Advances in Retinal Tissue Engineering

Detalhes bibliográficos
Autor(a) principal: Trese, Matthew
Data de Publicação: 2012
Outros Autores: Regatieri, Caio V. [UNIFESP], Young, Michael J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.3390/ma5010108
http://repositorio.unifesp.br/handle/11600/34403
Resumo: Retinal degenerations cause permanent visual loss and affect millions world-wide. Current treatment strategies, such as gene therapy and anti-angiogenic drugs, merely delay disease progression. Research is underway which aims to regenerate the diseased retina by transplanting a variety of cell types, including embryonic stem cells, fetal cells, progenitor cells and induced pluripotent stem cells. Initial retinal transplantation studies injected stem and progenitor cells into the vitreous or subretinal space with the hope that these donor cells would migrate to the site of retinal degeneration, integrate within the host retina and restore functional vision. Despite promising outcomes, these studies showed that the bolus injection technique gave rise to poorly localized tissue grafts. Subsequently, retinal tissue engineers have drawn upon the success of bone, cartilage and vasculature tissue engineering by employing a polymeric tissue engineering approach. This review will describe the evolution of retinal tissue engineering to date, with particular emphasis on the types of polymers that have routinely been used in recent investigations. Further, this review will show that the field of retinal tissue engineering will require new types of materials and fabrication techniques that optimize the survival, differentiation and delivery of retinal transplant cells.
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spelling Advances in Retinal Tissue Engineeringretinal engineeringpoly(lactic-co-glycolic acid) (PLGA)poly(lactic acid) (PLLA)poly(glycerol-sebacate) (PGS)poly(caprolactone) (PCL)Retinal degenerations cause permanent visual loss and affect millions world-wide. Current treatment strategies, such as gene therapy and anti-angiogenic drugs, merely delay disease progression. Research is underway which aims to regenerate the diseased retina by transplanting a variety of cell types, including embryonic stem cells, fetal cells, progenitor cells and induced pluripotent stem cells. Initial retinal transplantation studies injected stem and progenitor cells into the vitreous or subretinal space with the hope that these donor cells would migrate to the site of retinal degeneration, integrate within the host retina and restore functional vision. Despite promising outcomes, these studies showed that the bolus injection technique gave rise to poorly localized tissue grafts. Subsequently, retinal tissue engineers have drawn upon the success of bone, cartilage and vasculature tissue engineering by employing a polymeric tissue engineering approach. This review will describe the evolution of retinal tissue engineering to date, with particular emphasis on the types of polymers that have routinely been used in recent investigations. Further, this review will show that the field of retinal tissue engineering will require new types of materials and fabrication techniques that optimize the survival, differentiation and delivery of retinal transplant cells.Harvard Univ, Sch Med, Dept Ophthalmol, Schepens Eye Res Inst, Boston, MA 02114 USABoston Univ, Dept Grad Med Sci, Boston, MA 02215 USAUniversidade Federal de São Paulo, Dept Ophthalmol, BR-09210170 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Ophthalmol, BR-09210170 São Paulo, BrazilWeb of ScienceMdpi AgHarvard UnivBoston UnivUniversidade Federal de São Paulo (UNIFESP)Trese, MatthewRegatieri, Caio V. [UNIFESP]Young, Michael J.2016-01-24T14:17:39Z2016-01-24T14:17:39Z2012-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion108-120application/pdfhttp://dx.doi.org/10.3390/ma5010108Materials. Basel: Mdpi Ag, v. 5, n. 1, p. 108-120, 2012.10.3390/ma4010108WOS000300722400006.pdf1996-1944http://repositorio.unifesp.br/handle/11600/34403WOS:000300722400006engMaterialsinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-31T23:33:35Zoai:repositorio.unifesp.br/:11600/34403Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-31T23:33:35Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Advances in Retinal Tissue Engineering
title Advances in Retinal Tissue Engineering
spellingShingle Advances in Retinal Tissue Engineering
Trese, Matthew
retinal engineering
poly(lactic-co-glycolic acid) (PLGA)
poly(lactic acid) (PLLA)
poly(glycerol-sebacate) (PGS)
poly(caprolactone) (PCL)
title_short Advances in Retinal Tissue Engineering
title_full Advances in Retinal Tissue Engineering
title_fullStr Advances in Retinal Tissue Engineering
title_full_unstemmed Advances in Retinal Tissue Engineering
title_sort Advances in Retinal Tissue Engineering
author Trese, Matthew
author_facet Trese, Matthew
Regatieri, Caio V. [UNIFESP]
Young, Michael J.
author_role author
author2 Regatieri, Caio V. [UNIFESP]
Young, Michael J.
author2_role author
author
dc.contributor.none.fl_str_mv Harvard Univ
Boston Univ
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Trese, Matthew
Regatieri, Caio V. [UNIFESP]
Young, Michael J.
dc.subject.por.fl_str_mv retinal engineering
poly(lactic-co-glycolic acid) (PLGA)
poly(lactic acid) (PLLA)
poly(glycerol-sebacate) (PGS)
poly(caprolactone) (PCL)
topic retinal engineering
poly(lactic-co-glycolic acid) (PLGA)
poly(lactic acid) (PLLA)
poly(glycerol-sebacate) (PGS)
poly(caprolactone) (PCL)
description Retinal degenerations cause permanent visual loss and affect millions world-wide. Current treatment strategies, such as gene therapy and anti-angiogenic drugs, merely delay disease progression. Research is underway which aims to regenerate the diseased retina by transplanting a variety of cell types, including embryonic stem cells, fetal cells, progenitor cells and induced pluripotent stem cells. Initial retinal transplantation studies injected stem and progenitor cells into the vitreous or subretinal space with the hope that these donor cells would migrate to the site of retinal degeneration, integrate within the host retina and restore functional vision. Despite promising outcomes, these studies showed that the bolus injection technique gave rise to poorly localized tissue grafts. Subsequently, retinal tissue engineers have drawn upon the success of bone, cartilage and vasculature tissue engineering by employing a polymeric tissue engineering approach. This review will describe the evolution of retinal tissue engineering to date, with particular emphasis on the types of polymers that have routinely been used in recent investigations. Further, this review will show that the field of retinal tissue engineering will require new types of materials and fabrication techniques that optimize the survival, differentiation and delivery of retinal transplant cells.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-01
2016-01-24T14:17:39Z
2016-01-24T14:17:39Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3390/ma5010108
Materials. Basel: Mdpi Ag, v. 5, n. 1, p. 108-120, 2012.
10.3390/ma4010108
WOS000300722400006.pdf
1996-1944
http://repositorio.unifesp.br/handle/11600/34403
WOS:000300722400006
url http://dx.doi.org/10.3390/ma5010108
http://repositorio.unifesp.br/handle/11600/34403
identifier_str_mv Materials. Basel: Mdpi Ag, v. 5, n. 1, p. 108-120, 2012.
10.3390/ma4010108
WOS000300722400006.pdf
1996-1944
WOS:000300722400006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Materials
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 108-120
application/pdf
dc.publisher.none.fl_str_mv Mdpi Ag
publisher.none.fl_str_mv Mdpi Ag
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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