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A novel inducible haematopoietic cell‐depleting mouse model for chimeric complementation of blood cells

Haematopoietic stem cell transplantation (HSCT) is widely used in regenerative medicine. HSCT can be used not only to treat certain types of blood cancer and immune disorders but also to induce immune tolerance in organ transplantation. However, the inadequacy of HSCs available for transplantation i...

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Detalles Bibliográficos
Autores principales: Cao, Weiyun, Cao, Jiani, Li, Xing, Xu, Haoyu, Tian, Jiayi, Li, Xiaoyan, Wang, Fengchao, Zhao, Tongbiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212702/
https://www.ncbi.nlm.nih.gov/pubmed/37199017
http://dx.doi.org/10.1111/cpr.13472
Descripción
Sumario:Haematopoietic stem cell transplantation (HSCT) is widely used in regenerative medicine. HSCT can be used not only to treat certain types of blood cancer and immune disorders but also to induce immune tolerance in organ transplantation. However, the inadequacy of HSCs available for transplantation is still a major hurdle for clinical applications. Here, we established a novel inducible haematopoietic cell‐depleting mouse model and tested the feasibility of using chimeric complementation to regenerate HSCs and their progeny cells. Large populations of syngeneic and major histocompatibility‐mismatched haematopoietic cells were successfully regenerated by this model. The stable allogeneic chimeric mice maintained a substantial population of donor HSCs and Tregs, which indicated that the donor allogeneic HSCs successfully repopulated the recipient blood system, and the regenerated donor Tregs played essential roles in establishing immune tolerance in the allogeneic recipients. In addition, rat blood cells were detected in this model after xenotransplantation of rat whole bone marrow (BM) or Lin(−) BM cells. This mouse model holds promise for regenerating xenogeneic blood cells, including human haematopoietic cells.