Three-dimensional in vitro culture of endometrial explants mimics the early stages of endometriosis
To reproduce the earliest phases of endometriosis using a new in vitro model in which cells from a cultured endometrial fragment can proliferate, invade, reconstitute new endometrial-like tissue, and generate blood vessels. Experimental in vitro study. A hospital-based academic research institute. F...
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Veröffentlicht in: | Fertility and sterility 2003-11, Vol.80 (5), p.1137-1143 |
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creator | Fasciani, Alessandro Bocci, Guido Xu, Jing Bielecki, Ryszard Greenblatt, Ellen Leyland, Nicholas Casper, Robert F |
description | To reproduce the earliest phases of endometriosis using a new in vitro model in which cells from a cultured endometrial fragment can proliferate, invade, reconstitute new endometrial-like tissue, and generate blood vessels.
Experimental in vitro study.
A hospital-based academic research institute.
Five normal ovulating women undergoing surgery for various benign gynecological indications.
Endometrial samples obtained from the fundus of the uterine cavity were placed in a three-dimensional fibrin matrix culture system.
Degree of proliferation of stromal cells and invasion of the fibrin matrix, gland, and stroma formation, vessel sprouting, and immunohistochemical characterization of various cellular components.
During the first week of culture, an endometrial cell outgrowth was observed from the original fragments in 120 of 144 wells (83.3%). Subsequently, cell outgrowths could be quantified in 132 (91.6%), 129 (89.5%), and 127 (88.1%) of the wells after 15, 60, and 90 days, respectively. An invasion of the matrix by the human endometrial cells led to the formation of tubular structures that coalesced into tissue, architecturally resembling endometrium and in which the glands were immunohistochemically positive for cytokeratin. New capillaries, immunohistochemically positive for CD31 and vimentin, sprouted from the endometrial outgrowths at the beginning of the fifth week of culture.
These data show that cells from endometrial explants can proliferate and invade a fibrin matrix in vitro generating new glands, stroma, and vessels consistent with endometriosis. The three-dimensional fibrin matrix used in the present study provides an opportunity to observe the earliest biological events of endometriosis in a quantifiable way. |
doi_str_mv | 10.1016/S0015-0282(03)02164-2 |
format | Article |
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Experimental in vitro study.
A hospital-based academic research institute.
Five normal ovulating women undergoing surgery for various benign gynecological indications.
Endometrial samples obtained from the fundus of the uterine cavity were placed in a three-dimensional fibrin matrix culture system.
Degree of proliferation of stromal cells and invasion of the fibrin matrix, gland, and stroma formation, vessel sprouting, and immunohistochemical characterization of various cellular components.
During the first week of culture, an endometrial cell outgrowth was observed from the original fragments in 120 of 144 wells (83.3%). Subsequently, cell outgrowths could be quantified in 132 (91.6%), 129 (89.5%), and 127 (88.1%) of the wells after 15, 60, and 90 days, respectively. An invasion of the matrix by the human endometrial cells led to the formation of tubular structures that coalesced into tissue, architecturally resembling endometrium and in which the glands were immunohistochemically positive for cytokeratin. New capillaries, immunohistochemically positive for CD31 and vimentin, sprouted from the endometrial outgrowths at the beginning of the fifth week of culture.
These data show that cells from endometrial explants can proliferate and invade a fibrin matrix in vitro generating new glands, stroma, and vessels consistent with endometriosis. The three-dimensional fibrin matrix used in the present study provides an opportunity to observe the earliest biological events of endometriosis in a quantifiable way.</description><identifier>ISSN: 0015-0282</identifier><identifier>EISSN: 1556-5653</identifier><identifier>DOI: 10.1016/S0015-0282(03)02164-2</identifier><identifier>PMID: 14607564</identifier><identifier>CODEN: FESTAS</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>angiogenesis ; Biological and medical sciences ; Cell Division ; Culture Techniques ; cytokeratin ; Endometriosis ; Endometriosis - pathology ; Endometrium - blood supply ; Endometrium - cytology ; Endometrium - metabolism ; Endometrium - pathology ; Female ; Female genital diseases ; fibrin matrix ; Gynecology. Andrology. Obstetrics ; Histological Techniques ; Humans ; Image Processing, Computer-Assisted ; Immunohistochemistry ; in vitro ; invasion ; Medical sciences ; Neovascularization, Physiologic ; Non tumoral diseases ; Platelet Endothelial Cell Adhesion Molecule-1 - metabolism ; Time Factors ; vimentin ; Vimentin - metabolism</subject><ispartof>Fertility and sterility, 2003-11, Vol.80 (5), p.1137-1143</ispartof><rights>2003 American Society for Reproductive Medicine</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-170c8406c68ec5039f26d3ec7bab61e1ab091dbc95dc18fccdc9a6e543591bc53</citedby><cites>FETCH-LOGICAL-c438t-170c8406c68ec5039f26d3ec7bab61e1ab091dbc95dc18fccdc9a6e543591bc53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0015028203021642$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15265605$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14607564$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fasciani, Alessandro</creatorcontrib><creatorcontrib>Bocci, Guido</creatorcontrib><creatorcontrib>Xu, Jing</creatorcontrib><creatorcontrib>Bielecki, Ryszard</creatorcontrib><creatorcontrib>Greenblatt, Ellen</creatorcontrib><creatorcontrib>Leyland, Nicholas</creatorcontrib><creatorcontrib>Casper, Robert F</creatorcontrib><title>Three-dimensional in vitro culture of endometrial explants mimics the early stages of endometriosis</title><title>Fertility and sterility</title><addtitle>Fertil Steril</addtitle><description>To reproduce the earliest phases of endometriosis using a new in vitro model in which cells from a cultured endometrial fragment can proliferate, invade, reconstitute new endometrial-like tissue, and generate blood vessels.
Experimental in vitro study.
A hospital-based academic research institute.
Five normal ovulating women undergoing surgery for various benign gynecological indications.
Endometrial samples obtained from the fundus of the uterine cavity were placed in a three-dimensional fibrin matrix culture system.
Degree of proliferation of stromal cells and invasion of the fibrin matrix, gland, and stroma formation, vessel sprouting, and immunohistochemical characterization of various cellular components.
During the first week of culture, an endometrial cell outgrowth was observed from the original fragments in 120 of 144 wells (83.3%). Subsequently, cell outgrowths could be quantified in 132 (91.6%), 129 (89.5%), and 127 (88.1%) of the wells after 15, 60, and 90 days, respectively. An invasion of the matrix by the human endometrial cells led to the formation of tubular structures that coalesced into tissue, architecturally resembling endometrium and in which the glands were immunohistochemically positive for cytokeratin. New capillaries, immunohistochemically positive for CD31 and vimentin, sprouted from the endometrial outgrowths at the beginning of the fifth week of culture.
These data show that cells from endometrial explants can proliferate and invade a fibrin matrix in vitro generating new glands, stroma, and vessels consistent with endometriosis. The three-dimensional fibrin matrix used in the present study provides an opportunity to observe the earliest biological events of endometriosis in a quantifiable way.</description><subject>angiogenesis</subject><subject>Biological and medical sciences</subject><subject>Cell Division</subject><subject>Culture Techniques</subject><subject>cytokeratin</subject><subject>Endometriosis</subject><subject>Endometriosis - pathology</subject><subject>Endometrium - blood supply</subject><subject>Endometrium - cytology</subject><subject>Endometrium - metabolism</subject><subject>Endometrium - pathology</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>fibrin matrix</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Histological Techniques</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Immunohistochemistry</subject><subject>in vitro</subject><subject>invasion</subject><subject>Medical sciences</subject><subject>Neovascularization, Physiologic</subject><subject>Non tumoral diseases</subject><subject>Platelet Endothelial Cell Adhesion Molecule-1 - metabolism</subject><subject>Time Factors</subject><subject>vimentin</subject><subject>Vimentin - metabolism</subject><issn>0015-0282</issn><issn>1556-5653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMFu1DAQhi0EotvCI4B8AZVDyjiOneRUoQooUqUeKGfLmUyoURIvHqeib0-2u6Li1NMc5vtnfn1CvFFwpkDZj98BlCmgbMpT0B-gVLYqymdio4yxhbFGPxebf8iROGb-BQBW1eVLcaQqC7Wx1UbgzW0iKvow0cwhzn6UYZZ3IacocRnzkkjGQdLcx4lyCuue_mxHP2eWU5gCssy3JMmn8V5y9j-J_-MjB34lXgx-ZHp9mCfix5fPNxeXxdX1128Xn64KrHSTC1UDNhVYtA2hAd0Ope01Yd35zipSvoNW9R22pkfVDIg9tt6SqbRpVYdGn4j3-7vbFH8vxNlNgZHGtS3FhV2tdF03ulpBswcxReZEg9umMPl07xS4nV33YNft1DnQ7sGuK9fc28ODpZuof0wddK7AuwPgGf04JD9j4EfOlNZY2DU933O06rgLlBxjoBmpD4kwuz6GJ6r8BflLmH8</recordid><startdate>20031101</startdate><enddate>20031101</enddate><creator>Fasciani, Alessandro</creator><creator>Bocci, Guido</creator><creator>Xu, Jing</creator><creator>Bielecki, Ryszard</creator><creator>Greenblatt, Ellen</creator><creator>Leyland, Nicholas</creator><creator>Casper, Robert F</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20031101</creationdate><title>Three-dimensional in vitro culture of endometrial explants mimics the early stages of endometriosis</title><author>Fasciani, Alessandro ; Bocci, Guido ; Xu, Jing ; Bielecki, Ryszard ; Greenblatt, Ellen ; Leyland, Nicholas ; Casper, Robert F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-170c8406c68ec5039f26d3ec7bab61e1ab091dbc95dc18fccdc9a6e543591bc53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>angiogenesis</topic><topic>Biological and medical sciences</topic><topic>Cell Division</topic><topic>Culture Techniques</topic><topic>cytokeratin</topic><topic>Endometriosis</topic><topic>Endometriosis - pathology</topic><topic>Endometrium - blood supply</topic><topic>Endometrium - cytology</topic><topic>Endometrium - metabolism</topic><topic>Endometrium - pathology</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>fibrin matrix</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Histological Techniques</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted</topic><topic>Immunohistochemistry</topic><topic>in vitro</topic><topic>invasion</topic><topic>Medical sciences</topic><topic>Neovascularization, Physiologic</topic><topic>Non tumoral diseases</topic><topic>Platelet Endothelial Cell Adhesion Molecule-1 - metabolism</topic><topic>Time Factors</topic><topic>vimentin</topic><topic>Vimentin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fasciani, Alessandro</creatorcontrib><creatorcontrib>Bocci, Guido</creatorcontrib><creatorcontrib>Xu, Jing</creatorcontrib><creatorcontrib>Bielecki, Ryszard</creatorcontrib><creatorcontrib>Greenblatt, Ellen</creatorcontrib><creatorcontrib>Leyland, Nicholas</creatorcontrib><creatorcontrib>Casper, Robert F</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Fertility and sterility</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fasciani, Alessandro</au><au>Bocci, Guido</au><au>Xu, Jing</au><au>Bielecki, Ryszard</au><au>Greenblatt, Ellen</au><au>Leyland, Nicholas</au><au>Casper, Robert F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Three-dimensional in vitro culture of endometrial explants mimics the early stages of endometriosis</atitle><jtitle>Fertility and sterility</jtitle><addtitle>Fertil Steril</addtitle><date>2003-11-01</date><risdate>2003</risdate><volume>80</volume><issue>5</issue><spage>1137</spage><epage>1143</epage><pages>1137-1143</pages><issn>0015-0282</issn><eissn>1556-5653</eissn><coden>FESTAS</coden><abstract>To reproduce the earliest phases of endometriosis using a new in vitro model in which cells from a cultured endometrial fragment can proliferate, invade, reconstitute new endometrial-like tissue, and generate blood vessels.
Experimental in vitro study.
A hospital-based academic research institute.
Five normal ovulating women undergoing surgery for various benign gynecological indications.
Endometrial samples obtained from the fundus of the uterine cavity were placed in a three-dimensional fibrin matrix culture system.
Degree of proliferation of stromal cells and invasion of the fibrin matrix, gland, and stroma formation, vessel sprouting, and immunohistochemical characterization of various cellular components.
During the first week of culture, an endometrial cell outgrowth was observed from the original fragments in 120 of 144 wells (83.3%). Subsequently, cell outgrowths could be quantified in 132 (91.6%), 129 (89.5%), and 127 (88.1%) of the wells after 15, 60, and 90 days, respectively. An invasion of the matrix by the human endometrial cells led to the formation of tubular structures that coalesced into tissue, architecturally resembling endometrium and in which the glands were immunohistochemically positive for cytokeratin. New capillaries, immunohistochemically positive for CD31 and vimentin, sprouted from the endometrial outgrowths at the beginning of the fifth week of culture.
These data show that cells from endometrial explants can proliferate and invade a fibrin matrix in vitro generating new glands, stroma, and vessels consistent with endometriosis. The three-dimensional fibrin matrix used in the present study provides an opportunity to observe the earliest biological events of endometriosis in a quantifiable way.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>14607564</pmid><doi>10.1016/S0015-0282(03)02164-2</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | angiogenesis Biological and medical sciences Cell Division Culture Techniques cytokeratin Endometriosis Endometriosis - pathology Endometrium - blood supply Endometrium - cytology Endometrium - metabolism Endometrium - pathology Female Female genital diseases fibrin matrix Gynecology. Andrology. Obstetrics Histological Techniques Humans Image Processing, Computer-Assisted Immunohistochemistry in vitro invasion Medical sciences Neovascularization, Physiologic Non tumoral diseases Platelet Endothelial Cell Adhesion Molecule-1 - metabolism Time Factors vimentin Vimentin - metabolism |
title | Three-dimensional in vitro culture of endometrial explants mimics the early stages of endometriosis |
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