Topic Highlight
Copyright ©2014 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Stem Cells. Jan 26, 2014; 6(1): 11-23
Published online Jan 26, 2014. doi: 10.4252/wjsc.v6.i1.11
Neural differentiation from pluripotent stem cells: The role of natural and synthetic extracellular matrix
Yan Li, Meimei Liu, Yuanwei Yan, Shang-Tian Yang
Yan Li, Yuanwei Yan, Department of Chemical and Biomedical Engineering, FAMU-FSU College of Engineering, Florida State University, Tallahassee, FL 32310, United States
Meimei Liu, Shang-Tian Yang, Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH 43210, United States
Author contributions: Li Y prepared the original draft; Liu M and Yan Y contributed to writing and editing some sections in the manuscript; Yang ST revised and finalized the manuscript.
Supported by FSU start up fund and FSU Research Foundation GAP award; partial support from National Science Foundation, No.1342192
Correspondence to: Shang-Tian Yang, Professor, Department of Chemical and Biomolecular Engineering, The Ohio State University, 140 West 19th Ave, Columbus, OH 43210, United States. yang.15@osu.edu
Telephone: +1-614-2926611 Fax +1-614-2923769
Received: October 1, 2013
Revised: October 23, 2013
Accepted: November 2, 2013
Published online: January 26, 2014
Processing time: 137 Days and 4.8 Hours
Abstract

Neural cells differentiated from pluripotent stem cells (PSCs), including both embryonic stem cells and induced pluripotent stem cells, provide a powerful tool for drug screening, disease modeling and regenerative medicine. High-purity oligodendrocyte progenitor cells (OPCs) and neural progenitor cells (NPCs) have been derived from PSCs recently due to the advancements in understanding the developmental signaling pathways. Extracellular matrices (ECM) have been shown to play important roles in regulating the survival, proliferation, and differentiation of neural cells. To improve the function and maturation of the derived neural cells from PSCs, understanding the effects of ECM over the course of neural differentiation of PSCs is critical. During neural differentiation of PSCs, the cells are sensitive to the properties of natural or synthetic ECMs, including biochemical composition, biomechanical properties, and structural/topographical features. This review summarizes recent advances in neural differentiation of human PSCs into OPCs and NPCs, focusing on the role of ECM in modulating the composition and function of the differentiated cells. Especially, the importance of using three-dimensional ECM scaffolds to simulate the in vivo microenvironment for neural differentiation of PSCs is highlighted. Future perspectives including the immediate applications of PSC-derived neural cells in drug screening and disease modeling are also discussed.

Keywords: Pluripotent stem cells; Neural differentiation; Extracellular matrix; Three-dimensional; Drug screening

Core tip: Neural cells derived from human pluripotent stem cells (hPSCs), including oligodendrocyte progenitor cells and neural progenitor cells, emerge as an unlimited and physiologically relevant cell source for drug screening, disease modeling, and regenerative medicine. Natural and synthetic extracellular matrices play an important role in regulating neural differentiation, cell migration, and the derived neural cell maturation. Recent advances in neural differentiation of hPSCs on extracellular matrices in 2-D and 3-D systems are reviewed in this paper. The immediate applications of the derived neural cells in drug screening and disease modeling are also discussed.