An intracellular anion channel critical for pigmentation

被引:109
作者
Bellono, Nicholas W. [1 ]
Escobar, Iliana E. [1 ]
Lefkovith, Ariel J. [2 ,3 ]
Marks, Michael S. [2 ,3 ]
Oancea, Elena [1 ]
机构
[1] Brown Univ, Dept Mol Pharmacol Physiol & Biotechnol, Providence, RI 02912 USA
[2] Univ Penn, Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Childrens Hosp Philadelphia, Dept Physiol, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
PINK-EYED DILUTION; OCULOCUTANEOUS ALBINISM TYPE-2; P-GENE; OCULAR ALBINISM; MELANOSOME MATURATION; BAFILOMYCIN A1; PRADER-WILLI; OCA2; TYROSINASE; MUTATIONS;
D O I
10.7554/eLife.04543
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
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.
引用
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页数:16
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