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ISSN: 2155-9864

Journal of Blood Disorders & Transfusion
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Research Article

Feeder-Free Derivation of Functional Platelets from Human Induced Pluripotent Stem Cells

Pei-Ju Sung, Sayandip Mukherjee, Michael P Blundell and Adrian J Thrasher*

Centre for Immunodeficiency, UCL Institute of Child Health, 30 Guilford Street, WC1N 1EH, London, UK

Corresponding Author:
Adrian J Thrasher
Centre for Immunodeficiency
UCL Institute of Child Health
30 Guilford Street, WC1N 1EH
London, UK
Tel: 0044 207 813 8490
E-mail: [email protected]

Received Date: June 13, 2013; Accepted Date: August 07, 2013; Published Date: August 09, 2013

Citation: Sung PJ, Mukherjee S, Blundell MP, Thrasher AJ (2013) Feeder-Free Derivation of Functional Platelets from Human Induced Pluripotent Stem Cells. J Blood Disord Transfus 4:153. doi: 10.4172/2155-9864.1000153

Copyright: © 2013 Sung PJ, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Derivation of patient specific induced pluripotent stem cells, in combination with directed platelet differentiation, provides a promising platform to study human thrombopoiesis or platelet disorders, and has clear potential for future clinical applications. However, efficient differentiation of human induced pluripotent stem cells (iPSCs) into functional blood cells remains challenging. In this study, we report a novel protocol for the generation of CD41a+, CD42b+, and CD61+ functional platelets from human iPSCs under feeder-free culture conditions. Platelets derived from this feeder-free system showed similar fibrinogen binding activity after agonist stimulation when compared to platelets derived from a previously reported cell line co culture system. Evidence showed these culture-derived platelets responded to different agonist stimulation by increased expression of activation markers (CD62P and PAC1) as expected. Together, these results provide an important step towards generating in vitro functional platelets from an unlimited source of patient-specific induced pluripotent stem cells using an animal component-free culture system.

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