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
Hauptverfasser: 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
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container_end_page 1454
container_issue 5
container_start_page 1448
container_title Fertility and sterility
container_volume 93
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. 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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><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. 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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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source MEDLINE; Elsevier ScienceDirect Journals Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
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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