Transition of Phenotypic Dimorphism with Regard to Spontaneous Sister Chromatid Exchange in Epstein‐Barr Virus‐transformed Bloom's Syndrome Lymphoblastoid Cell Lines
We recently established four lymphoblastoid cell lines (LCLs) by infecting the peripheral blood of four Japanese patients suffering from Bloom's syndrome (BS) with Epstein‐Barr virus (EBV). During the course of propagating these cell lines, two of them exhibited dimorphism regarding spontaneous...
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Veröffentlicht in: | Cancer science 1992-07, Vol.83 (7), p.729-735 |
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description | We recently established four lymphoblastoid cell lines (LCLs) by infecting the peripheral blood of four Japanese patients suffering from Bloom's syndrome (BS) with Epstein‐Barr virus (EBV). During the course of propagating these cell lines, two of them exhibited dimorphism regarding spontaneous sister chromatid exchange (SCE), i.e., a mixed population consisted of cells with extremely high SCE levels characteristic of BS and cells with low SCE levels indistinguishable from that of normal control cells. On the other hand, the other two cell lines maintained a monomorphic population with high SCE levels at least until 30 weeks after EBV infection. The proportion of the cells with high SCE levels in the cell lines with dual phenotype declined as the population doubling numbers (PDN) increased with time and they became ultimately undetectable. The proportion of cells with low SCE levels at the time of EBV infection was estimated in one of these LCLs as 0.075% by extrapolating the linear regression of the logit for the proportion plotted against PDN. In view of the well‐known stability of the monomorphic phenotype in representative BS LCLs during extended cultivation, together with the present observations on the dual phenotype, we conclude that the frequent establishment of BS LCLs exclusively with low spontaneous SCE levels is attributable to the various proportions of low‐SCE cells existing in vivo in the B‐lymphocytes pool of BS individuals and to the selective pressure against the high‐SCE cells in in vitro cultures. |
doi_str_mv | 10.1111/j.1349-7006.1992.tb01973.x |
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During the course of propagating these cell lines, two of them exhibited dimorphism regarding spontaneous sister chromatid exchange (SCE), i.e., a mixed population consisted of cells with extremely high SCE levels characteristic of BS and cells with low SCE levels indistinguishable from that of normal control cells. On the other hand, the other two cell lines maintained a monomorphic population with high SCE levels at least until 30 weeks after EBV infection. The proportion of the cells with high SCE levels in the cell lines with dual phenotype declined as the population doubling numbers (PDN) increased with time and they became ultimately undetectable. The proportion of cells with low SCE levels at the time of EBV infection was estimated in one of these LCLs as 0.075% by extrapolating the linear regression of the logit for the proportion plotted against PDN. In view of the well‐known stability of the monomorphic phenotype in representative BS LCLs during extended cultivation, together with the present observations on the dual phenotype, we conclude that the frequent establishment of BS LCLs exclusively with low spontaneous SCE levels is attributable to the various proportions of low‐SCE cells existing in vivo in the B‐lymphocytes pool of BS individuals and to the selective pressure against the high‐SCE cells in in vitro cultures.</description><identifier>ISSN: 0910-5050</identifier><identifier>ISSN: 1347-9032</identifier><identifier>EISSN: 1349-7006</identifier><identifier>EISSN: 1876-4673</identifier><identifier>DOI: 10.1111/j.1349-7006.1992.tb01973.x</identifier><identifier>PMID: 1325430</identifier><identifier>CODEN: GANNA2</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Biological and medical sciences ; Bloom Syndrome - blood ; Bloom Syndrome - microbiology ; Bloom Syndrome - pathology ; Bloom's syndrome ; Cell Division - physiology ; Cell Transformation, Viral - genetics ; Cells, Cultured ; Child ; Complex syndromes ; Dimorphism ; EBV‐transformed lymphoblastoid cell ; Epstein-Barr virus ; Female ; Herpesvirus 4, Human - genetics ; Humans ; Key words ; Lymphoblastoid cell lines ; Lymphocytes ; Lymphocytes - microbiology ; Lymphocytes - pathology ; Lymphocytes - physiology ; Lymphocytes B ; Male ; Medical genetics ; Medical sciences ; Peripheral blood ; Phenotype ; Phenotypes ; Polymorphism, Genetic - genetics ; Population decline ; Proliferative advantage ; Sister chromatid exchange ; Sister Chromatid Exchange - genetics ; Somatic mosaicism</subject><ispartof>Cancer science, 1992-07, Vol.83 (7), p.729-735</ispartof><rights>1993 INIST-CNRS</rights><rights>Copyright John Wiley & Sons, Inc. Jul 1992</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5339-721c2a0fd43c8a695686d83b604dfb2e6e71b6cef174eb72092b08ab46e53e3f3</citedby><cites>FETCH-LOGICAL-c5339-721c2a0fd43c8a695686d83b604dfb2e6e71b6cef174eb72092b08ab46e53e3f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918926/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918926/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,1411,27901,27902,45550,45551,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4305962$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1325430$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tatsumi, Kouichi</creatorcontrib><creatorcontrib>Kurihara, Takayuki</creatorcontrib><creatorcontrib>Arita, Izumi</creatorcontrib><creatorcontrib>Tatsumi‐Miyajima, Junko</creatorcontrib><title>Transition of Phenotypic Dimorphism with Regard to Spontaneous Sister Chromatid Exchange in Epstein‐Barr Virus‐transformed Bloom's Syndrome Lymphoblastoid Cell Lines</title><title>Cancer science</title><addtitle>Jpn J Cancer Res</addtitle><description>We recently established four lymphoblastoid cell lines (LCLs) by infecting the peripheral blood of four Japanese patients suffering from Bloom's syndrome (BS) with Epstein‐Barr virus (EBV). During the course of propagating these cell lines, two of them exhibited dimorphism regarding spontaneous sister chromatid exchange (SCE), i.e., a mixed population consisted of cells with extremely high SCE levels characteristic of BS and cells with low SCE levels indistinguishable from that of normal control cells. On the other hand, the other two cell lines maintained a monomorphic population with high SCE levels at least until 30 weeks after EBV infection. The proportion of the cells with high SCE levels in the cell lines with dual phenotype declined as the population doubling numbers (PDN) increased with time and they became ultimately undetectable. The proportion of cells with low SCE levels at the time of EBV infection was estimated in one of these LCLs as 0.075% by extrapolating the linear regression of the logit for the proportion plotted against PDN. In view of the well‐known stability of the monomorphic phenotype in representative BS LCLs during extended cultivation, together with the present observations on the dual phenotype, we conclude that the frequent establishment of BS LCLs exclusively with low spontaneous SCE levels is attributable to the various proportions of low‐SCE cells existing in vivo in the B‐lymphocytes pool of BS individuals and to the selective pressure against the high‐SCE cells in in vitro cultures.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Bloom Syndrome - blood</subject><subject>Bloom Syndrome - microbiology</subject><subject>Bloom Syndrome - pathology</subject><subject>Bloom's syndrome</subject><subject>Cell Division - physiology</subject><subject>Cell Transformation, Viral - genetics</subject><subject>Cells, Cultured</subject><subject>Child</subject><subject>Complex syndromes</subject><subject>Dimorphism</subject><subject>EBV‐transformed lymphoblastoid cell</subject><subject>Epstein-Barr virus</subject><subject>Female</subject><subject>Herpesvirus 4, Human - genetics</subject><subject>Humans</subject><subject>Key words</subject><subject>Lymphoblastoid cell lines</subject><subject>Lymphocytes</subject><subject>Lymphocytes - microbiology</subject><subject>Lymphocytes - pathology</subject><subject>Lymphocytes - physiology</subject><subject>Lymphocytes B</subject><subject>Male</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Peripheral blood</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Polymorphism, Genetic - genetics</subject><subject>Population decline</subject><subject>Proliferative advantage</subject><subject>Sister chromatid exchange</subject><subject>Sister Chromatid Exchange - genetics</subject><subject>Somatic mosaicism</subject><issn>0910-5050</issn><issn>1347-9032</issn><issn>1349-7006</issn><issn>1876-4673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqVUsuO0zAUjRBo6Ax8ApIFCFYtfsROPAukmVIeUiUQM7C1HMdpXCV2sN2Zdscn8Bv8Fl-Co1YdYIc3lnXOPT73nptlTxGcoXRerWeI5HxaQMhmiHM8ixVEvCCz7b1scoTuZxPIEZxSSOHD7DSENYSogAyfZCeIYJoTOMl-Xntpg4nGWeAa8KnV1sXdYBR4Y3rnh9aEHtya2ILPeiV9DaIDV4OzUVrtNgFcmRC1B_PWu15GU4PFVrXSrjQwFiyGBBr76_uPS-k9-Gr8JqRHHL9snO91DS475_qXSWdn6yShwXLXD62rOhmiS3Jz3XVgaawOj7IHjeyCfny4z7IvbxfX8_fT5cd3H-YXy6mihKTOMVJYwqbOiSol45SVrC5JxWBeNxXWTBeoYko3qMh1VWDIcQVLWeVMU6JJQ86y13vdYVMlh0rb5LcTgze99DvhpBF_I9a0YuVuBOWo5JglgRcHAe--bXSIojdBpT72IxMFQRRRWCTis3-Ia7fxNjUncJ6yorDEMLHO9yzlXQheN0crCIpxHcRajJmLMXMxroM4rIPYpuInfzZzV7rPP-HPD7gMSnZNSkaZcKQlCuUM383k1nR69x8GxPxiUWBOfgOU79hk</recordid><startdate>199207</startdate><enddate>199207</enddate><creator>Tatsumi, Kouichi</creator><creator>Kurihara, Takayuki</creator><creator>Arita, Izumi</creator><creator>Tatsumi‐Miyajima, Junko</creator><general>Blackwell Publishing Ltd</general><general>Japanese Cancer Association</general><general>John Wiley & Sons, Inc</general><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>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>199207</creationdate><title>Transition of Phenotypic Dimorphism with Regard to Spontaneous Sister Chromatid Exchange in Epstein‐Barr Virus‐transformed Bloom's Syndrome Lymphoblastoid Cell Lines</title><author>Tatsumi, Kouichi ; Kurihara, Takayuki ; Arita, Izumi ; Tatsumi‐Miyajima, Junko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5339-721c2a0fd43c8a695686d83b604dfb2e6e71b6cef174eb72092b08ab46e53e3f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Bloom Syndrome - blood</topic><topic>Bloom Syndrome - microbiology</topic><topic>Bloom Syndrome - pathology</topic><topic>Bloom's syndrome</topic><topic>Cell Division - physiology</topic><topic>Cell Transformation, Viral - genetics</topic><topic>Cells, Cultured</topic><topic>Child</topic><topic>Complex syndromes</topic><topic>Dimorphism</topic><topic>EBV‐transformed lymphoblastoid cell</topic><topic>Epstein-Barr virus</topic><topic>Female</topic><topic>Herpesvirus 4, Human - genetics</topic><topic>Humans</topic><topic>Key words</topic><topic>Lymphoblastoid cell lines</topic><topic>Lymphocytes</topic><topic>Lymphocytes - microbiology</topic><topic>Lymphocytes - pathology</topic><topic>Lymphocytes - physiology</topic><topic>Lymphocytes B</topic><topic>Male</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Peripheral blood</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Polymorphism, Genetic - genetics</topic><topic>Population decline</topic><topic>Proliferative advantage</topic><topic>Sister chromatid exchange</topic><topic>Sister Chromatid Exchange - genetics</topic><topic>Somatic mosaicism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tatsumi, Kouichi</creatorcontrib><creatorcontrib>Kurihara, Takayuki</creatorcontrib><creatorcontrib>Arita, Izumi</creatorcontrib><creatorcontrib>Tatsumi‐Miyajima, Junko</creatorcontrib><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>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tatsumi, Kouichi</au><au>Kurihara, Takayuki</au><au>Arita, Izumi</au><au>Tatsumi‐Miyajima, Junko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transition of Phenotypic Dimorphism with Regard to Spontaneous Sister Chromatid Exchange in Epstein‐Barr Virus‐transformed Bloom's Syndrome Lymphoblastoid Cell Lines</atitle><jtitle>Cancer science</jtitle><addtitle>Jpn J Cancer Res</addtitle><date>1992-07</date><risdate>1992</risdate><volume>83</volume><issue>7</issue><spage>729</spage><epage>735</epage><pages>729-735</pages><issn>0910-5050</issn><issn>1347-9032</issn><eissn>1349-7006</eissn><eissn>1876-4673</eissn><coden>GANNA2</coden><abstract>We recently established four lymphoblastoid cell lines (LCLs) by infecting the peripheral blood of four Japanese patients suffering from Bloom's syndrome (BS) with Epstein‐Barr virus (EBV). During the course of propagating these cell lines, two of them exhibited dimorphism regarding spontaneous sister chromatid exchange (SCE), i.e., a mixed population consisted of cells with extremely high SCE levels characteristic of BS and cells with low SCE levels indistinguishable from that of normal control cells. On the other hand, the other two cell lines maintained a monomorphic population with high SCE levels at least until 30 weeks after EBV infection. The proportion of the cells with high SCE levels in the cell lines with dual phenotype declined as the population doubling numbers (PDN) increased with time and they became ultimately undetectable. The proportion of cells with low SCE levels at the time of EBV infection was estimated in one of these LCLs as 0.075% by extrapolating the linear regression of the logit for the proportion plotted against PDN. In view of the well‐known stability of the monomorphic phenotype in representative BS LCLs during extended cultivation, together with the present observations on the dual phenotype, we conclude that the frequent establishment of BS LCLs exclusively with low spontaneous SCE levels is attributable to the various proportions of low‐SCE cells existing in vivo in the B‐lymphocytes pool of BS individuals and to the selective pressure against the high‐SCE cells in in vitro cultures.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1325430</pmid><doi>10.1111/j.1349-7006.1992.tb01973.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Biological and medical sciences Bloom Syndrome - blood Bloom Syndrome - microbiology Bloom Syndrome - pathology Bloom's syndrome Cell Division - physiology Cell Transformation, Viral - genetics Cells, Cultured Child Complex syndromes Dimorphism EBV‐transformed lymphoblastoid cell Epstein-Barr virus Female Herpesvirus 4, Human - genetics Humans Key words Lymphoblastoid cell lines Lymphocytes Lymphocytes - microbiology Lymphocytes - pathology Lymphocytes - physiology Lymphocytes B Male Medical genetics Medical sciences Peripheral blood Phenotype Phenotypes Polymorphism, Genetic - genetics Population decline Proliferative advantage Sister chromatid exchange Sister Chromatid Exchange - genetics Somatic mosaicism |
title | Transition of Phenotypic Dimorphism with Regard to Spontaneous Sister Chromatid Exchange in Epstein‐Barr Virus‐transformed Bloom's Syndrome Lymphoblastoid Cell Lines |
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