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人类造血干细胞中存活、增殖与状态控制的解离

Dissociation of Survival, Proliferation, and State Control in Human Hematopoietic Stem Cells.

作者信息

Knapp David J H F, Hammond Colin A, Miller Paul H, Rabu Gabrielle M, Beer Philip A, Ricicova Marketa, Lecault Véronique, Da Costa Daniel, VanInsberghe Michael, Cheung Alice M, Pellacani Davide, Piret James, Hansen Carl, Eaves Connie J

机构信息

Terry Fox Laboratory, British Columbia Cancer Agency, BC Cancer Research Centre, 675 West 10(th) Avenue, Vancouver, BC V5Z 1L3, Canada.

AbCellera Biologics Inc, Vancouver, BC V6T 1Z4, Canada.

出版信息

Stem Cell Reports. 2017 Jan 10;8(1):152-162. doi: 10.1016/j.stemcr.2016.12.003.

Abstract

The role of growth factors (GFs) in controlling the biology of human hematopoietic stem cells (HSCs) remains limited by a lack of information concerning the individual and combined effects of GFs directly on the survival, Mitogenesis, and regenerative activity of highly purified human HSCs. We show that the initial input HSC activity of such a purified starting population of human cord blood cells can be fully maintained over a 21-day period in serum-free medium containing five GFs alone. HSC survival was partially supported by any one of these GFs, but none were essential, and different combinations of GFs variably stimulated HSC proliferation. However, serial transplantability was not detectably compromised by many conditions that reduced human HSC proliferation and/or survival. These results demonstrate the dissociated control of these three human HSC bio-responses, and set the stage for future improvements in strategies to modify and expand human HSCs ex vivo.

摘要

生长因子(GFs)在控制人类造血干细胞(HSCs)生物学特性方面的作用,因缺乏关于生长因子直接对高度纯化的人类造血干细胞的存活、有丝分裂和再生活性的个体及联合效应的信息而受到限制。我们发现,在仅含有五种生长因子的无血清培养基中,这种纯化的人类脐带血细胞起始群体的初始输入造血干细胞活性在21天内可得到充分维持。这些生长因子中的任何一种都能部分支持造血干细胞的存活,但没有一种是必需的,不同组合的生长因子对造血干细胞增殖的刺激程度各不相同。然而,许多降低人类造血干细胞增殖和/或存活的条件并未明显损害其连续移植能力。这些结果证明了对人类造血干细胞这三种生物学反应的解离控制,并为未来改进体外修饰和扩增人类造血干细胞的策略奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815b/5233451/9a115a2cf8eb/fx1.jpg

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