Household laundry detergents disrupt barrier integrity and induce inflammation in mouse and human skin

Author:

Rinaldi Arturo O.1ORCID,Li Manru1,Barletta Elena1ORCID,D'Avino Paolo1,Yazici Duygu1,Pat Yagiz1,Ward Siobhan12,Burla Daniel1,Tan Ge1ORCID,Askary Nima3,Larsson Rasmus3,Bost Jeremy3,Babayev Huseyn1,Dhir Raja4,Gaudenzio Nicolas56,Akdis Mubeccel1ORCID,Nadeau Kari7ORCID,Akdis Cezmi A.12ORCID,Mitamura Yasutaka1ORCID

Affiliation:

1. Swiss Institute of Allergy and Asthma Research (SIAF), University Zurich Davos Switzerland

2. Christine Kühne – Center for Allergy Research and Education (CK‐CARE) Davos Switzerland

3. SciBase AB Sundbyberg Sweden

4. SEED, Inc, Co Los Angeles California USA

5. Toulouse Institute for Infectious and Inflammatory Diseases (Infinity), INSERM UMR1291, CNRS UMR5051 University Toulouse III Toulouse France

6. Genoskin SAS Toulouse France

7. Department of Environmental Studies Harvard T.H. Chan School of Public Health Cambridge Massachusetts USA

Abstract

AbstractBackgroundEpithelial barrier impairment is associated with many skin and mucosal inflammatory disorders. Laundry detergents have been demonstrated to affect epithelial barrier function in vitro using air–liquid interface cultures of human epithelial cells.MethodsBack skin of C57BL/6 mice was treated with two household laundry detergents at several dilutions. Barrier function was assessed by electric impedance spectroscopy (EIS) and transepidermal water loss (TEWL) measurements after the 4 h of treatments with detergents. RNA sequencing (RNA‐seq) and targeted multiplex proteomics analyses in skin biopsy samples were performed. The 6‐h treatment effect of laundry detergent and sodium dodecyl sulfate (SDS) was investigated on ex vivo human skin.ResultsDetergent‐treated skin showed a significant EIS reduction and TEWL increase compared to untreated skin, with a relatively higher sensitivity and dose–response in EIS. The RNA‐seq showed the reduction of the expression of several genes essential for skin barrier integrity, such as tight junctions and adherens junction proteins. In contrast, keratinization, lipid metabolic processes, and epidermal cell differentiation were upregulated. Proteomics analysis showed that the detergents treatment generally downregulated cell adhesion‐related proteins, such as epithelial cell adhesion molecule and contactin‐1, and upregulated proinflammatory proteins, such as interleukin 6 and interleukin 1 beta. Both detergent and SDS led to a significant decrease in EIS values in the ex vivo human skin model.ConclusionThe present study demonstrated that laundry detergents and its main component, SDS impaired the epidermal barrier in vivo and ex vivo human skin. Daily detergent exposure may cause skin barrier disruption and may contribute to the development of atopic diseases.

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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