Reproductive biology. Endometrial angiogenesis throughout the human menstrual cycle
BACKGROUND: The timing and mechanisms of new blood vessel formation in the endometrium during the menstrual cycle are still largely unknown. In the present study we used the chick embryo chorioallantoic membrane (CAM) as an in-vivo assay for angiogenesis to assess the angiogenic potential of endomet...
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Veröffentlicht in: | Human reproduction (Oxford) 2001-08, Vol.16 (8), p.1557 |
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creator | Maas, Jacques W M Groothuis, Patrick G Dunselman, Gerard A J Anton F.P.M. de Goeij Harry A.J.Struyker Boudier Evers, Johannes L H |
description | BACKGROUND: The timing and mechanisms of new blood vessel formation in the endometrium during the menstrual cycle are still largely unknown. In the present study we used the chick embryo chorioallantoic membrane (CAM) as an in-vivo assay for angiogenesis to assess the angiogenic potential of endometrium obtained at different stages of the menstrual cycle. METHODS: Endometrial fragments were explanted onto the CAM and, after 4 days of incubation, slides of the treated area were taken in ovo through a microscope for computerized image analysis. The vascular density index (VDI), a stereological estimate of vessel number and length, was obtained by counting the intersections of vessels with five concentric circles of a circular grid superimposed on the computerized image. RESULTS: We demonstrated that human endometrium has angiogenic potential throughout the menstrual cycle. Furthermore, there was a significant difference in angiogenic response between the stages of the menstrual cycle (P = 0.01). The VDIs of the early proliferative, early and late secretory stage were significantly higher than the VDI of the late proliferative phase. CONCLUSIONS: Elongation of existing vessels during the early proliferative phase as well as growth and coiling of the spiral vessels during the secretory phase may demand far higher angiogenic activity than outgrowth and maintenance of vessels during the late proliferative phase. |
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Endometrial angiogenesis throughout the human menstrual cycle</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Oxford University Press Journals All Titles (1996-Current)</source><creator>Maas, Jacques W M ; Groothuis, Patrick G ; Dunselman, Gerard A J ; Anton F.P.M. de Goeij ; Harry A.J.Struyker Boudier ; Evers, Johannes L H</creator><creatorcontrib>Maas, Jacques W M ; Groothuis, Patrick G ; Dunselman, Gerard A J ; Anton F.P.M. de Goeij ; Harry A.J.Struyker Boudier ; Evers, Johannes L H</creatorcontrib><description>BACKGROUND: The timing and mechanisms of new blood vessel formation in the endometrium during the menstrual cycle are still largely unknown. In the present study we used the chick embryo chorioallantoic membrane (CAM) as an in-vivo assay for angiogenesis to assess the angiogenic potential of endometrium obtained at different stages of the menstrual cycle. METHODS: Endometrial fragments were explanted onto the CAM and, after 4 days of incubation, slides of the treated area were taken in ovo through a microscope for computerized image analysis. The vascular density index (VDI), a stereological estimate of vessel number and length, was obtained by counting the intersections of vessels with five concentric circles of a circular grid superimposed on the computerized image. RESULTS: We demonstrated that human endometrium has angiogenic potential throughout the menstrual cycle. Furthermore, there was a significant difference in angiogenic response between the stages of the menstrual cycle (P = 0.01). The VDIs of the early proliferative, early and late secretory stage were significantly higher than the VDI of the late proliferative phase. CONCLUSIONS: Elongation of existing vessels during the early proliferative phase as well as growth and coiling of the spiral vessels during the secretory phase may demand far higher angiogenic activity than outgrowth and maintenance of vessels during the late proliferative phase.</description><identifier>ISSN: 0268-1161</identifier><identifier>EISSN: 1460-2350</identifier><identifier>CODEN: HRUPF8</identifier><language>eng</language><publisher>Oxford: Oxford Publishing Limited (England)</publisher><ispartof>Human reproduction (Oxford), 2001-08, Vol.16 (8), p.1557</ispartof><rights>Copyright Oxford University Press(England) Aug 2001</rights><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>314,777,781</link.rule.ids></links><search><creatorcontrib>Maas, Jacques W M</creatorcontrib><creatorcontrib>Groothuis, Patrick G</creatorcontrib><creatorcontrib>Dunselman, Gerard A J</creatorcontrib><creatorcontrib>Anton F.P.M. de Goeij</creatorcontrib><creatorcontrib>Harry A.J.Struyker Boudier</creatorcontrib><creatorcontrib>Evers, Johannes L H</creatorcontrib><title>Reproductive biology. Endometrial angiogenesis throughout the human menstrual cycle</title><title>Human reproduction (Oxford)</title><description>BACKGROUND: The timing and mechanisms of new blood vessel formation in the endometrium during the menstrual cycle are still largely unknown. In the present study we used the chick embryo chorioallantoic membrane (CAM) as an in-vivo assay for angiogenesis to assess the angiogenic potential of endometrium obtained at different stages of the menstrual cycle. METHODS: Endometrial fragments were explanted onto the CAM and, after 4 days of incubation, slides of the treated area were taken in ovo through a microscope for computerized image analysis. The vascular density index (VDI), a stereological estimate of vessel number and length, was obtained by counting the intersections of vessels with five concentric circles of a circular grid superimposed on the computerized image. RESULTS: We demonstrated that human endometrium has angiogenic potential throughout the menstrual cycle. Furthermore, there was a significant difference in angiogenic response between the stages of the menstrual cycle (P = 0.01). The VDIs of the early proliferative, early and late secretory stage were significantly higher than the VDI of the late proliferative phase. 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Endometrial angiogenesis throughout the human menstrual cycle</title><author>Maas, Jacques W M ; Groothuis, Patrick G ; Dunselman, Gerard A J ; Anton F.P.M. de Goeij ; Harry A.J.Struyker Boudier ; Evers, Johannes L H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_2119070793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maas, Jacques W M</creatorcontrib><creatorcontrib>Groothuis, Patrick G</creatorcontrib><creatorcontrib>Dunselman, Gerard A J</creatorcontrib><creatorcontrib>Anton F.P.M. de Goeij</creatorcontrib><creatorcontrib>Harry A.J.Struyker Boudier</creatorcontrib><creatorcontrib>Evers, Johannes L H</creatorcontrib><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maas, Jacques W M</au><au>Groothuis, Patrick G</au><au>Dunselman, Gerard A J</au><au>Anton F.P.M. de Goeij</au><au>Harry A.J.Struyker Boudier</au><au>Evers, Johannes L H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reproductive biology. Endometrial angiogenesis throughout the human menstrual cycle</atitle><jtitle>Human reproduction (Oxford)</jtitle><date>2001-08-01</date><risdate>2001</risdate><volume>16</volume><issue>8</issue><spage>1557</spage><pages>1557-</pages><issn>0268-1161</issn><eissn>1460-2350</eissn><coden>HRUPF8</coden><abstract>BACKGROUND: The timing and mechanisms of new blood vessel formation in the endometrium during the menstrual cycle are still largely unknown. In the present study we used the chick embryo chorioallantoic membrane (CAM) as an in-vivo assay for angiogenesis to assess the angiogenic potential of endometrium obtained at different stages of the menstrual cycle. METHODS: Endometrial fragments were explanted onto the CAM and, after 4 days of incubation, slides of the treated area were taken in ovo through a microscope for computerized image analysis. The vascular density index (VDI), a stereological estimate of vessel number and length, was obtained by counting the intersections of vessels with five concentric circles of a circular grid superimposed on the computerized image. RESULTS: We demonstrated that human endometrium has angiogenic potential throughout the menstrual cycle. Furthermore, there was a significant difference in angiogenic response between the stages of the menstrual cycle (P = 0.01). The VDIs of the early proliferative, early and late secretory stage were significantly higher than the VDI of the late proliferative phase. CONCLUSIONS: Elongation of existing vessels during the early proliferative phase as well as growth and coiling of the spiral vessels during the secretory phase may demand far higher angiogenic activity than outgrowth and maintenance of vessels during the late proliferative phase.</abstract><cop>Oxford</cop><pub>Oxford Publishing Limited (England)</pub></addata></record> |
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title | Reproductive biology. Endometrial angiogenesis throughout the human menstrual cycle |
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