Comparative effect of cadmium on osteoblastic cells and osteoclastic cells
Cadmium(Cd) has been thought to disturb the bone metabolism directly. The mechanism for the bone lesion is unknown, however. To examine the effects of cadmium on bone metabolism, we compared its effects on osteoblasts and osteoclasts in vitro. We used an established cell line, MC3T3-E1, as osteoblas...
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Veröffentlicht in: | Archives of toxicology 1993, Vol.67 (5), p.352-357 |
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description | Cadmium(Cd) has been thought to disturb the bone metabolism directly. The mechanism for the bone lesion is unknown, however. To examine the effects of cadmium on bone metabolism, we compared its effects on osteoblasts and osteoclasts in vitro. We used an established cell line, MC3T3-E1, as osteoblasts and tartrate resistant acid phosphatase (TRACP)-positive multi-nucleated cells (MNC) formed by a bone marrow culture system as osteoclasts. Alkaline phosphatase (ALP) activity was decreased by 10(-7) M Cd and DNA content and hydroxyproline content of osteoblastic cells were decreased by 10(-5) M Cd. Cadmium at 10(-7) M inhibited the osteoclastic cell formation from mouse bone marrow in the presence of 10(-8) M 1 alpha, 25(OH)2 vitamin D3. A 100-fold higher concentration of zinc(Zn) simultaneously added to the cadmium-containing medium prevented the toxicity of cadmium to osteoclastic cells as observed in the culture of osteoblastic cells. These results indicate that both bone formation and bone resorption are inhibited by cadmium. The responses of osteoclasts and osteoblasts to cadmium in this culture system were the same and the responses of cadmium-damaged osteoblasts and osteoclasts to zinc were also similar. These results suggest that another mechanism by which cadmium could cause bone damage should be considered in addition to the specific induction of osteoclastic cells by Cd. |
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The mechanism for the bone lesion is unknown, however. To examine the effects of cadmium on bone metabolism, we compared its effects on osteoblasts and osteoclasts in vitro. We used an established cell line, MC3T3-E1, as osteoblasts and tartrate resistant acid phosphatase (TRACP)-positive multi-nucleated cells (MNC) formed by a bone marrow culture system as osteoclasts. Alkaline phosphatase (ALP) activity was decreased by 10(-7) M Cd and DNA content and hydroxyproline content of osteoblastic cells were decreased by 10(-5) M Cd. Cadmium at 10(-7) M inhibited the osteoclastic cell formation from mouse bone marrow in the presence of 10(-8) M 1 alpha, 25(OH)2 vitamin D3. A 100-fold higher concentration of zinc(Zn) simultaneously added to the cadmium-containing medium prevented the toxicity of cadmium to osteoclastic cells as observed in the culture of osteoblastic cells. These results indicate that both bone formation and bone resorption are inhibited by cadmium. The responses of osteoclasts and osteoblasts to cadmium in this culture system were the same and the responses of cadmium-damaged osteoblasts and osteoclasts to zinc were also similar. These results suggest that another mechanism by which cadmium could cause bone damage should be considered in addition to the specific induction of osteoclastic cells by Cd.</description><identifier>ISSN: 0340-5761</identifier><identifier>EISSN: 1432-0738</identifier><identifier>DOI: 10.1007/BF01973707</identifier><identifier>PMID: 8368944</identifier><identifier>CODEN: ARTODN</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Acid Phosphatase - metabolism ; Alkaline Phosphatase - metabolism ; Animals ; Biological and medical sciences ; Bone Marrow Cells ; Cadmium - toxicity ; Cell Line ; Cells, Cultured ; Chemical and industrial products toxicology. Toxic occupational diseases ; Collagen - metabolism ; DNA - metabolism ; Histocytochemistry ; Hydroxyproline - metabolism ; Isoenzymes - metabolism ; Male ; Medical sciences ; Metals and various inorganic compounds ; Mice ; Mice, Inbred Strains ; Osteoblasts - drug effects ; Osteoclasts - drug effects ; Proteins - metabolism ; Tartrate-Resistant Acid Phosphatase ; Taurine - pharmacology ; Toxicology ; Zinc - pharmacology</subject><ispartof>Archives of toxicology, 1993, Vol.67 (5), p.352-357</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-67ad636e0024b99f25e82ccafb0187b7d789fd159c08fb56bebfbab63d64f92c3</citedby><cites>FETCH-LOGICAL-c384t-67ad636e0024b99f25e82ccafb0187b7d789fd159c08fb56bebfbab63d64f92c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4800180$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8368944$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>IWAMI, K</creatorcontrib><creatorcontrib>MORIYAMA, T</creatorcontrib><title>Comparative effect of cadmium on osteoblastic cells and osteoclastic cells</title><title>Archives of toxicology</title><addtitle>Arch Toxicol</addtitle><description>Cadmium(Cd) has been thought to disturb the bone metabolism directly. The mechanism for the bone lesion is unknown, however. To examine the effects of cadmium on bone metabolism, we compared its effects on osteoblasts and osteoclasts in vitro. We used an established cell line, MC3T3-E1, as osteoblasts and tartrate resistant acid phosphatase (TRACP)-positive multi-nucleated cells (MNC) formed by a bone marrow culture system as osteoclasts. Alkaline phosphatase (ALP) activity was decreased by 10(-7) M Cd and DNA content and hydroxyproline content of osteoblastic cells were decreased by 10(-5) M Cd. Cadmium at 10(-7) M inhibited the osteoclastic cell formation from mouse bone marrow in the presence of 10(-8) M 1 alpha, 25(OH)2 vitamin D3. A 100-fold higher concentration of zinc(Zn) simultaneously added to the cadmium-containing medium prevented the toxicity of cadmium to osteoclastic cells as observed in the culture of osteoblastic cells. These results indicate that both bone formation and bone resorption are inhibited by cadmium. The responses of osteoclasts and osteoblasts to cadmium in this culture system were the same and the responses of cadmium-damaged osteoblasts and osteoclasts to zinc were also similar. These results suggest that another mechanism by which cadmium could cause bone damage should be considered in addition to the specific induction of osteoclastic cells by Cd.</description><subject>Acid Phosphatase - metabolism</subject><subject>Alkaline Phosphatase - metabolism</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Cells</subject><subject>Cadmium - toxicity</subject><subject>Cell Line</subject><subject>Cells, Cultured</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Collagen - metabolism</subject><subject>DNA - metabolism</subject><subject>Histocytochemistry</subject><subject>Hydroxyproline - metabolism</subject><subject>Isoenzymes - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metals and various inorganic compounds</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Osteoblasts - drug effects</subject><subject>Osteoclasts - drug effects</subject><subject>Proteins - metabolism</subject><subject>Tartrate-Resistant Acid Phosphatase</subject><subject>Taurine - pharmacology</subject><subject>Toxicology</subject><subject>Zinc - pharmacology</subject><issn>0340-5761</issn><issn>1432-0738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEtLw0AUhQdRaq1u3AtZiAsheiczmcfSFuuDghtdh3lCJMnUmUTw35vSUF1dOOfjcPkQusRwhwH4_XINWHLCgR-hOaakyIETcYzmQCjkJWf4FJ2l9AmACyHJDM0EYUJSOkevq9BuVVR9_e0y570zfRZ8ZpRt66HNQpeF1LugG5X62mTGNU3KVGf3sfkfn6MTr5rkLqa7QB_rx_fVc755e3pZPWxyQwTtc8aVZYQ5gIJqKX1ROlEYo7wGLLjmlgvpLS6lAeF1ybTTXivNiGXUy8KQBbrZ725j-Bpc6qu2TrsPVOfCkCrMmCQcwwje7kETQ0rR-Wob61bFnwpDtRNX_Ykb4atpddCtswd0MjX211OvklGNj6ozdTpgVIxyBZBfTlt1Tg</recordid><startdate>1993</startdate><enddate>1993</enddate><creator>IWAMI, K</creator><creator>MORIYAMA, T</creator><general>Springer</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>1993</creationdate><title>Comparative effect of cadmium on osteoblastic cells and osteoclastic cells</title><author>IWAMI, K ; MORIYAMA, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-67ad636e0024b99f25e82ccafb0187b7d789fd159c08fb56bebfbab63d64f92c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Acid Phosphatase - metabolism</topic><topic>Alkaline Phosphatase - metabolism</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Cells</topic><topic>Cadmium - toxicity</topic><topic>Cell Line</topic><topic>Cells, Cultured</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Collagen - metabolism</topic><topic>DNA - metabolism</topic><topic>Histocytochemistry</topic><topic>Hydroxyproline - metabolism</topic><topic>Isoenzymes - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metals and various inorganic compounds</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Osteoblasts - drug effects</topic><topic>Osteoclasts - drug effects</topic><topic>Proteins - metabolism</topic><topic>Tartrate-Resistant Acid Phosphatase</topic><topic>Taurine - pharmacology</topic><topic>Toxicology</topic><topic>Zinc - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>IWAMI, K</creatorcontrib><creatorcontrib>MORIYAMA, T</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 & Calcified Tissue Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Archives of toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>IWAMI, K</au><au>MORIYAMA, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative effect of cadmium on osteoblastic cells and osteoclastic cells</atitle><jtitle>Archives of toxicology</jtitle><addtitle>Arch Toxicol</addtitle><date>1993</date><risdate>1993</risdate><volume>67</volume><issue>5</issue><spage>352</spage><epage>357</epage><pages>352-357</pages><issn>0340-5761</issn><eissn>1432-0738</eissn><coden>ARTODN</coden><abstract>Cadmium(Cd) has been thought to disturb the bone metabolism directly. The mechanism for the bone lesion is unknown, however. To examine the effects of cadmium on bone metabolism, we compared its effects on osteoblasts and osteoclasts in vitro. We used an established cell line, MC3T3-E1, as osteoblasts and tartrate resistant acid phosphatase (TRACP)-positive multi-nucleated cells (MNC) formed by a bone marrow culture system as osteoclasts. Alkaline phosphatase (ALP) activity was decreased by 10(-7) M Cd and DNA content and hydroxyproline content of osteoblastic cells were decreased by 10(-5) M Cd. Cadmium at 10(-7) M inhibited the osteoclastic cell formation from mouse bone marrow in the presence of 10(-8) M 1 alpha, 25(OH)2 vitamin D3. A 100-fold higher concentration of zinc(Zn) simultaneously added to the cadmium-containing medium prevented the toxicity of cadmium to osteoclastic cells as observed in the culture of osteoblastic cells. These results indicate that both bone formation and bone resorption are inhibited by cadmium. The responses of osteoclasts and osteoblasts to cadmium in this culture system were the same and the responses of cadmium-damaged osteoblasts and osteoclasts to zinc were also similar. These results suggest that another mechanism by which cadmium could cause bone damage should be considered in addition to the specific induction of osteoclastic cells by Cd.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>8368944</pmid><doi>10.1007/BF01973707</doi><tpages>6</tpages></addata></record> |
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subjects | Acid Phosphatase - metabolism Alkaline Phosphatase - metabolism Animals Biological and medical sciences Bone Marrow Cells Cadmium - toxicity Cell Line Cells, Cultured Chemical and industrial products toxicology. Toxic occupational diseases Collagen - metabolism DNA - metabolism Histocytochemistry Hydroxyproline - metabolism Isoenzymes - metabolism Male Medical sciences Metals and various inorganic compounds Mice Mice, Inbred Strains Osteoblasts - drug effects Osteoclasts - drug effects Proteins - metabolism Tartrate-Resistant Acid Phosphatase Taurine - pharmacology Toxicology Zinc - pharmacology |
title | Comparative effect of cadmium on osteoblastic cells and osteoclastic cells |
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