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Mast cell chymase is increased in chronic atopic dermatitis but not in psoriasis

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Abstract

Mast cell chymase is a chymotrypsin-like serine proteinase primarily stored in secretory mast cell granules. Mast cell chymase has various effects on angiotensin, metalloproteases, lipoproteins, procollagen, neuropeptides and cytokines. Recent studies have demonstrated that chymase inhibitors inhibit skin inflammation. In this study we sought to determine the role of mast cell chymase in atopic dermatitis (AD) in comparison with its role in psoriasis and normal skin. Skin biopsy specimens were obtained from non-lesional and lesional skin of patients with chronic AD and psoriasis and from normal skin of non-atopic and non-psoriatic controls. The number of mast cells containing chymase was determined by immunohistochemistry using a chymase-specific monoclonal antibody. A significantly (P<0.05) enhanced number of chymase-positive cells was found in lesional AD skin as compared to normal skin as well as to lesional and non-lesional skin of patients with psoriasis. A significant (P<0.05) increase in the number of chymase-positive cells was also found in non-lesional AD skin in comparison to psoriasis. An enhanced, albeit not statistically significant difference was noted in non-lesional AD skin as compared to normal skin. In conclusion, these results suggest that mast cell chymase may play an integral part in eliciting and maintaining cutaneous inflammation in AD but not in psoriasis. The increased proteinase activity of mast cell chymase may also be involved in promoting a skin barrier defect in AD, which subsequently enhances the skin’s permeability to allergens and microbes and thereby aggravates the eczema.

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References

  1. Leung DY, Boguniewicz M, Howell MD, et al (2004) New insights into atopic dermatitis. J Clin Invest 113:651–657

    Google Scholar 

  2. Mihm MC Jr, Soter NA, Dvorak HF, et al (1976) The structure of normal skin and the morphology of atopic eczema. J Invest Dermatol 67:305–312

    Google Scholar 

  3. Fukami H, Okunishi H, Miyazaki M (1998) Chymase: its pathophysiological roles and inhibitors. Curr Pharm Des 4:439–453

    Google Scholar 

  4. Mao XQ, Shirakawa T, Yoshikawa T, et al (1996) Association between genetic variants of mast-cell chymase and eczema. Lancet 348:581–583

    Google Scholar 

  5. Forrest S, Dunn K, Elliott K, et al (1999) Identifying genes predisposing to atopic eczema. J Allergy Clin Immunol 104:1066–1070

    Google Scholar 

  6. Kawashima T, Noguchi E, Arinami T, et al (1998) No evidence for an association between a variant of the mast cell chymase gene and atopic dermatitis based on case-control and haplotype-relative-risk analyses. Hum Hered 48:271–274

    Google Scholar 

  7. Hanifin J, Rajka G (1980) Diagnostic features of atopic dermatitis. Acta Derm Venereol 92:4–47

    Google Scholar 

  8. Jarvikallio A, Naukkarinen A, Harvima IT, et al (1997) Quantitative analysis of tryptase- and chymase-containing mast cells in atopic dermatitis and nummular eczema. Br J Dermatol 136:871–877

    Google Scholar 

  9. Weber A, Knop J, Maurer M (2003) Pattern analysis of human cutaneous mast cell populations by total body surface mapping. Br J Dermatol 148:224–228

    Google Scholar 

  10. Wintroub BU, Schechter NB, Lazarus GS, et al (1984) Angiotensin I conversion by human and rat chymotryptic proteinases. J Invest Dermatol 83:336–339

    Google Scholar 

  11. Mizutani H, Schechter N, Lazarus G, et al (1991) Rapid and specific conversion of precursor interleukin 1 beta (IL-1 beta) to an active IL-1 species by human mast cell chymase. J Exp Med 174:821–825

    Google Scholar 

  12. Tomimori Y, Tsuruoka N, Fukami H, et al (2002) Role of mast cell chymase in allergen-induced biphasic skin reaction. Biochem Pharmacol 64:1187–1193

    Google Scholar 

  13. Nomura I, Gao B, Boguniewicz M, et al (2003) Distinct patterns of gene expression in the skin lesions of atopic dermatitis and psoriasis: a gene microarray analysis. J Allergy Clin Immunol 112:1195–1202

    Google Scholar 

  14. Harvima IT, Haapanen L, Ackermann L, et al (1999) Decreased chymase activity is associated with increased levels of protease inhibitors in mast cells of psoriatic lesions. Acta Derm Venereol 79:98–104

    Google Scholar 

  15. Rukwied R, Lischetzki G, McGlone F, et al (2000) Mast cell mediators other than histamine induce pruritus in atopic dermatitis patients: a dermal microdialysis study. Br J Dermatol 142:1114–1120

    Google Scholar 

  16. Algermissen B, Sitzmann J, Nurnberg W, et al (2000) Distribution and potential biologic function of the thrombin receptor PAR-1 on human keratinocytes. Arch Dermatol Res 292:488–495

    Google Scholar 

  17. Schechter NM, Brass LF, Lavker RM, et al (1998) Reaction of mast cell proteases tryptase and chymase with protease activated receptors (PARs) on keratinocytes and fibroblasts. J Cell Physiol 176:365–373

    Google Scholar 

  18. Komatsu N, Takata M, Otsuki N, et al (2002) Elevated stratum corneum hydrolytic activity in Netherton syndrome suggests an inhibitory regulation of desquamation by SPINK5-derived peptides. J Invest Dermatol 118:436–443

    Article  CAS  PubMed  Google Scholar 

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Correspondence to Nikhil Yawalkar.

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Badertscher, K., Brönnimann, M., Karlen, S. et al. Mast cell chymase is increased in chronic atopic dermatitis but not in psoriasis. Arch Dermatol Res 296, 503–506 (2005). https://doi.org/10.1007/s00403-005-0542-3

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  • DOI: https://doi.org/10.1007/s00403-005-0542-3

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