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CD44 standard and variant isoform expression in normal human skin appendages and epidermis
Authors:Walter K. F. Seelentag  Ursula Günthert  Parvin Saremaslani  Eva Futo  Madeleine Pfaltz  Philipp U. Heitz  Jürgen Roth
Affiliation:(1) Division of Cell and Molecular Pathology, University of Zürich, Schmelzbergstrasse 12, CH-8091 Zürich, Switzerland Tel. +41-1-255.40.51; Fax +41-1-255.44.07 e-mail seelewa@pathol.unizh.ch, CH;(2) Basel Institute for Immunology, Basel, Switzerland, CH;(3) Department of Pathology, University of Zürich, Switzerland, CH;(4) Institute for Clinical Pathology, University of Zürich, Switzerland, CH
Abstract:
 CD44 isoforms have been implicated in tumor progression and metastasis formation. This study presents a thorough immunohistochemical analysis of CD44 standard and isoform expression in normal human skin appendages and epidermis applying monoclonal antibodies against CD44s, CD44v3, -v4, -v5, -v6, and -v9. An improved immunohistochemical protocol with microwave-based antigen retrieval in paraffin sections and heavy metal amplification of the diaminobenzidine reaction product provided enhanced resolution and sensitivity as compared to studies on frozen sections. The hair follicle, the seborrheic and eccrine sweat glands were strongly positive for all CD44 isoforms studied. In the latter, the clear cells but not the dark (intercalated) cells were positive. The sudoriferous ducts adjacent to the glands were weakly positive for all CD44 isoforms and strongly positive near the skin surface. In the apocrine glands, the basal cells showed only a moderate positivity. The myoepithelial cells expressed only CD44s. In the epidermis, all CD44 isoforms were detectable, with strongest CD44 immunostaining in the lower third of the stratum spinosum and weaker staining in the stratum basale and the upper two-thirds of the stratum granulosum. The stratum granulosum and corneum were unreactive. Thus, a regional and cell type-specific CD44 expression was revealed. Accepted: 10 May 1996
Keywords:
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