Nantes Université, CHU Nantes, INSERM, Center for Research in Transplantation and Translational Immunology, UMR 1064, Nantes, France.
Nantes Université, CHU Nantes, INSERM, CNRS, BioCore, Nantes, France.
Nat Protoc. 2022 Dec;17(12):2760-2783. doi: 10.1038/s41596-022-00744-0. Epub 2022 Oct 14.
Cell reprogramming has allowed unprecedented access to human development, from virtually any genome. However, reprogramming yields pluripotent stem cells that can differentiate into all cells that form a fetus, but not extraembryonic annexes. Therefore, a cellular model allowing study of placental development from a broad genomic repertoire is lacking. Here, we describe an optimized protocol to reprogram somatic cells into human induced trophoblast stem cells (hiTSCs) and convert pluripotent stem cells into human converted TSCs (hcTSCs). This protocol enables much-needed genome-specific placental disease modeling. We also detail extravillous trophoblast and syncytiotrophoblast differentiation protocols from hiTSCs and hcTSCs, a necessary step to validate these cells. In total, this protocol takes 4 months and requires advanced cell culture skills, comparable to those necessary for somatic cell reprogramming into human induced pluripotent stem cells.
细胞重编程使人们能够以前所未有的方式深入了解人类的发育过程,几乎可以从任何基因组中获取信息。然而,重编程得到的多能干细胞可以分化为形成胎儿的所有细胞,但不能形成胚胎外附属物。因此,目前缺乏一种能够基于广泛基因组资源库来研究胎盘发育的细胞模型。在这里,我们描述了一种优化的方案,可以将体细胞重编程为人类诱导滋养层干细胞(hiTSC),并将多能干细胞转化为人类转化滋养层干细胞(hcTSC)。该方案能够实现对胎盘疾病进行急需的基因组特异性建模。我们还详细介绍了 hiTSC 和 hcTSC 来源的绒毛外滋养层和合体滋养层分化方案,这是验证这些细胞的必要步骤。总的来说,该方案需要 4 个月的时间,并且需要先进的细胞培养技能,与体细胞重编程为人类诱导多能干细胞所需的技能相当。