
经过 6 次传代,无血清培养中生长的细胞中有 93%通过流式细胞术检测为 VE-钙黏蛋白阳性、CD-31 阳性和 CD45 阴性,符合已知的 EC 特征。从培养第 4 天开始,我们观察到与在凝胶或 Matrigel 上培养的卵泡相比,与 AOEC 共培养的卵泡的卵泡和卵母细胞生长速度明显更快。培养 14 天后,73%的初级卵泡和 83%的次级卵泡与 AOEC 共培养存活,而大多数在凝胶或 Matrigel 上培养的卵泡发生了闭锁。
这是首次成功分离和培养卵巢 ECs 的报道。我们认为,与激活的卵巢 EC 共培养可促进早期卵泡的发育和存活。该模型是体外成熟早期卵泡和未来探索内皮-卵泡通讯的新平台。
早期卵泡的体外发育需要复杂的生长因子和信号相互作用,这些信号是发育所必需的。内皮细胞 (ECs) 可能分泌参与器官再生的重要“旁分泌因子”。我们证明,与卵巢 EC 共培养可使小鼠卵巢初级和早期次级卵泡在体外培养。