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Keratin expression in the normal nail unit: markers of regional differentiation.

Abstract:
Differentiation within the nail unit was examined using a range of antikeratin monoclonal antibodies including the recently described antibody LHTric-1, specific to the acidic hair-type keratin Ha1. Keratinocytes of the nail matrix, nail bed and the digit pulp were characterized by different patterns of keratin expression. Nail matrix was the sole site of expression of Ha1, which colocalized in suprabasal matrix epidermis with epidermal keratins K1 and K10. Small amounts of K17 were found at the apex of the matrix in some cases. K6 and K16 were found where the epidermal surface folds forwards to become the ventral aspect of the proximal nail fold. The nail bed was distinguished by the absence of hair-type keratin Ha1 and the absence of markers of cornified epidermis and mucosal differentiation K1/K10 and K4/K13, respectively, while K6, K16 and K17 were detected. The basal keratin conformation marker, LH6, was expressed suprabasally throughout the nail bed. This complement of keratins exists in the nail bed in the absence of notable proliferative activity, and suggests a state of minimally developed differentiation which may be afforded by the physical or biological properties of the overlying nail. Keratins, K6, K16 and K17 were all found in the digit pulp in limited amounts, possibly in association with the epidermal component of the eccrine duct. The simple epithelial keratins, K7, K8 and K18, were found in small amounts in the specimens from younger individuals, mainly in epibasal cells of the apex of the matrix and in putative Merkel cells.
Publication status:
Published

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Publisher copy:
10.1046/j.1365-2133.2000.03246.x

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Journal:
British journal of dermatology More from this journal
Volume:
142
Issue:
1
Pages:
89-96
Publication date:
2000-01-01
DOI:
EISSN:
1365-2133
ISSN:
0007-0963


Language:
English
Keywords:
Pubs id:
pubs:25090
UUID:
uuid:d5a84f19-1115-4ff6-ac14-3bd12e566246
Local pid:
pubs:25090
Source identifiers:
25090
Deposit date:
2012-12-19

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