Change of proinflammatory cytokines follows certain patterns after induction of endometriosis in a mouse model
Objective To examine the change in proinflammatory cytokines in the pathologic processes of endometriosis in mice. Design A dynamic study on a murine model of endometriosis. Setting Medical school. Animal(s) Female BALB/c mice. Intervention(s) Endometriosis was induced by injecting endometrial fragm...
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Veröffentlicht in: | Fertility and sterility 2010-03, Vol.93 (5), p.1448-1454 |
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creator | Chen, Qiong-Hua, Ph.D Zhou, Wei-Dong, Ph.D Su, Zhi-Ying, M.D Huang, Qian-Sheng, Ph.D Jiang, Jin-Na, M.D Chen, Qing-Xi, Ph.D |
description | Objective To examine the change in proinflammatory cytokines in the pathologic processes of endometriosis in mice. Design A dynamic study on a murine model of endometriosis. Setting Medical school. Animal(s) Female BALB/c mice. Intervention(s) Endometriosis was induced by injecting endometrial fragments of syngenic mice into the peritoneal cavity of model mice; in control group, phosphate-buffered saline instead of fragments was injected. The peritoneal fluid and the endometriotic lesions were harvested 1 to 21 days after the induction. Main Outcome Measure(s) The endometriotic lesions were weighed, the gene and protein levels of some proinflammatory cytokines, including interleukin 1β, tumor necrosis factor α, vascular endothelial growth factor, and monocyte chemoattractant protein 1, were determined by real-time quantitative polymerase chain reaction and enzyme-linked immunosorbent assay, respectively. Result(s) The levels of these cytokines reached the first peak on the first day and no endometriotic lesions were found. The lesions began to appear on the second day, presenting red color during the initial 6 days, and then they turned dark-red, brown, or bluish. The adhesion took place on the 9th day, and all the lesions evolved into white or transparent cysts on the 15th day. Corresponding to these changes, the second and the third peaks were identified during the 3rd–6th day and the 12th-15th day, respectively. Conclusion(s) The change pattern of cytokines over time might bear some relationship with the development and progression of the endometriosis. |
doi_str_mv | 10.1016/j.fertnstert.2009.02.013 |
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Design A dynamic study on a murine model of endometriosis. Setting Medical school. Animal(s) Female BALB/c mice. Intervention(s) Endometriosis was induced by injecting endometrial fragments of syngenic mice into the peritoneal cavity of model mice; in control group, phosphate-buffered saline instead of fragments was injected. The peritoneal fluid and the endometriotic lesions were harvested 1 to 21 days after the induction. Main Outcome Measure(s) The endometriotic lesions were weighed, the gene and protein levels of some proinflammatory cytokines, including interleukin 1β, tumor necrosis factor α, vascular endothelial growth factor, and monocyte chemoattractant protein 1, were determined by real-time quantitative polymerase chain reaction and enzyme-linked immunosorbent assay, respectively. Result(s) The levels of these cytokines reached the first peak on the first day and no endometriotic lesions were found. The lesions began to appear on the second day, presenting red color during the initial 6 days, and then they turned dark-red, brown, or bluish. The adhesion took place on the 9th day, and all the lesions evolved into white or transparent cysts on the 15th day. Corresponding to these changes, the second and the third peaks were identified during the 3rd–6th day and the 12th-15th day, respectively. Conclusion(s) The change pattern of cytokines over time might bear some relationship with the development and progression of the endometriosis.</description><identifier>ISSN: 0015-0282</identifier><identifier>EISSN: 1556-5653</identifier><identifier>DOI: 10.1016/j.fertnstert.2009.02.013</identifier><identifier>PMID: 19342044</identifier><identifier>CODEN: FESTAS</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Ascitic Fluid - immunology ; Biological and medical sciences ; Biomarkers - metabolism ; Chemokine CCL2 - metabolism ; Cytokines - genetics ; Cytokines - metabolism ; Disease Models, Animal ; Endometriosis ; Endometriosis - immunology ; Endometriosis - pathology ; Endometrium - immunology ; Endometrium - pathology ; Endometrium - transplantation ; Enzyme-Linked Immunosorbent Assay ; Female ; Female genital diseases ; Gynecology. Andrology. Obstetrics ; IL-1β ; Inflammation Mediators - metabolism ; Interleukin-1beta - metabolism ; Internal Medicine ; MCP-1 ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Non tumoral diseases ; Obstetrics and Gynecology ; pathogenesis ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - metabolism ; Time Factors ; TNF-α ; Tumor Necrosis Factor-alpha - metabolism ; Vascular Endothelial Growth Factor A - metabolism ; VEGF</subject><ispartof>Fertility and sterility, 2010-03, Vol.93 (5), p.1448-1454</ispartof><rights>American Society for Reproductive Medicine</rights><rights>2010 American Society for Reproductive Medicine</rights><rights>2015 INIST-CNRS</rights><rights>Copyright 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c574t-997c71fbf2a0a1998f13f1b62ec8754f509cb81e8ff119cf115d0bba4ac833fb3</citedby><cites>FETCH-LOGICAL-c574t-997c71fbf2a0a1998f13f1b62ec8754f509cb81e8ff119cf115d0bba4ac833fb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0015028209003604$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22540445$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19342044$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Qiong-Hua, Ph.D</creatorcontrib><creatorcontrib>Zhou, Wei-Dong, Ph.D</creatorcontrib><creatorcontrib>Su, Zhi-Ying, M.D</creatorcontrib><creatorcontrib>Huang, Qian-Sheng, Ph.D</creatorcontrib><creatorcontrib>Jiang, Jin-Na, M.D</creatorcontrib><creatorcontrib>Chen, Qing-Xi, Ph.D</creatorcontrib><title>Change of proinflammatory cytokines follows certain patterns after induction of endometriosis in a mouse model</title><title>Fertility and sterility</title><addtitle>Fertil Steril</addtitle><description>Objective To examine the change in proinflammatory cytokines in the pathologic processes of endometriosis in mice. Design A dynamic study on a murine model of endometriosis. Setting Medical school. Animal(s) Female BALB/c mice. Intervention(s) Endometriosis was induced by injecting endometrial fragments of syngenic mice into the peritoneal cavity of model mice; in control group, phosphate-buffered saline instead of fragments was injected. The peritoneal fluid and the endometriotic lesions were harvested 1 to 21 days after the induction. Main Outcome Measure(s) The endometriotic lesions were weighed, the gene and protein levels of some proinflammatory cytokines, including interleukin 1β, tumor necrosis factor α, vascular endothelial growth factor, and monocyte chemoattractant protein 1, were determined by real-time quantitative polymerase chain reaction and enzyme-linked immunosorbent assay, respectively. Result(s) The levels of these cytokines reached the first peak on the first day and no endometriotic lesions were found. The lesions began to appear on the second day, presenting red color during the initial 6 days, and then they turned dark-red, brown, or bluish. The adhesion took place on the 9th day, and all the lesions evolved into white or transparent cysts on the 15th day. Corresponding to these changes, the second and the third peaks were identified during the 3rd–6th day and the 12th-15th day, respectively. Conclusion(s) The change pattern of cytokines over time might bear some relationship with the development and progression of the endometriosis.</description><subject>Animals</subject><subject>Ascitic Fluid - immunology</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - metabolism</subject><subject>Chemokine CCL2 - metabolism</subject><subject>Cytokines - genetics</subject><subject>Cytokines - metabolism</subject><subject>Disease Models, Animal</subject><subject>Endometriosis</subject><subject>Endometriosis - immunology</subject><subject>Endometriosis - pathology</subject><subject>Endometrium - immunology</subject><subject>Endometrium - pathology</subject><subject>Endometrium - transplantation</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>IL-1β</subject><subject>Inflammation Mediators - metabolism</subject><subject>Interleukin-1beta - metabolism</subject><subject>Internal Medicine</subject><subject>MCP-1</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Non tumoral diseases</subject><subject>Obstetrics and Gynecology</subject><subject>pathogenesis</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - metabolism</subject><subject>Time Factors</subject><subject>TNF-α</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><subject>VEGF</subject><issn>0015-0282</issn><issn>1556-5653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkjGP1DAQhSME4paDv4DcIKqEsR0ncYMEK-BOOokCqC3HGYP3EnuxHdD-exztipOoaGYKf2_e-GmqilBoKNDuzaGxGLNPudSGAcgGWAOUP6p2VIiuFp3gj6sdABU1sIFdVc9SOgBAR3v2tLqikrcM2nZX-f0P7b8jCZYcY3DeznpZdA7xRMwph3vnMREb5jn8TsQUO-08OepcnH0i2pZOnJ9Wk13w2xT0U1gwRxeSS-WJaLKENWGpE87PqydWzwlfXPp19e3jh6_7m_ru86fb_bu72oi-zbWUvempHS3ToKmUg6Xc0rFjaIZetFaANONAcbCWUmlKEROMo261GTi3I7-uXp_nlk_9XDFltbhkcJ61x7KN6jnvh0FIVsjhTJoYUopo1TG6RceToqC2sNVBPYSttrAVMFXCLtKXF5N1XHB6EF7SLcCrC6CT0bON2huX_nKMibZgonDvzxyWSH45jCoZh97g5CKarKbg_mebt_8MMbPzrvje4wnTIazRl8gVVakI1JftOLbbAAnAO2j5HxTSupQ</recordid><startdate>20100315</startdate><enddate>20100315</enddate><creator>Chen, Qiong-Hua, Ph.D</creator><creator>Zhou, Wei-Dong, Ph.D</creator><creator>Su, Zhi-Ying, M.D</creator><creator>Huang, Qian-Sheng, Ph.D</creator><creator>Jiang, Jin-Na, M.D</creator><creator>Chen, Qing-Xi, Ph.D</creator><general>Elsevier Inc</general><general>Elsevier</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>20100315</creationdate><title>Change of proinflammatory cytokines follows certain patterns after induction of endometriosis in a mouse model</title><author>Chen, Qiong-Hua, Ph.D ; Zhou, Wei-Dong, Ph.D ; Su, Zhi-Ying, M.D ; Huang, Qian-Sheng, Ph.D ; Jiang, Jin-Na, M.D ; Chen, Qing-Xi, Ph.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-997c71fbf2a0a1998f13f1b62ec8754f509cb81e8ff119cf115d0bba4ac833fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Ascitic Fluid - immunology</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - metabolism</topic><topic>Chemokine CCL2 - metabolism</topic><topic>Cytokines - genetics</topic><topic>Cytokines - metabolism</topic><topic>Disease Models, Animal</topic><topic>Endometriosis</topic><topic>Endometriosis - immunology</topic><topic>Endometriosis - pathology</topic><topic>Endometrium - immunology</topic><topic>Endometrium - pathology</topic><topic>Endometrium - transplantation</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>IL-1β</topic><topic>Inflammation Mediators - metabolism</topic><topic>Interleukin-1beta - metabolism</topic><topic>Internal Medicine</topic><topic>MCP-1</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Non tumoral diseases</topic><topic>Obstetrics and Gynecology</topic><topic>pathogenesis</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - metabolism</topic><topic>Time Factors</topic><topic>TNF-α</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><topic>VEGF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Qiong-Hua, Ph.D</creatorcontrib><creatorcontrib>Zhou, Wei-Dong, Ph.D</creatorcontrib><creatorcontrib>Su, Zhi-Ying, M.D</creatorcontrib><creatorcontrib>Huang, Qian-Sheng, Ph.D</creatorcontrib><creatorcontrib>Jiang, Jin-Na, M.D</creatorcontrib><creatorcontrib>Chen, Qing-Xi, Ph.D</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>Chen, Qiong-Hua, Ph.D</au><au>Zhou, Wei-Dong, Ph.D</au><au>Su, Zhi-Ying, M.D</au><au>Huang, Qian-Sheng, Ph.D</au><au>Jiang, Jin-Na, M.D</au><au>Chen, Qing-Xi, Ph.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Change of proinflammatory cytokines follows certain patterns after induction of endometriosis in a mouse model</atitle><jtitle>Fertility and sterility</jtitle><addtitle>Fertil Steril</addtitle><date>2010-03-15</date><risdate>2010</risdate><volume>93</volume><issue>5</issue><spage>1448</spage><epage>1454</epage><pages>1448-1454</pages><issn>0015-0282</issn><eissn>1556-5653</eissn><coden>FESTAS</coden><abstract>Objective To examine the change in proinflammatory cytokines in the pathologic processes of endometriosis in mice. Design A dynamic study on a murine model of endometriosis. Setting Medical school. Animal(s) Female BALB/c mice. Intervention(s) Endometriosis was induced by injecting endometrial fragments of syngenic mice into the peritoneal cavity of model mice; in control group, phosphate-buffered saline instead of fragments was injected. The peritoneal fluid and the endometriotic lesions were harvested 1 to 21 days after the induction. Main Outcome Measure(s) The endometriotic lesions were weighed, the gene and protein levels of some proinflammatory cytokines, including interleukin 1β, tumor necrosis factor α, vascular endothelial growth factor, and monocyte chemoattractant protein 1, were determined by real-time quantitative polymerase chain reaction and enzyme-linked immunosorbent assay, respectively. Result(s) The levels of these cytokines reached the first peak on the first day and no endometriotic lesions were found. The lesions began to appear on the second day, presenting red color during the initial 6 days, and then they turned dark-red, brown, or bluish. The adhesion took place on the 9th day, and all the lesions evolved into white or transparent cysts on the 15th day. Corresponding to these changes, the second and the third peaks were identified during the 3rd–6th day and the 12th-15th day, respectively. Conclusion(s) The change pattern of cytokines over time might bear some relationship with the development and progression of the endometriosis.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>19342044</pmid><doi>10.1016/j.fertnstert.2009.02.013</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Ascitic Fluid - immunology Biological and medical sciences Biomarkers - metabolism Chemokine CCL2 - metabolism Cytokines - genetics Cytokines - metabolism Disease Models, Animal Endometriosis Endometriosis - immunology Endometriosis - pathology Endometrium - immunology Endometrium - pathology Endometrium - transplantation Enzyme-Linked Immunosorbent Assay Female Female genital diseases Gynecology. Andrology. Obstetrics IL-1β Inflammation Mediators - metabolism Interleukin-1beta - metabolism Internal Medicine MCP-1 Medical sciences Mice Mice, Inbred BALB C Non tumoral diseases Obstetrics and Gynecology pathogenesis Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - metabolism Time Factors TNF-α Tumor Necrosis Factor-alpha - metabolism Vascular Endothelial Growth Factor A - metabolism VEGF |
title | Change of proinflammatory cytokines follows certain patterns after induction of endometriosis in a mouse model |
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