Kaewsakulthong Woratree, Pasala Ajay Ratan, Hanotaux Justine, Hasan Tanvir, Maganti Harinad B
Canadian Blood Services, Centre for Innovation, Ottawa, ON, Canada.
Biochemistry, Microbiology and Immunology Department, University of Ottawa, Ottawa, ON, Canada.
Methods Mol Biol. 2025;2960:147-157. doi: 10.1007/7651_2024_582.
The insufficient number of hematopoietic stem cells (HSCs) poses a significant challenge for successful hematopoietic stem cell transplantation and gene-based therapies. To address this issue, ex vivo expansion of HSCs has been developed, improving engraftment and reducing morbidity risks in hematological disorders. Small molecules, known as stem cell agonists (SCAs), have been utilized to promote HSC expansion and have been implemented in clinical trials. While most HSC expansion protocols focus on the single use of SCAs, we describe a protocol using an optimized small molecule cocktail (SMC), X2A, to robustly enhance HSC yield. This protocol is applicable to human CD34+ hematopoietic stem and progenitor cells (HSPCs) derived from both umbilical cord blood and peripheral blood. In addition to the ex vivo HSC expansion protocol, we detail the CD34+ HSPC isolation technique and flow cytometry methods to characterize HSPC sub-populations from cell cultures. This culture protocol serves as a robust tool for pre-clinical studies in HSPCs and provides a foundation for further modifications to meet specific research needs.
造血干细胞(HSC)数量不足对成功进行造血干细胞移植和基于基因的治疗构成了重大挑战。为了解决这个问题,已经开发了造血干细胞的体外扩增方法,可改善植入情况并降低血液系统疾病中的发病风险。被称为干细胞激动剂(SCA)的小分子已被用于促进造血干细胞的扩增,并已在临床试验中应用。虽然大多数造血干细胞扩增方案侧重于单一使用干细胞激动剂,但我们描述了一种使用优化的小分子混合物(SMC)X2A来强劲提高造血干细胞产量的方案。该方案适用于源自脐带血和外周血的人类CD34+造血干细胞和祖细胞(HSPC)。除了体外造血干细胞扩增方案外,我们还详细介绍了CD34+ HSPC分离技术和流式细胞术方法,以表征细胞培养物中的HSPC亚群。该培养方案是HSPC临床前研究的有力工具,并为进一步修改以满足特定研究需求奠定了基础。