» Articles » PMID: 27183391

Oxidative Stress and Dysfunctional NRF2 Underlie Pachyonychia Congenita Phenotypes

Overview
Journal J Clin Invest
Specialty General Medicine
Date 2016 May 17
PMID 27183391
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

Palmoplantar keratoderma (PPK) are debilitating lesions that arise in individuals with pachyonychia congenita (PC) and feature upregulation of danger-associated molecular patterns and skin barrier regulators. The defining features of PC-associated PPK are reproduced in mice null for keratin 16 (Krt16), which is commonly mutated in PC patients. Here, we have shown that PPK onset is preceded by oxidative stress in footpad skin of Krt16-/- mice and correlates with an inability of keratinocytes to sustain nuclear factor erythroid-derived 2 related factor 2-dependent (NRF2-dependent) synthesis of the cellular antioxidant glutathione (GSH). Additionally, examination of plantar skin biopsies from individuals with PC confirmed the presence of high levels of hypophosphorylated NRF2 in lesional tissue. In Krt16-/- mice, genetic ablation of Nrf2 worsened spontaneous skin lesions and accelerated PPK development in footpad skin. Hypoactivity of NRF2 in Krt16-/- footpad skin correlated with decreased levels or activity of upstream NRF2 activators, including PKCδ, receptor for activated C kinase 1 (RACK1), and p21. Topical application of the NRF2 activator sulforaphane to the footpad of Krt16-/- mice prevented the development of PPK and normalized redox balance via regeneration of GSH from existing cellular pools. Together, these findings point to oxidative stress and dysfunctional NRF2 as contributors to PPK pathogenesis, identify K16 as a regulator of NRF2 activation, and suggest that pharmacological activation of NRF2 should be further explored for PC treatment.

Citing Articles

Treatment of palmoplantar keratoderma in a patient with ichthyosis with topical tapinarof.

Robinson S, Kranseler J, Rosmarin D JAAD Case Rep. 2024; 45:66-67.

PMID: 38389856 PMC: 10882012. DOI: 10.1016/j.jdcr.2024.01.017.


Significance of stress keratin expression in normal and diseased epithelia.

Cohen E, Johnson C, Wasikowski R, Billi A, Tsoi L, Kahlenberg J iScience. 2024; 27(2):108805.

PMID: 38299111 PMC: 10828818. DOI: 10.1016/j.isci.2024.108805.


Vascular Endothelial Growth Factor A VEGFA Inhibition: An Effective Treatment Strategy for Psoriasis.

Chen Y, Tai Z, Zhu C, Yu Q, Zhu Q, Chen Z Int J Mol Sci. 2024; 25(1).

PMID: 38203230 PMC: 10778864. DOI: 10.3390/ijms25010059.


Role of Phytochemicals in Skin Photoprotection Regulation of Nrf2.

Chaiprasongsuk A, Panich U Front Pharmacol. 2022; 13:823881.

PMID: 35645796 PMC: 9133606. DOI: 10.3389/fphar.2022.823881.


Redox signaling at the crossroads of human health and disease.

Zuo J, Zhang Z, Luo M, Zhou L, Nice E, Zhang W MedComm (2020). 2022; 3(2):e127.

PMID: 35386842 PMC: 8971743. DOI: 10.1002/mco2.127.


References
1.
Omary M, Coulombe P, McLean W . Intermediate filament proteins and their associated diseases. N Engl J Med. 2004; 351(20):2087-100. DOI: 10.1056/NEJMra040319. View

2.
Lessard J, Coulombe P . Keratin 16-null mice develop palmoplantar keratoderma, a hallmark feature of pachyonychia congenita and related disorders. J Invest Dermatol. 2012; 132(5):1384-91. PMC: 3326191. DOI: 10.1038/jid.2012.6. View

3.
Leachman S, Hickerson R, Schwartz M, Bullough E, Hutcherson S, Boucher K . First-in-human mutation-targeted siRNA phase Ib trial of an inherited skin disorder. Mol Ther. 2009; 18(2):442-6. PMC: 2839285. DOI: 10.1038/mt.2009.273. View

4.
Lushchak V . Glutathione homeostasis and functions: potential targets for medical interventions. J Amino Acids. 2012; 2012:736837. PMC: 3303626. DOI: 10.1155/2012/736837. View

5.
Goldberg I, Fruchter D, Meilick A, Schwartz M, Sprecher E . Best treatment practices for pachyonychia congenita. J Eur Acad Dermatol Venereol. 2013; 28(3):279-85. DOI: 10.1111/jdv.12098. View