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NNT mediates redox-dependent pigmentation via a UVB- and MITF-independent mechanism.
- 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.)
- Subjects :
- Animals
Cell Line
Cohort Studies
Cyclic AMP metabolism
DNA Damage
Enzyme Inhibitors chemistry
Enzyme Inhibitors pharmacology
Genetic Predisposition to Disease
Humans
Melanocytes drug effects
Melanocytes metabolism
Melanosomes drug effects
Melanosomes metabolism
Melanosomes radiation effects
Mice
Mice, Inbred C57BL
Mitochondria drug effects
Mitochondria metabolism
Monophenol Monooxygenase genetics
Monophenol Monooxygenase metabolism
NADP Transhydrogenases antagonists & inhibitors
Oxidation-Reduction drug effects
Oxidation-Reduction radiation effects
Polymorphism, Single Nucleotide genetics
Proteasome Endopeptidase Complex metabolism
Proteolysis drug effects
Proteolysis radiation effects
RNA, Messenger genetics
RNA, Messenger metabolism
Skin Pigmentation drug effects
Skin Pigmentation genetics
Ubiquitin metabolism
Zebrafish
Microphthalmia-Associated Transcription Factor metabolism
NADP Transhydrogenases metabolism
Skin Pigmentation radiation effects
Ultraviolet Rays
Subjects
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