Advances in Retinal Tissue Engineering
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , |
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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Repositório Institucional da UNIFESP |
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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 |
_version_ |
1814268403596132352 |