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Pregled bibliografske jedinice broj: 958056

Early-life regional and temporal variation in filaggrin-derived natural moisturizing factor, filaggrin-processing enzyme activity, corneocyte phenotypes and plasmin activity: implications for atopic dermatitis


McAleer, M.A.; Jakaša, Ivone; Raj, N.; O'Donnell, C.P.F.; Lane, M.E.; Rawlings, A.V.; Voegeli, R.; McLean, W.H.I.; Kezic, S.; Irvine, A.D.
Early-life regional and temporal variation in filaggrin-derived natural moisturizing factor, filaggrin-processing enzyme activity, corneocyte phenotypes and plasmin activity: implications for atopic dermatitis // British journal of dermatology, 179 (2018), 2; 431-441 doi:10.1111/bjd.16691 (međunarodna recenzija, članak, znanstveni)


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Naslov
Early-life regional and temporal variation in filaggrin-derived natural moisturizing factor, filaggrin-processing enzyme activity, corneocyte phenotypes and plasmin activity: implications for atopic dermatitis
(Early-life regional and temporal variation in filaggrin-derived natural moisturizing factor, filaggrin-processing enzyme activity, corneocyte phenotypes and plasmin activity: implications for atopic dermatitis)

Autori
McAleer, M.A. ; Jakaša, Ivone ; Raj, N. ; O'Donnell, C.P.F. ; Lane, M.E. ; Rawlings, A.V. ; Voegeli, R. ; McLean, W.H.I. ; Kezic, S. ; Irvine, A.D.

Izvornik
British journal of dermatology (0007-0963) 179 (2018), 2; 431-441

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
atopic dermatitis ; NMF ; imflammatory mediators ; bleomycin hydrolase ; plasmin

Sažetak
Background Filaggrin is central to the pathogenesis of atopic dermatitis (AD). The cheeks are a common initiation site of infantile AD. Regional and temporal expression of levels of filaggrin degradation products [natural moisturizing factors (NMFs)], activities of filaggrin-processing enzymes [bleomycin hydrolase (BH) and calpain-1 (C-1)] and plasmin, and corneocyte envelope (CE) maturity in early life are largely unknown. Objectives We conducted a cross-sectional, observational study investigating regional and age-dependent variations in NMF levels, activity of proteases and CE maturity in stratum corneum (SC) from infants to determine whether these factors could explain the observed predilection sites for AD in early life. Methods We measured NMF using a tape-stripping method at seven sites in the SC of 129 children (aged < 12 months to 72 months) and in three sites in 56 neonates and infants (< 48 h to 3 months). In 37 of these neonates and infants, corneocyte size, maturity, BH, C-1 and plasmin activities were determined. Results NMF levels are low at birth and increase with age. Cheek SC, compared with elbow flexure and nasal tip, has the lowest NMF in the first year of life and is the slowest to reach stable levels. Cheek corneocytes remain immature. Plasmin, BH and C-1 activities are all elevated by 1 month of age in exposed cheek skin, but not in elbow skin. Conclusions Regional and temporal differences in NMF levels, CE maturity and protease activities may explain the predilection for AD to affect the cheeks initially and are supportive of this site as key for allergen priming in early childhood. These observations will help design early intervention and treatment strategies for AD.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Kliničke medicinske znanosti



POVEZANOST RADA


Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb

Profili:

Avatar Url Ivone Jakasa (autor)

Poveznice na cjeloviti tekst rada:

doi onlinelibrary.wiley.com

Citiraj ovu publikaciju:

McAleer, M.A.; Jakaša, Ivone; Raj, N.; O'Donnell, C.P.F.; Lane, M.E.; Rawlings, A.V.; Voegeli, R.; McLean, W.H.I.; Kezic, S.; Irvine, A.D.
Early-life regional and temporal variation in filaggrin-derived natural moisturizing factor, filaggrin-processing enzyme activity, corneocyte phenotypes and plasmin activity: implications for atopic dermatitis // British journal of dermatology, 179 (2018), 2; 431-441 doi:10.1111/bjd.16691 (međunarodna recenzija, članak, znanstveni)
McAleer, M., Jakaša, I., Raj, N., O'Donnell, C., Lane, M., Rawlings, A., Voegeli, R., McLean, W., Kezic, S. & Irvine, A. (2018) Early-life regional and temporal variation in filaggrin-derived natural moisturizing factor, filaggrin-processing enzyme activity, corneocyte phenotypes and plasmin activity: implications for atopic dermatitis. British journal of dermatology, 179 (2), 431-441 doi:10.1111/bjd.16691.
@article{article, author = {McAleer, M.A. and Jaka\v{s}a, Ivone and Raj, N. and O'Donnell, C.P.F. and Lane, M.E. and Rawlings, A.V. and Voegeli, R. and McLean, W.H.I. and Kezic, S. and Irvine, A.D.}, year = {2018}, pages = {431-441}, DOI = {10.1111/bjd.16691}, keywords = {atopic dermatitis, NMF, imflammatory mediators, bleomycin hydrolase, plasmin}, journal = {British journal of dermatology}, doi = {10.1111/bjd.16691}, volume = {179}, number = {2}, issn = {0007-0963}, title = {Early-life regional and temporal variation in filaggrin-derived natural moisturizing factor, filaggrin-processing enzyme activity, corneocyte phenotypes and plasmin activity: implications for atopic dermatitis}, keyword = {atopic dermatitis, NMF, imflammatory mediators, bleomycin hydrolase, plasmin} }
@article{article, author = {McAleer, M.A. and Jaka\v{s}a, Ivone and Raj, N. and O'Donnell, C.P.F. and Lane, M.E. and Rawlings, A.V. and Voegeli, R. and McLean, W.H.I. and Kezic, S. and Irvine, A.D.}, year = {2018}, pages = {431-441}, DOI = {10.1111/bjd.16691}, keywords = {atopic dermatitis, NMF, imflammatory mediators, bleomycin hydrolase, plasmin}, journal = {British journal of dermatology}, doi = {10.1111/bjd.16691}, volume = {179}, number = {2}, issn = {0007-0963}, title = {Early-life regional and temporal variation in filaggrin-derived natural moisturizing factor, filaggrin-processing enzyme activity, corneocyte phenotypes and plasmin activity: implications for atopic dermatitis}, keyword = {atopic dermatitis, NMF, imflammatory mediators, bleomycin hydrolase, plasmin} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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