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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/78670

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network_name_str CONICET Digital (CONICET)
spelling 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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