Involvement of the corticotropin-releasing hormone system in the pathogenesis of acne vulgaris
- PMID: 19077080
- DOI: 10.1111/j.1365-2133.2008.08959.x
Involvement of the corticotropin-releasing hormone system in the pathogenesis of acne vulgaris
Abstract
Background: The sebaceous gland exhibits an independent peripheral endocrine function and expresses receptors for neuropeptides. Previous reports have confirmed the presence of a complete corticotropin-releasing hormone (CRH) system in human sebocytes in vitro. The capability of hypothalamic CRH to induce lipid synthesis, induce steroidogenesis and interact with testosterone and growth hormone implicates a possibility of its involvement in the clinical development of acne.
Objectives: The purpose of the study was to detect expression changes of CRH/CRH binding protein (CRHBP)/CRH receptors (CRHRs) in acne-involved skin, especially in the sebaceous glands.
Methods: Expression of CRH/CRHBP/CRHRs was analysed by immunohistochemistry in biopsies from facial skin of 33 patients with acne, noninvolved thigh skin of the same patients and normal skin of eight age-matched healthy volunteers.
Results: Very strong positive reaction for CRH was observed in acne-involved skin in all types of sebaceous gland cells, irrespective of their differentiation stage, whereas in noninvolved and normal skin sebaceous glands exhibited a weaker CRH staining depending upon the differentiation stage of sebocytes. The strongest reaction for CRHBP in acne-involved sebaceous glands was in differentiating sebocytes. CRHR-1 and CRHR-2 exhibited the strongest expression in sweat glands and sebaceous glands, respectively.
Conclusions: Expression of the complete CRH system is abundant in acne-involved skin, especially in the sebaceous glands, possibly activating pathways which affect immune and inflammatory processes leading to the development and stress-induced exacerbation of acne.
Comment in
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On the role of the corticotropin-releasing hormone signalling system in the aetiology of inflammatory skin disorders.Br J Dermatol. 2009 Feb;160(2):229-32. doi: 10.1111/j.1365-2133.2008.08958.x. Br J Dermatol. 2009. PMID: 19187344 Free PMC article.
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