Aihara Ayako, Koike Tomo, Abe Natsuki, Nakamura Sou, Sawaguchi Akira, Nakamura Takanori, Sugimoto Naoshi, Nakauchi Hiromitsu, Nishino Taito, Eto Koji
Biological Research Laboratories, Nissan Chemical Industries Ltd., Saitama, Japan.
Department of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto, Japan.
Blood Adv. 2017 Feb 28;1(7):468-476. doi: 10.1182/bloodadvances.2016000844.
Signaling by thrombopoietin (TPO) in complex with its receptor, c-MPL, is critical for hematopoietic stem cell (HSC) homeostasis and platelet generation. Here we show that TA-316, a novel chemically synthesized c-MPL agonist (CMA), is useful for ex vivo platelet generation from human-induced pluripotent stem (iPS) cell-derived immortalized megakaryocyte progenitor cell lines (imMKCLs). Moreover, the generation is clinically applicable, because self-renewal expansion and platelet release is tightly controllable. TA-316 but not eltrombopag, another CMA, promoted both the self-renewal and maturation of imMKCLs, leading to more than a twofold higher platelet production than that achieved with recombinant human TPO (rhTPO). Interestingly, TA-316 seemed to favor MK-biased differentiation from bone marrow CD34 HSC/progenitors and imMKCLs through the upregulation of vascular endothelial growth factor A and fibroblast growth factor 2. This result suggests TA-316 could facilitate the development of an efficient and useful system to expand platelets from imMKCLs.
血小板生成素(TPO)与其受体c-MPL形成的复合物所介导的信号传导,对于造血干细胞(HSC)的稳态维持和血小板生成至关重要。在此,我们表明TA-316,一种新型化学合成的c-MPL激动剂(CMA),可用于从人诱导多能干细胞(iPS)衍生的永生化巨核细胞祖细胞系(imMKCLs)中体外生成血小板。此外,这种生成在临床上是可行的,因为自我更新扩增和血小板释放是可控的。TA-316而非另一种CMA艾曲泊帕,促进了imMKCLs的自我更新和成熟,导致血小板生成量比重组人TPO(rhTPO)高出两倍多。有趣的是,TA-316似乎通过上调血管内皮生长因子A和成纤维细胞生长因子2,有利于骨髓CD34 HSC/祖细胞和imMKCLs向巨核细胞偏向性分化。这一结果表明TA-316有助于开发一种高效且有用的系统,以从imMKCLs中扩增血小板。