Two‐pore channel 2 is required for soluble adenylyl cyclase‐dependent regulation of melanosomal pH and melanin synthesis

Author:

Zhou Dalee1,Eraslan Zuhal1,Miller Dawson2,Taylor Isobel2,You Jaewon1,Grondin Samuel J.2,Vega Martha3,Manga Prashiela3,Goff Philip S.4ORCID,Sviderskaya Elena V.4,Gross Steven S.2,Chen Qiuying2,Zippin Jonathan H.12ORCID

Affiliation:

1. Department of Dermatology Weill Cornell Medical College of Cornell University New York New York USA

2. Department of Pharmacology Weill Cornell Medical College of Cornell University New York New York USA

3. The Ronald O. Perelman Department of Dermatology New York University School of Medicine New York New York USA

4. Cell Biology Research Section, Molecular and Clinical Sciences Research Institute St George's University of London London UK

Abstract

AbstractMelanosomal pH is important for the synthesis of melanin as the rate‐limiting enzyme, tyrosinase, is very pH‐sensitive. The soluble adenylyl cyclase (sAC) signaling pathway was recently identified as a regulator of melanosomal pH in melanocytes; however, the melanosomal proteins critical for sAC‐dependent regulation of melanosomal pH were undefined. We now systematically examine four well‐characterized melanosomal membrane proteins to determine whether any of them are required for sAC‐dependent regulation of melanosomal pH. We find that OA1, OCA2, and SLC45A2 are dispensable for sAC‐dependent regulation of melanosomal pH. In contrast, TPC2 activity is required for sAC‐dependent regulation of melanosomal pH and melanin synthesis. In addition, activation of TPC2 by NAADP‐AM rescues melanosomal pH alkalinization and reduces melanin synthesis following pharmacologic or genetic inhibition of sAC signaling. These studies establish TPC2 as a critical melanosomal protein for sAC‐dependent regulation of melanosomal pH and pigmentation.

Funder

Dermatology Foundation

Pfizer

National Cancer Institute

National Institute of Arthritis and Musculoskeletal and Skin Diseases

National Institute of Environmental Health Sciences

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

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