An intracellular anion channel critical for pigmentation

Author:

Bellono Nicholas W1,Escobar Iliana E1,Lefkovith Ariel J23,Marks Michael S23,Oancea Elena1

Affiliation:

1. Department of Molecular Pharmacology, Physiology and Biotechnology, Brown University, Providence, United States

2. Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, United States

3. Department of Physiology, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, United States

Abstract

Intracellular ion channels are essential regulators of organellar and cellular function, yet the molecular identity and physiological role of many of these channels remains elusive. In particular, no ion channel has been characterized in melanosomes, organelles that produce and store the major mammalian pigment melanin. Defects in melanosome function cause albinism, characterized by vision and pigmentation deficits, impaired retinal development, and increased susceptibility to skin and eye cancers. The most common form of albinism is caused by mutations in oculocutaneous albinism II (OCA2), a melanosome-specific transmembrane protein with unknown function. Here we used direct patch-clamp of skin and eye melanosomes to identify a novel chloride-selective anion conductance mediated by OCA2 and required for melanin production. Expression of OCA2 increases organelle pH, suggesting that the chloride channel might regulate melanin synthesis by modulating melanosome pH. Thus, a melanosomal anion channel that requires OCA2 is essential for skin and eye pigmentation.

Funder

National Science Foundation

National Institute of General Medical Sciences

National Institute of Arthritis and Musculoskeletal and Skin Diseases

National Eye Institute

Brown University

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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