Toward in Vitro Production of Platelet from Induced Pluripotent Stem Cells

被引:4
|
作者
Izady, Elaheh [1 ]
Saltanatpour, Zohreh [1 ,2 ]
Liu, Li-Ping [3 ]
Alizadeh, Akram [4 ]
Hamidieh, Amir Ali [1 ,2 ]
机构
[1] Univ Tehran Med Sci, Stem Cell & Regenerat Med Ctr Excellence, Tehran, Iran
[2] Univ Tehran Med Sci, Pediat Cell & Gene Therapy Res Ctr, Gene Cell & Tissue Res Inst, Tehran, Iran
[3] Jiangsu Univ, Affiliated Hosp, Inst Regenerat Med, Zhenjiang 212001, Jiangsu, Peoples R China
[4] Semnan Univ Med Sci, Nervous Syst Stem Cells Res Ctr, Semnan, Iran
关键词
Stem cells; Induced Pluripotent Stem Cell (iPSC); Platelet (PLT); In Vitro Production; Megakaryocyte (MK); EX-VIVO EXPANSION; FUNCTIONAL PLATELETS; HUMAN FIBROBLASTS; PROGENITOR CELLS; CORD BLOOD; GENERATION; MEGAKARYOCYTES; DIFFERENTIATION; SYSTEM; REFRACTORINESS;
D O I
10.1007/s12015-022-10366-4
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Platelets (PLTs) are small anucleate blood cells that release from polyploidy megakaryocytes(MKs). PLT transfusion is standard therapy to prevent hemorrhage. PLT transfusion is donor-dependent way which have limitations including the inadequate donor blood supply, poor quality, and issues related to infection and immunity. Overcoming these obstacles is possible with in vitro production of human PLTs. Currently several cells have been considered as source to in vitro production of PLTs such as hematopoietic stem cells (HSCs), embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs). However, HSCs are a limited source for PLT production and large-scale expansion of HSC-derived PLT remains difficult. Alternative sources can be ESCs which have unlimited expansion capacity. But ESCs have ethical issues related to destroying human embryos. iPSCs are considered as an ideal unlimited source for PLT production. They are able to differentiate into any cells and have the capacity of self-renewal. Moreover, iPSCs can be acquired from any donor and easily manipulated. Due to new advances in development of MK cell lines, bioreactors, feeder cell-free production and the ability of large scale generation, iPSC-based PLTs are moving toward clinical applicability and considering the minimal risk of alloimmunization and tumorigenesis of these products, there is great hopefulness they will become the standard source for blood transfusions in the future. This review will focus on how to progress of in vitro generation of PLT from stem cell especially iPSCs and some of the successful strategies that can be easily used in clinic will be described.
引用
收藏
页码:2376 / 2387
页数:12
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