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Bisphenol A in combination with insulin can accelerate the conversion of 3T3-L1 fibroblasts to adipocytes
The confluent cultures of 3T3-L1 fibroblasts were treated with or without bisphenol A (BPA) for 2 days and subsequently treated with insulin (INS) alone for 9 days. When BPA was absent during the first 2-day treatment period, the cultures contained 1.6 microg/microg DNA of triacylglycerol (TG), 202...
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Published in: | Journal of lipid research 2002-05, Vol.43 (5), p.676-684 |
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container_title | Journal of lipid research |
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creator | Masuno, Hiroshi Kidani, Teruki Sekiya, Keizo Sakayama, Kenshi Shiosaka, Takahiko Yamamoto, Haruyasu Honda, Katsuhisa |
description | The confluent cultures of 3T3-L1 fibroblasts were treated with or without bisphenol A (BPA) for 2 days and subsequently treated with insulin (INS) alone for 9 days. When BPA was absent during the first 2-day treatment period, the cultures contained 1.6 microg/microg DNA of triacylglycerol (TG), 202 mU/mg DNA of lipoprotein lipase (LPL) activity, and 462 nmol/min/mg DNA of glycerol-3-phosphate dehydrogenase (GPDH) activity. The presence of BPA during the same period caused a 150% increase in the TG content, a 60% increase in the LPL activity, and a 500% increase in the GPDH activity. Thus, BPA by itself can trigger 3T3-L1 fibroblasts to differentiate into adipocytes. Next, the confluent cultures were treated with BPA for 2 days and subsequently treated with a combination of INS and BPA for 9 days. The simultaneous presence of BPA with INS caused a 370% increase in the TG content, a 200% increase in the LPL activity, and a 225% increase in the GPDH activity compared with the cultures treated with INS alone. The amount of [(3)H]thymidine incorporated into DNA was lower in the cultures treated with INS in the presence of BPA than in those treated with INS alone, indicating that BPA has an anti-proliferative activity on 3T3-L1 cells. Taken together, our results indicate that BPA in combination with INS can accelerate the adipocyte conversion. |
doi_str_mv | 10.1016/S0022-2275(20)30108-5 |
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When BPA was absent during the first 2-day treatment period, the cultures contained 1.6 microg/microg DNA of triacylglycerol (TG), 202 mU/mg DNA of lipoprotein lipase (LPL) activity, and 462 nmol/min/mg DNA of glycerol-3-phosphate dehydrogenase (GPDH) activity. The presence of BPA during the same period caused a 150% increase in the TG content, a 60% increase in the LPL activity, and a 500% increase in the GPDH activity. Thus, BPA by itself can trigger 3T3-L1 fibroblasts to differentiate into adipocytes. Next, the confluent cultures were treated with BPA for 2 days and subsequently treated with a combination of INS and BPA for 9 days. The simultaneous presence of BPA with INS caused a 370% increase in the TG content, a 200% increase in the LPL activity, and a 225% increase in the GPDH activity compared with the cultures treated with INS alone. The amount of [(3)H]thymidine incorporated into DNA was lower in the cultures treated with INS in the presence of BPA than in those treated with INS alone, indicating that BPA has an anti-proliferative activity on 3T3-L1 cells. Taken together, our results indicate that BPA in combination with INS can accelerate the adipocyte conversion.</description><identifier>ISSN: 0022-2275</identifier><identifier>DOI: 10.1016/S0022-2275(20)30108-5</identifier><identifier>PMID: 11971937</identifier><language>eng</language><publisher>United States: Elsevier</publisher><subject>3T3 Cells ; 3T3-L1 adipocytes ; Adipocytes - cytology ; Adipocytes - drug effects ; Adipocytes - physiology ; Animals ; Benzhydryl Compounds ; Cell Differentiation - drug effects ; DNA - biosynthesis ; environmental endocrine disrupting chemical ; Estrogens, Non-Steroidal - pharmacology ; Fibroblasts - cytology ; Fibroblasts - drug effects ; Fibroblasts - physiology ; glycerol-3-phosphate dehydrogenase ; Glycerolphosphate Dehydrogenase - metabolism ; Insulin - pharmacology ; lipoprotein lipase ; Lipoprotein Lipase - metabolism ; Mice ; Phenols - pharmacology ; Proliferating Cell Nuclear Antigen - analysis ; Thymidine - metabolism ; triacylglycerol accumulation ; Triglycerides - metabolism</subject><ispartof>Journal of lipid research, 2002-05, Vol.43 (5), p.676-684</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-7e3edf9bb3ec11236f52139fa2eec787c4707ea555db625808bb11ef6ea4f6013</citedby><cites>FETCH-LOGICAL-c443t-7e3edf9bb3ec11236f52139fa2eec787c4707ea555db625808bb11ef6ea4f6013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11971937$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Masuno, Hiroshi</creatorcontrib><creatorcontrib>Kidani, Teruki</creatorcontrib><creatorcontrib>Sekiya, Keizo</creatorcontrib><creatorcontrib>Sakayama, Kenshi</creatorcontrib><creatorcontrib>Shiosaka, Takahiko</creatorcontrib><creatorcontrib>Yamamoto, Haruyasu</creatorcontrib><creatorcontrib>Honda, Katsuhisa</creatorcontrib><title>Bisphenol A in combination with insulin can accelerate the conversion of 3T3-L1 fibroblasts to adipocytes</title><title>Journal of lipid research</title><addtitle>J Lipid Res</addtitle><description>The confluent cultures of 3T3-L1 fibroblasts were treated with or without bisphenol A (BPA) for 2 days and subsequently treated with insulin (INS) alone for 9 days. When BPA was absent during the first 2-day treatment period, the cultures contained 1.6 microg/microg DNA of triacylglycerol (TG), 202 mU/mg DNA of lipoprotein lipase (LPL) activity, and 462 nmol/min/mg DNA of glycerol-3-phosphate dehydrogenase (GPDH) activity. The presence of BPA during the same period caused a 150% increase in the TG content, a 60% increase in the LPL activity, and a 500% increase in the GPDH activity. Thus, BPA by itself can trigger 3T3-L1 fibroblasts to differentiate into adipocytes. Next, the confluent cultures were treated with BPA for 2 days and subsequently treated with a combination of INS and BPA for 9 days. The simultaneous presence of BPA with INS caused a 370% increase in the TG content, a 200% increase in the LPL activity, and a 225% increase in the GPDH activity compared with the cultures treated with INS alone. The amount of [(3)H]thymidine incorporated into DNA was lower in the cultures treated with INS in the presence of BPA than in those treated with INS alone, indicating that BPA has an anti-proliferative activity on 3T3-L1 cells. Taken together, our results indicate that BPA in combination with INS can accelerate the adipocyte conversion.</description><subject>3T3 Cells</subject><subject>3T3-L1 adipocytes</subject><subject>Adipocytes - cytology</subject><subject>Adipocytes - drug effects</subject><subject>Adipocytes - physiology</subject><subject>Animals</subject><subject>Benzhydryl Compounds</subject><subject>Cell Differentiation - drug effects</subject><subject>DNA - biosynthesis</subject><subject>environmental endocrine disrupting chemical</subject><subject>Estrogens, Non-Steroidal - pharmacology</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - drug effects</subject><subject>Fibroblasts - physiology</subject><subject>glycerol-3-phosphate dehydrogenase</subject><subject>Glycerolphosphate Dehydrogenase - metabolism</subject><subject>Insulin - pharmacology</subject><subject>lipoprotein lipase</subject><subject>Lipoprotein Lipase - metabolism</subject><subject>Mice</subject><subject>Phenols - pharmacology</subject><subject>Proliferating Cell Nuclear Antigen - analysis</subject><subject>Thymidine - metabolism</subject><subject>triacylglycerol accumulation</subject><subject>Triglycerides - metabolism</subject><issn>0022-2275</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpFkE1PGzEQhn1oVWjan1DkIxy2eOz1en2kiLZIkThAz5Y_xo3RZh3Zpoh_302C4DTSO_M-Iz2EfAP2HRgMl_eMcd5xruQ5ZxeCARs7-YGcvsUn5HOtj4xB3w_wiZwAaAVaqFOSfqS62-CcJ3pF00x93ro025byTJ9T2yxZfZr2CztT6z1OWGxD2ja43M7_sNT9aY5UPIhuDTQmV7KbbG2VtkxtSLvsXxrWL-RjtFPFr69zRf78vHm4_t2t737dXl-tO9_3onUKBYaonRPoAbgYouQgdLQc0atR-V4xhVZKGdzA5chG5wAwDmj7ODAQK3J75IZsH82upK0tLybbZA5BLn-NLS35CY1WNoxca2H5uDzXLojRBwAbhiFyPS4seWT5kmstGN94wMxevTmoN3vHhjNzUG_k0js79nZPbovhvfXqXfwHGM2BZQ</recordid><startdate>20020501</startdate><enddate>20020501</enddate><creator>Masuno, Hiroshi</creator><creator>Kidani, Teruki</creator><creator>Sekiya, Keizo</creator><creator>Sakayama, Kenshi</creator><creator>Shiosaka, Takahiko</creator><creator>Yamamoto, Haruyasu</creator><creator>Honda, Katsuhisa</creator><general>Elsevier</general><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>DOA</scope></search><sort><creationdate>20020501</creationdate><title>Bisphenol A in combination with insulin can accelerate the conversion of 3T3-L1 fibroblasts to adipocytes</title><author>Masuno, Hiroshi ; Kidani, Teruki ; Sekiya, Keizo ; Sakayama, Kenshi ; Shiosaka, Takahiko ; Yamamoto, Haruyasu ; Honda, Katsuhisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-7e3edf9bb3ec11236f52139fa2eec787c4707ea555db625808bb11ef6ea4f6013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>3T3 Cells</topic><topic>3T3-L1 adipocytes</topic><topic>Adipocytes - cytology</topic><topic>Adipocytes - drug effects</topic><topic>Adipocytes - physiology</topic><topic>Animals</topic><topic>Benzhydryl Compounds</topic><topic>Cell Differentiation - drug effects</topic><topic>DNA - biosynthesis</topic><topic>environmental endocrine disrupting chemical</topic><topic>Estrogens, Non-Steroidal - pharmacology</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - drug effects</topic><topic>Fibroblasts - physiology</topic><topic>glycerol-3-phosphate dehydrogenase</topic><topic>Glycerolphosphate Dehydrogenase - metabolism</topic><topic>Insulin - pharmacology</topic><topic>lipoprotein lipase</topic><topic>Lipoprotein Lipase - metabolism</topic><topic>Mice</topic><topic>Phenols - pharmacology</topic><topic>Proliferating Cell Nuclear Antigen - analysis</topic><topic>Thymidine - metabolism</topic><topic>triacylglycerol accumulation</topic><topic>Triglycerides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Masuno, Hiroshi</creatorcontrib><creatorcontrib>Kidani, Teruki</creatorcontrib><creatorcontrib>Sekiya, Keizo</creatorcontrib><creatorcontrib>Sakayama, Kenshi</creatorcontrib><creatorcontrib>Shiosaka, Takahiko</creatorcontrib><creatorcontrib>Yamamoto, Haruyasu</creatorcontrib><creatorcontrib>Honda, Katsuhisa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of lipid research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Masuno, Hiroshi</au><au>Kidani, Teruki</au><au>Sekiya, Keizo</au><au>Sakayama, Kenshi</au><au>Shiosaka, Takahiko</au><au>Yamamoto, Haruyasu</au><au>Honda, Katsuhisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bisphenol A in combination with insulin can accelerate the conversion of 3T3-L1 fibroblasts to adipocytes</atitle><jtitle>Journal of lipid research</jtitle><addtitle>J Lipid Res</addtitle><date>2002-05-01</date><risdate>2002</risdate><volume>43</volume><issue>5</issue><spage>676</spage><epage>684</epage><pages>676-684</pages><issn>0022-2275</issn><abstract>The confluent cultures of 3T3-L1 fibroblasts were treated with or without bisphenol A (BPA) for 2 days and subsequently treated with insulin (INS) alone for 9 days. When BPA was absent during the first 2-day treatment period, the cultures contained 1.6 microg/microg DNA of triacylglycerol (TG), 202 mU/mg DNA of lipoprotein lipase (LPL) activity, and 462 nmol/min/mg DNA of glycerol-3-phosphate dehydrogenase (GPDH) activity. The presence of BPA during the same period caused a 150% increase in the TG content, a 60% increase in the LPL activity, and a 500% increase in the GPDH activity. Thus, BPA by itself can trigger 3T3-L1 fibroblasts to differentiate into adipocytes. Next, the confluent cultures were treated with BPA for 2 days and subsequently treated with a combination of INS and BPA for 9 days. The simultaneous presence of BPA with INS caused a 370% increase in the TG content, a 200% increase in the LPL activity, and a 225% increase in the GPDH activity compared with the cultures treated with INS alone. The amount of [(3)H]thymidine incorporated into DNA was lower in the cultures treated with INS in the presence of BPA than in those treated with INS alone, indicating that BPA has an anti-proliferative activity on 3T3-L1 cells. Taken together, our results indicate that BPA in combination with INS can accelerate the adipocyte conversion.</abstract><cop>United States</cop><pub>Elsevier</pub><pmid>11971937</pmid><doi>10.1016/S0022-2275(20)30108-5</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3T3 Cells 3T3-L1 adipocytes Adipocytes - cytology Adipocytes - drug effects Adipocytes - physiology Animals Benzhydryl Compounds Cell Differentiation - drug effects DNA - biosynthesis environmental endocrine disrupting chemical Estrogens, Non-Steroidal - pharmacology Fibroblasts - cytology Fibroblasts - drug effects Fibroblasts - physiology glycerol-3-phosphate dehydrogenase Glycerolphosphate Dehydrogenase - metabolism Insulin - pharmacology lipoprotein lipase Lipoprotein Lipase - metabolism Mice Phenols - pharmacology Proliferating Cell Nuclear Antigen - analysis Thymidine - metabolism triacylglycerol accumulation Triglycerides - metabolism |
title | Bisphenol A in combination with insulin can accelerate the conversion of 3T3-L1 fibroblasts to adipocytes |
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