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Increased keratinocyte proliferation initiated through downregulation of desmoplakin by RNA interference

Journal Article · · Experimental Cell Research
OSTI ID:20955488
 [1];  [2];  [1]
  1. Centre for Tumour Biology, Institute of Cancer and CR-UK Clinical Centre, Barts and The London, Queen Mary's School of Medicine and Dentistry, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ (United Kingdom)
  2. Centre for Cutaneous Research, Barts and The London, Queen Mary's School of Medicine and Dentistry, 4 Newark Street, London E1 2AT (United Kingdom)

The intercellular adhesive junction desmosomes are essential for the maintenance of tissue structure and integrity in skin. Desmoplakin (Dp) is a major obligate plaque protein which plays a fundamental role in anchoring intermediate filaments to desmosomal cadherins. Evidence from hereditary human disease caused by mutations in the gene encoding Dp, e.g. Dp haploinsufficiency, suggests that alterations in Dp expression result not only in the disruption of tissue structure and integrity but also could evoke changes in keratinocyte proliferation. We have used transient RNA interference (RNAi) to downregulate Dp specifically in HaCaT keratinocytes. We showed that this Dp downregulation also caused reduced expression of several other desmosomal proteins. Increased cell proliferation and enhanced G{sub 1}-to-S-phase entry in the cell cycle, as monitored by colonial cellular density and BrdU incorporation, were seen in Dp RNAi-treated cells. These proliferative changes were associated with elevated phospho-ERK1/2 and phospho-Akt levels. Furthermore, this increase in phospho-ERK/1/2 and phospho-Akt levels was sustained in Dp RNAi-treated cells at confluence whereas in control cells there was a significant reduction in phosphorylation of ERK1/2. This study indicates that Dp may participate in the regulation of keratinocyte cell proliferation by, in part at least, regulating cell cycle progression.

OSTI ID:
20955488
Journal Information:
Experimental Cell Research, Journal Name: Experimental Cell Research Journal Issue: 11 Vol. 313; ISSN 0014-4827; ISSN ECREAL
Country of Publication:
United States
Language:
English

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