期刊
HUMAN MOLECULAR GENETICS
卷 17, 期 17, 页码 2723-2737出版社
OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddn174
关键词
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资金
- Intramural Research Program of the NIH
- National Heart, Lung, and Blood Institute (NHLBI)
- NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [ZIAHL000140, ZICHL005906, Z01HL005906, Z01HL000140] Funding Source: NIH RePORTER
Mutations in Mucolipin 1 (MCOLN1) have been linked to mucolipidosis type IV (MLIV), a lysosomal storage disease characterized by several neurological and ophthalmological abnormalities. It has been proposed that MCOLN1 might regulate transport of membrane components in the late endosomal-lysosomal pathway; however, the mechanisms by which defects of MCOLN1 function result in mental and psychomotor retardation remain largely unknown. In this study, we show constitutive activation of autophagy in fibroblasts obtained from MLIV patients. Accumulation of autophagosomes in MLIV cells was due to the increased de novo autophagosome formation and to delayed fusion of autophagosomes with late endosomes/lysosomes. Impairment of the autophagic pathway led to increased levels and aggregation of p62, suggesting that abnormal accumulation of ubiquitin proteins may contribute to the neurodegeneration observed in MLIV patients. In addition, we found that delivery of platelet-derived growth factor receptor to lysosomes is delayed in MCOLN1-deficient cells, suggesting that MCOLN1 is necessary for efficient fusion of both autophagosomes and late endosomes with lysosomes. Our data are in agreement with recent evidence showing that autophagic defects may be a common characteristic of many neurodegenerative disorders.
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