Centre for Stem Cell Research (CSCR), A unit of InStem Bengaluru, Christian Medical College campus, Vellore, 632002, Tamil Nadu, India.
Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India.
Stem Cell Res Ther. 2024 Sep 27;15(1):319. doi: 10.1186/s13287-024-03927-6.
Hematopoietic stem cells (HSCs) have emerged as one of the most therapeutically significant adult stem cells, paving way for a range of novel curative regimens over decades. HSCs are transplanted, either directly or post restorative genetic engineering in order to repopulate a healthy hematopoietic homeostasis in patients with disorders affecting the blood and immune cells. Despite being an extensively studied system, the maintenance and expansion of functional HSCs ex vivo remains a major bottleneck. The challenge primarily stems from difficulties in reproducing HSC self-renewal divisions and gradual depletion of stemness characters, in vitro. Refining the in vitro culture can be particularly beneficial in the case of cord blood HSCs (CB-HSCs), as inadequate numbers in a single umbilical cord limits its therapeutic potential. In recent years, molecular dissection of HSC stemness has significantly improved in vitro hematopoietic stem and progenitor cells (HSPCs) culture. Despite such significant progress, lacunae exist in fully understanding all the underlying mechanisms and their interplay active in bona fide HSCs, and how it transforms when cells proliferate in culture. A new groundbreaking study titled "MYCT1 controls environmental sensing in human haematopoietic stem cells", published in Nature in June 2024, sheds light on this complex field. Through a series of experiments, including knock-down, overexpression, single-cell RNA sequencing, and transplantation, the study identifies a previously unknown role of the MYC target 1 (MYCT1) protein in HSC maintenance. This protein acts as a crucial regulator of human HSCs, with high expression in primitive HSCs and subsequently downregulated during ex vivo culture. The study reveals that MYCT1 plays a vital role in moderating endocytosis and environmental sensing in HSCs, processes thereby essential for maintaining HSC stemness and function. This commentary will discuss the implications of the new findings for cord blood expansion in cell therapies and HSPC culture for gene therapy applications, providing valuable insights for the field of hematopoietic regenerative medicine.
造血干细胞(HSCs)已成为最具治疗意义的成人干细胞之一,为几十年来一系列新的治疗方案铺平了道路。HSCs 被移植,无论是直接移植还是经过修复基因工程的移植,目的都是为了在影响血液和免疫细胞的疾病患者中重新建立健康的造血稳态。尽管这是一个被广泛研究的系统,但体外维持和扩增功能性 HSCs 仍然是一个主要的瓶颈。这个挑战主要源于在体外难以复制 HSC 自我更新分裂和逐渐耗尽干细胞特性。改进体外培养对于脐带血 HSCs(CB-HSCs)尤其有益,因为单个脐带中的数量不足限制了其治疗潜力。近年来,对 HSC 干细胞特性的分子剖析显著改善了体外造血干细胞和祖细胞(HSPCs)的培养。尽管取得了如此显著的进展,但在充分了解所有潜在机制及其在真正的 HSCs 中的相互作用以及细胞在培养中增殖时如何转化方面仍存在空白。2024 年 6 月发表在《自然》杂志上的一项题为“MYCT1 控制人类造血干细胞的环境感应”的开创性研究填补了这一空白。该研究通过一系列实验,包括敲低、过表达、单细胞 RNA 测序和移植,确定了 MYC 靶 1(MYCT1)蛋白在 HSC 维持中的一个以前未知的作用。这种蛋白质是人类 HSCs 的关键调节因子,在原始 HSCs 中高表达,随后在体外培养中下调。该研究揭示了 MYCT1 在调节 HSCs 内吞作用和环境感应中的重要作用,这些过程对于维持 HSC 干细胞特性和功能至关重要。这篇评论将讨论新发现对细胞疗法中脐带血扩增和基因治疗应用中 HSPC 培养的意义,为造血再生医学领域提供有价值的见解。