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K15
Expression Implies Lateral Differentiation within Stratified Epithelial
Basal Cells
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Rebecca M. Porter,
Declan P. Lunny, Patricia H. Ogden, Susan M. Morley, W. H. Irwin McLean,
Alan Evans, Dolores L. Harrison, Elizabeth L. Rugg, and E. Birgitte Lane
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CRC Cell
Structure Research Group (RMP, DPL, PHO, SMM, WHIM, ELR, EBL), University
of Dundee, Dundee, Epithelial Genetics Group (WHIM) and Department of Molecular
and Cellular Pathology (AE), Ninewells Medical School, Dundee, ICRF Clare
Hall Laboratories (DLH), Hertfordshire, and Centre for Cutaneous Research
(ELR), St Bartholomew\'s and the Royal London Hospital School of Medicine
and Dentistry, London, United Kingdom
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Keratins are intermediate filament proteins whose expression in epithelial
tissues is closely linked to their differentiated state. The greatest
complexity of this expression is seen in the epidermis and associated
structures. The critical basal (proliferative) cell layer expresses the
major keratin pair, K5 and K14, but it also expresses an additional type
I keratin, K15, about which far less is known. We have compared the expression
of K15 with K14 in normal, pathological, and tissue culture contexts;
distinct differences in their expression patterns have been observed that
imply different regulation and function for these two genes. K15 appears
to be preferentially expressed in stable or slowly turning over basal
cells. In steady-state epidermis, K15 is present in higher amounts in
basal cells of thin skin but in lower amounts in the rapidly turning over
thick plantar skin. Although remaining high in basal cell carcinomas (noninvasive)
it is suppressed in squamous cell carcinomas (which frequently metastasize).
Wounding-stimulated epidermis loses K15 expression, whereas K14 is unchanged.
In cultured keratinocytes, K15 levels are suppressed until the culture
stratifies, whereas K14 is constitutively expressed throughout. Therefore,
unlike K14, which appears to be a fundamental component of all keratinocytes,
K15 expression appears to be more tightly coupled to a mature basal keratinocyte
phenotype.
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