Development of a New Conditionally Immortalized Human Liver Sinusoidal Endothelial Cells
Liver sinusoidal endothelial cells (LSECs), which are specialized endothelial cells that line liver sinusoids, have been reported to participate in a variety of liver functions, such as blood macromolecule clearance and factor VIII production. In addition, LSECs play crucial roles in liver regenerat...
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Veröffentlicht in: | Biological & pharmaceutical bulletin 2018/03/01, Vol.41(3), pp.440-444 |
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creator | Zhu, Meiyan Koibuchi, Akira Ide, Hideyuki Morio, Hanae Shibuya, Minaka Kamiichi, Atsuko Tsubota, Akihito Anzai, Naohiko Akita, Hidetaka Chiba, Kan Furihata, Tomomi |
description | Liver sinusoidal endothelial cells (LSECs), which are specialized endothelial cells that line liver sinusoids, have been reported to participate in a variety of liver functions, such as blood macromolecule clearance and factor VIII production. In addition, LSECs play crucial roles in liver regeneration following acute liver injury, as well as the development and progression of liver diseases or drug-induced hepatotoxicity. However, the molecular mechanisms underlying their roles remain mostly unknown. Therefore, in order to contribute to the clarification of those mechanisms, herein we report on the development of a new immortalized human LSEC (HLSEC) line. To produce this cell line, two immortalized genes were introduced into the primary HLSECs, which eventually resulted in the establishment of the HLSEC/conditionally immortalized, clone-J (HLSEC/ciJ). Consistent with the two-immortalized gene expression, HLSEC/ciJ showed excellent proliferation activity. Additionally, the results of gene expression analyses showed that several LSEC (as well as pan-endothelial) marker mRNAs and proteins were clearly expressed in HLSEC/ciJ. Furthermore, we found that adherence junction proteins were localized at the cell border in the HLSEC/ciJ monolayer, and that the cells exhibited a tube-like structure formation property. Taken together, the results obtained thus far indicate that we have successfully immortalized HLSECs, resulting in creation of HLSEC/ciJ, a cell line that possesses infinite proliferation ability while retaining possession of at least some HLSEC features. We believe that the HLSEC/ciJ have the potential to provide a valuable and unlimited alternative source of HLSECs for use in liver/LSEC physiology/pathophysiology, pharmacology, and toxicology studies. |
doi_str_mv | 10.1248/bpb.b17-00661 |
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In addition, LSECs play crucial roles in liver regeneration following acute liver injury, as well as the development and progression of liver diseases or drug-induced hepatotoxicity. However, the molecular mechanisms underlying their roles remain mostly unknown. Therefore, in order to contribute to the clarification of those mechanisms, herein we report on the development of a new immortalized human LSEC (HLSEC) line. To produce this cell line, two immortalized genes were introduced into the primary HLSECs, which eventually resulted in the establishment of the HLSEC/conditionally immortalized, clone-J (HLSEC/ciJ). Consistent with the two-immortalized gene expression, HLSEC/ciJ showed excellent proliferation activity. Additionally, the results of gene expression analyses showed that several LSEC (as well as pan-endothelial) marker mRNAs and proteins were clearly expressed in HLSEC/ciJ. Furthermore, we found that adherence junction proteins were localized at the cell border in the HLSEC/ciJ monolayer, and that the cells exhibited a tube-like structure formation property. Taken together, the results obtained thus far indicate that we have successfully immortalized HLSECs, resulting in creation of HLSEC/ciJ, a cell line that possesses infinite proliferation ability while retaining possession of at least some HLSEC features. We believe that the HLSEC/ciJ have the potential to provide a valuable and unlimited alternative source of HLSECs for use in liver/LSEC physiology/pathophysiology, pharmacology, and toxicology studies.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.b17-00661</identifier><identifier>PMID: 29491221</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Coagulation factors ; Endothelial cells ; Gene expression ; Hepatocytes ; Hepatotoxicity ; immortalized cell ; in vitro liver model ; Liver ; Liver diseases ; liver sinusoidal endothelial cell ; Molecular modelling ; Pharmacology ; Proteins ; Toxicology</subject><ispartof>Biological and Pharmaceutical Bulletin, 2018/03/01, Vol.41(3), pp.440-444</ispartof><rights>2018 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c702t-ddb65af9e6f53513b7567c831c0914c18edb0cde01da351c52c3576c581dddc03</citedby><cites>FETCH-LOGICAL-c702t-ddb65af9e6f53513b7567c831c0914c18edb0cde01da351c52c3576c581dddc03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1883,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29491221$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Meiyan</creatorcontrib><creatorcontrib>Koibuchi, Akira</creatorcontrib><creatorcontrib>Ide, Hideyuki</creatorcontrib><creatorcontrib>Morio, Hanae</creatorcontrib><creatorcontrib>Shibuya, Minaka</creatorcontrib><creatorcontrib>Kamiichi, Atsuko</creatorcontrib><creatorcontrib>Tsubota, Akihito</creatorcontrib><creatorcontrib>Anzai, Naohiko</creatorcontrib><creatorcontrib>Akita, Hidetaka</creatorcontrib><creatorcontrib>Chiba, Kan</creatorcontrib><creatorcontrib>Furihata, Tomomi</creatorcontrib><creatorcontrib>Research Center for Medical Science</creatorcontrib><creatorcontrib>and (cCore Research Facilities for Basic Science (Division of Molecular Cell Biology</creatorcontrib><creatorcontrib>bDepartment of Pharmacology</creatorcontrib><creatorcontrib>The Jikei University School of Medicine</creatorcontrib><creatorcontrib>Graduate School of Pharmaceutical Sciences</creatorcontrib><creatorcontrib>Chiba University</creatorcontrib><creatorcontrib>Graduate School of Medicine</creatorcontrib><creatorcontrib>Chiba Uiversity</creatorcontrib><creatorcontrib>aLaboratory of Pharmacology and Toxicology</creatorcontrib><title>Development of a New Conditionally Immortalized Human Liver Sinusoidal Endothelial Cells</title><title>Biological & pharmaceutical bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>Liver sinusoidal endothelial cells (LSECs), which are specialized endothelial cells that line liver sinusoids, have been reported to participate in a variety of liver functions, such as blood macromolecule clearance and factor VIII production. In addition, LSECs play crucial roles in liver regeneration following acute liver injury, as well as the development and progression of liver diseases or drug-induced hepatotoxicity. However, the molecular mechanisms underlying their roles remain mostly unknown. Therefore, in order to contribute to the clarification of those mechanisms, herein we report on the development of a new immortalized human LSEC (HLSEC) line. To produce this cell line, two immortalized genes were introduced into the primary HLSECs, which eventually resulted in the establishment of the HLSEC/conditionally immortalized, clone-J (HLSEC/ciJ). Consistent with the two-immortalized gene expression, HLSEC/ciJ showed excellent proliferation activity. Additionally, the results of gene expression analyses showed that several LSEC (as well as pan-endothelial) marker mRNAs and proteins were clearly expressed in HLSEC/ciJ. Furthermore, we found that adherence junction proteins were localized at the cell border in the HLSEC/ciJ monolayer, and that the cells exhibited a tube-like structure formation property. Taken together, the results obtained thus far indicate that we have successfully immortalized HLSECs, resulting in creation of HLSEC/ciJ, a cell line that possesses infinite proliferation ability while retaining possession of at least some HLSEC features. We believe that the HLSEC/ciJ have the potential to provide a valuable and unlimited alternative source of HLSECs for use in liver/LSEC physiology/pathophysiology, pharmacology, and toxicology studies.</description><subject>Coagulation factors</subject><subject>Endothelial cells</subject><subject>Gene expression</subject><subject>Hepatocytes</subject><subject>Hepatotoxicity</subject><subject>immortalized cell</subject><subject>in vitro liver model</subject><subject>Liver</subject><subject>Liver diseases</subject><subject>liver sinusoidal endothelial cell</subject><subject>Molecular modelling</subject><subject>Pharmacology</subject><subject>Proteins</subject><subject>Toxicology</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdkM1v1DAQxS0EotvCkSuKxIVLisefyRFtS1tpBQdA4mY5tkO9cuzFTorKX19vtywSl7Gl99ObNw-hN4DPgbDuw7AbzgeQLcZCwDO0Aspkywnw52iFe-haAbw7QaelbDHGEhP6Ep2QnvVACKzQjwt350LaTS7OTRob3Xx2v5t1itbPPkUdwn1zM00pzzr4P84218ukY7Pxdy43X31cSvJWh-Yy2jTfuuDrf-1CKK_Qi1GH4l4_vWfo-6fLb-vrdvPl6mb9cdOammVurR0E12PvxMgpBzpILqTpKJganhnonB2wsQ6D1VU3nBjKpTC8A2utwfQMvT_47nL6tbgyq8kXUxPo6NJSFMG450IQ2lX03X_oNi253lgpwoASITtWqfZAmZxKyW5Uu-wnne8VYLWvXNXKVa1cPVZe-bdPrsswOXuk_3ZcgasDUFVvdEgx-Oj-7TZFDj6FVKNCV00ZYKowAYUZw_vBKKZSUlKd1genbZn1T3dcpfPsTXCPwRgouh_HgEfV3OqsXKQP0x-qXQ</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Zhu, Meiyan</creator><creator>Koibuchi, Akira</creator><creator>Ide, Hideyuki</creator><creator>Morio, Hanae</creator><creator>Shibuya, Minaka</creator><creator>Kamiichi, Atsuko</creator><creator>Tsubota, Akihito</creator><creator>Anzai, Naohiko</creator><creator>Akita, Hidetaka</creator><creator>Chiba, Kan</creator><creator>Furihata, Tomomi</creator><general>The Pharmaceutical Society of Japan</general><general>Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>2018</creationdate><title>Development of a New Conditionally Immortalized Human Liver Sinusoidal Endothelial Cells</title><author>Zhu, Meiyan ; 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In addition, LSECs play crucial roles in liver regeneration following acute liver injury, as well as the development and progression of liver diseases or drug-induced hepatotoxicity. However, the molecular mechanisms underlying their roles remain mostly unknown. Therefore, in order to contribute to the clarification of those mechanisms, herein we report on the development of a new immortalized human LSEC (HLSEC) line. To produce this cell line, two immortalized genes were introduced into the primary HLSECs, which eventually resulted in the establishment of the HLSEC/conditionally immortalized, clone-J (HLSEC/ciJ). Consistent with the two-immortalized gene expression, HLSEC/ciJ showed excellent proliferation activity. Additionally, the results of gene expression analyses showed that several LSEC (as well as pan-endothelial) marker mRNAs and proteins were clearly expressed in HLSEC/ciJ. Furthermore, we found that adherence junction proteins were localized at the cell border in the HLSEC/ciJ monolayer, and that the cells exhibited a tube-like structure formation property. Taken together, the results obtained thus far indicate that we have successfully immortalized HLSECs, resulting in creation of HLSEC/ciJ, a cell line that possesses infinite proliferation ability while retaining possession of at least some HLSEC features. We believe that the HLSEC/ciJ have the potential to provide a valuable and unlimited alternative source of HLSECs for use in liver/LSEC physiology/pathophysiology, pharmacology, and toxicology studies.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>29491221</pmid><doi>10.1248/bpb.b17-00661</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; EZB-FREE-00999 freely available EZB journals; Free Full-Text Journals in Chemistry |
subjects | Coagulation factors Endothelial cells Gene expression Hepatocytes Hepatotoxicity immortalized cell in vitro liver model Liver Liver diseases liver sinusoidal endothelial cell Molecular modelling Pharmacology Proteins Toxicology |
title | Development of a New Conditionally Immortalized Human Liver Sinusoidal Endothelial Cells |
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