OP9 基质细胞分泌的因子可延缓成体红系细胞的分化,并增加其体外扩增潜能。

Secretory factors from OP9 stromal cells delay differentiation and increase the expansion potential of adult erythroid cells in vitro.

机构信息

Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

School of Biochemistry, Faculty of Biomedical Sciences, University of Bristol, Bristol, United Kingdom.

出版信息

Sci Rep. 2018 Jan 31;8(1):1983. doi: 10.1038/s41598-018-20491-1.

Abstract

Development of in vitro culture systems for the generation of red blood cells is a goal of scientists globally with the aim of producing clinical grade products for transfusion. Although mature reticulocytes can be efficiently generated by such systems, the numbers produced fall short of that required for therapeutics, due to limited proliferative capacity of the erythroblasts. To overcome this hurdle, approaches are required to increase the expansion potential of such culture systems. The OP9 mouse stromal cell line is known to promote haematopoietic differentiation of pluripotent stem cells, however an effect of OP9 cells on erythropoiesis has not been explored. In this study, we show not only OP9 co-culture, but factors secreted by OP9 cells in isolation increase the proliferative potential of adult erythroid cells by delaying differentiation and hence maintaining self-renewing cells for an extended duration. The number of reticulocytes obtained was increased by approximately 3.5-fold, bringing it closer to that required for a therapeutic product. To identify the factors responsible, we analysed the OP9 cell secretome using comparative proteomics, identifying 18 candidate proteins. These data reveal the potential to increase erythroid cell numbers from in vitro culture systems without the need for genetic manipulation or co-culture.

摘要

体外培养系统生成红细胞是全球科学家的目标,旨在生产用于输血的临床级产品。尽管此类系统可以有效地生成成熟的网织红细胞,但由于红细胞生成前体细胞的增殖能力有限,产生的数量仍不足以满足治疗需求。为了克服这一障碍,需要采用方法来增加此类培养系统的扩增潜力。OP9 小鼠基质细胞系已知可促进多能干细胞的造血分化,但 OP9 细胞对红细胞生成的影响尚未得到探索。在这项研究中,我们不仅证明了 OP9 共培养,而且 OP9 细胞分泌的因子在单独培养时也通过延迟分化来增加成体红细胞的增殖潜力,从而延长自我更新细胞的维持时间。获得的网织红细胞数量增加了约 3.5 倍,接近治疗产品所需的数量。为了确定负责的因子,我们使用比较蛋白质组学分析了 OP9 细胞的分泌组,鉴定出 18 种候选蛋白。这些数据表明有可能在无需遗传操作或共培养的情况下,从体外培养系统中增加红细胞数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b0/5792592/1ff0909d1cb1/41598_2018_20491_Fig1_HTML.jpg

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