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Liver fibrosis in vitro: Cell culture models and precision-cut liver slices
Chronic liver injury of various etiologies can cause liver fibrosis, which is characterized by the progressive accumulation of connective tissue in the liver. As no effective treatment for liver fibrosis is available yet, extensive research is ongoing to further study the mechanisms underlying the d...
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Published in: | Toxicology in vitro 2007-06, Vol.21 (4), p.545-557 |
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container_title | Toxicology in vitro |
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creator | Van de Bovenkamp, M. Groothuis, G.M.M. Meijer, D.K.F. Olinga, P. |
description | Chronic liver injury of various etiologies can cause liver fibrosis, which is characterized by the progressive accumulation of connective tissue in the liver. As no effective treatment for liver fibrosis is available yet, extensive research is ongoing to further study the mechanisms underlying the development of disease- or toxicity-induced liver fibrosis and to identify potential pro- or anti-fibrotic properties of compounds. This review gives an overview of the
in vitro methods that are currently available for this purpose. The first focus is on cell culture models, since the majority of
in vitro research uses these systems. Both primary cells and cell lines as well as the use of different culture matrices and co-culture models are discussed. Second, the use of precision-cut liver slices, which recently came into attention as
in vitro model for the study of fibrosis, is discussed. The overview clearly shows that continuous optimization and adaptation have extended the potential of
in vitro models for liver fibrosis during the past years. By combining the use of the different cell and tissue culture models, the mechanisms underlying multicellular fibrosis development can be studied
in vitro and potential pro- or anti-fibrotic properties of compounds can be identified both on single liver cell types and in human liver tissue. |
doi_str_mv | 10.1016/j.tiv.2006.12.009 |
format | article |
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in vitro methods that are currently available for this purpose. The first focus is on cell culture models, since the majority of
in vitro research uses these systems. Both primary cells and cell lines as well as the use of different culture matrices and co-culture models are discussed. Second, the use of precision-cut liver slices, which recently came into attention as
in vitro model for the study of fibrosis, is discussed. The overview clearly shows that continuous optimization and adaptation have extended the potential of
in vitro models for liver fibrosis during the past years. By combining the use of the different cell and tissue culture models, the mechanisms underlying multicellular fibrosis development can be studied
in vitro and potential pro- or anti-fibrotic properties of compounds can be identified both on single liver cell types and in human liver tissue.</description><identifier>ISSN: 0887-2333</identifier><identifier>EISSN: 1879-3177</identifier><identifier>DOI: 10.1016/j.tiv.2006.12.009</identifier><identifier>PMID: 17289342</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Cell Line ; Cell lines ; Cells, Cultured ; Coculture Techniques ; Cytological Techniques ; Extracellular matrix ; Extracellular Matrix - pathology ; Extracellular Matrix - physiology ; Fibrosis ; Hepatic stellate cells ; Hepatocytes - pathology ; Humans ; Liver Cirrhosis - pathology ; Organ Culture Techniques ; Precision-cut liver slices</subject><ispartof>Toxicology in vitro, 2007-06, Vol.21 (4), p.545-557</ispartof><rights>2007 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c407t-6414de4c58730c5b20cdd68998806610d5d9bceb6eed616ce2050ed4051cf0f63</citedby><cites>FETCH-LOGICAL-c407t-6414de4c58730c5b20cdd68998806610d5d9bceb6eed616ce2050ed4051cf0f63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17289342$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Van de Bovenkamp, M.</creatorcontrib><creatorcontrib>Groothuis, G.M.M.</creatorcontrib><creatorcontrib>Meijer, D.K.F.</creatorcontrib><creatorcontrib>Olinga, P.</creatorcontrib><title>Liver fibrosis in vitro: Cell culture models and precision-cut liver slices</title><title>Toxicology in vitro</title><addtitle>Toxicol In Vitro</addtitle><description>Chronic liver injury of various etiologies can cause liver fibrosis, which is characterized by the progressive accumulation of connective tissue in the liver. As no effective treatment for liver fibrosis is available yet, extensive research is ongoing to further study the mechanisms underlying the development of disease- or toxicity-induced liver fibrosis and to identify potential pro- or anti-fibrotic properties of compounds. This review gives an overview of the
in vitro methods that are currently available for this purpose. The first focus is on cell culture models, since the majority of
in vitro research uses these systems. Both primary cells and cell lines as well as the use of different culture matrices and co-culture models are discussed. Second, the use of precision-cut liver slices, which recently came into attention as
in vitro model for the study of fibrosis, is discussed. The overview clearly shows that continuous optimization and adaptation have extended the potential of
in vitro models for liver fibrosis during the past years. By combining the use of the different cell and tissue culture models, the mechanisms underlying multicellular fibrosis development can be studied
in vitro and potential pro- or anti-fibrotic properties of compounds can be identified both on single liver cell types and in human liver tissue.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Cell lines</subject><subject>Cells, Cultured</subject><subject>Coculture Techniques</subject><subject>Cytological Techniques</subject><subject>Extracellular matrix</subject><subject>Extracellular Matrix - pathology</subject><subject>Extracellular Matrix - physiology</subject><subject>Fibrosis</subject><subject>Hepatic stellate cells</subject><subject>Hepatocytes - pathology</subject><subject>Humans</subject><subject>Liver Cirrhosis - pathology</subject><subject>Organ Culture Techniques</subject><subject>Precision-cut liver slices</subject><issn>0887-2333</issn><issn>1879-3177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp9kDtPwzAUhS0EglL4ASzIE1vCtZ04Dkyo4iUqscBsJfaN5CqPYieR-Pe4tBIb012-c3TuR8gVg5QBk7ebdHRzygFkyngKUB6RBVNFmQhWFMdkAUoVCRdCnJHzEDYAkCsOp-SMFVyVIuML8rZ2M3rauNoPwQXqejq70Q93dIVtS83UjpNH2g0W20Cr3tKtR-OCG_rETCNtf-OhdQbDBTlpqjbg5eEuyefT48fqJVm_P7-uHtaJyaAYE5mxzGJmclUIMHnNwVgrVVkqBVIysLkta4O1RLSSSYMcckCbQc5MA40US3Kz79364WvCMOrOBRPnVj0OU9AcGAeViQiyPWjic8Fjo7fedZX_1gz0zqDe6GhQ7wxqxnU0GDPXh_Kp7tD-JQ7KInC_B6IQnB16HYzD3qB10cyo7eD-qf8B13mBSQ</recordid><startdate>20070601</startdate><enddate>20070601</enddate><creator>Van de Bovenkamp, M.</creator><creator>Groothuis, G.M.M.</creator><creator>Meijer, D.K.F.</creator><creator>Olinga, P.</creator><general>Elsevier Ltd</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>7QO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20070601</creationdate><title>Liver fibrosis in vitro: Cell culture models and precision-cut liver slices</title><author>Van de Bovenkamp, M. ; Groothuis, G.M.M. ; Meijer, D.K.F. ; Olinga, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c407t-6414de4c58730c5b20cdd68998806610d5d9bceb6eed616ce2050ed4051cf0f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Cell lines</topic><topic>Cells, Cultured</topic><topic>Coculture Techniques</topic><topic>Cytological Techniques</topic><topic>Extracellular matrix</topic><topic>Extracellular Matrix - pathology</topic><topic>Extracellular Matrix - physiology</topic><topic>Fibrosis</topic><topic>Hepatic stellate cells</topic><topic>Hepatocytes - pathology</topic><topic>Humans</topic><topic>Liver Cirrhosis - pathology</topic><topic>Organ Culture Techniques</topic><topic>Precision-cut liver slices</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Van de Bovenkamp, M.</creatorcontrib><creatorcontrib>Groothuis, G.M.M.</creatorcontrib><creatorcontrib>Meijer, D.K.F.</creatorcontrib><creatorcontrib>Olinga, P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Toxicology in vitro</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Van de Bovenkamp, M.</au><au>Groothuis, G.M.M.</au><au>Meijer, D.K.F.</au><au>Olinga, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Liver fibrosis in vitro: Cell culture models and precision-cut liver slices</atitle><jtitle>Toxicology in vitro</jtitle><addtitle>Toxicol In Vitro</addtitle><date>2007-06-01</date><risdate>2007</risdate><volume>21</volume><issue>4</issue><spage>545</spage><epage>557</epage><pages>545-557</pages><issn>0887-2333</issn><eissn>1879-3177</eissn><abstract>Chronic liver injury of various etiologies can cause liver fibrosis, which is characterized by the progressive accumulation of connective tissue in the liver. As no effective treatment for liver fibrosis is available yet, extensive research is ongoing to further study the mechanisms underlying the development of disease- or toxicity-induced liver fibrosis and to identify potential pro- or anti-fibrotic properties of compounds. This review gives an overview of the
in vitro methods that are currently available for this purpose. The first focus is on cell culture models, since the majority of
in vitro research uses these systems. Both primary cells and cell lines as well as the use of different culture matrices and co-culture models are discussed. Second, the use of precision-cut liver slices, which recently came into attention as
in vitro model for the study of fibrosis, is discussed. The overview clearly shows that continuous optimization and adaptation have extended the potential of
in vitro models for liver fibrosis during the past years. By combining the use of the different cell and tissue culture models, the mechanisms underlying multicellular fibrosis development can be studied
in vitro and potential pro- or anti-fibrotic properties of compounds can be identified both on single liver cell types and in human liver tissue.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>17289342</pmid><doi>10.1016/j.tiv.2006.12.009</doi><tpages>13</tpages></addata></record> |
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subjects | Animals Cell Line Cell lines Cells, Cultured Coculture Techniques Cytological Techniques Extracellular matrix Extracellular Matrix - pathology Extracellular Matrix - physiology Fibrosis Hepatic stellate cells Hepatocytes - pathology Humans Liver Cirrhosis - pathology Organ Culture Techniques Precision-cut liver slices |
title | Liver fibrosis in vitro: Cell culture models and precision-cut liver slices |
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