Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, 19839-63113 Tehran, Iran.
Reproductive Biotechnology Research Center, Aviccena Research Institute, ACECR, 14115-343 Tehran, Iran.
ACS Biomater Sci Eng. 2020 Oct 12;6(10):5823-5832. doi: 10.1021/acsbiomaterials.0c00893. Epub 2020 Sep 18.
Engineering of 3D substrates with maximum similarity to seminiferous tubules would help to produce functional sperm cells from stem cells. Here, we present a 3D electrospun gelatin (EG) substrate seeded with Sertoli cells and determine its potential for guided differentiation of embryonic stem cells (ESCs) toward germline cells. The EG was fabricated by electrospinning, and its morphology under SEM, as well as cytobiocompatibility for Sertoli cells and ESCs, was confirmed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide and cell attachment assay. Embryoid bodies (EBs) were formed from ESCs and co-cultured with Sertoli cells, induced with BMP4 for 3 and 7 consecutive days to induce the differentiation of EBs toward germline cells. The differentiation was investigated by immunocytochemistry (ICC), flow cytometry, and RT-PCR in four experimental groups of EBs (EBs cultured in gelatin-coated cell culture plates); Scaffold/EB (EBs cultured on EG); ESCs/Ser (EBs and Sertoli cells co-cultured on gelatin-coated cell culture plates without EG); and Scaffold/EB/Ser (EBs and Sertoli cells co-cultured on EG). All experimental groups exhibited a significantly increased MVH (germline-specific marker) and decreased c-KIT (stemness marker) expression when compared with the EB group. ICC and flow cytometry revealed that Scaffold/EB/Ser had the highest level of MVH and the lowest c-KIT expression at both 3 and 7 days postdifferentiation compared with other groups. RT-PCR results showed a significant increase in the germline marker () and a significant decrease in the ESC stemness marker () in Scaffold/EB compared to the EB group. The germline markers , , , , , and were significantly increased in Scaffold/EB/Ser compared to the Scaffold/EB group. Our findings revealed that the EG scaffold can provide an excellent substrate biomimicking the micro/nanostructure of native seminiferous tubules and a platform for Sertoli cell-EB communication required for growth and differentiation of ESCs into germline cells.
工程化的 3D 基底与曲细精管具有最大的相似性,有助于从干细胞中产生功能性精子。在这里,我们提出了一种 3D 静电纺丝明胶(EG)基底,其上接种了支持细胞,并确定了其引导胚胎干细胞(ESCs)向生殖细胞分化的潜力。通过静电纺丝制备 EG,并通过 SEM 观察其形态,以及通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐和细胞附着试验证实其对支持细胞和 ESCs 的细胞相容性。从 ESCs 形成类胚体(EBs),并与支持细胞共培养,用 BMP4 诱导 3 和 7 天连续诱导 EBs 向生殖细胞分化。通过免疫细胞化学(ICC)、流式细胞术和 RT-PCR 在 EBs 的四个实验组(在明胶包被的细胞培养板中培养的 EBs;支架/EB;在明胶包被的细胞培养板上培养的 EBs 和支持细胞没有 EG);支架/EB/Ser(在 EG 上共培养的 EBs 和支持细胞)进行分化研究。与 EB 组相比,所有实验组的 MVH(生殖细胞特异性标志物)表达显著增加,而 c-KIT(干性标志物)表达显著降低。ICC 和流式细胞术显示,与其他组相比,支架/EB/Ser 在分化后 3 天和 7 天的 MVH 表达最高,c-KIT 表达最低。RT-PCR 结果显示,与 EB 组相比,支架/EB 组的生殖细胞标志物()显著增加,ESC 干性标志物()显著降低。与支架/EB 组相比,支架/EB/Ser 组的生殖细胞标志物、、、、、和 显著增加。我们的研究结果表明,EG 支架可以提供一个极好的基底,模拟天然曲细精管的微/纳米结构,并为支持细胞-类胚体通讯提供一个平台,促进 ESCs 生长和分化为生殖细胞。