Bovine and porcine fibroblasts can be immortalized with intact karyotype by the expression of mutant cyclin dependent kinase 4, cyclin D, and telomerase
•Mutant CDK4, cyclin D1, and hTERT immortalize bovine and porcine fibroblasts.•Immortalized fibroblasts maintained normal diploid karyotypes at 98–100%.•Immortalized livestock cells indicate conserved cell cycle networks across species. Cattle and pigs comprise the most economically important livest...
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Veröffentlicht in: | Journal of biotechnology 2014-04, Vol.176, p.50-57 |
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creator | Donai, Kenichiro Kiyono, Tohru Eitsuka, Takahiro Guo, Yijie Kuroda, Kengo Sone, Hideko Isogai, Emiko Fukuda, Tomokazu |
description | •Mutant CDK4, cyclin D1, and hTERT immortalize bovine and porcine fibroblasts.•Immortalized fibroblasts maintained normal diploid karyotypes at 98–100%.•Immortalized livestock cells indicate conserved cell cycle networks across species.
Cattle and pigs comprise the most economically important livestock. Despite their importance, cultured cells from these species, which are useful for physiological analyses, are quite limited in cell banks. One of the reasons for the limited number of cell lines is the difficulty in their establishment. To overcome limitations in cell-line establishment, we attempted to immortalize bovine and porcine fibroblasts by transduction of multiple cell cycle regulators (mutant cyclin dependent kinase 4, cyclin D and telomerase reverse transcriptase). The transduced cells continued to display a stable proliferation rate and did not show cellular senescence. Furthermore, cell cycle assays showed that induction of these exogenous genes enhanced turnover of the cell cycle, especially at the G1-S phase. Furthermore, our established cell lines maintained normal diploid karyotypes at 98–100%. Our study demonstrated that bypassing p16/Rb-mediated cell arrest and activation of telomerase activity enabled efficient establishment of immortalized bovine- and porcine-derived fibroblasts. The high efficiency of establishing cell lines suggests that the networks of cell cycle regulators, especially p16/Rb-associated cell cycle arrest, have been conserved during evolution of humans, cattle, and pigs. |
doi_str_mv | 10.1016/j.jbiotec.2014.02.017 |
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Cattle and pigs comprise the most economically important livestock. Despite their importance, cultured cells from these species, which are useful for physiological analyses, are quite limited in cell banks. One of the reasons for the limited number of cell lines is the difficulty in their establishment. To overcome limitations in cell-line establishment, we attempted to immortalize bovine and porcine fibroblasts by transduction of multiple cell cycle regulators (mutant cyclin dependent kinase 4, cyclin D and telomerase reverse transcriptase). The transduced cells continued to display a stable proliferation rate and did not show cellular senescence. Furthermore, cell cycle assays showed that induction of these exogenous genes enhanced turnover of the cell cycle, especially at the G1-S phase. Furthermore, our established cell lines maintained normal diploid karyotypes at 98–100%. Our study demonstrated that bypassing p16/Rb-mediated cell arrest and activation of telomerase activity enabled efficient establishment of immortalized bovine- and porcine-derived fibroblasts. The high efficiency of establishing cell lines suggests that the networks of cell cycle regulators, especially p16/Rb-associated cell cycle arrest, have been conserved during evolution of humans, cattle, and pigs.</description><identifier>ISSN: 0168-1656</identifier><identifier>EISSN: 1873-4863</identifier><identifier>DOI: 10.1016/j.jbiotec.2014.02.017</identifier><identifier>PMID: 24589663</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Activation ; Animals ; Biotechnology ; Cattle ; Cell Cycle ; Cell Line ; Cell Proliferation ; Cellular ; Cellular senescence ; Cyclin D - genetics ; Cyclin D - metabolism ; Cyclin-Dependent Kinase 4 - genetics ; Cyclin-Dependent Kinase 4 - metabolism ; Diploidy ; Economics ; Embryo, Mammalian - cytology ; Fibroblasts ; Fibroblasts - cytology ; Fibroblasts - metabolism ; Immortalization ; Karyotype ; Kinases ; Livestock ; Regulators ; Swine ; Telomerase ; Telomerase - genetics ; Telomerase - metabolism ; Transduction, Genetic</subject><ispartof>Journal of biotechnology, 2014-04, Vol.176, p.50-57</ispartof><rights>2014 Elsevier B.V.</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-d0e4af3447a778c6ceac7d9f28340a3dfa4d0005a13b36052db7c94f49502d543</citedby><cites>FETCH-LOGICAL-c501t-d0e4af3447a778c6ceac7d9f28340a3dfa4d0005a13b36052db7c94f49502d543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jbiotec.2014.02.017$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24589663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Donai, Kenichiro</creatorcontrib><creatorcontrib>Kiyono, Tohru</creatorcontrib><creatorcontrib>Eitsuka, Takahiro</creatorcontrib><creatorcontrib>Guo, Yijie</creatorcontrib><creatorcontrib>Kuroda, Kengo</creatorcontrib><creatorcontrib>Sone, Hideko</creatorcontrib><creatorcontrib>Isogai, Emiko</creatorcontrib><creatorcontrib>Fukuda, Tomokazu</creatorcontrib><title>Bovine and porcine fibroblasts can be immortalized with intact karyotype by the expression of mutant cyclin dependent kinase 4, cyclin D, and telomerase</title><title>Journal of biotechnology</title><addtitle>J Biotechnol</addtitle><description>•Mutant CDK4, cyclin D1, and hTERT immortalize bovine and porcine fibroblasts.•Immortalized fibroblasts maintained normal diploid karyotypes at 98–100%.•Immortalized livestock cells indicate conserved cell cycle networks across species.
Cattle and pigs comprise the most economically important livestock. Despite their importance, cultured cells from these species, which are useful for physiological analyses, are quite limited in cell banks. One of the reasons for the limited number of cell lines is the difficulty in their establishment. To overcome limitations in cell-line establishment, we attempted to immortalize bovine and porcine fibroblasts by transduction of multiple cell cycle regulators (mutant cyclin dependent kinase 4, cyclin D and telomerase reverse transcriptase). The transduced cells continued to display a stable proliferation rate and did not show cellular senescence. Furthermore, cell cycle assays showed that induction of these exogenous genes enhanced turnover of the cell cycle, especially at the G1-S phase. Furthermore, our established cell lines maintained normal diploid karyotypes at 98–100%. Our study demonstrated that bypassing p16/Rb-mediated cell arrest and activation of telomerase activity enabled efficient establishment of immortalized bovine- and porcine-derived fibroblasts. The high efficiency of establishing cell lines suggests that the networks of cell cycle regulators, especially p16/Rb-associated cell cycle arrest, have been conserved during evolution of humans, cattle, and pigs.</description><subject>Activation</subject><subject>Animals</subject><subject>Biotechnology</subject><subject>Cattle</subject><subject>Cell Cycle</subject><subject>Cell Line</subject><subject>Cell Proliferation</subject><subject>Cellular</subject><subject>Cellular senescence</subject><subject>Cyclin D - genetics</subject><subject>Cyclin D - metabolism</subject><subject>Cyclin-Dependent Kinase 4 - genetics</subject><subject>Cyclin-Dependent Kinase 4 - metabolism</subject><subject>Diploidy</subject><subject>Economics</subject><subject>Embryo, Mammalian - cytology</subject><subject>Fibroblasts</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - metabolism</subject><subject>Immortalization</subject><subject>Karyotype</subject><subject>Kinases</subject><subject>Livestock</subject><subject>Regulators</subject><subject>Swine</subject><subject>Telomerase</subject><subject>Telomerase - genetics</subject><subject>Telomerase - metabolism</subject><subject>Transduction, Genetic</subject><issn>0168-1656</issn><issn>1873-4863</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctu1DAUhi0EotPCI4C8ZNEMvsbJCtFSLlIlNrC2HPtE9TSxg-0pDE_C4-Jhpmxn5SOf79z-H6FXlKwpoe3bzXoz-FjArhmhYk3YmlD1BK1op3gjupY_RavKdQ1tZXuGznPeEEJEL-lzdMaE7Pq25Sv05yo--ADYBIeXmOw-Hv2Q4jCZXDK2JuABsJ_nmIqZ_G9w-Kcvd9iHYmzB9ybtYtktgIcdLneA4deSIGcfA44jnrfFhILtzk4-YAcLBAf1494HkwGLy8fUh8t_KxSY4gyp5l6gZ6OZMrw8vhfo-8ebb9efm9uvn75cv79trCS0NI6AMCMXQhmlOttaMFa5fmQdF8RwNxrh6t3SUD7wlkjmBmV7MVYhCHNS8Av05tB3SfHHFnLRs88WpskEiNusq4RS9ZRUtU6jquWtrPhpVFLGmOr7fVd5QG2KOScY9ZL8XGXVlOi91Xqjj1brvdWaMF2trnWvjyO2wwzuf9WjtxV4dwCgyvfgIelsPQQLziewRbvoT4z4Cy2rvog</recordid><startdate>20140420</startdate><enddate>20140420</enddate><creator>Donai, Kenichiro</creator><creator>Kiyono, Tohru</creator><creator>Eitsuka, Takahiro</creator><creator>Guo, Yijie</creator><creator>Kuroda, Kengo</creator><creator>Sone, Hideko</creator><creator>Isogai, Emiko</creator><creator>Fukuda, Tomokazu</creator><general>Elsevier B.V</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>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7U5</scope><scope>L7M</scope></search><sort><creationdate>20140420</creationdate><title>Bovine and porcine fibroblasts can be immortalized with intact karyotype by the expression of mutant cyclin dependent kinase 4, cyclin D, and telomerase</title><author>Donai, Kenichiro ; Kiyono, Tohru ; Eitsuka, Takahiro ; Guo, Yijie ; Kuroda, Kengo ; Sone, Hideko ; Isogai, Emiko ; Fukuda, Tomokazu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-d0e4af3447a778c6ceac7d9f28340a3dfa4d0005a13b36052db7c94f49502d543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Activation</topic><topic>Animals</topic><topic>Biotechnology</topic><topic>Cattle</topic><topic>Cell Cycle</topic><topic>Cell Line</topic><topic>Cell Proliferation</topic><topic>Cellular</topic><topic>Cellular senescence</topic><topic>Cyclin D - genetics</topic><topic>Cyclin D - metabolism</topic><topic>Cyclin-Dependent Kinase 4 - genetics</topic><topic>Cyclin-Dependent Kinase 4 - metabolism</topic><topic>Diploidy</topic><topic>Economics</topic><topic>Embryo, Mammalian - cytology</topic><topic>Fibroblasts</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - metabolism</topic><topic>Immortalization</topic><topic>Karyotype</topic><topic>Kinases</topic><topic>Livestock</topic><topic>Regulators</topic><topic>Swine</topic><topic>Telomerase</topic><topic>Telomerase - genetics</topic><topic>Telomerase - metabolism</topic><topic>Transduction, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Donai, Kenichiro</creatorcontrib><creatorcontrib>Kiyono, Tohru</creatorcontrib><creatorcontrib>Eitsuka, Takahiro</creatorcontrib><creatorcontrib>Guo, Yijie</creatorcontrib><creatorcontrib>Kuroda, Kengo</creatorcontrib><creatorcontrib>Sone, Hideko</creatorcontrib><creatorcontrib>Isogai, Emiko</creatorcontrib><creatorcontrib>Fukuda, Tomokazu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Donai, Kenichiro</au><au>Kiyono, Tohru</au><au>Eitsuka, Takahiro</au><au>Guo, Yijie</au><au>Kuroda, Kengo</au><au>Sone, Hideko</au><au>Isogai, Emiko</au><au>Fukuda, Tomokazu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bovine and porcine fibroblasts can be immortalized with intact karyotype by the expression of mutant cyclin dependent kinase 4, cyclin D, and telomerase</atitle><jtitle>Journal of biotechnology</jtitle><addtitle>J Biotechnol</addtitle><date>2014-04-20</date><risdate>2014</risdate><volume>176</volume><spage>50</spage><epage>57</epage><pages>50-57</pages><issn>0168-1656</issn><eissn>1873-4863</eissn><abstract>•Mutant CDK4, cyclin D1, and hTERT immortalize bovine and porcine fibroblasts.•Immortalized fibroblasts maintained normal diploid karyotypes at 98–100%.•Immortalized livestock cells indicate conserved cell cycle networks across species.
Cattle and pigs comprise the most economically important livestock. Despite their importance, cultured cells from these species, which are useful for physiological analyses, are quite limited in cell banks. One of the reasons for the limited number of cell lines is the difficulty in their establishment. To overcome limitations in cell-line establishment, we attempted to immortalize bovine and porcine fibroblasts by transduction of multiple cell cycle regulators (mutant cyclin dependent kinase 4, cyclin D and telomerase reverse transcriptase). The transduced cells continued to display a stable proliferation rate and did not show cellular senescence. Furthermore, cell cycle assays showed that induction of these exogenous genes enhanced turnover of the cell cycle, especially at the G1-S phase. Furthermore, our established cell lines maintained normal diploid karyotypes at 98–100%. Our study demonstrated that bypassing p16/Rb-mediated cell arrest and activation of telomerase activity enabled efficient establishment of immortalized bovine- and porcine-derived fibroblasts. The high efficiency of establishing cell lines suggests that the networks of cell cycle regulators, especially p16/Rb-associated cell cycle arrest, have been conserved during evolution of humans, cattle, and pigs.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>24589663</pmid><doi>10.1016/j.jbiotec.2014.02.017</doi><tpages>8</tpages></addata></record> |
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subjects | Activation Animals Biotechnology Cattle Cell Cycle Cell Line Cell Proliferation Cellular Cellular senescence Cyclin D - genetics Cyclin D - metabolism Cyclin-Dependent Kinase 4 - genetics Cyclin-Dependent Kinase 4 - metabolism Diploidy Economics Embryo, Mammalian - cytology Fibroblasts Fibroblasts - cytology Fibroblasts - metabolism Immortalization Karyotype Kinases Livestock Regulators Swine Telomerase Telomerase - genetics Telomerase - metabolism Transduction, Genetic |
title | Bovine and porcine fibroblasts can be immortalized with intact karyotype by the expression of mutant cyclin dependent kinase 4, cyclin D, and telomerase |
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