Background:
Caveolin-1 is a key structural and functional protein for plasmalemmal invaginations termed caveolae. caveolin-1 is known to modulate multiple signal-transducing pathways involved in cell differentiation and proliferation. psoriasis is viewed as a multifactorial pathology characterized by keratinocyte hyperproliferation and abnormal cell maturation. we hypothesized that loss of caveolin-1 within epidermal keratinocytes may contribute to the development and/or progression of the psoriatic phenotype.
Objectives:
To examine the expression and spatial distribution of caveolin-1 in skin biopsies from normal subjects and in patients with psoriasis.
Methods:
Using immunohistochemical methods caveolin-1 protein expression was assayed in two independent patient groups. firstly, a retrospective analysis was conducted on archival skin samples obtained from nine normal subjects and from involved tissue of 12 patients with psoriasis. following this, a prospectively designed study was conducted in 10 further patients with active psoriasis and involving caveolin-1 staining of biopsy tissue from the uninvolved, advancing edge and lesional skin tissue from within the same subject.
Results:
In normal skin or uninvolved skin from psoriasis patients intense caveolin-1 staining was present throughout full-thickness epidermis. in 20 of the 22 patient cases (combined retrospective and prospective samples) caveolin-1 protein was significantly reduced and consistently showed very weak or absent staining within the hyperproliferative basal cell layers of the psoriatic plaque (p < 0.002 for retrospective archival study and p < 0.01 for prospectively designed study). comparisons between caveolin-1 staining in uninvolved tissue and at the advancing edge of a migrating plaque were more equivocal (p > 0.05).
Conclusions:
The findings of this study are consistent with a downregulation of caveolin-1 that may serve as an aetiological factor in the development and/or progression of psoriasis. further mechanistic investigations are required with the potential that caveolin-1 protein may be a novel target for therapy of psoriasis.