Female Gender Attenuates Cytokine and Chemokine Expression and Leukocyte Recruitment in Experimental Rodent Abdominal Aortic Aneurysms
: Female gender appears to be protective in the development of abdominal aortic aneurysms (AAAs). This study sought to identify gender differences in cytokine and chemokine expression in an experimental rodent AAA model. Male and female rodent aortas were perfused with either saline (control) or el...
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Veröffentlicht in: | Annals of the New York Academy of Sciences 2006-11, Vol.1085 (1), p.367-379 |
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creator | SINHA, INDRANIL CHO, BRENDA S. ROELOFS, KAREN J. STANLEY, JAMES C. HENKE, PETER K. UPCHURCH Jr, GILBERT R. |
description | : Female gender appears to be protective in the development of abdominal aortic aneurysms (AAAs). This study sought to identify gender differences in cytokine and chemokine expression in an experimental rodent AAA model. Male and female rodent aortas were perfused with either saline (control) or elastase to induce AAA formation. Aortic diameter was determined and aortic tissue was harvested on postperfusion days 4 and 7. Cytokine and chemokine gene expression was examined using focused gene arrays. Immunohistochemistry was used to quantify aortic leukocyte infiltration. Data were analyzed by Student's t‐tests and ANOVA.
Elastase‐perfused female rodents developed significantly smaller aneurysms compared to males by day 7 (93 ± 10% vs. 201 ± 25%, P= 0.003). Elastase‐perfused female aortas exhibited a fivefold decrease in expression of the BMP family and ligands of the TNF superfamily compared to males. In addition, the expression of members of the TGF β and VEGF families were three to fourfold lower in female elastase‐perfused aortas compared to males. Multiple members of the interleukin, CC chemokine receptor, and CC ligand families were detectable in only the male elastase‐perfused aortas. Female elastase‐perfused aortas demonstrated a corollary twofold lower neutrophil count (females: 17.5 ± 1.1 PMN/HPF; males: 41 ± 5.2 neutrophils/HPF, P= 0.01) and a 1.5‐fold lower macrophage count (females: 12 ± 1.1 macrophages/HPF; males: 17.5 ± 1.1 macrophages/HPF, P= 0.003) compared to male elastase‐perfused aortas.
This study documents decreased expression of multiple cytokines and chemokines and diminished leukocyte trafficking in female rat aortas compared to male aortas following elastase perfusion. These genes may contribute to the gender disparity seen in AAA formation. |
doi_str_mv | 10.1196/annals.1383.027 |
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Elastase‐perfused female rodents developed significantly smaller aneurysms compared to males by day 7 (93 ± 10% vs. 201 ± 25%, P= 0.003). Elastase‐perfused female aortas exhibited a fivefold decrease in expression of the BMP family and ligands of the TNF superfamily compared to males. In addition, the expression of members of the TGF β and VEGF families were three to fourfold lower in female elastase‐perfused aortas compared to males. Multiple members of the interleukin, CC chemokine receptor, and CC ligand families were detectable in only the male elastase‐perfused aortas. Female elastase‐perfused aortas demonstrated a corollary twofold lower neutrophil count (females: 17.5 ± 1.1 PMN/HPF; males: 41 ± 5.2 neutrophils/HPF, P= 0.01) and a 1.5‐fold lower macrophage count (females: 12 ± 1.1 macrophages/HPF; males: 17.5 ± 1.1 macrophages/HPF, P= 0.003) compared to male elastase‐perfused aortas.
This study documents decreased expression of multiple cytokines and chemokines and diminished leukocyte trafficking in female rat aortas compared to male aortas following elastase perfusion. These genes may contribute to the gender disparity seen in AAA formation.</description><identifier>ISSN: 0077-8923</identifier><identifier>EISSN: 1749-6632</identifier><identifier>EISSN: 1930-6547</identifier><identifier>DOI: 10.1196/annals.1383.027</identifier><identifier>PMID: 17182958</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>AAAs ; Animals ; Aortic Aneurysm, Abdominal - immunology ; Aortic Aneurysm, Abdominal - metabolism ; Aortic Aneurysm, Abdominal - pathology ; Cell Movement ; chemokine ; cytokine ; Cytokines - chemistry ; Cytokines - metabolism ; Disease Models, Animal ; Female ; gender ; gene array ; Gene Expression Regulation ; Leukocytes - cytology ; Leukocytes - metabolism ; Macrophages - immunology ; Male ; Neutrophil Infiltration ; Oligonucleotide Array Sequence Analysis ; Perfusion ; Rats ; Rats, Sprague-Dawley ; Sex Characteristics ; Time Factors</subject><ispartof>Annals of the New York Academy of Sciences, 2006-11, Vol.1085 (1), p.367-379</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4807-b12cd60a3bde369b7e98d63c49b1383f9459a411e7f4f1f2e3f7271992a361663</citedby><cites>FETCH-LOGICAL-c4807-b12cd60a3bde369b7e98d63c49b1383f9459a411e7f4f1f2e3f7271992a361663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1196%2Fannals.1383.027$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1196%2Fannals.1383.027$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17182958$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SINHA, INDRANIL</creatorcontrib><creatorcontrib>CHO, BRENDA S.</creatorcontrib><creatorcontrib>ROELOFS, KAREN J.</creatorcontrib><creatorcontrib>STANLEY, JAMES C.</creatorcontrib><creatorcontrib>HENKE, PETER K.</creatorcontrib><creatorcontrib>UPCHURCH Jr, GILBERT R.</creatorcontrib><title>Female Gender Attenuates Cytokine and Chemokine Expression and Leukocyte Recruitment in Experimental Rodent Abdominal Aortic Aneurysms</title><title>Annals of the New York Academy of Sciences</title><addtitle>Ann N Y Acad Sci</addtitle><description>: Female gender appears to be protective in the development of abdominal aortic aneurysms (AAAs). This study sought to identify gender differences in cytokine and chemokine expression in an experimental rodent AAA model. Male and female rodent aortas were perfused with either saline (control) or elastase to induce AAA formation. Aortic diameter was determined and aortic tissue was harvested on postperfusion days 4 and 7. Cytokine and chemokine gene expression was examined using focused gene arrays. Immunohistochemistry was used to quantify aortic leukocyte infiltration. Data were analyzed by Student's t‐tests and ANOVA.
Elastase‐perfused female rodents developed significantly smaller aneurysms compared to males by day 7 (93 ± 10% vs. 201 ± 25%, P= 0.003). Elastase‐perfused female aortas exhibited a fivefold decrease in expression of the BMP family and ligands of the TNF superfamily compared to males. In addition, the expression of members of the TGF β and VEGF families were three to fourfold lower in female elastase‐perfused aortas compared to males. Multiple members of the interleukin, CC chemokine receptor, and CC ligand families were detectable in only the male elastase‐perfused aortas. Female elastase‐perfused aortas demonstrated a corollary twofold lower neutrophil count (females: 17.5 ± 1.1 PMN/HPF; males: 41 ± 5.2 neutrophils/HPF, P= 0.01) and a 1.5‐fold lower macrophage count (females: 12 ± 1.1 macrophages/HPF; males: 17.5 ± 1.1 macrophages/HPF, P= 0.003) compared to male elastase‐perfused aortas.
This study documents decreased expression of multiple cytokines and chemokines and diminished leukocyte trafficking in female rat aortas compared to male aortas following elastase perfusion. These genes may contribute to the gender disparity seen in AAA formation.</description><subject>AAAs</subject><subject>Animals</subject><subject>Aortic Aneurysm, Abdominal - immunology</subject><subject>Aortic Aneurysm, Abdominal - metabolism</subject><subject>Aortic Aneurysm, Abdominal - pathology</subject><subject>Cell Movement</subject><subject>chemokine</subject><subject>cytokine</subject><subject>Cytokines - chemistry</subject><subject>Cytokines - metabolism</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>gender</subject><subject>gene array</subject><subject>Gene Expression Regulation</subject><subject>Leukocytes - cytology</subject><subject>Leukocytes - metabolism</subject><subject>Macrophages - immunology</subject><subject>Male</subject><subject>Neutrophil Infiltration</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Perfusion</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sex Characteristics</subject><subject>Time Factors</subject><issn>0077-8923</issn><issn>1749-6632</issn><issn>1930-6547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtv1DAUhS0EotPCmh3Kil2mfiR-LKNRO0UailQeBTaWk9wIM4kztR3R_IH-bpJmBMuysq793XN9z0HoDcFrQhQ_N86ZNqwJk2yNqXiGVkRkKuWc0edohbEQqVSUnaDTEH5hTKjMxEt0QgSRVOVyhR4uoTMtJFtwNfikiBHcYCKEZDPGfm8dJMbVyeYndEt1cX_wEILt3ePDDoZ9X40Rkhuo_GBjBy4m1s0ceDtXpk1u-nq-Lsq67-z046TofbRVUjgY_Bi68Aq9aKZF4PXxPENfLi8-b67S3cft-02xS6tMYpGWhFY1x4aVNTCuSgFK1pxVmSpnCxqV5cpkhIBosoY0FFgjqCBKUcM4mVw5Q-8W3YPv7wYIUXc2VNC2xkE_BM0l5ZxT8iRIcS4FlvQ_QJpnWM6jzxew8n0IHhp9mPwxftQE6zlMvYSp5030FObU8fYoPZQd1P_4Y3oTwBbgt21hfEpPX38vPj3KpkuXDRHu_3YZv9dcMJHr2-utvv1x9VV8-JZpwf4A6wm9Kg</recordid><startdate>200611</startdate><enddate>200611</enddate><creator>SINHA, INDRANIL</creator><creator>CHO, BRENDA S.</creator><creator>ROELOFS, KAREN J.</creator><creator>STANLEY, JAMES C.</creator><creator>HENKE, PETER K.</creator><creator>UPCHURCH Jr, GILBERT R.</creator><general>Blackwell Publishing Inc</general><scope>BSCLL</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200611</creationdate><title>Female Gender Attenuates Cytokine and Chemokine Expression and Leukocyte Recruitment in Experimental Rodent Abdominal Aortic Aneurysms</title><author>SINHA, INDRANIL ; CHO, BRENDA S. ; ROELOFS, KAREN J. ; STANLEY, JAMES C. ; HENKE, PETER K. ; UPCHURCH Jr, GILBERT R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4807-b12cd60a3bde369b7e98d63c49b1383f9459a411e7f4f1f2e3f7271992a361663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>AAAs</topic><topic>Animals</topic><topic>Aortic Aneurysm, Abdominal - immunology</topic><topic>Aortic Aneurysm, Abdominal - metabolism</topic><topic>Aortic Aneurysm, Abdominal - pathology</topic><topic>Cell Movement</topic><topic>chemokine</topic><topic>cytokine</topic><topic>Cytokines - chemistry</topic><topic>Cytokines - metabolism</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>gender</topic><topic>gene array</topic><topic>Gene Expression Regulation</topic><topic>Leukocytes - cytology</topic><topic>Leukocytes - metabolism</topic><topic>Macrophages - immunology</topic><topic>Male</topic><topic>Neutrophil Infiltration</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Perfusion</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sex Characteristics</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SINHA, INDRANIL</creatorcontrib><creatorcontrib>CHO, BRENDA S.</creatorcontrib><creatorcontrib>ROELOFS, KAREN J.</creatorcontrib><creatorcontrib>STANLEY, JAMES C.</creatorcontrib><creatorcontrib>HENKE, PETER K.</creatorcontrib><creatorcontrib>UPCHURCH Jr, GILBERT R.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of the New York Academy of Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SINHA, INDRANIL</au><au>CHO, BRENDA S.</au><au>ROELOFS, KAREN J.</au><au>STANLEY, JAMES C.</au><au>HENKE, PETER K.</au><au>UPCHURCH Jr, GILBERT R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Female Gender Attenuates Cytokine and Chemokine Expression and Leukocyte Recruitment in Experimental Rodent Abdominal Aortic Aneurysms</atitle><jtitle>Annals of the New York Academy of Sciences</jtitle><addtitle>Ann N Y Acad Sci</addtitle><date>2006-11</date><risdate>2006</risdate><volume>1085</volume><issue>1</issue><spage>367</spage><epage>379</epage><pages>367-379</pages><issn>0077-8923</issn><eissn>1749-6632</eissn><eissn>1930-6547</eissn><abstract>: Female gender appears to be protective in the development of abdominal aortic aneurysms (AAAs). This study sought to identify gender differences in cytokine and chemokine expression in an experimental rodent AAA model. Male and female rodent aortas were perfused with either saline (control) or elastase to induce AAA formation. Aortic diameter was determined and aortic tissue was harvested on postperfusion days 4 and 7. Cytokine and chemokine gene expression was examined using focused gene arrays. Immunohistochemistry was used to quantify aortic leukocyte infiltration. Data were analyzed by Student's t‐tests and ANOVA.
Elastase‐perfused female rodents developed significantly smaller aneurysms compared to males by day 7 (93 ± 10% vs. 201 ± 25%, P= 0.003). Elastase‐perfused female aortas exhibited a fivefold decrease in expression of the BMP family and ligands of the TNF superfamily compared to males. In addition, the expression of members of the TGF β and VEGF families were three to fourfold lower in female elastase‐perfused aortas compared to males. Multiple members of the interleukin, CC chemokine receptor, and CC ligand families were detectable in only the male elastase‐perfused aortas. Female elastase‐perfused aortas demonstrated a corollary twofold lower neutrophil count (females: 17.5 ± 1.1 PMN/HPF; males: 41 ± 5.2 neutrophils/HPF, P= 0.01) and a 1.5‐fold lower macrophage count (females: 12 ± 1.1 macrophages/HPF; males: 17.5 ± 1.1 macrophages/HPF, P= 0.003) compared to male elastase‐perfused aortas.
This study documents decreased expression of multiple cytokines and chemokines and diminished leukocyte trafficking in female rat aortas compared to male aortas following elastase perfusion. These genes may contribute to the gender disparity seen in AAA formation.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>17182958</pmid><doi>10.1196/annals.1383.027</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | AAAs Animals Aortic Aneurysm, Abdominal - immunology Aortic Aneurysm, Abdominal - metabolism Aortic Aneurysm, Abdominal - pathology Cell Movement chemokine cytokine Cytokines - chemistry Cytokines - metabolism Disease Models, Animal Female gender gene array Gene Expression Regulation Leukocytes - cytology Leukocytes - metabolism Macrophages - immunology Male Neutrophil Infiltration Oligonucleotide Array Sequence Analysis Perfusion Rats Rats, Sprague-Dawley Sex Characteristics Time Factors |
title | Female Gender Attenuates Cytokine and Chemokine Expression and Leukocyte Recruitment in Experimental Rodent Abdominal Aortic Aneurysms |
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