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Novel role for caspase recruitment domain family member 14 and its genetic variant rs11652075 in skin filaggrin homeostasis - 03/02/22

Doi : 10.1016/j.jaci.2021.07.003 
Stanley B. DeVore, MS a, b, Mariana L. Stevens, PhD b, Hua He, MS c, Jocelyn M. Biagini, PhD a, b, John W. Kroner, MS b, Lisa J. Martin, PhD a, c, Gurjit K. Khurana Hershey, MD, PhD a, b,
a Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio 
b Division of Asthma Research, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio 
c Division of Human Genetics, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio 

Corresponding author: Gurjit K. Khurana Hershey, MD, PhD, 3333 Burnet Ave, MLC 7037, Cincinnati, OH 45229.3333 Burnet AveMLC 7037CincinnatiOH45229

Abstract

Background

Low epidermal filaggrin (FLG) is a risk factor for atopic dermatitis (AD) and allergic comorbidity. FLG mutations do not fully explain the variation in epidermal FLG levels, highlighting that other genetic loci may also regulate FLG expression.

Objective

We sought to identify genetic loci that regulate FLG expression and elucidate their functional and mechanistic consequences.

Methods

A genome-wide association study of quantified skin FLG expression in lesional and baseline non(never)-lesional skin of children with AD in the Mechanisms of Progression of Atopic Dermatitis to Asthma in Children cohort was conducted. Clustered regularly interspaced short palindromic repeat approaches were used to create isogenic human keratinocytes differing only at the identified variant rs11652075, and caspase recruitment domain family member 14 (CARD14)-deficient keratinocytes for subsequent mechanistic studies.

Results

The genome-wide association study identified the CARD14 rs11652075 variant to be associated with FLG expression in non(never)-lesional skin of children with AD. Rs11652075 is a CARD14 expression quantitative trait locus in human skin and primary human keratinocytes. The T variant destroys a functional cytosine-phosphate-guanine site, resulting in reduced cytosine-phosphate-guanine methylation at this site (but not neighboring sites) in TT and CT compared with CC primary human keratinocytes and Mechanisms of Progression of Atopic Dermatitis to Asthma in Children children’s skin samples, and rs11652075 increases CARD14 expression in an allele-specific fashion. Furthermore, studies in clustered regularly interspaced short palindromic repeat-generated CC and TT isogenic keratinocytes, as well as CARD14-haplosufficient and deficient keratinocytes, reveal that IL-17A regulates FLG expression via CARD14, and that the underlying mechanisms are dependent on the rs11652075 genotype.

Conclusions

Our study identifies CARD14 as a novel regulator of FLG expression in the skin of children with AD. Furthermore, CARD14 regulates skin FLG homeostasis in an rs11652075-dependent fashion.

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Key words : Atopic dermatitis, filaggrin, CARD14, GWAS, skin, gene, skin barrier

Abbreviations used : AD, BCL10, CARD14, Cas9, CBM, CCL20, CpG, CRISPR-Cas9, CXCL8, eQTL, FLG, GWAS, MALT1, MAPK, MPAACH, NF-kB, SNP


Mappa


 This work was supported by the National Institutes of Health (grant no, U19AI70235 to G.K.K.H., J.M.B., and L.J.M.). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
 Disclosure of potential conflict of interest: The authors declare that they have no relevant conflicts of interest.


© 2021  American Academy of Allergy, Asthma & Immunology. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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Vol 149 - N° 2

P. 708-717 - Febbraio 2022 Ritorno al numero
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