Retinoic acid treatment induces type X collagen gene expression in cultured chick chondrocytes

The vitamin A derivative retinoic acid (RA) is widely thought to be involved in cartilage development, but its precise roles and mechanisms of action in this complex process remain unclear. We have tested the hypothesis that RA is involved in chondrocyte maturation during endochondral ossification a...

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Veröffentlicht in:Experimental cell research 1991-07, Vol.195 (1), p.38-46
Hauptverfasser: Pacifici, Maurizio, Golden, Eleanor B., Iwamoto, Masahiro, Adams, Sherrill L.
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creator Pacifici, Maurizio
Golden, Eleanor B.
Iwamoto, Masahiro
Adams, Sherrill L.
description The vitamin A derivative retinoic acid (RA) is widely thought to be involved in cartilage development, but its precise roles and mechanisms of action in this complex process remain unclear. We have tested the hypothesis that RA is involved in chondrocyte maturation during endochondral ossification and, in particular, is an inducer of maturation-associated traits such as type X collagen and alkaline phosphatase. Immature chondrocytes isolated from the caudal region of Day 19 chick embryo sterna were seeded in secondary monolayer cultures and treated either with a high dose (100 n M) or with physiological doses (10–35 n M) of RA for up to 3 days. We found that after an initial lag of about 24 h, physiological doses of RA indeed induced type X collagen gene expression in the immature cells. This induction was not accompanied by obvious changes in expression of the type II collagen and large aggregating proteoglycan core protein genes. As revealed by immunocytochemistry, 30–35% of the cells in cultures treated with RA for 3 days were engaged in type X collagen production. Interestingly, these cells were relatively similar in size to chondrocytes in which no type X collagen was detected, suggesting that chondrocytes can initiate type X collagen production independent of cell hypertrophy. RA treatment also led to increased alkaline phosphatase activity occurring as early as 24 h after the start of treatment. The data in this study indicate that RA may have a role in endochondral ossification as an inducer/promoter of maturation-associated traits during chondrocyte maturation.
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We have tested the hypothesis that RA is involved in chondrocyte maturation during endochondral ossification and, in particular, is an inducer of maturation-associated traits such as type X collagen and alkaline phosphatase. Immature chondrocytes isolated from the caudal region of Day 19 chick embryo sterna were seeded in secondary monolayer cultures and treated either with a high dose (100 n M) or with physiological doses (10–35 n M) of RA for up to 3 days. We found that after an initial lag of about 24 h, physiological doses of RA indeed induced type X collagen gene expression in the immature cells. This induction was not accompanied by obvious changes in expression of the type II collagen and large aggregating proteoglycan core protein genes. As revealed by immunocytochemistry, 30–35% of the cells in cultures treated with RA for 3 days were engaged in type X collagen production. Interestingly, these cells were relatively similar in size to chondrocytes in which no type X collagen was detected, suggesting that chondrocytes can initiate type X collagen production independent of cell hypertrophy. RA treatment also led to increased alkaline phosphatase activity occurring as early as 24 h after the start of treatment. 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We have tested the hypothesis that RA is involved in chondrocyte maturation during endochondral ossification and, in particular, is an inducer of maturation-associated traits such as type X collagen and alkaline phosphatase. Immature chondrocytes isolated from the caudal region of Day 19 chick embryo sterna were seeded in secondary monolayer cultures and treated either with a high dose (100 n M) or with physiological doses (10–35 n M) of RA for up to 3 days. We found that after an initial lag of about 24 h, physiological doses of RA indeed induced type X collagen gene expression in the immature cells. This induction was not accompanied by obvious changes in expression of the type II collagen and large aggregating proteoglycan core protein genes. As revealed by immunocytochemistry, 30–35% of the cells in cultures treated with RA for 3 days were engaged in type X collagen production. Interestingly, these cells were relatively similar in size to chondrocytes in which no type X collagen was detected, suggesting that chondrocytes can initiate type X collagen production independent of cell hypertrophy. RA treatment also led to increased alkaline phosphatase activity occurring as early as 24 h after the start of treatment. The data in this study indicate that RA may have a role in endochondral ossification as an inducer/promoter of maturation-associated traits during chondrocyte maturation.</description><subject>Alkaline Phosphatase - metabolism</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Cartilage - cytology</subject><subject>Cartilage - physiology</subject><subject>Cell Differentiation - drug effects</subject><subject>Cells, Cultured</subject><subject>Chickens</subject><subject>Collagen - genetics</subject><subject>Collagen - immunology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Fluorescent Antibody Technique</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression - drug effects</subject><subject>Other biological molecules</subject><subject>Proteoglycans - genetics</subject><subject>RNA, Messenger - genetics</subject><subject>Tretinoin - pharmacology</subject><issn>0014-4827</issn><issn>1090-2422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE2LFDEQhoO4rLOr_0AhB1nWQ2sqSXfSF2FZ_BhYEETBkyFdXa3Rns6YpMX59_Y4wxzXQ6UO9byV4mHsKYiXIKB5JQToSltprlt40Qrdmmr9gK1AtKKSWsqHbHVCHrGLnH8IIayF5pydS1HX0ugV-_qRSphiQO4x9Lwk8mVDU-Fh6mekzMtuS_wLxziO_htNfCni9GebKOcQp4XjOI9lTtRz_B7w5_LGqU8Rd4XyY3Y2-DHTk2O_ZJ_fvvl0-766-_BufXtzV6EGU6rBk607oZREZU0jwdekhUEwtq5773ULBjo1NN5i14EZht60SwKbDiV0g7pkV4e92xR_zZSL24SMtNw8UZyzs6JRYFT9XxAa0EoZuYD6AGKKOSca3DaFjU87B8Lt_bu9XLeX61pw__y79RJ7dtw_dxvqT6Gj8GX-_Dj3Gf04JD9hyCdM19q2av_76wNGi7TfgZLLGGhC6kMiLK6P4f47_gI9SaI2</recordid><startdate>19910701</startdate><enddate>19910701</enddate><creator>Pacifici, Maurizio</creator><creator>Golden, Eleanor B.</creator><creator>Iwamoto, Masahiro</creator><creator>Adams, Sherrill L.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</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>7QP</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>19910701</creationdate><title>Retinoic acid treatment induces type X collagen gene expression in cultured chick chondrocytes</title><author>Pacifici, Maurizio ; Golden, Eleanor B. ; Iwamoto, Masahiro ; Adams, Sherrill L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-fae85b0332c387621a5e407c17855daa49171b3f6a8cbb17ffd7985bc6bc21bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Alkaline Phosphatase - metabolism</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Cartilage - cytology</topic><topic>Cartilage - physiology</topic><topic>Cell Differentiation - drug effects</topic><topic>Cells, Cultured</topic><topic>Chickens</topic><topic>Collagen - genetics</topic><topic>Collagen - immunology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Fluorescent Antibody Technique</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression - drug effects</topic><topic>Other biological molecules</topic><topic>Proteoglycans - genetics</topic><topic>RNA, Messenger - genetics</topic><topic>Tretinoin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pacifici, Maurizio</creatorcontrib><creatorcontrib>Golden, Eleanor B.</creatorcontrib><creatorcontrib>Iwamoto, Masahiro</creatorcontrib><creatorcontrib>Adams, Sherrill L.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental cell research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pacifici, Maurizio</au><au>Golden, Eleanor B.</au><au>Iwamoto, Masahiro</au><au>Adams, Sherrill L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retinoic acid treatment induces type X collagen gene expression in cultured chick chondrocytes</atitle><jtitle>Experimental cell research</jtitle><addtitle>Exp Cell Res</addtitle><date>1991-07-01</date><risdate>1991</risdate><volume>195</volume><issue>1</issue><spage>38</spage><epage>46</epage><pages>38-46</pages><issn>0014-4827</issn><eissn>1090-2422</eissn><coden>ECREAL</coden><abstract>The vitamin A derivative retinoic acid (RA) is widely thought to be involved in cartilage development, but its precise roles and mechanisms of action in this complex process remain unclear. 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Interestingly, these cells were relatively similar in size to chondrocytes in which no type X collagen was detected, suggesting that chondrocytes can initiate type X collagen production independent of cell hypertrophy. RA treatment also led to increased alkaline phosphatase activity occurring as early as 24 h after the start of treatment. The data in this study indicate that RA may have a role in endochondral ossification as an inducer/promoter of maturation-associated traits during chondrocyte maturation.</abstract><cop>Orlando, FL</cop><pub>Elsevier Inc</pub><pmid>2055274</pmid><doi>10.1016/0014-4827(91)90497-I</doi><tpages>9</tpages></addata></record>
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subjects Alkaline Phosphatase - metabolism
Analytical, structural and metabolic biochemistry
Animals
Biological and medical sciences
Blotting, Northern
Cartilage - cytology
Cartilage - physiology
Cell Differentiation - drug effects
Cells, Cultured
Chickens
Collagen - genetics
Collagen - immunology
Dose-Response Relationship, Drug
Fluorescent Antibody Technique
Fundamental and applied biological sciences. Psychology
Gene Expression - drug effects
Other biological molecules
Proteoglycans - genetics
RNA, Messenger - genetics
Tretinoin - pharmacology
title Retinoic acid treatment induces type X collagen gene expression in cultured chick chondrocytes
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