PMEL Amyloid Fibril Formation: The Bright Steps of Pigmentation

被引:80
作者
Bissig, Christin [1 ,2 ]
Rochin, Leila [3 ]
van Niel, Guillaume [1 ,2 ]
机构
[1] Paris Sci & Lettres Res Univ, Inst Curie, Ctr Rech, UMR144, 26 Rue ULM, F-75231 Paris, France
[2] CNRS, UMR144, F-75248 Paris, France
[3] Univ Liverpool, Inst Translat Med, Dept Cellular & Mol Physiol, Liverpool L69 3BX, Merseyside, England
基金
瑞士国家科学基金会;
关键词
melanosome; PMEL; amyloid; pigmentation; fibril formation; melanocyte; secretases; apolipoprotein E; SOLUBLE-PROTEIN OLIGOMERS; ALZHEIMERS-DISEASE; REPEAT DOMAIN; MEMBRANE-PROTEINS; PRECURSOR PROTEIN; BETA-SECRETASE; HUMAN MELANOCYTES; APOLIPOPROTEIN-E; SILVER MUTATION; ESCRT MACHINERY;
D O I
10.3390/ijms17091438
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In pigment cells, melanin synthesis takes place in specialized organelles, called melanosomes. The biogenesis and maturation of melanosomes is initiated by an unpigmented step that takes place prior to the initiation of melanin synthesis and leads to the formation of luminal fibrils deriving from the pigment cell-specific pre-melanosomal protein (PMEL). In the lumen of melanosomes, PMEL fibrils optimize sequestration and condensation of the pigment melanin. Interestingly, PMEL fibrils have been described to adopt a typical amyloid-like structure. In contrast to pathological amyloids often associated with neurodegenerative diseases, PMEL fibrils represent an emergent category of physiological amyloids due to their beneficial cellular functions. The formation of PMEL fibrils within melanosomes is tightly regulated by diverse mechanisms, such as PMEL traffic, cleavage and sorting. These mechanisms revealed increasing analogies between the formation of physiological PMEL fibrils and pathological amyloid fibrils. In this review we summarize the known mechanisms of PMEL fibrillation and discuss how the recent understanding of physiological PMEL amyloid formation may help to shed light on processes involved in pathological amyloid formation.
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页数:14
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