Expression of Endo180 is spatially and temporally regulated during wound healing.

Abstract

AIMS:

Interactions of cells with the extracellular matrix are important for normal wound healing and may play a role in scar formation. Remarkably, wound healing in human gingiva does not result in scar formation and serves as a model for wound regeneration. Endo180 (CD280) is a cell surface receptor that has novel functions to regulate cell migration and bind and internalize collagens that are key processes in wound healing. The aim of this study was to examine the expression of Endo180 during gingival wound regeneration.

METHODS AND RESULTS:

Biopsies were collected from normal human gingiva and 1-60 days after wounding and expression of Endo180 was analysed by immunostaining. Expression of Endo180 by cultured fibroblasts and keratinocytes was studied by immunoblotting and semiquantitative reverse transcriptase-polymerase chain reaction. In normal gingiva, Endo180 was expressed by basal epithelial cells, fibroblasts, myofibroblasts, pericytes, macrophages and endothelial cells. In wounds, Endo180 expression was spatiotemporally increased in the migrating and differentiating wound epithelium, in subsets of myofibroblasts, pericytes, macrophages and endothelial cells. Growth factors involved in wound healing up-regulated the expression of Endo180 in keratinocytes and fibroblasts.

CONCLUSIONS:

The findings suggest that Endo180 plays a role in re-epithelialization and connective tissue remodelling during wound regeneration.

• Authors: H A Honardoust, G Jiang, L Koivisto, D Wienke, C M Isacke, H Larjava, L Häkkinen
• Journal: Histopathology (Histopathology) Vol. 49 Issue 6 Pg. 634-48 (Dec 2006) ISSN: 0309-0167 [Print] England
• PMID: 17163848 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Endo180
• RNA, Messenger
• Receptors, Mitogen

Topics

• Cells, Cultured
• Endothelium, Vascular (metabolism, pathology)
• Epithelial Cells (metabolism, pathology)
• Fibroblasts (metabolism, pathology)
• Fluorescent Antibody Technique, Indirect
• Gene Expression Regulation
• Gingiva (injuries, metabolism, pathology)
• Humans
• Keratinocytes (metabolism, pathology)
• Macrophages (metabolism, pathology)
• Pericytes (metabolism, pathology)
• RNA, Messenger (metabolism)
• Receptors, Mitogen (genetics, metabolism)
• Time Factors
• Wound Healing (physiology)