Lens Cell Populations Studied in Human Donor Capsular Bags with Implanted Intraocular Lenses
Posterior capsule opacification is an ongoing cellular redistribution process. The level of viable cell coverage was therefore determined in human donor capsular bags with implanted intraocular lenses, and cellular morphology and ultrastructure were investigated in relation to cell type and level of...
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Veröffentlicht in: | Investigative ophthalmology & visual science 2000-04, Vol.41 (5), p.1130-1141 |
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description | Posterior capsule opacification is an ongoing cellular redistribution process. The level of viable cell coverage was therefore determined in human donor capsular bags with implanted intraocular lenses, and cellular morphology and ultrastructure were investigated in relation to cell type and level of differentiation.
Donor capsular bags, retrieved at intervals of 4 months to 13 years after surgery, were investigated by phase optics before fixation. Postfixation techniques included scanning electron microscopy and transmission electron microscopy of sections and immunofluorescent staining of cytoskeletal proteins in wholemounts.
All the capsular bags contained a large population of viable cells on the capsular surfaces. Cells on the anterior face of the anterior capsule and in the spaces around the intraocular lens had an elongated morphology and expressed alpha-smooth muscle actin. The cells formed light-scattering, multilayered aggregates and strands that were surrounded by layers of extracellular matrix. The regions between the intraocular lens and the equator of the bags were populated by monolayers of epithelial cells of normal morphology and ultrastructure, on both the anterior and posterior capsules. In some regions the apical surfaces of the two epithelial monolayers were in contact, and in some parts of the equatorial regions, differentiation of cells into well-organized fiberlike cells was evident.
Human capsular bags contain a large population of viable cells for many years after cataract surgery. Cells in the regions around the intraocular lens undergo transition to a mesenchymal type. Cells peripheral to these regions can form a stable closed microenvironment in which both normal epithelial morphology and differentiation to fiberlike cells are maintained. |
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Donor capsular bags, retrieved at intervals of 4 months to 13 years after surgery, were investigated by phase optics before fixation. Postfixation techniques included scanning electron microscopy and transmission electron microscopy of sections and immunofluorescent staining of cytoskeletal proteins in wholemounts.
All the capsular bags contained a large population of viable cells on the capsular surfaces. Cells on the anterior face of the anterior capsule and in the spaces around the intraocular lens had an elongated morphology and expressed alpha-smooth muscle actin. The cells formed light-scattering, multilayered aggregates and strands that were surrounded by layers of extracellular matrix. The regions between the intraocular lens and the equator of the bags were populated by monolayers of epithelial cells of normal morphology and ultrastructure, on both the anterior and posterior capsules. In some regions the apical surfaces of the two epithelial monolayers were in contact, and in some parts of the equatorial regions, differentiation of cells into well-organized fiberlike cells was evident.
Human capsular bags contain a large population of viable cells for many years after cataract surgery. Cells in the regions around the intraocular lens undergo transition to a mesenchymal type. Cells peripheral to these regions can form a stable closed microenvironment in which both normal epithelial morphology and differentiation to fiberlike cells are maintained.</description><identifier>ISSN: 0146-0404</identifier><identifier>EISSN: 1552-5783</identifier><identifier>PMID: 10752951</identifier><language>eng</language><publisher>United States: ARVO</publisher><subject>Actins - metabolism ; Adolescent ; Adult ; Aged ; Aged, 80 and over ; Aquaporins ; Cataract Extraction ; Cell Differentiation ; Child ; Epithelial Cells - metabolism ; Epithelial Cells - ultrastructure ; Eye Proteins - metabolism ; Fluorescent Antibody Technique, Indirect ; Humans ; Lens Capsule, Crystalline - cytology ; Lens Capsule, Crystalline - metabolism ; Lens Implantation, Intraocular ; Membrane Glycoproteins ; Microscopy, Electron, Scanning ; Middle Aged ; Tissue Donors ; Vimentin - metabolism</subject><ispartof>Investigative ophthalmology & visual science, 2000-04, Vol.41 (5), p.1130-1141</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10752951$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marcantonio, Julia M</creatorcontrib><creatorcontrib>Rakic, Jean-Marie</creatorcontrib><creatorcontrib>Vrensen, Gijs F. J. M</creatorcontrib><creatorcontrib>Duncan, George</creatorcontrib><title>Lens Cell Populations Studied in Human Donor Capsular Bags with Implanted Intraocular Lenses</title><title>Investigative ophthalmology & visual science</title><addtitle>Invest Ophthalmol Vis Sci</addtitle><description>Posterior capsule opacification is an ongoing cellular redistribution process. The level of viable cell coverage was therefore determined in human donor capsular bags with implanted intraocular lenses, and cellular morphology and ultrastructure were investigated in relation to cell type and level of differentiation.
Donor capsular bags, retrieved at intervals of 4 months to 13 years after surgery, were investigated by phase optics before fixation. Postfixation techniques included scanning electron microscopy and transmission electron microscopy of sections and immunofluorescent staining of cytoskeletal proteins in wholemounts.
All the capsular bags contained a large population of viable cells on the capsular surfaces. Cells on the anterior face of the anterior capsule and in the spaces around the intraocular lens had an elongated morphology and expressed alpha-smooth muscle actin. The cells formed light-scattering, multilayered aggregates and strands that were surrounded by layers of extracellular matrix. The regions between the intraocular lens and the equator of the bags were populated by monolayers of epithelial cells of normal morphology and ultrastructure, on both the anterior and posterior capsules. In some regions the apical surfaces of the two epithelial monolayers were in contact, and in some parts of the equatorial regions, differentiation of cells into well-organized fiberlike cells was evident.
Human capsular bags contain a large population of viable cells for many years after cataract surgery. Cells in the regions around the intraocular lens undergo transition to a mesenchymal type. Cells peripheral to these regions can form a stable closed microenvironment in which both normal epithelial morphology and differentiation to fiberlike cells are maintained.</description><subject>Actins - metabolism</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aquaporins</subject><subject>Cataract Extraction</subject><subject>Cell Differentiation</subject><subject>Child</subject><subject>Epithelial Cells - metabolism</subject><subject>Epithelial Cells - ultrastructure</subject><subject>Eye Proteins - metabolism</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Humans</subject><subject>Lens Capsule, Crystalline - cytology</subject><subject>Lens Capsule, Crystalline - metabolism</subject><subject>Lens Implantation, Intraocular</subject><subject>Membrane Glycoproteins</subject><subject>Microscopy, Electron, Scanning</subject><subject>Middle Aged</subject><subject>Tissue Donors</subject><subject>Vimentin - metabolism</subject><issn>0146-0404</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1LxDAQhoMo7rr6FyQnb4VMmmzao9aPXVhQUG9CSJpkG-mXSUvx31t1xdPAO8888M4RWgLnNOEiS4_RkgBbJ4QRtkBnMb4TQgEoOUULIILTnMMSve1sG3Fh6xo_df1Yq8F3c_A8jMZbg32LN2OjWnzbtV3AherjzAR8o_YRT36o8Lbpa9UOM7tth6C68mf_bbXxHJ04VUd7cZgr9Hp_91Jskt3jw7a43iUVTbMhAQLrnGqngGRM59qIkuU605nNjBI5d4anlDsHwgjNLLPC8XK-AePKlDiWrtDVr7cP3cdo4yAbH8u5k2ptN0YpgBDCGczg5QEcdWON7INvVPiUf__4N1V-X00-WBkbVdczDnKaJgaSS4CUpF-MJmqd</recordid><startdate>20000401</startdate><enddate>20000401</enddate><creator>Marcantonio, Julia M</creator><creator>Rakic, Jean-Marie</creator><creator>Vrensen, Gijs F. J. M</creator><creator>Duncan, George</creator><general>ARVO</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20000401</creationdate><title>Lens Cell Populations Studied in Human Donor Capsular Bags with Implanted Intraocular Lenses</title><author>Marcantonio, Julia M ; Rakic, Jean-Marie ; Vrensen, Gijs F. J. M ; Duncan, George</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h238t-101692bfa1084b9bd7c49b8b8e8da795fd5325ff17d7b4e4e7f5c0161dfc30f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Actins - metabolism</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aquaporins</topic><topic>Cataract Extraction</topic><topic>Cell Differentiation</topic><topic>Child</topic><topic>Epithelial Cells - metabolism</topic><topic>Epithelial Cells - ultrastructure</topic><topic>Eye Proteins - metabolism</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Humans</topic><topic>Lens Capsule, Crystalline - cytology</topic><topic>Lens Capsule, Crystalline - metabolism</topic><topic>Lens Implantation, Intraocular</topic><topic>Membrane Glycoproteins</topic><topic>Microscopy, Electron, Scanning</topic><topic>Middle Aged</topic><topic>Tissue Donors</topic><topic>Vimentin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marcantonio, Julia M</creatorcontrib><creatorcontrib>Rakic, Jean-Marie</creatorcontrib><creatorcontrib>Vrensen, Gijs F. J. M</creatorcontrib><creatorcontrib>Duncan, George</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Investigative ophthalmology & visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marcantonio, Julia M</au><au>Rakic, Jean-Marie</au><au>Vrensen, Gijs F. J. M</au><au>Duncan, George</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lens Cell Populations Studied in Human Donor Capsular Bags with Implanted Intraocular Lenses</atitle><jtitle>Investigative ophthalmology & visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>2000-04-01</date><risdate>2000</risdate><volume>41</volume><issue>5</issue><spage>1130</spage><epage>1141</epage><pages>1130-1141</pages><issn>0146-0404</issn><eissn>1552-5783</eissn><abstract>Posterior capsule opacification is an ongoing cellular redistribution process. The level of viable cell coverage was therefore determined in human donor capsular bags with implanted intraocular lenses, and cellular morphology and ultrastructure were investigated in relation to cell type and level of differentiation.
Donor capsular bags, retrieved at intervals of 4 months to 13 years after surgery, were investigated by phase optics before fixation. Postfixation techniques included scanning electron microscopy and transmission electron microscopy of sections and immunofluorescent staining of cytoskeletal proteins in wholemounts.
All the capsular bags contained a large population of viable cells on the capsular surfaces. Cells on the anterior face of the anterior capsule and in the spaces around the intraocular lens had an elongated morphology and expressed alpha-smooth muscle actin. The cells formed light-scattering, multilayered aggregates and strands that were surrounded by layers of extracellular matrix. The regions between the intraocular lens and the equator of the bags were populated by monolayers of epithelial cells of normal morphology and ultrastructure, on both the anterior and posterior capsules. In some regions the apical surfaces of the two epithelial monolayers were in contact, and in some parts of the equatorial regions, differentiation of cells into well-organized fiberlike cells was evident.
Human capsular bags contain a large population of viable cells for many years after cataract surgery. Cells in the regions around the intraocular lens undergo transition to a mesenchymal type. Cells peripheral to these regions can form a stable closed microenvironment in which both normal epithelial morphology and differentiation to fiberlike cells are maintained.</abstract><cop>United States</cop><pub>ARVO</pub><pmid>10752951</pmid><tpages>12</tpages></addata></record> |
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subjects | Actins - metabolism Adolescent Adult Aged Aged, 80 and over Aquaporins Cataract Extraction Cell Differentiation Child Epithelial Cells - metabolism Epithelial Cells - ultrastructure Eye Proteins - metabolism Fluorescent Antibody Technique, Indirect Humans Lens Capsule, Crystalline - cytology Lens Capsule, Crystalline - metabolism Lens Implantation, Intraocular Membrane Glycoproteins Microscopy, Electron, Scanning Middle Aged Tissue Donors Vimentin - metabolism |
title | Lens Cell Populations Studied in Human Donor Capsular Bags with Implanted Intraocular Lenses |
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