Necessity of Enzymatic Activity of Alkaline Phosphatase for Mineralization of Osteoblastic Cells
Alkaline phosphatase (ALP) is supposed to be important for bone formation; however, its role is not clear. In this study, we examined the importance of enzymatic activity of ALP and anchoring of ALP protein to the cells for mineralization of an osteoblastic cell line, MC3T3-E1. While we cultured the...
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Veröffentlicht in: | Japanese Journal of Pharmacology 2002, Vol.88(3), pp.262-269 |
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description | Alkaline phosphatase (ALP) is supposed to be important for bone formation; however, its role is not clear. In this study, we examined the importance of enzymatic activity of ALP and anchoring of ALP protein to the cells for mineralization of an osteoblastic cell line, MC3T3-E1. While we cultured the cells in the presence of tetramisole, an inhibitor of ALP activity, ALP protein was expressed at a similar level to that in the control. Although tetramisole showed no effect on cell growth and increased hydroxyproline accumulation, it decreased the osteocalcin production and the accumulation of calcium and phosphate in the matrices. Tetramisole also inhibited mineralized nodule formation, which was observed by optical microscopy and detected by Von Kossa staining. On the other hand, when ALP protein was released from the cell membranes with the use of phosphatidylinositol-specific phospholipase C, no marked changes were detected in hydroxyproline, calcium and phosphate accumulations in the matrices at late calcification stage, which was consistent with the morphological findings. These results clearly show that enzymatic activity of ALP is necessary for mineralization of MC3T3-E1 cells, but not the presence of ALP protein or anchoring of ALP to the cells. |
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In this study, we examined the importance of enzymatic activity of ALP and anchoring of ALP protein to the cells for mineralization of an osteoblastic cell line, MC3T3-E1. While we cultured the cells in the presence of tetramisole, an inhibitor of ALP activity, ALP protein was expressed at a similar level to that in the control. Although tetramisole showed no effect on cell growth and increased hydroxyproline accumulation, it decreased the osteocalcin production and the accumulation of calcium and phosphate in the matrices. Tetramisole also inhibited mineralized nodule formation, which was observed by optical microscopy and detected by Von Kossa staining. On the other hand, when ALP protein was released from the cell membranes with the use of phosphatidylinositol-specific phospholipase C, no marked changes were detected in hydroxyproline, calcium and phosphate accumulations in the matrices at late calcification stage, which was consistent with the morphological findings. These results clearly show that enzymatic activity of ALP is necessary for mineralization of MC3T3-E1 cells, but not the presence of ALP protein or anchoring of ALP to the cells.</description><identifier>ISSN: 0021-5198</identifier><identifier>EISSN: 1347-3506</identifier><identifier>DOI: 10.1254/jjp.88.262</identifier><identifier>PMID: 11949880</identifier><language>eng</language><publisher>Japan: The Japanese Pharmacological Society</publisher><subject>Alkaline phosphatase ; Alkaline Phosphatase - metabolism ; Animals ; Calcification, Physiologic - physiology ; Calcium - metabolism ; Cell Line ; Cell Membrane - drug effects ; Cell Membrane - metabolism ; Hydroxyproline - metabolism ; Mice ; Mineralization ; Osteoblastic cell ; Osteoblasts - metabolism ; Osteoblasts - physiology ; Osteocalcin - metabolism ; Phosphates - metabolism ; Phosphatidylinositol Diacylglycerol-Lyase ; Phosphatidylinositol-specific phospholipase C ; Phosphoinositide Phospholipase C ; Tetramisole ; Tetramisole - pharmacology ; Type C Phospholipases - metabolism</subject><ispartof>The Japanese Journal of Pharmacology, 2002, Vol.88(3), pp.262-269</ispartof><rights>2002 Elsevier B.V.</rights><rights>The Japanese Pharmacological Society 2002</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c699t-6d28760b1fecffcb31ad1a9eea242aa35770a4db98f0cb3660c721eda4b119a23</citedby><cites>FETCH-LOGICAL-c699t-6d28760b1fecffcb31ad1a9eea242aa35770a4db98f0cb3660c721eda4b119a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1882,4023,27922,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11949880$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sugawara, Yuki</creatorcontrib><creatorcontrib>Suzuki, Kuniaki</creatorcontrib><creatorcontrib>Koshikawa, Mino</creatorcontrib><creatorcontrib>Ando, Masaki</creatorcontrib><creatorcontrib>Iida, Junichiro</creatorcontrib><creatorcontrib>Graduate School of Dental Medicine</creatorcontrib><creatorcontrib>Department of Oral Functional Science (Section of Orthodontics</creatorcontrib><creatorcontrib>Department of Oral Pathobiological Science (Section of Dental Pharmacology</creatorcontrib><creatorcontrib>Hokkaido University</creatorcontrib><title>Necessity of Enzymatic Activity of Alkaline Phosphatase for Mineralization of Osteoblastic Cells</title><title>Japanese Journal of Pharmacology</title><addtitle>Jpn.J.Pharmacol.</addtitle><description>Alkaline phosphatase (ALP) is supposed to be important for bone formation; however, its role is not clear. In this study, we examined the importance of enzymatic activity of ALP and anchoring of ALP protein to the cells for mineralization of an osteoblastic cell line, MC3T3-E1. While we cultured the cells in the presence of tetramisole, an inhibitor of ALP activity, ALP protein was expressed at a similar level to that in the control. Although tetramisole showed no effect on cell growth and increased hydroxyproline accumulation, it decreased the osteocalcin production and the accumulation of calcium and phosphate in the matrices. Tetramisole also inhibited mineralized nodule formation, which was observed by optical microscopy and detected by Von Kossa staining. On the other hand, when ALP protein was released from the cell membranes with the use of phosphatidylinositol-specific phospholipase C, no marked changes were detected in hydroxyproline, calcium and phosphate accumulations in the matrices at late calcification stage, which was consistent with the morphological findings. These results clearly show that enzymatic activity of ALP is necessary for mineralization of MC3T3-E1 cells, but not the presence of ALP protein or anchoring of ALP to the cells.</description><subject>Alkaline phosphatase</subject><subject>Alkaline Phosphatase - metabolism</subject><subject>Animals</subject><subject>Calcification, Physiologic - physiology</subject><subject>Calcium - metabolism</subject><subject>Cell Line</subject><subject>Cell Membrane - drug effects</subject><subject>Cell Membrane - metabolism</subject><subject>Hydroxyproline - metabolism</subject><subject>Mice</subject><subject>Mineralization</subject><subject>Osteoblastic cell</subject><subject>Osteoblasts - metabolism</subject><subject>Osteoblasts - physiology</subject><subject>Osteocalcin - metabolism</subject><subject>Phosphates - metabolism</subject><subject>Phosphatidylinositol Diacylglycerol-Lyase</subject><subject>Phosphatidylinositol-specific phospholipase C</subject><subject>Phosphoinositide Phospholipase C</subject><subject>Tetramisole</subject><subject>Tetramisole - pharmacology</subject><subject>Type C Phospholipases - metabolism</subject><issn>0021-5198</issn><issn>1347-3506</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkE1v1DAQhi0Eokvhwg9AOXGolMV2vpwTWq1aQGopB3p2J86YdcjGwc5W2v56JsoWLr145Jl33pl5GHsv-FrIIv_UdeNaqbUs5Qu2EllepVnBy5dsxbkUaSFqdcbexNjRV3GRv2ZnQtR5rRRfsfvvaDBGNx0Tb5PL4fG4h8mZZGMm93DKbvrf0LsBkx87H8cdTBAxsT4kN5QMVHqkFj_M0ts4oW96iLPHFvs-vmWvLPQR353iObu7uvy5_Zpe3375tt1cp6as6yktW6mqkjfCorHWNJmAVkCNCDKXAFlRVRzytqmV5VQtS24qKbCFvKFjQGbn7OPiOwb_54Bx0nsXDW0AA_pD1JUo6lKoWXixCE3wMQa0egxuD-GoBdczT008tVKaeJL4w8n10Oyx_S89ASTB1SKgqjPQ-2EmpTt_CAOdq40tu86PvZZEX3M-91DINSf7-akFp6HzpM-LURcn-IX_JkEglD0-LZUtz9z8VDE7CBoHcsgXByTMDw6DjsbhYGixgGbSrXfPnfgXsH6xyQ</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>Sugawara, Yuki</creator><creator>Suzuki, Kuniaki</creator><creator>Koshikawa, Mino</creator><creator>Ando, Masaki</creator><creator>Iida, Junichiro</creator><general>The Japanese Pharmacological Society</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope></search><sort><creationdate>2002</creationdate><title>Necessity of Enzymatic Activity of Alkaline Phosphatase for Mineralization of Osteoblastic Cells</title><author>Sugawara, Yuki ; Suzuki, Kuniaki ; Koshikawa, Mino ; Ando, Masaki ; Iida, Junichiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c699t-6d28760b1fecffcb31ad1a9eea242aa35770a4db98f0cb3660c721eda4b119a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Alkaline phosphatase</topic><topic>Alkaline Phosphatase - metabolism</topic><topic>Animals</topic><topic>Calcification, Physiologic - physiology</topic><topic>Calcium - metabolism</topic><topic>Cell Line</topic><topic>Cell Membrane - drug effects</topic><topic>Cell Membrane - metabolism</topic><topic>Hydroxyproline - metabolism</topic><topic>Mice</topic><topic>Mineralization</topic><topic>Osteoblastic cell</topic><topic>Osteoblasts - metabolism</topic><topic>Osteoblasts - physiology</topic><topic>Osteocalcin - metabolism</topic><topic>Phosphates - metabolism</topic><topic>Phosphatidylinositol Diacylglycerol-Lyase</topic><topic>Phosphatidylinositol-specific phospholipase C</topic><topic>Phosphoinositide Phospholipase C</topic><topic>Tetramisole</topic><topic>Tetramisole - pharmacology</topic><topic>Type C Phospholipases - metabolism</topic><toplevel>online_resources</toplevel><creatorcontrib>Sugawara, Yuki</creatorcontrib><creatorcontrib>Suzuki, Kuniaki</creatorcontrib><creatorcontrib>Koshikawa, Mino</creatorcontrib><creatorcontrib>Ando, Masaki</creatorcontrib><creatorcontrib>Iida, Junichiro</creatorcontrib><creatorcontrib>Graduate School of Dental Medicine</creatorcontrib><creatorcontrib>Department of Oral Functional Science (Section of Orthodontics</creatorcontrib><creatorcontrib>Department of Oral Pathobiological Science (Section of Dental Pharmacology</creatorcontrib><creatorcontrib>Hokkaido University</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Japanese Journal of Pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sugawara, Yuki</au><au>Suzuki, Kuniaki</au><au>Koshikawa, Mino</au><au>Ando, Masaki</au><au>Iida, Junichiro</au><aucorp>Graduate School of Dental Medicine</aucorp><aucorp>Department of Oral Functional Science (Section of Orthodontics</aucorp><aucorp>Department of Oral Pathobiological Science (Section of Dental Pharmacology</aucorp><aucorp>Hokkaido University</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Necessity of Enzymatic Activity of Alkaline Phosphatase for Mineralization of Osteoblastic Cells</atitle><jtitle>Japanese Journal of Pharmacology</jtitle><addtitle>Jpn.J.Pharmacol.</addtitle><date>2002</date><risdate>2002</risdate><volume>88</volume><issue>3</issue><spage>262</spage><epage>269</epage><pages>262-269</pages><issn>0021-5198</issn><eissn>1347-3506</eissn><abstract>Alkaline phosphatase (ALP) is supposed to be important for bone formation; however, its role is not clear. In this study, we examined the importance of enzymatic activity of ALP and anchoring of ALP protein to the cells for mineralization of an osteoblastic cell line, MC3T3-E1. While we cultured the cells in the presence of tetramisole, an inhibitor of ALP activity, ALP protein was expressed at a similar level to that in the control. Although tetramisole showed no effect on cell growth and increased hydroxyproline accumulation, it decreased the osteocalcin production and the accumulation of calcium and phosphate in the matrices. Tetramisole also inhibited mineralized nodule formation, which was observed by optical microscopy and detected by Von Kossa staining. On the other hand, when ALP protein was released from the cell membranes with the use of phosphatidylinositol-specific phospholipase C, no marked changes were detected in hydroxyproline, calcium and phosphate accumulations in the matrices at late calcification stage, which was consistent with the morphological findings. These results clearly show that enzymatic activity of ALP is necessary for mineralization of MC3T3-E1 cells, but not the presence of ALP protein or anchoring of ALP to the cells.</abstract><cop>Japan</cop><pub>The Japanese Pharmacological Society</pub><pmid>11949880</pmid><doi>10.1254/jjp.88.262</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alkaline phosphatase Alkaline Phosphatase - metabolism Animals Calcification, Physiologic - physiology Calcium - metabolism Cell Line Cell Membrane - drug effects Cell Membrane - metabolism Hydroxyproline - metabolism Mice Mineralization Osteoblastic cell Osteoblasts - metabolism Osteoblasts - physiology Osteocalcin - metabolism Phosphates - metabolism Phosphatidylinositol Diacylglycerol-Lyase Phosphatidylinositol-specific phospholipase C Phosphoinositide Phospholipase C Tetramisole Tetramisole - pharmacology Type C Phospholipases - metabolism |
title | Necessity of Enzymatic Activity of Alkaline Phosphatase for Mineralization of Osteoblastic Cells |
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