Literature DB >> 1372096

A comparison of the response of unstimulated and stimulated T-lymphocytes and fibroblasts from normal, xeroderma pigmentosum and trichothiodystrophy donors to the lethal action of UV-C.

C F Arlett1, S A Harcourt, J Cole, M H Green, A V Anstey.   

Abstract

Unstimulated T-lymphocytes from normal donors are significantly more sensitive to the lethal effects of UV-C than either stimulated T-lymphocytes or fibroblasts as judged by colony-forming ability. Data from other studies suggest that excision repair is more effective in stimulated than unstimulated T-lymphocytes leading to the prediction that these differences in survival should be minimal in cells established from excision defective donors. The prediction was met with XP6BR, a donor of unknown complementation group. For 3 XP's from complementation group D, however, enhanced survival in stimulated T-cells was observed. With cells from an excision-defective TTD who was included in complementation group D of XP both fibroblasts and unstimulated T-lymphocytes were hypersensitive. For a second excision defective TTD patient who was excluded from complementation group D, the unstimulated T-lymphocytes were more resistant than those of normal donors although the fibroblasts were hypersensitive. These results suggest that the in vitro response of stimulated T-lymphocytes or fibroblasts may not reflect the in vivo response of cells, as measured by the response of unstimulated T-lymphocytes.

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Year:  1992        PMID: 1372096     DOI: 10.1016/0921-8777(92)90074-d

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  4 in total

1.  Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.

Authors:  E M Taylor; B C Broughton; E Botta; M Stefanini; A Sarasin; N G Jaspers; H Fawcett; S A Harcourt; C F Arlett; A R Lehmann
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-05       Impact factor: 11.205

2.  Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.

Authors:  W Vermeulen; R J Scott; S Rodgers; H J Müller; J Cole; C F Arlett; W J Kleijer; D Bootsma; J H Hoeijmakers; G Weeda
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

3.  Xeroderma pigmentosum variant: 5 years of tumour suppression by etretinate.

Authors:  J Berth-Jones; J Cole; A R Lehmann; C F Arlett; R A Graham-Brown
Journal:  J R Soc Med       Date:  1993-06       Impact factor: 18.000

4.  Hypomorphic PCNA mutation underlies a human DNA repair disorder.

Authors:  Emma L Baple; Helen Chambers; Harold E Cross; Heather Fawcett; Yuka Nakazawa; Barry A Chioza; Gaurav V Harlalka; Sahar Mansour; Ajith Sreekantan-Nair; Michael A Patton; Martina Muggenthaler; Phillip Rich; Karin Wagner; Roselyn Coblentz; Constance K Stein; James I Last; A Malcolm R Taylor; Andrew P Jackson; Tomoo Ogi; Alan R Lehmann; Catherine M Green; Andrew H Crosby
Journal:  J Clin Invest       Date:  2014-06-09       Impact factor: 14.808

  4 in total

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