Chronic ethanol administration impairs the binding and endocytosis of asialo-orosomucoid in isolated hepatocytes
We have examined the effect of ethanol administration on receptor-mediated endocytosis of asialo-orosomucoid by isolated hepatocytes. Significantly less ligand was bound, internalized, and degraded by hepatocytes isolated from rats fed an ethanol diet for 5-7 weeks than by cells isolated from chow-f...
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Veröffentlicht in: | The Journal of biological chemistry 1987-02, Vol.262 (6), p.2704-2710 |
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description | We have examined the effect of ethanol administration on receptor-mediated endocytosis of asialo-orosomucoid by isolated hepatocytes. Significantly less ligand was bound, internalized, and degraded by hepatocytes isolated from rats fed an ethanol diet for 5-7 weeks than by cells isolated from chow-fed or pair-fed controls. Reduced binding was shown to be primarily due to a decreased number of cell surface receptors rather than to a lowered affinity of the receptor for its ligand. This reduction in cell surface receptors resulted in a marked inhibition of internalization and degradation of ligand by hepatocytes from the ethanol-fed rats. In addition, a defect in the initial stages of receptor-ligand internalization was also indicated, since less surface-bound ligand was internalized and subsequently degraded in cells from the ethanol-treated animals as compared to controls. Rates of internalization and degradation of internalized ligand were, however, similar for all three groups, suggesting that neither degradation per se nor rate of delivery of internalized ligand to the lysosomes was affected by ethanol feeding. Receptor recycling was impaired in ethanol-fed rats, as indicated by a decrease in the binding site number after stimulation of endocytosis for 120 min when compared to initial binding capacity. Receptor recycling was not impaired in hepatocytes from control animals. These results indicate that chronic ethanol feeding impairs the process of receptor-mediated endocytosis by the liver; the major cause of this impairment appears to be due to a decreased number of cell surface asialoglycoprotein receptors in the ethanol-fed animals, along with a decreased ability of these cells to internalize all of the surface-bound ligand. |
doi_str_mv | 10.1016/S0021-9258(18)61564-9 |
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Significantly less ligand was bound, internalized, and degraded by hepatocytes isolated from rats fed an ethanol diet for 5-7 weeks than by cells isolated from chow-fed or pair-fed controls. Reduced binding was shown to be primarily due to a decreased number of cell surface receptors rather than to a lowered affinity of the receptor for its ligand. This reduction in cell surface receptors resulted in a marked inhibition of internalization and degradation of ligand by hepatocytes from the ethanol-fed rats. In addition, a defect in the initial stages of receptor-ligand internalization was also indicated, since less surface-bound ligand was internalized and subsequently degraded in cells from the ethanol-treated animals as compared to controls. Rates of internalization and degradation of internalized ligand were, however, similar for all three groups, suggesting that neither degradation per se nor rate of delivery of internalized ligand to the lysosomes was affected by ethanol feeding. Receptor recycling was impaired in ethanol-fed rats, as indicated by a decrease in the binding site number after stimulation of endocytosis for 120 min when compared to initial binding capacity. Receptor recycling was not impaired in hepatocytes from control animals. These results indicate that chronic ethanol feeding impairs the process of receptor-mediated endocytosis by the liver; the major cause of this impairment appears to be due to a decreased number of cell surface asialoglycoprotein receptors in the ethanol-fed animals, along with a decreased ability of these cells to internalize all of the surface-bound ligand.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1016/S0021-9258(18)61564-9</identifier><identifier>PMID: 3818618</identifier><identifier>CODEN: JBCHA3</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Animals ; asialo-orosomucoid ; Asialoglycoprotein Receptor ; Asialoglycoproteins ; Binding Sites ; Biological and medical sciences ; Cell physiology ; cell surface ; Endocytosis ; ethanol ; Ethanol - pharmacology ; Fundamental and applied biological sciences. Psychology ; hepatocytes ; Humans ; Kinetics ; Liver - cytology ; Liver - metabolism ; Molecular and cellular biology ; Orosomucoid - analogs & derivatives ; Orosomucoid - metabolism ; Rats ; receptors ; Receptors, Immunologic - metabolism</subject><ispartof>The Journal of biological chemistry, 1987-02, Vol.262 (6), p.2704-2710</ispartof><rights>1987 © 1987 ASBMB. 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Significantly less ligand was bound, internalized, and degraded by hepatocytes isolated from rats fed an ethanol diet for 5-7 weeks than by cells isolated from chow-fed or pair-fed controls. Reduced binding was shown to be primarily due to a decreased number of cell surface receptors rather than to a lowered affinity of the receptor for its ligand. This reduction in cell surface receptors resulted in a marked inhibition of internalization and degradation of ligand by hepatocytes from the ethanol-fed rats. In addition, a defect in the initial stages of receptor-ligand internalization was also indicated, since less surface-bound ligand was internalized and subsequently degraded in cells from the ethanol-treated animals as compared to controls. Rates of internalization and degradation of internalized ligand were, however, similar for all three groups, suggesting that neither degradation per se nor rate of delivery of internalized ligand to the lysosomes was affected by ethanol feeding. Receptor recycling was impaired in ethanol-fed rats, as indicated by a decrease in the binding site number after stimulation of endocytosis for 120 min when compared to initial binding capacity. Receptor recycling was not impaired in hepatocytes from control animals. These results indicate that chronic ethanol feeding impairs the process of receptor-mediated endocytosis by the liver; the major cause of this impairment appears to be due to a decreased number of cell surface asialoglycoprotein receptors in the ethanol-fed animals, along with a decreased ability of these cells to internalize all of the surface-bound ligand.</description><subject>Animals</subject><subject>asialo-orosomucoid</subject><subject>Asialoglycoprotein Receptor</subject><subject>Asialoglycoproteins</subject><subject>Binding Sites</subject><subject>Biological and medical sciences</subject><subject>Cell physiology</subject><subject>cell surface</subject><subject>Endocytosis</subject><subject>ethanol</subject><subject>Ethanol - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>hepatocytes</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Liver - cytology</subject><subject>Liver - metabolism</subject><subject>Molecular and cellular biology</subject><subject>Orosomucoid - analogs & derivatives</subject><subject>Orosomucoid - metabolism</subject><subject>Rats</subject><subject>receptors</subject><subject>Receptors, Immunologic - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2LFDEQhhtR1nH1JywEEdFDa5Lu9CSnRQa_YMGDCt5Ckq5sl3QnbZJR9t-b2RnmurnkUM-bqtTTNFeMvmOUDe-_U8pZq7iQb5h8OzAx9K161GwYlV3bCfbrcbM5I0-bZzn_pvX0il00F51kcmBy06y7KcWAjkCZTIgzMeOCAXNJpmAMBJfVYMqkTEAshhHDLTFhJBDG6O5KzJhJ9MRkNHNsY4o5LnsXcSRYwznOpsBIJlhNOfCQnzdPvJkzvDjdl83PTx9_7L60N98-f919uGldr_rSCiGplw6oGaQCyrzjTKiOK9WD9BasdMIxaT2n3govvfLU-ApYJa2zvLtsXh_fXVP8s4dc9ILZwTybAHGf9XbbU0Z7-SDIeiE73g0VFEfQ1V_mBF6vCReT7jSj-qBE3yvRh31rJvW9Eq1q7urUYG8XGM-pk4Naf3Wqm-zM7JMJDvMZk7xKE4f2L4_YhLfTP0ygLUY3waL5wPWg-Zb2Fbo-QlBX-xch6ewQgoOxBlzRY8QHpv0PPSe2Hg</recordid><startdate>19870225</startdate><enddate>19870225</enddate><creator>Casey, C.A.</creator><creator>Kragskow, S.L.</creator><creator>Sorrell, M.F.</creator><creator>Tuma, D.J.</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><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>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19870225</creationdate><title>Chronic ethanol administration impairs the binding and endocytosis of asialo-orosomucoid in isolated hepatocytes</title><author>Casey, C.A. ; Kragskow, S.L. ; Sorrell, M.F. ; Tuma, D.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-5580f8ce0a689e01fc215932994e8fbeb8c5c18bf20fb5f8f9f0af932b98bcb23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Animals</topic><topic>asialo-orosomucoid</topic><topic>Asialoglycoprotein Receptor</topic><topic>Asialoglycoproteins</topic><topic>Binding Sites</topic><topic>Biological and medical sciences</topic><topic>Cell physiology</topic><topic>cell surface</topic><topic>Endocytosis</topic><topic>ethanol</topic><topic>Ethanol - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>hepatocytes</topic><topic>Humans</topic><topic>Kinetics</topic><topic>Liver - cytology</topic><topic>Liver - metabolism</topic><topic>Molecular and cellular biology</topic><topic>Orosomucoid - analogs & derivatives</topic><topic>Orosomucoid - metabolism</topic><topic>Rats</topic><topic>receptors</topic><topic>Receptors, Immunologic - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Casey, C.A.</creatorcontrib><creatorcontrib>Kragskow, S.L.</creatorcontrib><creatorcontrib>Sorrell, M.F.</creatorcontrib><creatorcontrib>Tuma, D.J.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Casey, C.A.</au><au>Kragskow, S.L.</au><au>Sorrell, M.F.</au><au>Tuma, D.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronic ethanol administration impairs the binding and endocytosis of asialo-orosomucoid in isolated hepatocytes</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1987-02-25</date><risdate>1987</risdate><volume>262</volume><issue>6</issue><spage>2704</spage><epage>2710</epage><pages>2704-2710</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><coden>JBCHA3</coden><abstract>We have examined the effect of ethanol administration on receptor-mediated endocytosis of asialo-orosomucoid by isolated hepatocytes. Significantly less ligand was bound, internalized, and degraded by hepatocytes isolated from rats fed an ethanol diet for 5-7 weeks than by cells isolated from chow-fed or pair-fed controls. Reduced binding was shown to be primarily due to a decreased number of cell surface receptors rather than to a lowered affinity of the receptor for its ligand. This reduction in cell surface receptors resulted in a marked inhibition of internalization and degradation of ligand by hepatocytes from the ethanol-fed rats. In addition, a defect in the initial stages of receptor-ligand internalization was also indicated, since less surface-bound ligand was internalized and subsequently degraded in cells from the ethanol-treated animals as compared to controls. Rates of internalization and degradation of internalized ligand were, however, similar for all three groups, suggesting that neither degradation per se nor rate of delivery of internalized ligand to the lysosomes was affected by ethanol feeding. Receptor recycling was impaired in ethanol-fed rats, as indicated by a decrease in the binding site number after stimulation of endocytosis for 120 min when compared to initial binding capacity. Receptor recycling was not impaired in hepatocytes from control animals. These results indicate that chronic ethanol feeding impairs the process of receptor-mediated endocytosis by the liver; the major cause of this impairment appears to be due to a decreased number of cell surface asialoglycoprotein receptors in the ethanol-fed animals, along with a decreased ability of these cells to internalize all of the surface-bound ligand.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>3818618</pmid><doi>10.1016/S0021-9258(18)61564-9</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals asialo-orosomucoid Asialoglycoprotein Receptor Asialoglycoproteins Binding Sites Biological and medical sciences Cell physiology cell surface Endocytosis ethanol Ethanol - pharmacology Fundamental and applied biological sciences. Psychology hepatocytes Humans Kinetics Liver - cytology Liver - metabolism Molecular and cellular biology Orosomucoid - analogs & derivatives Orosomucoid - metabolism Rats receptors Receptors, Immunologic - metabolism |
title | Chronic ethanol administration impairs the binding and endocytosis of asialo-orosomucoid in isolated hepatocytes |
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