TY - JOUR
T1 - Mouse retinal progenitor cell dynamics on electrospun poly(ε- caprolactone)
AU - Cai, Sophie
AU - Smith, Meghan Elisabeth
AU - Redenti, Stephen Michael
AU - Wnek, Gary Edmund
AU - Young, Michael Joseph
N1 - Funding Information:
S. C. and M. E. S. contributed equally. We thank James Swift for assistance with SEM imaging and Randy Huang from the Schepens Flow Cytometry Facility for assistance with FACS enrichment. We would also like to thank the National Eye Institute, Discovery Eye Foundation, and Lincy Foundation for funding support.
PY - 2012
Y1 - 2012
N2 - Age-related macular degeneration, retinitis pigmentosa and glaucoma are among the many retinal degenerative diseases where retinal cell death leads to irreversible vision loss and blindness. Working toward a cell-replacement-based therapy for such diseases, a number of research groups have recently evaluated the feasibility of using retinal progenitor cells (RPCs) cultured and transplanted on biodegradable polymer substrates to replace damaged retinal tissue. Appropriate polymer substrate design is essential to providing a three-dimensional environment that can facilitate cell adhesion, proliferation and post-transplantation migration into the host environment. In this study, we have designed and fabricated a novel, ultra-thin electrospun poly(ε-caprolactone) (PCL) scaffold with microscale fiber diameters, appropriate porosity for infiltration by RPCs, and biologically compatible mechanical characteristics. We have verified that our electrospun PCL scaffold supports robust mouse RPC proliferation, adhesion, and differentiation in vitro, as well as migration into mouse retinal explants. These promising results make PCL a strong candidate for further development as a cell transplantation substrate in retinal regenerative research.
AB - Age-related macular degeneration, retinitis pigmentosa and glaucoma are among the many retinal degenerative diseases where retinal cell death leads to irreversible vision loss and blindness. Working toward a cell-replacement-based therapy for such diseases, a number of research groups have recently evaluated the feasibility of using retinal progenitor cells (RPCs) cultured and transplanted on biodegradable polymer substrates to replace damaged retinal tissue. Appropriate polymer substrate design is essential to providing a three-dimensional environment that can facilitate cell adhesion, proliferation and post-transplantation migration into the host environment. In this study, we have designed and fabricated a novel, ultra-thin electrospun poly(ε-caprolactone) (PCL) scaffold with microscale fiber diameters, appropriate porosity for infiltration by RPCs, and biologically compatible mechanical characteristics. We have verified that our electrospun PCL scaffold supports robust mouse RPC proliferation, adhesion, and differentiation in vitro, as well as migration into mouse retinal explants. These promising results make PCL a strong candidate for further development as a cell transplantation substrate in retinal regenerative research.
KW - Biocompatibility
KW - Electrospinning
KW - Polycaprolactone
KW - Progenitor cell
KW - Retina
KW - Scaffold
UR - http://www.scopus.com/inward/record.url?scp=84867218392&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84867218392&partnerID=8YFLogxK
U2 - 10.1163/092050611X584388
DO - 10.1163/092050611X584388
M3 - Article
C2 - 21781383
AN - SCOPUS:84867218392
SN - 0920-5063
VL - 23
SP - 1451
EP - 1465
JO - Journal of Biomaterials Science, Polymer Edition
JF - Journal of Biomaterials Science, Polymer Edition
IS - 11
ER -