Literature DB >> 12473057

Evidence that the keratinocyte colony number is genetically controlled.

Natalia V Popova1, Kimberly A Tryson, Kai Q Wu, Rebecca J Morris.   

Abstract

We tested five inbred strains and two outbred stocks of female mice in a quantitative assay for clonogenic keratinocytes from the cutaneous epithelium. We found three significantly different subsets of colony counts such that: C57BL/6 C3H = DBA/2 = SENCAR = BALB/c > FVB = CD(-1) in culture conditions optimized for CD(-1) 0. C57BL/6 and BALB/c, two inbred parental strains, were chosen for further analysis. The F1 generation of these two parental strains had an intermediate number of colonies. The keratinocyte colony number from the two backcross generations was significantly different, while the colony number in the F2 generation was intermediate between the two backcrosses. We conclude that the number of keratinocyte colonies represents a new genetically definable quantitative trait. Analysis suggests that this trait is multigenic where the genes have an additive but not necessarily equal effect. We have therefore laid the foundation for identifying these stem cell regulatory genes, which may provide a new perspective on the mechanism of carcinogenesis and a new target for gene therapy.

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Year:  2002        PMID: 12473057     DOI: 10.1034/j.1600-0625.2002.110602.x

Source DB:  PubMed          Journal:  Exp Dermatol        ISSN: 0906-6705            Impact factor:   3.960


  3 in total

Review 1.  Keratinocyte stem cells and the targets for nonmelanoma skin cancer.

Authors:  Ashok Singh; Heuijoon Park; Thaned Kangsamaksin; Anupama Singh; Nyssa Readio; Rebecca J Morris
Journal:  Photochem Photobiol       Date:  2012-01-31       Impact factor: 3.421

2.  An activating beta1 integrin mutation increases the conversion of benign to malignant skin tumors.

Authors:  Manuela Ferreira; Hironobu Fujiwara; Kazumasa Morita; Fiona M Watt
Journal:  Cancer Res       Date:  2009-02-03       Impact factor: 12.701

3.  Comparison of Human Dermal Fibroblasts and HaCat Cells Cultured in Medium with or without Serum via a Generic Tissue Engineering Research Platform.

Authors:  Christopher Michael Gabbott; Tao Sun
Journal:  Int J Mol Sci       Date:  2018-01-28       Impact factor: 5.923

  3 in total

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