TY - JOUR
T1 - Engineering cell-material interfaces for long-term expansion of human pluripotent stem cells
AU - Chang, Chien Wen
AU - Hwang, Yongsung
AU - Brafman, Dave
AU - Hagan, Thomas
AU - Phung, Catherine
AU - Varghese, Shyni
N1 - Funding Information:
We acknowledge Profs. S. Chien and G. Arya for valuable discussions. We also thank the financial support from California Institute of Regenerative Medicine ( RN2-00945 and RT2-01889 ).
PY - 2013/1
Y1 - 2013/1
N2 - Cost-effective and scalable synthetic matrices that support long-term expansion of human pluripotent stem cells (hPSCs) have many applications, ranging from drug screening platforms to regenerative medicine. Here, we report the development of a hydrogel-based matrix containing synthetic heparin-mimicking moieties that supports the long-term expansion of hPSCs (≥20 passages) in a chemically defined medium. HPSCs expanded on this synthetic matrix maintained their characteristic morphology, colony forming ability, karyotypic stability, and differentiation potential. We also used the synthetic matrix as a platform to investigate the effects of various physicochemical properties of the extracellular environment on the adhesion, growth, and self-renewal of hPSCs. The observed cellular responses can be explained in terms of matrix interface-mediated binding of extracellular matrix proteins, growth factors, and other cell-secreted factors, which create an instructive microenvironment to support self-renewal of hPSCs. These synthetic matrices, which comprise of " off-the-shelf" components and are easy to synthesize, provide an ideal tool to elucidate the molecular mechanisms that control stem cell fate.
AB - Cost-effective and scalable synthetic matrices that support long-term expansion of human pluripotent stem cells (hPSCs) have many applications, ranging from drug screening platforms to regenerative medicine. Here, we report the development of a hydrogel-based matrix containing synthetic heparin-mimicking moieties that supports the long-term expansion of hPSCs (≥20 passages) in a chemically defined medium. HPSCs expanded on this synthetic matrix maintained their characteristic morphology, colony forming ability, karyotypic stability, and differentiation potential. We also used the synthetic matrix as a platform to investigate the effects of various physicochemical properties of the extracellular environment on the adhesion, growth, and self-renewal of hPSCs. The observed cellular responses can be explained in terms of matrix interface-mediated binding of extracellular matrix proteins, growth factors, and other cell-secreted factors, which create an instructive microenvironment to support self-renewal of hPSCs. These synthetic matrices, which comprise of " off-the-shelf" components and are easy to synthesize, provide an ideal tool to elucidate the molecular mechanisms that control stem cell fate.
KW - Embryonic stem cells
KW - Human pluripotent stem cells
KW - Physicochemical cues
KW - Self-renewal
KW - Synthetic heparin mimics
KW - Synthetic matrices
UR - http://www.scopus.com/inward/record.url?scp=84870336498&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84870336498&partnerID=8YFLogxK
U2 - 10.1016/j.biomaterials.2012.10.020
DO - 10.1016/j.biomaterials.2012.10.020
M3 - Article
C2 - 23131532
AN - SCOPUS:84870336498
SN - 0142-9612
VL - 34
SP - 912
EP - 921
JO - Biomaterials
JF - Biomaterials
IS - 4
ER -