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NNT mediates redox-dependent pigmentation via a UVB- and MITF-independent mechanism.

Authors :
Allouche J
Rachmin I
Adhikari K
Pardo LM
Lee JH
McConnell AM
Kato S
Fan S
Kawakami A
Suita Y
Wakamatsu K
Igras V
Zhang J
Navarro PP
Lugo CM
Noonan HR
Christie KA
Itin K
Mujahid N
Lo JA
Won CH
Evans CL
Weng QY
Wang H
Osseiran S
Lovas A
Németh I
Cozzio A
Navarini AA
Hsiao JJ
Nguyen N
Kemény LV
Iliopoulos O
Berking C
Ruzicka T
Gonzalez-José R
Bortolini MC
Canizales-Quinteros S
Acuna-Alonso V
Gallo C
Poletti G
Bedoya G
Rothhammer F
Ito S
Schiaffino MV
Chao LH
Kleinstiver BP
Tishkoff S
Zon LI
Nijsten T
Ruiz-Linares A
Fisher DE
Roider E
Source :
Cell [Cell] 2021 Aug 05; Vol. 184 (16), pp. 4268-4283.e20. Date of Electronic Publication: 2021 Jul 06.
Publication Year :
2021

Abstract

Ultraviolet (UV) light and incompletely understood genetic and epigenetic variations determine skin color. Here we describe an UV- and microphthalmia-associated transcription factor (MITF)-independent mechanism of skin pigmentation. Targeting the mitochondrial redox-regulating enzyme nicotinamide nucleotide transhydrogenase (NNT) resulted in cellular redox changes that affect tyrosinase degradation. These changes regulate melanosome maturation and, consequently, eumelanin levels and pigmentation. Topical application of small-molecule inhibitors yielded skin darkening in human skin, and mice with decreased NNT function displayed increased pigmentation. Additionally, genetic modification of NNT in zebrafish alters melanocytic pigmentation. Analysis of four diverse human cohorts revealed significant associations of skin color, tanning, and sun protection use with various single-nucleotide polymorphisms within NNT. NNT levels were independent of UVB irradiation and redox modulation. Individuals with postinflammatory hyperpigmentation or lentigines displayed decreased skin NNT levels, suggesting an NNT-driven, redox-dependent pigmentation mechanism that can be targeted with NNT-modifying topical drugs for medical and cosmetic purposes.<br />Competing Interests: Declaration of interests D.E.F. and E.R. have a patent filed on “Methods and compositions for enhancing skin pigmentation” (publication number WO/2016/077817, May 19, 2016.). D.E.F. has a financial interest in Soltego, Inc., a company developing SIK inhibitors for topical skin darkening treatments that might be used for a broad set of human applications. D.E.F.’s interests were reviewed and are managed by Massachusetts General Hospital and Partners HealthCare in accordance with their conflict-of-interest policies. B.P.K. is an inventor on patents and patent applications filed by Mass General Brigham that describe genome engineering technologies. B.P.K. consults for Avectas Inc., ElevateBio, and EcoR1 capital and is an advisor to Acrigen Biosciences. Q.Y.W. is a shareholder in Mymiel Skincare. L.I.Z. is a founder and stockholder of Fate Therapeutics, CAMP4 Therapeutics, Amagma Therapeutics, and Scholar Rock. He is a consultant for Celularity and Cellarity. H.W. is an employee and shareholder of Johnson and Johnson.<br /> (Copyright © 2021 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-4172
Volume :
184
Issue :
16
Database :
MEDLINE
Journal :
Cell
Publication Type :
Academic Journal
Accession number :
34233163
Full Text :
https://doi.org/10.1016/j.cell.2021.06.022