A method for inducing differentiation of human pluripotent stem cells into bone marrow stromal cells and use thereof
By differentiating human pluripotent stem cells into endothelial cells and inducing endothelial-mesenchymal transition using TGF-β, the problem of obtaining bone marrow stromal cells has been solved. The obtained BMSCs have a stable phenotype and mature function, promote the proliferation and differentiation of hematopoietic stem cells, delay aging, and have broad clinical application potential.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- THE HONG KONG POLYTECHNIC UNIV SHENZHEN RES INST
- Filing Date
- 2026-02-06
- Publication Date
- 2026-06-09
AI Technical Summary
In existing technologies, the acquisition of bone marrow stromal cells has problems such as invasive operations, limited donor sources, low purity, and high heterogeneity. In addition, the differentiation technology of human pluripotent stem cells is not efficient, making it difficult to obtain phenotypically mature and functionally complete BMSCs, which limits their preparation and application on a clinical scale.
By simulating the physiological development process, human pluripotent stem cells are first differentiated into endothelial cells, and then TGF-β is used to induce endothelial-mesenchymal transition (EndMT) to efficiently obtain phenotypically stable and functionally mature bone marrow stromal cells. CD31+ endothelial cells are used as precursors, and the TGF-β-induced endothelial-mesenchymal transition (EndMT) pathway is utilized to achieve efficient and stable preparation of BMSCs.
The obtained bone marrow stromal cells have a stable phenotype and low heterogeneity, which can effectively promote the proliferation and multi-lineage differentiation of hematopoietic stem cells, delay aging, and have a significant ability to promote the expansion of immune cells. They have good application prospects in the fields of hematopoietic reconstitution, intervention of aging-related blood diseases, and immunomodulatory therapy.
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