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Synthesis and Secretion of Lipoproteins by Human Hepatocytes in Culture

Confluent monolayers of normal human hepatocytes obtained by collagenase perfusion of liver fragments were incubated in a serum-free medium. Intracellular apolipoproteins apo AI, apo C, apo B, and apo E were detected between Day 1 and Day 6 of the culture by immunoenzymatic staining using polyclonal...

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Published in:In Vitro Cellular & Developmental Biology 1988-02, Vol.24 (2), p.85-90
Main Authors: M. E. Bouma, M. Pessah, Renaud, G., N. Amit, D. Catala, R. Infante
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description Confluent monolayers of normal human hepatocytes obtained by collagenase perfusion of liver fragments were incubated in a serum-free medium. Intracellular apolipoproteins apo AI, apo C, apo B, and apo E were detected between Day 1 and Day 6 of the culture by immunoenzymatic staining using polyclonal antibodies directed against these apoproteins and monoclonal antibodies directed against both forms of apo B (B100 and B48). Translation of mRNA isolated from these hepatocytes in an acellular system revealed that apo AI and apo E were synthesized as the precusor forms of mature plasma apo AI and apo E. Three lipoprotein fractions corresponding to the density of very low density lipoprotein (VLDL), low density lipoprotein (LDL), and high density lipoprotein (HDL) were isolated from the medium at Day 5 of culture and examined by electron microscopy after negative staining. VLDL and LDL particles are similar in size and shape to plasma lipoproteins; spherical HDL are larger than normal plasma particles isolated at the same density. Their protein represented 44, 19.5, and 36.5% respectively, of the total lipoprotein protein. The secretion rate of VLDL protein corresponded to that measured in primary cultures of rat hepatocytes. After incorporation of$[^3H]glycerol$, more than 92% of the$[^3H]triglyceride$secreted into the medium was recovered in the VLDL fraction. These results demonstrate that primary cultures of normal human hepatocytes are able to synthesize and secrete lipoproteins and thus could be a useful model to study lipoprotein metabolism in human liver.
doi_str_mv 10.1007/BF02623884
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E. Bouma ; M. Pessah ; Renaud, G. ; N. Amit ; D. Catala ; R. Infante</creator><creatorcontrib>M. E. Bouma ; M. Pessah ; Renaud, G. ; N. Amit ; D. Catala ; R. Infante</creatorcontrib><description>Confluent monolayers of normal human hepatocytes obtained by collagenase perfusion of liver fragments were incubated in a serum-free medium. Intracellular apolipoproteins apo AI, apo C, apo B, and apo E were detected between Day 1 and Day 6 of the culture by immunoenzymatic staining using polyclonal antibodies directed against these apoproteins and monoclonal antibodies directed against both forms of apo B (B100 and B48). Translation of mRNA isolated from these hepatocytes in an acellular system revealed that apo AI and apo E were synthesized as the precusor forms of mature plasma apo AI and apo E. Three lipoprotein fractions corresponding to the density of very low density lipoprotein (VLDL), low density lipoprotein (LDL), and high density lipoprotein (HDL) were isolated from the medium at Day 5 of culture and examined by electron microscopy after negative staining. VLDL and LDL particles are similar in size and shape to plasma lipoproteins; spherical HDL are larger than normal plasma particles isolated at the same density. Their protein represented 44, 19.5, and 36.5% respectively, of the total lipoprotein protein. The secretion rate of VLDL protein corresponded to that measured in primary cultures of rat hepatocytes. After incorporation of$[^3H]glycerol$, more than 92% of the$[^3H]triglyceride$secreted into the medium was recovered in the VLDL fraction. 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Hybridization. Fusion ; Cell Survival ; Cells, Cultured ; Electrophoresis, Polyacrylamide Gel ; Eukaryotic cell cultures ; Fundamental and applied biological sciences. Psychology ; HDL lipoproteins ; Hepatocellular carcinoma ; Hepatocytes ; Histocytochemistry ; Humans ; Immunoassay ; Immunoenzyme Techniques ; Lipids ; Lipoproteins ; Lipoproteins - biosynthesis ; Lipoproteins - secretion ; Lipoproteins, HDL - biosynthesis ; Lipoproteins, HDL - secretion ; Lipoproteins, LDL - biosynthesis ; Lipoproteins, LDL - secretion ; Lipoproteins, VLDL - biosynthesis ; Lipoproteins, VLDL - secretion ; Liver ; Liver - cytology ; Liver - metabolism ; Liver - secretion ; Methods. Procedures. 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E. Bouma</creatorcontrib><creatorcontrib>M. Pessah</creatorcontrib><creatorcontrib>Renaud, G.</creatorcontrib><creatorcontrib>N. Amit</creatorcontrib><creatorcontrib>D. Catala</creatorcontrib><creatorcontrib>R. Infante</creatorcontrib><title>Synthesis and Secretion of Lipoproteins by Human Hepatocytes in Culture</title><title>In Vitro Cellular &amp; Developmental Biology</title><addtitle>In Vitro Cell Dev Biol</addtitle><description>Confluent monolayers of normal human hepatocytes obtained by collagenase perfusion of liver fragments were incubated in a serum-free medium. Intracellular apolipoproteins apo AI, apo C, apo B, and apo E were detected between Day 1 and Day 6 of the culture by immunoenzymatic staining using polyclonal antibodies directed against these apoproteins and monoclonal antibodies directed against both forms of apo B (B100 and B48). Translation of mRNA isolated from these hepatocytes in an acellular system revealed that apo AI and apo E were synthesized as the precusor forms of mature plasma apo AI and apo E. Three lipoprotein fractions corresponding to the density of very low density lipoprotein (VLDL), low density lipoprotein (LDL), and high density lipoprotein (HDL) were isolated from the medium at Day 5 of culture and examined by electron microscopy after negative staining. VLDL and LDL particles are similar in size and shape to plasma lipoproteins; spherical HDL are larger than normal plasma particles isolated at the same density. Their protein represented 44, 19.5, and 36.5% respectively, of the total lipoprotein protein. The secretion rate of VLDL protein corresponded to that measured in primary cultures of rat hepatocytes. After incorporation of$[^3H]glycerol$, more than 92% of the$[^3H]triglyceride$secreted into the medium was recovered in the VLDL fraction. 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Fusion</topic><topic>Cell Survival</topic><topic>Cells, Cultured</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Eukaryotic cell cultures</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>HDL lipoproteins</topic><topic>Hepatocellular carcinoma</topic><topic>Hepatocytes</topic><topic>Histocytochemistry</topic><topic>Humans</topic><topic>Immunoassay</topic><topic>Immunoenzyme Techniques</topic><topic>Lipids</topic><topic>Lipoproteins</topic><topic>Lipoproteins - biosynthesis</topic><topic>Lipoproteins - secretion</topic><topic>Lipoproteins, HDL - biosynthesis</topic><topic>Lipoproteins, HDL - secretion</topic><topic>Lipoproteins, LDL - biosynthesis</topic><topic>Lipoproteins, LDL - secretion</topic><topic>Lipoproteins, VLDL - biosynthesis</topic><topic>Lipoproteins, VLDL - secretion</topic><topic>Liver</topic><topic>Liver - cytology</topic><topic>Liver - metabolism</topic><topic>Liver - secretion</topic><topic>Methods. Procedures. Technologies</topic><topic>Miscellaneous</topic><topic>Models, Biological</topic><topic>Molecular and cellular biology</topic><topic>Monoclonal antibodies</topic><topic>Polyclonal antibodies</topic><topic>Protein Biosynthesis</topic><topic>RNA, Messenger - genetics</topic><topic>Secretion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>M. E. Bouma</creatorcontrib><creatorcontrib>M. Pessah</creatorcontrib><creatorcontrib>Renaud, G.</creatorcontrib><creatorcontrib>N. Amit</creatorcontrib><creatorcontrib>D. Catala</creatorcontrib><creatorcontrib>R. 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Infante</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Secretion of Lipoproteins by Human Hepatocytes in Culture</atitle><jtitle>In Vitro Cellular &amp; Developmental Biology</jtitle><addtitle>In Vitro Cell Dev Biol</addtitle><date>1988-02-01</date><risdate>1988</risdate><volume>24</volume><issue>2</issue><spage>85</spage><epage>90</epage><pages>85-90</pages><issn>0883-8364</issn><eissn>2327-431X</eissn><eissn>1475-2689</eissn><coden>ICDBEO</coden><abstract>Confluent monolayers of normal human hepatocytes obtained by collagenase perfusion of liver fragments were incubated in a serum-free medium. Intracellular apolipoproteins apo AI, apo C, apo B, and apo E were detected between Day 1 and Day 6 of the culture by immunoenzymatic staining using polyclonal antibodies directed against these apoproteins and monoclonal antibodies directed against both forms of apo B (B100 and B48). Translation of mRNA isolated from these hepatocytes in an acellular system revealed that apo AI and apo E were synthesized as the precusor forms of mature plasma apo AI and apo E. Three lipoprotein fractions corresponding to the density of very low density lipoprotein (VLDL), low density lipoprotein (LDL), and high density lipoprotein (HDL) were isolated from the medium at Day 5 of culture and examined by electron microscopy after negative staining. VLDL and LDL particles are similar in size and shape to plasma lipoproteins; spherical HDL are larger than normal plasma particles isolated at the same density. Their protein represented 44, 19.5, and 36.5% respectively, of the total lipoprotein protein. The secretion rate of VLDL protein corresponded to that measured in primary cultures of rat hepatocytes. After incorporation of$[^3H]glycerol$, more than 92% of the$[^3H]triglyceride$secreted into the medium was recovered in the VLDL fraction. These results demonstrate that primary cultures of normal human hepatocytes are able to synthesize and secrete lipoproteins and thus could be a useful model to study lipoprotein metabolism in human liver.</abstract><cop>Largo, MD</cop><pub>Tissue Culture Association, Inc</pub><pmid>3125144</pmid><doi>10.1007/BF02623884</doi><tpages>6</tpages></addata></record>
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identifier ISSN: 0883-8364
ispartof In Vitro Cellular & Developmental Biology, 1988-02, Vol.24 (2), p.85-90
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source Access via JSTOR; Springer LINK Archives
subjects Animal cells
Apolipoprotein A-I
Apolipoproteins - biosynthesis
Apolipoproteins - secretion
Apolipoproteins A - biosynthesis
Apolipoproteins A - secretion
Apolipoproteins B - biosynthesis
Apolipoproteins B - secretion
Apolipoproteins C - biosynthesis
Apolipoproteins C - secretion
Apolipoproteins E - biosynthesis
Apolipoproteins E - secretion
Apoproteins
Autoradiography
Biological and medical sciences
Biotechnology
Cell cultures. Hybridization. Fusion
Cell Survival
Cells, Cultured
Electrophoresis, Polyacrylamide Gel
Eukaryotic cell cultures
Fundamental and applied biological sciences. Psychology
HDL lipoproteins
Hepatocellular carcinoma
Hepatocytes
Histocytochemistry
Humans
Immunoassay
Immunoenzyme Techniques
Lipids
Lipoproteins
Lipoproteins - biosynthesis
Lipoproteins - secretion
Lipoproteins, HDL - biosynthesis
Lipoproteins, HDL - secretion
Lipoproteins, LDL - biosynthesis
Lipoproteins, LDL - secretion
Lipoproteins, VLDL - biosynthesis
Lipoproteins, VLDL - secretion
Liver
Liver - cytology
Liver - metabolism
Liver - secretion
Methods. Procedures. Technologies
Miscellaneous
Models, Biological
Molecular and cellular biology
Monoclonal antibodies
Polyclonal antibodies
Protein Biosynthesis
RNA, Messenger - genetics
Secretion
title Synthesis and Secretion of Lipoproteins by Human Hepatocytes in Culture
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