Osteoclast differentiation at growth plate cartilage–trabecular bone junction in newborn rat femur
Using 3-day-old newborn rats, we examined the differentiation processes of osteoclasts associated with the destruction of the femoral growth plate cartilage and primary trabecular bone. In the growth plate cartilage, thin mineralized areas were detected solely in the longitudinal septal cartilage ma...
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description | Using 3-day-old newborn rats, we examined the differentiation processes of osteoclasts associated with the destruction of the femoral growth plate cartilage and primary trabecular bone. In the growth plate cartilage, thin mineralized areas were detected solely in the longitudinal septal cartilage matrix in the hypertrophic zone, but the transverse septal cartilage matrix between adjacent chondrocytic lacunae within a row of chondrocytes remained unmineralized. The longitudinal septal cartilage between adjacent rows of chondrocytes appeared to persist, forming the walls of opened lacunar canals. Consistent with the removal of the transverse septal cartilage matrix, the longitudinal canals of opened chondrocytic lacunae were deeply invaded by capillary vessels, mononuclear cells and multinucleated pre-osteoclasts lacking a ruffled border. CD34-positive endothelial cells of capillary vessels deeply penetrated into the transverse septal cartilage matrix facing the medullary cavity and the opened chondrocytic lacunae. ED1-positive monocytes/macrophages were distributed at the chondro–osseous junction, but they were distant from the erosive front of the transverse septa. Tartrate-resistant acid phosphatase-positive multinucleated pre-osteoclasts lacking a ruffled border and differentiated osteoclasts with a ruffled border were localized mainly at two locations: the chondro–osseous junction and the growth front of primary bone trabeculae. Osteoclasts were located on the type-I collagen-positive bone trabeculae close to the growth plate, but they appeared to be distant from the type-II collagen-positive cartilage matrix. Even within opened chondrocytic lacunae, when osteoclasts were distant from the cartilage and bone matrix, they lacked polarized cytoplasmic organization and a ruffled border. The osteoclasts located in the remaining septal cartilage also exhibited neither a ruffled border nor a clear zone. Osteoclasts with a prominent ruffled border and clear zone were located in bone matrix covering the remaining septal cartilage. These results suggest that osteoclasts require hydroxyapatite crystals and bone matrix constituents for ruffled border formation and are not involved in resorption of the unmineralized transverse and mineralized longitudinal septal cartilage without covering bone matrix at the chondro–osseous junction. |
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In the growth plate cartilage, thin mineralized areas were detected solely in the longitudinal septal cartilage matrix in the hypertrophic zone, but the transverse septal cartilage matrix between adjacent chondrocytic lacunae within a row of chondrocytes remained unmineralized. The longitudinal septal cartilage between adjacent rows of chondrocytes appeared to persist, forming the walls of opened lacunar canals. Consistent with the removal of the transverse septal cartilage matrix, the longitudinal canals of opened chondrocytic lacunae were deeply invaded by capillary vessels, mononuclear cells and multinucleated pre-osteoclasts lacking a ruffled border. CD34-positive endothelial cells of capillary vessels deeply penetrated into the transverse septal cartilage matrix facing the medullary cavity and the opened chondrocytic lacunae. ED1-positive monocytes/macrophages were distributed at the chondro–osseous junction, but they were distant from the erosive front of the transverse septa. Tartrate-resistant acid phosphatase-positive multinucleated pre-osteoclasts lacking a ruffled border and differentiated osteoclasts with a ruffled border were localized mainly at two locations: the chondro–osseous junction and the growth front of primary bone trabeculae. Osteoclasts were located on the type-I collagen-positive bone trabeculae close to the growth plate, but they appeared to be distant from the type-II collagen-positive cartilage matrix. Even within opened chondrocytic lacunae, when osteoclasts were distant from the cartilage and bone matrix, they lacked polarized cytoplasmic organization and a ruffled border. The osteoclasts located in the remaining septal cartilage also exhibited neither a ruffled border nor a clear zone. Osteoclasts with a prominent ruffled border and clear zone were located in bone matrix covering the remaining septal cartilage. These results suggest that osteoclasts require hydroxyapatite crystals and bone matrix constituents for ruffled border formation and are not involved in resorption of the unmineralized transverse and mineralized longitudinal septal cartilage without covering bone matrix at the chondro–osseous junction.</description><identifier>ISSN: 0022-0744</identifier><identifier>EISSN: 1477-9986</identifier><identifier>EISSN: 2050-5701</identifier><identifier>DOI: 10.1093/jmicro/52.6.493</identifier><identifier>PMID: 14756237</identifier><language>eng</language><publisher>Japan: Oxford University Press</publisher><subject>Animals ; Animals, Newborn ; Antigens, CD34 - metabolism ; Bone and Bones - cytology ; Bone and Bones - physiology ; Bone Development ; CD34 ; Cell Differentiation ; Collagen Type I - metabolism ; ED1 ; Endothelium, Vascular ; Femur - cytology ; Femur - growth & development ; Growth Plate - cytology ; Immunohistochemistry ; Microscopy, Electron ; osteoclast ; Osteoclasts - cytology ; Rats ; Rats, Sprague-Dawley ; TRAP ; type-I collagen ; type-II collagen</subject><ispartof>Journal of electron microscopy, 2003-12, Vol.52 (6), p.493-502</ispartof><rights>Copyright Oxford University Press(England) Dec 2003</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-1c09eb5247db5d2f63fa412ba8c3f7f7756cddaebe45c3aad548cfc9f2904e93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14756237$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sawae, Yoshiko</creatorcontrib><creatorcontrib>Sahara, Takako</creatorcontrib><creatorcontrib>Sasaki, Takahisa</creatorcontrib><title>Osteoclast differentiation at growth plate cartilage–trabecular bone junction in newborn rat femur</title><title>Journal of electron microscopy</title><addtitle>J Electron Microsc (Tokyo)</addtitle><description>Using 3-day-old newborn rats, we examined the differentiation processes of osteoclasts associated with the destruction of the femoral growth plate cartilage and primary trabecular bone. In the growth plate cartilage, thin mineralized areas were detected solely in the longitudinal septal cartilage matrix in the hypertrophic zone, but the transverse septal cartilage matrix between adjacent chondrocytic lacunae within a row of chondrocytes remained unmineralized. The longitudinal septal cartilage between adjacent rows of chondrocytes appeared to persist, forming the walls of opened lacunar canals. Consistent with the removal of the transverse septal cartilage matrix, the longitudinal canals of opened chondrocytic lacunae were deeply invaded by capillary vessels, mononuclear cells and multinucleated pre-osteoclasts lacking a ruffled border. CD34-positive endothelial cells of capillary vessels deeply penetrated into the transverse septal cartilage matrix facing the medullary cavity and the opened chondrocytic lacunae. ED1-positive monocytes/macrophages were distributed at the chondro–osseous junction, but they were distant from the erosive front of the transverse septa. Tartrate-resistant acid phosphatase-positive multinucleated pre-osteoclasts lacking a ruffled border and differentiated osteoclasts with a ruffled border were localized mainly at two locations: the chondro–osseous junction and the growth front of primary bone trabeculae. Osteoclasts were located on the type-I collagen-positive bone trabeculae close to the growth plate, but they appeared to be distant from the type-II collagen-positive cartilage matrix. Even within opened chondrocytic lacunae, when osteoclasts were distant from the cartilage and bone matrix, they lacked polarized cytoplasmic organization and a ruffled border. The osteoclasts located in the remaining septal cartilage also exhibited neither a ruffled border nor a clear zone. Osteoclasts with a prominent ruffled border and clear zone were located in bone matrix covering the remaining septal cartilage. These results suggest that osteoclasts require hydroxyapatite crystals and bone matrix constituents for ruffled border formation and are not involved in resorption of the unmineralized transverse and mineralized longitudinal septal cartilage without covering bone matrix at the chondro–osseous junction.</description><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Antigens, CD34 - metabolism</subject><subject>Bone and Bones - cytology</subject><subject>Bone and Bones - physiology</subject><subject>Bone Development</subject><subject>CD34</subject><subject>Cell Differentiation</subject><subject>Collagen Type I - metabolism</subject><subject>ED1</subject><subject>Endothelium, Vascular</subject><subject>Femur - cytology</subject><subject>Femur - growth & development</subject><subject>Growth Plate - cytology</subject><subject>Immunohistochemistry</subject><subject>Microscopy, Electron</subject><subject>osteoclast</subject><subject>Osteoclasts - cytology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>TRAP</subject><subject>type-I collagen</subject><subject>type-II collagen</subject><issn>0022-0744</issn><issn>1477-9986</issn><issn>2050-5701</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc-KFDEQh4Mo7uzo2ZsED-6pZ_K3M32UYdcVVhZhQfES0unKmrE7GZM0qzffwTf0SYzOoOBBT3Wor35U1YfQE0pWlHR8vZu8TXEt2apdiY7fQwsqlGq6btPeRwtCGGuIEuIEnea8I4QqQclDdFIh2TKuFmi4zgWiHU0uePDOQYJQvCk-BmwKvk3xrnzA-9EUwNak4kdzC9-_fivJ9GDn0STcxwB4Nwf7a8gHHOCujyngVAMcTHN6hB44M2Z4fKxLdHNxfrO9bK6uX77avrhqrBCyNNSSDnrJhBp6OTDXcmcEZb3ZWO6UU3VnOwwGehDScmMGKTbW2c6xjgjo-BKdHWL3KX6aIRc9-WxhHE2AOGetBK93E7qp5PN_k1SyjgryX5ARySSpr1yiZ3-BuzinUK_VjKq6OpOyQusDVJ3lnMDpffKTSV80JfqnT33wqSXTra4-68TTY-zcTzD84Y8CK9AcAF89fv7dN-mjbhVXUl--e6_fkPatENsL_Zr_AIWFrtg</recordid><startdate>20031201</startdate><enddate>20031201</enddate><creator>Sawae, Yoshiko</creator><creator>Sahara, Takako</creator><creator>Sasaki, Takahisa</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7QP</scope><scope>7X8</scope></search><sort><creationdate>20031201</creationdate><title>Osteoclast differentiation at growth plate cartilage–trabecular bone junction in newborn rat femur</title><author>Sawae, Yoshiko ; Sahara, Takako ; Sasaki, Takahisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-1c09eb5247db5d2f63fa412ba8c3f7f7756cddaebe45c3aad548cfc9f2904e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Antigens, CD34 - metabolism</topic><topic>Bone and Bones - cytology</topic><topic>Bone and Bones - physiology</topic><topic>Bone Development</topic><topic>CD34</topic><topic>Cell Differentiation</topic><topic>Collagen Type I - metabolism</topic><topic>ED1</topic><topic>Endothelium, Vascular</topic><topic>Femur - cytology</topic><topic>Femur - growth & development</topic><topic>Growth Plate - cytology</topic><topic>Immunohistochemistry</topic><topic>Microscopy, Electron</topic><topic>osteoclast</topic><topic>Osteoclasts - cytology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>TRAP</topic><topic>type-I collagen</topic><topic>type-II collagen</topic><toplevel>online_resources</toplevel><creatorcontrib>Sawae, Yoshiko</creatorcontrib><creatorcontrib>Sahara, Takako</creatorcontrib><creatorcontrib>Sasaki, Takahisa</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>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of electron microscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sawae, Yoshiko</au><au>Sahara, Takako</au><au>Sasaki, Takahisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osteoclast differentiation at growth plate cartilage–trabecular bone junction in newborn rat femur</atitle><jtitle>Journal of electron microscopy</jtitle><addtitle>J Electron Microsc (Tokyo)</addtitle><date>2003-12-01</date><risdate>2003</risdate><volume>52</volume><issue>6</issue><spage>493</spage><epage>502</epage><pages>493-502</pages><issn>0022-0744</issn><eissn>1477-9986</eissn><eissn>2050-5701</eissn><abstract>Using 3-day-old newborn rats, we examined the differentiation processes of osteoclasts associated with the destruction of the femoral growth plate cartilage and primary trabecular bone. In the growth plate cartilage, thin mineralized areas were detected solely in the longitudinal septal cartilage matrix in the hypertrophic zone, but the transverse septal cartilage matrix between adjacent chondrocytic lacunae within a row of chondrocytes remained unmineralized. The longitudinal septal cartilage between adjacent rows of chondrocytes appeared to persist, forming the walls of opened lacunar canals. Consistent with the removal of the transverse septal cartilage matrix, the longitudinal canals of opened chondrocytic lacunae were deeply invaded by capillary vessels, mononuclear cells and multinucleated pre-osteoclasts lacking a ruffled border. CD34-positive endothelial cells of capillary vessels deeply penetrated into the transverse septal cartilage matrix facing the medullary cavity and the opened chondrocytic lacunae. ED1-positive monocytes/macrophages were distributed at the chondro–osseous junction, but they were distant from the erosive front of the transverse septa. Tartrate-resistant acid phosphatase-positive multinucleated pre-osteoclasts lacking a ruffled border and differentiated osteoclasts with a ruffled border were localized mainly at two locations: the chondro–osseous junction and the growth front of primary bone trabeculae. Osteoclasts were located on the type-I collagen-positive bone trabeculae close to the growth plate, but they appeared to be distant from the type-II collagen-positive cartilage matrix. Even within opened chondrocytic lacunae, when osteoclasts were distant from the cartilage and bone matrix, they lacked polarized cytoplasmic organization and a ruffled border. The osteoclasts located in the remaining septal cartilage also exhibited neither a ruffled border nor a clear zone. Osteoclasts with a prominent ruffled border and clear zone were located in bone matrix covering the remaining septal cartilage. These results suggest that osteoclasts require hydroxyapatite crystals and bone matrix constituents for ruffled border formation and are not involved in resorption of the unmineralized transverse and mineralized longitudinal septal cartilage without covering bone matrix at the chondro–osseous junction.</abstract><cop>Japan</cop><pub>Oxford University Press</pub><pmid>14756237</pmid><doi>10.1093/jmicro/52.6.493</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Animals, Newborn Antigens, CD34 - metabolism Bone and Bones - cytology Bone and Bones - physiology Bone Development CD34 Cell Differentiation Collagen Type I - metabolism ED1 Endothelium, Vascular Femur - cytology Femur - growth & development Growth Plate - cytology Immunohistochemistry Microscopy, Electron osteoclast Osteoclasts - cytology Rats Rats, Sprague-Dawley TRAP type-I collagen type-II collagen |
title | Osteoclast differentiation at growth plate cartilage–trabecular bone junction in newborn rat femur |
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