Literature DB >> 1325430

Transition of phenotypic dimorphism with regard to spontaneous sister chromatid exchange in Epstein-Barr virus-transformed Bloom's syndrome lymphoblastoid cell lines.

K Tatsumi1, T Kurihara, I Arita, J Tatsumi-Miyajima.   

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.

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Mesh:

Year:  1992        PMID: 1325430      PMCID: PMC5918926          DOI: 10.1111/j.1349-7006.1992.tb01973.x

Source DB:  PubMed          Journal:  Jpn J Cancer Res        ISSN: 0910-5050


Bloom's syndrome sister chromatid exchanges Epstein‐Barr virus phytohemagglutinm fluorescence plus Giemsa population doubling number
  27 in total

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Authors:  J G Hall
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

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Authors:  J German; H Takebe
Journal:  Clin Genet       Date:  1989-02       Impact factor: 4.438

3.  DNA ligase I deficiency in Bloom's syndrome.

Authors:  A E Willis; T Lindahl
Journal:  Nature       Date:  1987 Jan 22-28       Impact factor: 49.962

4.  Altered DNA ligase I activity in Bloom's syndrome cells.

Authors:  J Y Chan; F F Becker; J German; J H Ray
Journal:  Nature       Date:  1987 Jan 22-28       Impact factor: 49.962

5.  Ultraviolet light sensitivity and delayed DNA-chain maturation in Bloom's syndrome fibroblasts.

Authors:  F Gianneli; P F Benson; S A Pawsey; P E Polani
Journal:  Nature       Date:  1977-02-03       Impact factor: 49.962

6.  Dimorphism of sister chromatid exchange in Bloom's syndrome B- and T-cell lines transformed with Epstein-Barr and adult T-cell leukemia viruses.

Authors:  Y Shiraishi; S Yoshimoto; I Miyoshi; N Kondo; T Orii; A A Sandberg
Journal:  Cancer Res       Date:  1983-08       Impact factor: 12.701

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Authors:  S T Warren; R A Schultz; C C Chang; M H Wade; J E Trosko
Journal:  Proc Natl Acad Sci U S A       Date:  1981-05       Impact factor: 11.205

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Authors:  H Kawashima; T Sato; N Taniguchi; T Yagi; K Ishizaki; H Takebe
Journal:  Clin Genet       Date:  1980-02       Impact factor: 4.438

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Authors:  R Weksberg; C Smith; L Anson-Cartwright; K Maloney
Journal:  Am J Hum Genet       Date:  1988-06       Impact factor: 11.025

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Authors:  A B Krepinsky; J A Heddle; J German
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

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  1 in total

1.  An efficient method for routine Epstein-Barr virus immortalization of human B lymphocytes.

Authors:  F E Wall; R D Henkel; M P Stern; H B Jenson; M P Moyer
Journal:  In Vitro Cell Dev Biol Anim       Date:  1995-02       Impact factor: 2.416

  1 in total

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