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新型血小板生成素受体激动剂TA-316有助于人诱导多能干细胞生成血小板。

Novel TPO receptor agonist TA-316 contributes to platelet biogenesis from human iPS cells.

作者信息

Aihara Ayako, Koike Tomo, Abe Natsuki, Nakamura Sou, Sawaguchi Akira, Nakamura Takanori, Sugimoto Naoshi, Nakauchi Hiromitsu, Nishino Taito, Eto Koji

机构信息

Biological Research Laboratories, Nissan Chemical Industries Ltd., Saitama, Japan.

Department of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto, Japan.

出版信息

Blood Adv. 2017 Feb 28;1(7):468-476. doi: 10.1182/bloodadvances.2016000844.

DOI:10.1182/bloodadvances.2016000844
PMID:29296963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5738977/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d51/5738977/66651bc465ff/advances000844absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d51/5738977/66651bc465ff/advances000844absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d51/5738977/66651bc465ff/advances000844absf1.jpg

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Novel TPO receptor agonist TA-316 contributes to platelet biogenesis from human iPS cells.新型血小板生成素受体激动剂TA-316有助于人诱导多能干细胞生成血小板。
Blood Adv. 2017 Feb 28;1(7):468-476. doi: 10.1182/bloodadvances.2016000844.
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Blood. 2016 May 5;127(18):2231-40. doi: 10.1182/blood-2015-09-670208. Epub 2016 Mar 10.
2
Distinct routes of lineage development reshape the human blood hierarchy across ontogeny.不同的谱系发育途径重塑了个体发育过程中的人类血液层级结构。
Science. 2016 Jan 8;351(6269):aab2116. doi: 10.1126/science.aab2116. Epub 2015 Nov 5.
3
Overview of blood components and their preparation.
离体制造血小板:超越使用自体 iPSC 血小板的首例人体临床试验。
Int J Hematol. 2023 Mar;117(3):349-355. doi: 10.1007/s12185-022-03512-8. Epub 2022 Dec 27.
4
Production and nonclinical evaluation of an autologous iPSC-derived platelet product for the iPLAT1 clinical trial.自体 iPSC 来源血小板产品的生产和非临床评估用于 iPLAT1 临床试验。
Blood Adv. 2022 Dec 13;6(23):6056-6069. doi: 10.1182/bloodadvances.2022008512.
5
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Cells. 2021 Nov 19;10(11):3250. doi: 10.3390/cells10113250.
6
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Dev Growth Differ. 2021 Feb;63(2):178-186. doi: 10.1111/dgd.12711. Epub 2021 Mar 4.
7
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Cell Mol Life Sci. 2021 Apr;78(7):3385-3401. doi: 10.1007/s00018-020-03749-8. Epub 2021 Jan 13.
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5
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6
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9
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Proc Natl Acad Sci U S A. 2012 Aug 28;109(35):14019-23. doi: 10.1073/pnas.1212545109. Epub 2012 Aug 13.
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J Exp Med. 2010 Dec 20;207(13):2817-30. doi: 10.1084/jem.20100844. Epub 2010 Nov 22.