RPE cell and sheet properties in normal and diseased eyes
- Autores
- Rashid, Alia; Bhatia, Shagun K.; Mazzitello, Karina Irma; Chrenek, Micah A.; Zhang, Qing; Boatright, Jeffrey H.; Grossniklaus, Hans E.; Jiang, Yi; Nickerson, John M.
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Previous studies of human retinal pigment epithelium (RPE) morphology found spatial differences in density: a high density of cells in the macula, decreasing peripherally. Because the RPE sheet is not perfectly regular, we anticipate that there will be differences between conditions and when and where damage is most likely to begin. The purpose of this study is to establish relationships among RPE morphometrics in age, cell location, and disease of normal human and AMD eyes that highlight irregularities reflecting damage. Cadaveric eyes from 11 normal and 3 age-related macular degeneration (AMD) human donors ranging from 29 to 82 years of age were used. Borders of RPE cells were identified with phalloidin. RPE segmentation and analysis were conducted with CellProfiler. Exploration of spatial point patterns was conducted using the “spatstat” package of R. In the normal human eye, with increasing age, cell size increased, and cells lost their regular hexagonal shape. Cell density was higher in the macula versus periphery. AMD resulted in greater variability in size and shape of the RPE cell. Spatial point analysis revealed an ordered distribution of cells in normal and high spatial disorder in AMD eyes. Morphometrics of the RPE cell readily discriminate among young vs. old and normal vs. diseased in the human eye. The normal RPE sheet is organized in a regular array of cells, but AMD exhibited strong spatial irregularity. These findings reflect on the robust recovery of the RPE sheet after wounding and the circumstances under which it cannot recover.
Fil: Rashid, Alia. Emory University; Estados Unidos
Fil: Bhatia, Shagun K.. Emory University; Estados Unidos
Fil: Mazzitello, Karina Irma. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Mar del Plata; Argentina
Fil: Chrenek, Micah A.. Emory University; Estados Unidos
Fil: Zhang, Qing. Emory University; Estados Unidos
Fil: Boatright, Jeffrey H.. Emory University; Estados Unidos
Fil: Grossniklaus, Hans E.. Emory University; Estados Unidos
Fil: Jiang, Yi. Georgia State University; Estados Unidos
Fil: Nickerson, John M.. Emory Eye Center; Estados Unidos - Materia
-
Age Related Macular Degeneration (Amd)
Cadaveric Eyes
Cellprofiler
En Face
Flatmount
Macula
Nearest Neighbor Distance
Periphery
Retinal Pigmented Epithelium (Rpe)
Spatial Point Patterns
Spatstat - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/50712
Ver los metadatos del registro completo
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oai:ri.conicet.gov.ar:11336/50712 |
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CONICET Digital (CONICET) |
spelling |
RPE cell and sheet properties in normal and diseased eyesRashid, AliaBhatia, Shagun K.Mazzitello, Karina IrmaChrenek, Micah A.Zhang, QingBoatright, Jeffrey H.Grossniklaus, Hans E.Jiang, YiNickerson, John M.Age Related Macular Degeneration (Amd)Cadaveric EyesCellprofilerEn FaceFlatmountMaculaNearest Neighbor DistancePeripheryRetinal Pigmented Epithelium (Rpe)Spatial Point PatternsSpatstathttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Previous studies of human retinal pigment epithelium (RPE) morphology found spatial differences in density: a high density of cells in the macula, decreasing peripherally. Because the RPE sheet is not perfectly regular, we anticipate that there will be differences between conditions and when and where damage is most likely to begin. The purpose of this study is to establish relationships among RPE morphometrics in age, cell location, and disease of normal human and AMD eyes that highlight irregularities reflecting damage. Cadaveric eyes from 11 normal and 3 age-related macular degeneration (AMD) human donors ranging from 29 to 82 years of age were used. Borders of RPE cells were identified with phalloidin. RPE segmentation and analysis were conducted with CellProfiler. Exploration of spatial point patterns was conducted using the “spatstat” package of R. In the normal human eye, with increasing age, cell size increased, and cells lost their regular hexagonal shape. Cell density was higher in the macula versus periphery. AMD resulted in greater variability in size and shape of the RPE cell. Spatial point analysis revealed an ordered distribution of cells in normal and high spatial disorder in AMD eyes. Morphometrics of the RPE cell readily discriminate among young vs. old and normal vs. diseased in the human eye. The normal RPE sheet is organized in a regular array of cells, but AMD exhibited strong spatial irregularity. These findings reflect on the robust recovery of the RPE sheet after wounding and the circumstances under which it cannot recover.Fil: Rashid, Alia. Emory University; Estados UnidosFil: Bhatia, Shagun K.. Emory University; Estados UnidosFil: Mazzitello, Karina Irma. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Mar del Plata; ArgentinaFil: Chrenek, Micah A.. Emory University; Estados UnidosFil: Zhang, Qing. Emory University; Estados UnidosFil: Boatright, Jeffrey H.. Emory University; Estados UnidosFil: Grossniklaus, Hans E.. Emory University; Estados UnidosFil: Jiang, Yi. Georgia State University; Estados UnidosFil: Nickerson, John M.. Emory Eye Center; Estados UnidosSpringer Verlag Berlín2016-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/50712Rashid, Alia; Bhatia, Shagun K.; Mazzitello, Karina Irma; Chrenek, Micah A.; Zhang, Qing; et al.; RPE cell and sheet properties in normal and diseased eyes; Springer Verlag Berlín; Advances in Experimental Medicine and Biology; 854; 10-2016; 757-7630065-2598CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1007/978-3-319-17121-0_101info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/chapter/10.1007%2F978-3-319-17121-0_101info:eu-repo/semantics/altIdentifier/url/https://pubmed.ncbi.nlm.nih.gov/23692342/info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:28:06Zoai:ri.conicet.gov.ar:11336/50712instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:28:07.013CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
RPE cell and sheet properties in normal and diseased eyes |
title |
RPE cell and sheet properties in normal and diseased eyes |
spellingShingle |
RPE cell and sheet properties in normal and diseased eyes Rashid, Alia Age Related Macular Degeneration (Amd) Cadaveric Eyes Cellprofiler En Face Flatmount Macula Nearest Neighbor Distance Periphery Retinal Pigmented Epithelium (Rpe) Spatial Point Patterns Spatstat |
title_short |
RPE cell and sheet properties in normal and diseased eyes |
title_full |
RPE cell and sheet properties in normal and diseased eyes |
title_fullStr |
RPE cell and sheet properties in normal and diseased eyes |
title_full_unstemmed |
RPE cell and sheet properties in normal and diseased eyes |
title_sort |
RPE cell and sheet properties in normal and diseased eyes |
dc.creator.none.fl_str_mv |
Rashid, Alia Bhatia, Shagun K. Mazzitello, Karina Irma Chrenek, Micah A. Zhang, Qing Boatright, Jeffrey H. Grossniklaus, Hans E. Jiang, Yi Nickerson, John M. |
author |
Rashid, Alia |
author_facet |
Rashid, Alia Bhatia, Shagun K. Mazzitello, Karina Irma Chrenek, Micah A. Zhang, Qing Boatright, Jeffrey H. Grossniklaus, Hans E. Jiang, Yi Nickerson, John M. |
author_role |
author |
author2 |
Bhatia, Shagun K. Mazzitello, Karina Irma Chrenek, Micah A. Zhang, Qing Boatright, Jeffrey H. Grossniklaus, Hans E. Jiang, Yi Nickerson, John M. |
author2_role |
author author author author author author author author |
dc.subject.none.fl_str_mv |
Age Related Macular Degeneration (Amd) Cadaveric Eyes Cellprofiler En Face Flatmount Macula Nearest Neighbor Distance Periphery Retinal Pigmented Epithelium (Rpe) Spatial Point Patterns Spatstat |
topic |
Age Related Macular Degeneration (Amd) Cadaveric Eyes Cellprofiler En Face Flatmount Macula Nearest Neighbor Distance Periphery Retinal Pigmented Epithelium (Rpe) Spatial Point Patterns Spatstat |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Previous studies of human retinal pigment epithelium (RPE) morphology found spatial differences in density: a high density of cells in the macula, decreasing peripherally. Because the RPE sheet is not perfectly regular, we anticipate that there will be differences between conditions and when and where damage is most likely to begin. The purpose of this study is to establish relationships among RPE morphometrics in age, cell location, and disease of normal human and AMD eyes that highlight irregularities reflecting damage. Cadaveric eyes from 11 normal and 3 age-related macular degeneration (AMD) human donors ranging from 29 to 82 years of age were used. Borders of RPE cells were identified with phalloidin. RPE segmentation and analysis were conducted with CellProfiler. Exploration of spatial point patterns was conducted using the “spatstat” package of R. In the normal human eye, with increasing age, cell size increased, and cells lost their regular hexagonal shape. Cell density was higher in the macula versus periphery. AMD resulted in greater variability in size and shape of the RPE cell. Spatial point analysis revealed an ordered distribution of cells in normal and high spatial disorder in AMD eyes. Morphometrics of the RPE cell readily discriminate among young vs. old and normal vs. diseased in the human eye. The normal RPE sheet is organized in a regular array of cells, but AMD exhibited strong spatial irregularity. These findings reflect on the robust recovery of the RPE sheet after wounding and the circumstances under which it cannot recover. Fil: Rashid, Alia. Emory University; Estados Unidos Fil: Bhatia, Shagun K.. Emory University; Estados Unidos Fil: Mazzitello, Karina Irma. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Mar del Plata; Argentina Fil: Chrenek, Micah A.. Emory University; Estados Unidos Fil: Zhang, Qing. Emory University; Estados Unidos Fil: Boatright, Jeffrey H.. Emory University; Estados Unidos Fil: Grossniklaus, Hans E.. Emory University; Estados Unidos Fil: Jiang, Yi. Georgia State University; Estados Unidos Fil: Nickerson, John M.. Emory Eye Center; Estados Unidos |
description |
Previous studies of human retinal pigment epithelium (RPE) morphology found spatial differences in density: a high density of cells in the macula, decreasing peripherally. Because the RPE sheet is not perfectly regular, we anticipate that there will be differences between conditions and when and where damage is most likely to begin. The purpose of this study is to establish relationships among RPE morphometrics in age, cell location, and disease of normal human and AMD eyes that highlight irregularities reflecting damage. Cadaveric eyes from 11 normal and 3 age-related macular degeneration (AMD) human donors ranging from 29 to 82 years of age were used. Borders of RPE cells were identified with phalloidin. RPE segmentation and analysis were conducted with CellProfiler. Exploration of spatial point patterns was conducted using the “spatstat” package of R. In the normal human eye, with increasing age, cell size increased, and cells lost their regular hexagonal shape. Cell density was higher in the macula versus periphery. AMD resulted in greater variability in size and shape of the RPE cell. Spatial point analysis revealed an ordered distribution of cells in normal and high spatial disorder in AMD eyes. Morphometrics of the RPE cell readily discriminate among young vs. old and normal vs. diseased in the human eye. The normal RPE sheet is organized in a regular array of cells, but AMD exhibited strong spatial irregularity. These findings reflect on the robust recovery of the RPE sheet after wounding and the circumstances under which it cannot recover. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-10 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/50712 Rashid, Alia; Bhatia, Shagun K.; Mazzitello, Karina Irma; Chrenek, Micah A.; Zhang, Qing; et al.; RPE cell and sheet properties in normal and diseased eyes; Springer Verlag Berlín; Advances in Experimental Medicine and Biology; 854; 10-2016; 757-763 0065-2598 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/50712 |
identifier_str_mv |
Rashid, Alia; Bhatia, Shagun K.; Mazzitello, Karina Irma; Chrenek, Micah A.; Zhang, Qing; et al.; RPE cell and sheet properties in normal and diseased eyes; Springer Verlag Berlín; Advances in Experimental Medicine and Biology; 854; 10-2016; 757-763 0065-2598 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1007/978-3-319-17121-0_101 info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/chapter/10.1007%2F978-3-319-17121-0_101 info:eu-repo/semantics/altIdentifier/url/https://pubmed.ncbi.nlm.nih.gov/23692342/ |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Springer Verlag Berlín |
publisher.none.fl_str_mv |
Springer Verlag Berlín |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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score |
13.070432 |