Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis
- Autores
- Matturri, Luigi; Cazzullo, Alessandra; Turconi, Paola; Roncoroni, Lucia; Grana, Daniel Rodolfo; Milei, Jose
- Año de publicación
- 2000
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Chlamydia pneumoniae (CP), chromosomal alterations and apoptosis were suggested as contributing factors in the pathogenesis of atherosclerosis. Early (EP) and unstable plaques (UP) were studied in order to assess infiltrate composition, the apoptotic index, chromosome 7 stability and to investigate the concurrent presence of CP in EP and UP. Paraffin embedded sections of three iliac arteries and four aortas from young donors (EP), and four coronaries and nine carotid arteries (UP) were used. Aside from histological techniques, immunophenotypification for macrophages, T and B cells, smooth muscle and endothelial cells; FISH and DNA nick end labeling were performed. The amplifications with PCR for CP infection were negative in all specimens. In the EP, a focal myointimal thickening with foam cells and scarce smooth muscle cells was observed. Macrophages were most frequent in the intima (10.8%) while T and B cells were found in 2.3 and 1.5%. In the UP a thin cap covering a lipid-rich core with widespread vascularization and with severe luminal obstruction was observed. Macrophages were increased (21%), and T (1.5%) and B cells (3.5%) in the caps and inner areas of the lipid cores. At these sites, the FISH showed trisomy and tetrasomy of chromosome 7 and apoptosis was very frequent (10-30%). Macrophages in intimal lesions is one of the most prominent, consistent and permanent features in EP, and an elevated apoptotic index and chromosome 7 instability might contribute to evolution from stable to complicated plaques, while CP seems to play no role. However, further studies are needed with more cases to confirm this last observation. Copyright (C) 2000 Elsevier Science Ireland Ltd.
Fil: Matturri, Luigi. Università degli Studi di Milano; Italia. IRCCS Ospedale Maggiore; Italia
Fil: Cazzullo, Alessandra. Università degli Studi di Milano; Italia. IRCCS Ospedale Maggiore; Italia
Fil: Turconi, Paola. IRCCS Ospedale Maggiore; Italia. Università degli Studi di Milano; Italia
Fil: Roncoroni, Lucia. IRCCS Ospedale Maggiore; Italia. Università degli Studi di Milano; Italia
Fil: Grana, Daniel Rodolfo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Cardiológicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Cardiológicas; Argentina. Universidad del Salvador. Facultad de Medicina; Argentina
Fil: Milei, Jose. Universidad del Salvador. Facultad de Medicina; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Cardiológicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Cardiológicas; Argentina - Materia
-
Apoptosis
Atherosclerosis
Chlamydia Pneumoniae
Chromosome 7
Macrophage
Smooth Muscle Cell - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/39105
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Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosisMatturri, LuigiCazzullo, AlessandraTurconi, PaolaRoncoroni, LuciaGrana, Daniel RodolfoMilei, JoseApoptosisAtherosclerosisChlamydia PneumoniaeChromosome 7MacrophageSmooth Muscle Cellhttps://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Chlamydia pneumoniae (CP), chromosomal alterations and apoptosis were suggested as contributing factors in the pathogenesis of atherosclerosis. Early (EP) and unstable plaques (UP) were studied in order to assess infiltrate composition, the apoptotic index, chromosome 7 stability and to investigate the concurrent presence of CP in EP and UP. Paraffin embedded sections of three iliac arteries and four aortas from young donors (EP), and four coronaries and nine carotid arteries (UP) were used. Aside from histological techniques, immunophenotypification for macrophages, T and B cells, smooth muscle and endothelial cells; FISH and DNA nick end labeling were performed. The amplifications with PCR for CP infection were negative in all specimens. In the EP, a focal myointimal thickening with foam cells and scarce smooth muscle cells was observed. Macrophages were most frequent in the intima (10.8%) while T and B cells were found in 2.3 and 1.5%. In the UP a thin cap covering a lipid-rich core with widespread vascularization and with severe luminal obstruction was observed. Macrophages were increased (21%), and T (1.5%) and B cells (3.5%) in the caps and inner areas of the lipid cores. At these sites, the FISH showed trisomy and tetrasomy of chromosome 7 and apoptosis was very frequent (10-30%). Macrophages in intimal lesions is one of the most prominent, consistent and permanent features in EP, and an elevated apoptotic index and chromosome 7 instability might contribute to evolution from stable to complicated plaques, while CP seems to play no role. However, further studies are needed with more cases to confirm this last observation. Copyright (C) 2000 Elsevier Science Ireland Ltd.Fil: Matturri, Luigi. Università degli Studi di Milano; Italia. IRCCS Ospedale Maggiore; ItaliaFil: Cazzullo, Alessandra. Università degli Studi di Milano; Italia. IRCCS Ospedale Maggiore; ItaliaFil: Turconi, Paola. IRCCS Ospedale Maggiore; Italia. Università degli Studi di Milano; ItaliaFil: Roncoroni, Lucia. IRCCS Ospedale Maggiore; Italia. Università degli Studi di Milano; ItaliaFil: Grana, Daniel Rodolfo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Cardiológicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Cardiológicas; Argentina. Universidad del Salvador. Facultad de Medicina; ArgentinaFil: Milei, Jose. Universidad del Salvador. Facultad de Medicina; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Cardiológicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Cardiológicas; ArgentinaElsevier Ireland2000-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/pdfhttp://hdl.handle.net/11336/39105Matturri, Luigi; Cazzullo, Alessandra; Turconi, Paola; Roncoroni, Lucia; Grana, Daniel Rodolfo; et al.; Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis; Elsevier Ireland; International Journal of Cardiology; 75; 1; 8-2000; 23-330167-5273CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0167527300003065info:eu-repo/semantics/altIdentifier/doi/10.1016/S0167-5273(00)00306-5info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:22:56Zoai:ri.conicet.gov.ar:11336/39105instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:22:56.493CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis |
title |
Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis |
spellingShingle |
Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis Matturri, Luigi Apoptosis Atherosclerosis Chlamydia Pneumoniae Chromosome 7 Macrophage Smooth Muscle Cell |
title_short |
Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis |
title_full |
Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis |
title_fullStr |
Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis |
title_full_unstemmed |
Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis |
title_sort |
Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis |
dc.creator.none.fl_str_mv |
Matturri, Luigi Cazzullo, Alessandra Turconi, Paola Roncoroni, Lucia Grana, Daniel Rodolfo Milei, Jose |
author |
Matturri, Luigi |
author_facet |
Matturri, Luigi Cazzullo, Alessandra Turconi, Paola Roncoroni, Lucia Grana, Daniel Rodolfo Milei, Jose |
author_role |
author |
author2 |
Cazzullo, Alessandra Turconi, Paola Roncoroni, Lucia Grana, Daniel Rodolfo Milei, Jose |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Apoptosis Atherosclerosis Chlamydia Pneumoniae Chromosome 7 Macrophage Smooth Muscle Cell |
topic |
Apoptosis Atherosclerosis Chlamydia Pneumoniae Chromosome 7 Macrophage Smooth Muscle Cell |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Chlamydia pneumoniae (CP), chromosomal alterations and apoptosis were suggested as contributing factors in the pathogenesis of atherosclerosis. Early (EP) and unstable plaques (UP) were studied in order to assess infiltrate composition, the apoptotic index, chromosome 7 stability and to investigate the concurrent presence of CP in EP and UP. Paraffin embedded sections of three iliac arteries and four aortas from young donors (EP), and four coronaries and nine carotid arteries (UP) were used. Aside from histological techniques, immunophenotypification for macrophages, T and B cells, smooth muscle and endothelial cells; FISH and DNA nick end labeling were performed. The amplifications with PCR for CP infection were negative in all specimens. In the EP, a focal myointimal thickening with foam cells and scarce smooth muscle cells was observed. Macrophages were most frequent in the intima (10.8%) while T and B cells were found in 2.3 and 1.5%. In the UP a thin cap covering a lipid-rich core with widespread vascularization and with severe luminal obstruction was observed. Macrophages were increased (21%), and T (1.5%) and B cells (3.5%) in the caps and inner areas of the lipid cores. At these sites, the FISH showed trisomy and tetrasomy of chromosome 7 and apoptosis was very frequent (10-30%). Macrophages in intimal lesions is one of the most prominent, consistent and permanent features in EP, and an elevated apoptotic index and chromosome 7 instability might contribute to evolution from stable to complicated plaques, while CP seems to play no role. However, further studies are needed with more cases to confirm this last observation. Copyright (C) 2000 Elsevier Science Ireland Ltd. Fil: Matturri, Luigi. Università degli Studi di Milano; Italia. IRCCS Ospedale Maggiore; Italia Fil: Cazzullo, Alessandra. Università degli Studi di Milano; Italia. IRCCS Ospedale Maggiore; Italia Fil: Turconi, Paola. IRCCS Ospedale Maggiore; Italia. Università degli Studi di Milano; Italia Fil: Roncoroni, Lucia. IRCCS Ospedale Maggiore; Italia. Università degli Studi di Milano; Italia Fil: Grana, Daniel Rodolfo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Cardiológicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Cardiológicas; Argentina. Universidad del Salvador. Facultad de Medicina; Argentina Fil: Milei, Jose. Universidad del Salvador. Facultad de Medicina; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Cardiológicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Cardiológicas; Argentina |
description |
Chlamydia pneumoniae (CP), chromosomal alterations and apoptosis were suggested as contributing factors in the pathogenesis of atherosclerosis. Early (EP) and unstable plaques (UP) were studied in order to assess infiltrate composition, the apoptotic index, chromosome 7 stability and to investigate the concurrent presence of CP in EP and UP. Paraffin embedded sections of three iliac arteries and four aortas from young donors (EP), and four coronaries and nine carotid arteries (UP) were used. Aside from histological techniques, immunophenotypification for macrophages, T and B cells, smooth muscle and endothelial cells; FISH and DNA nick end labeling were performed. The amplifications with PCR for CP infection were negative in all specimens. In the EP, a focal myointimal thickening with foam cells and scarce smooth muscle cells was observed. Macrophages were most frequent in the intima (10.8%) while T and B cells were found in 2.3 and 1.5%. In the UP a thin cap covering a lipid-rich core with widespread vascularization and with severe luminal obstruction was observed. Macrophages were increased (21%), and T (1.5%) and B cells (3.5%) in the caps and inner areas of the lipid cores. At these sites, the FISH showed trisomy and tetrasomy of chromosome 7 and apoptosis was very frequent (10-30%). Macrophages in intimal lesions is one of the most prominent, consistent and permanent features in EP, and an elevated apoptotic index and chromosome 7 instability might contribute to evolution from stable to complicated plaques, while CP seems to play no role. However, further studies are needed with more cases to confirm this last observation. Copyright (C) 2000 Elsevier Science Ireland Ltd. |
publishDate |
2000 |
dc.date.none.fl_str_mv |
2000-08 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/39105 Matturri, Luigi; Cazzullo, Alessandra; Turconi, Paola; Roncoroni, Lucia; Grana, Daniel Rodolfo; et al.; Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis; Elsevier Ireland; International Journal of Cardiology; 75; 1; 8-2000; 23-33 0167-5273 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/39105 |
identifier_str_mv |
Matturri, Luigi; Cazzullo, Alessandra; Turconi, Paola; Roncoroni, Lucia; Grana, Daniel Rodolfo; et al.; Inflammatory cells, apoptosis and Chlamydia pneumoniae infection in atherosclerosis; Elsevier Ireland; International Journal of Cardiology; 75; 1; 8-2000; 23-33 0167-5273 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0167527300003065 info:eu-repo/semantics/altIdentifier/doi/10.1016/S0167-5273(00)00306-5 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/vnd.openxmlformats-officedocument.wordprocessingml.document application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier Ireland |
publisher.none.fl_str_mv |
Elsevier Ireland |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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13.070432 |