Immunolocalization of Epidermal Growth Factor Receptors in Normal Developing Human Skin

The embryogenesis of normal human skin is a complex process involving multiple cell types and developmentally regulated growth factors. The immunohistochemical localization of epidermal growth factor receptors (EGF-R) was studied in human fetal skin because this receptor modulates all known actions...

Full description

Saved in:
Bibliographic Details
Published inJournal of investigative dermatology Vol. 94; no. 6; pp. 742 - 748
Main Authors Nanney, Lillian B., Stoscheck, Christa M., Underwood, Robert A., Holbrook, Karen A., King, Lloyd E.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.06.1990
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The embryogenesis of normal human skin is a complex process involving multiple cell types and developmentally regulated growth factors. The immunohistochemical localization of epidermal growth factor receptors (EGF-R) was studied in human fetal skin because this receptor modulates all known actions of EGF and TGF-α. EGF-R are present in developing skin as early as the 42nd day of gestation. Immunoreactive EGF-R are present in keratinocytes, endothelial, and skeletal muscle cells. In contrast to normal adult human skin in which the EGF-R are primarily restricted to the basal and immediately suprabasal keratinocytes, the fetal epidermis showed a persistent expression of EGF-R in all cell layers. The absence of EGF-R on the outer, apical surface of periderm cells that are exposed to amniotic fluid was unexpected and may reflect down-regulation of EGF-R by EGF/TGF-α or related fetal growth factors present in amniotic fluid. The complex regulation of EGF-R in embryonic hair follicles and sebaceous glands indicates an active and perhaps regulatory role for EGF/TGF-α in the development and function of pilosebaceous glands as well as mammalian skin in general.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0022-202X
1523-1747
DOI:10.1111/1523-1747.ep12874601