Differentiation of human embryonic stem cells into clinically amenable keratinocytes in an autogenic environment

Fahad K. Kidwai, Hua Liu, Wei Seong Toh, Xin Fu, Doorgesh S. Jokhun, Mohammad M. Movahednia, Mingming Li, Yu Zou, Christopher A. Squier, Toan T. Phan, Tong Cao

Research output: Contribution to journalArticlepeer-review

28 Scopus citations


Human embryonic stem cells (hESCs)-derived keratinocytes hold great clinical and research potential. However, the current techniques are hampered by the use of xenogenic components that limits their clinical application. Here we demonstrated an efficient differentiation of H9 hESCs (H9-hESCs) into keratinocytes (H9-Kert) with the minimum use of animal-derived materials. For differentiation, we established two microenvironment systems originated from H9-hESCs (autogenic microenvironment). These autogenic microenvironment systems consist of an autogenic coculture system (ACC) and an autogenic feeder-free system (AFF). In addition, we showed a stage-specific effect of Activin in promoting keratinocyte differentiation from H9-hESCs while repressing the expression of early neural markers in the ACC system. Furthermore, we also explained the effect of Activin in construction of the AFF system made up of extracellular matrix similar to basement membrane extracted from H9-hESC-derived fibroblasts. H9-Kert differentiated in both systems expressed keratinocyte markers at mRNA and protein levels. H9-Kert were also able to undergo terminal differentiation in high Ca2+ medium. These findings support the transition toward the establishment of an animal-free microenvironment for successful differentiation of hESCs into keratinocytes for potential clinical application.

Original languageEnglish (US)
Pages (from-to)618-628
Number of pages11
JournalJournal of Investigative Dermatology
Issue number3
StatePublished - Mar 2013

Bibliographical note

Funding Information:
We acknowledge the expert assistance of Dr Sri Ram Gopu, Dr Kulsum Iqbal, and Mr Lu Qiqi for their helpful suggestions and comments on experimental design and result presentation. We also gratefully acknowledge the help from the Flow Cytometry Laboratory Unit, Confocal Unit in Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597. This work was partially supported by grants from the Ministry of Education of Singapore, NUS ARF grant numbers R221000023112 and R221000026112.

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