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
Hauptverfasser: Tatsumi, Kouichi, Kurihara, Takayuki, Arita, Izumi, Tatsumi‐Miyajima, Junko
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creator Tatsumi, Kouichi
Kurihara, Takayuki
Arita, Izumi
Tatsumi‐Miyajima, Junko
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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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 &amp; Sons, Inc. 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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 - 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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.</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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identifier ISSN: 0910-5050
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source MEDLINE; IngentaConnect Free/Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
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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