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Induction of human trophoblast stem cells.

Nature protocols (2022-10-15)
Gaël Castel, Laurent David
ZUSAMMENFASSUNG

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.

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Gelatine -Lösung, Type B, 2% in H2O, tissue culture grade, BioReagent, suitable for cell culture
Sigma-Aldrich
N-Acetyl-L-Cystein, BioReagent, suitable for cell culture
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Albumin aus Rinderserum, heat shock fraction, protease free, essentially globulin free, pH 7, ≥98%
Sigma-Aldrich
Humanplasma Fibronectin-aufgereinigtes Protein, from human plasma, liquid, 1 mg/mL (100 MG pack size is lyophilized), purified protein, suitable for cell culture
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Valproinsäure Natriumsalz, 98%
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Monoclonal Anti-GATA2 antibody produced in mouse, clone 2D11, purified immunoglobulin, buffered aqueous solution