Ex vivo expansion and functional activity preservation of adult hematopoietic stem cells by a diarylheptanoid from Curcuma comosa

造血 干细胞 CD90型 离体 CD38 川地34 生物 移植 细胞生物学 免疫学 癌症研究 骨髓 体内 医学 内科学 遗传学
作者
Nopmullee Tanhuad,Umnuaychoke Thongsa-ad,Nareerat Sutjarit,Ploychompoo Yoosabai,Wittaya Panvongsa,Sirapope Wongniam,Apichart Suksamrarn,Pawinee Piyachaturawat,Usanarat Anurathapan,Suparerk Borwornpinyo,Arthit Chairoungdua,Suradej Hongeng,Kanit Bhukhai
出处
期刊:Biomedicine & Pharmacotherapy [Elsevier BV]
卷期号:143: 112102-112102 被引量:8
标识
DOI:10.1016/j.biopha.2021.112102
摘要

Hematopoietic stem cells (HSCs, CD34+ cells) have shown therapeutic efficacy for transplantation in various hematological disorders. However, a large quantity of HSCs is required for transplantation. Therefore, strategies to increase HSC numbers and preserve HSC functions through ex vivo culture are critically required. Here, we report that expansion medium supplemented with ASPP 049, a diarylheptanoid isolated from Curcuma comosa, and a cocktail of cytokines markedly increased numbers of adult CD34+ cells. Interestingly, phenotypically defined primitive HSCs (CD34+CD38-CD90+) were significantly increased under ASPP 049 treatment relative to control. ASPP 049 treatment also improved two functional properties of HSCs, as evidenced by an increased number of CD34+CD38- cells in secondary culture (self-renewal) and the growth of colony-forming units as assessed by colony formation assay (multilineage differentiation). Transplantation of cultured CD34+ cells into immunodeficient mice demonstrated the long-term reconstitution and differentiation ability of ASPP 049-expanded cells. RNA sequencing and KEGG analysis revealed that Hippo signaling was the most likely pathway involved in the effects of ASPP 049. These results suggest that ASPP 049 improved ex vivo expansion and functional preservation of expanded HSCs. Our findings provide a rationale for the use of ASPP 049 to grow HSCs prior to hematological disease treatment.
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