Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage.
- Autores
- Anderson, H. Clarke; Hodges, Peter T.; Aguillera, Ximena; Missana, Liliana Raquel; Moylan, Paul E.
- Año de publicación
- 2000
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- We assessed the distribution and relative staining intensity of bone morphogenetic protein (BMP)-1–7 by immunohistochemistry in tibial growth plates, epiphyses, metaphyses, and articular cartilage in one 21-week and one 22-week human fetus and in five 10-week-old Sprague–Dawley rats. In the rats, articular cartilage was also examined. BMP proteins were mostly cytoplasmic, with negligible matrix staining. Highest BMP levels were seen in (a) hypertrophic and calcifying zone chondrocytes of growth plate (BMP-1–7), (b) osteoblasts and/or osteoprogenitor fibroblasts and vascular cells of the metaphyseal cortex and medulla (BMP-1–6), (c) osteoclasts of the metaphysis and epiphysis (BMP-1,-4,-5, and −6), and (d) mid to deep zone articular chondrocytes of weanling rats (BMP-1–7). BMP staining in osteoclasts, an unexpected finding, was consistently strong with BMP-4, −5, and −6 but was variable and dependent on osteoclast location with BMP-2,-3, and −7. BMP-1–7 were moderately to intensely stained in vascular canals of human fetal epiphyseal cartilage by endothelial cells and pericytes. BMP-1,-3,-5,-6, and −7 were localized in hypertrophic chondrocytes adjacent to cartilage canals. We conclude that BMP expression is associated with maturing chondrocytes of growth plate and articular cartilage, and may play a role in chondrocyte differentiation and/or apoptosis. BMP appears to be expressed by osteoclasts and might be involved in the intercellular “cross-talk” between osteoclasts and neighboring osteoprogenitor cells at sites of bone remodeling.
Fil: Anderson, H. Clarke. University of Kansas; Estados Unidos
Fil: Hodges, Peter T.. University of Kansas; Estados Unidos
Fil: Aguillera, Ximena. University of Kansas; Estados Unidos
Fil: Missana, Liliana Raquel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Planta Piloto de Procesos Industriales Microbiológicos; Argentina
Fil: Moylan, Paul E.. University of Kansas; Estados Unidos - Materia
-
Bone Morphogenetic Protein (Bmp)
Growth Plate,Metaphysis And Epiphysis
Human And Rat
Articular Cartilage. - 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:11336/78670
Ver los metadatos del registro completo
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Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage.Anderson, H. ClarkeHodges, Peter T.Aguillera, XimenaMissana, Liliana RaquelMoylan, Paul E.Bone Morphogenetic Protein (Bmp)Growth Plate,Metaphysis And EpiphysisHuman And RatArticular Cartilage.https://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3We assessed the distribution and relative staining intensity of bone morphogenetic protein (BMP)-1–7 by immunohistochemistry in tibial growth plates, epiphyses, metaphyses, and articular cartilage in one 21-week and one 22-week human fetus and in five 10-week-old Sprague–Dawley rats. In the rats, articular cartilage was also examined. BMP proteins were mostly cytoplasmic, with negligible matrix staining. Highest BMP levels were seen in (a) hypertrophic and calcifying zone chondrocytes of growth plate (BMP-1–7), (b) osteoblasts and/or osteoprogenitor fibroblasts and vascular cells of the metaphyseal cortex and medulla (BMP-1–6), (c) osteoclasts of the metaphysis and epiphysis (BMP-1,-4,-5, and −6), and (d) mid to deep zone articular chondrocytes of weanling rats (BMP-1–7). BMP staining in osteoclasts, an unexpected finding, was consistently strong with BMP-4, −5, and −6 but was variable and dependent on osteoclast location with BMP-2,-3, and −7. BMP-1–7 were moderately to intensely stained in vascular canals of human fetal epiphyseal cartilage by endothelial cells and pericytes. BMP-1,-3,-5,-6, and −7 were localized in hypertrophic chondrocytes adjacent to cartilage canals. We conclude that BMP expression is associated with maturing chondrocytes of growth plate and articular cartilage, and may play a role in chondrocyte differentiation and/or apoptosis. BMP appears to be expressed by osteoclasts and might be involved in the intercellular “cross-talk” between osteoclasts and neighboring osteoprogenitor cells at sites of bone remodeling.Fil: Anderson, H. Clarke. University of Kansas; Estados UnidosFil: Hodges, Peter T.. University of Kansas; Estados UnidosFil: Aguillera, Ximena. University of Kansas; Estados UnidosFil: Missana, Liliana Raquel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Planta Piloto de Procesos Industriales Microbiológicos; ArgentinaFil: Moylan, Paul E.. University of Kansas; Estados UnidosHistochemical Society2000-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/78670Anderson, H. Clarke; Hodges, Peter T.; Aguillera, Ximena; Missana, Liliana Raquel; Moylan, Paul E.; Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage.; Histochemical Society; The Journal of Histochemistry and Cytochemistry: Official Journal of the Histochemistry Society; 48; 11; 12-2000; 1493-15020022-1554CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://journals.sagepub.com/doi/pdf/10.1177/002215540004801106info:eu-repo/semantics/altIdentifier/doi/10.1177%2F002215540004801106info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:43:45Zoai:ri.conicet.gov.ar:11336/78670instacron: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:34982025-09-03 09:43:45.698CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage. |
title |
Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage. |
spellingShingle |
Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage. Anderson, H. Clarke Bone Morphogenetic Protein (Bmp) Growth Plate,Metaphysis And Epiphysis Human And Rat Articular Cartilage. |
title_short |
Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage. |
title_full |
Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage. |
title_fullStr |
Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage. |
title_full_unstemmed |
Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage. |
title_sort |
Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage. |
dc.creator.none.fl_str_mv |
Anderson, H. Clarke Hodges, Peter T. Aguillera, Ximena Missana, Liliana Raquel Moylan, Paul E. |
author |
Anderson, H. Clarke |
author_facet |
Anderson, H. Clarke Hodges, Peter T. Aguillera, Ximena Missana, Liliana Raquel Moylan, Paul E. |
author_role |
author |
author2 |
Hodges, Peter T. Aguillera, Ximena Missana, Liliana Raquel Moylan, Paul E. |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Bone Morphogenetic Protein (Bmp) Growth Plate,Metaphysis And Epiphysis Human And Rat Articular Cartilage. |
topic |
Bone Morphogenetic Protein (Bmp) Growth Plate,Metaphysis And Epiphysis Human And Rat Articular Cartilage. |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
We assessed the distribution and relative staining intensity of bone morphogenetic protein (BMP)-1–7 by immunohistochemistry in tibial growth plates, epiphyses, metaphyses, and articular cartilage in one 21-week and one 22-week human fetus and in five 10-week-old Sprague–Dawley rats. In the rats, articular cartilage was also examined. BMP proteins were mostly cytoplasmic, with negligible matrix staining. Highest BMP levels were seen in (a) hypertrophic and calcifying zone chondrocytes of growth plate (BMP-1–7), (b) osteoblasts and/or osteoprogenitor fibroblasts and vascular cells of the metaphyseal cortex and medulla (BMP-1–6), (c) osteoclasts of the metaphysis and epiphysis (BMP-1,-4,-5, and −6), and (d) mid to deep zone articular chondrocytes of weanling rats (BMP-1–7). BMP staining in osteoclasts, an unexpected finding, was consistently strong with BMP-4, −5, and −6 but was variable and dependent on osteoclast location with BMP-2,-3, and −7. BMP-1–7 were moderately to intensely stained in vascular canals of human fetal epiphyseal cartilage by endothelial cells and pericytes. BMP-1,-3,-5,-6, and −7 were localized in hypertrophic chondrocytes adjacent to cartilage canals. We conclude that BMP expression is associated with maturing chondrocytes of growth plate and articular cartilage, and may play a role in chondrocyte differentiation and/or apoptosis. BMP appears to be expressed by osteoclasts and might be involved in the intercellular “cross-talk” between osteoclasts and neighboring osteoprogenitor cells at sites of bone remodeling. Fil: Anderson, H. Clarke. University of Kansas; Estados Unidos Fil: Hodges, Peter T.. University of Kansas; Estados Unidos Fil: Aguillera, Ximena. University of Kansas; Estados Unidos Fil: Missana, Liliana Raquel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Planta Piloto de Procesos Industriales Microbiológicos; Argentina Fil: Moylan, Paul E.. University of Kansas; Estados Unidos |
description |
We assessed the distribution and relative staining intensity of bone morphogenetic protein (BMP)-1–7 by immunohistochemistry in tibial growth plates, epiphyses, metaphyses, and articular cartilage in one 21-week and one 22-week human fetus and in five 10-week-old Sprague–Dawley rats. In the rats, articular cartilage was also examined. BMP proteins were mostly cytoplasmic, with negligible matrix staining. Highest BMP levels were seen in (a) hypertrophic and calcifying zone chondrocytes of growth plate (BMP-1–7), (b) osteoblasts and/or osteoprogenitor fibroblasts and vascular cells of the metaphyseal cortex and medulla (BMP-1–6), (c) osteoclasts of the metaphysis and epiphysis (BMP-1,-4,-5, and −6), and (d) mid to deep zone articular chondrocytes of weanling rats (BMP-1–7). BMP staining in osteoclasts, an unexpected finding, was consistently strong with BMP-4, −5, and −6 but was variable and dependent on osteoclast location with BMP-2,-3, and −7. BMP-1–7 were moderately to intensely stained in vascular canals of human fetal epiphyseal cartilage by endothelial cells and pericytes. BMP-1,-3,-5,-6, and −7 were localized in hypertrophic chondrocytes adjacent to cartilage canals. We conclude that BMP expression is associated with maturing chondrocytes of growth plate and articular cartilage, and may play a role in chondrocyte differentiation and/or apoptosis. BMP appears to be expressed by osteoclasts and might be involved in the intercellular “cross-talk” between osteoclasts and neighboring osteoprogenitor cells at sites of bone remodeling. |
publishDate |
2000 |
dc.date.none.fl_str_mv |
2000-12 |
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/11336/78670 Anderson, H. Clarke; Hodges, Peter T.; Aguillera, Ximena; Missana, Liliana Raquel; Moylan, Paul E.; Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage.; Histochemical Society; The Journal of Histochemistry and Cytochemistry: Official Journal of the Histochemistry Society; 48; 11; 12-2000; 1493-1502 0022-1554 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/78670 |
identifier_str_mv |
Anderson, H. Clarke; Hodges, Peter T.; Aguillera, Ximena; Missana, Liliana Raquel; Moylan, Paul E.; Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis and articular cartilage.; Histochemical Society; The Journal of Histochemistry and Cytochemistry: Official Journal of the Histochemistry Society; 48; 11; 12-2000; 1493-1502 0022-1554 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://journals.sagepub.com/doi/pdf/10.1177/002215540004801106 info:eu-repo/semantics/altIdentifier/doi/10.1177%2F002215540004801106 |
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/pdf |
dc.publisher.none.fl_str_mv |
Histochemical Society |
publisher.none.fl_str_mv |
Histochemical Society |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842268620035457024 |
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12.885934 |