A mechanism of self-lipid endocytosis mediated by the receptor Mincle.
Proc Natl Acad Sci U S A
; 119(30): e2120489119, 2022 07 26.
Article
in En
| MEDLINE
| ID: mdl-35867828
ABSTRACT
Cellular lipid uptake (through endocytosis) is a basic physiological process. Dysregulation of this process underlies the pathogenesis of diseases such as atherosclerosis, obesity, diabetes, and cancer. However, to date, only some mechanisms of lipid endocytosis have been discovered. Here, we show a previously unknown mechanism of lipid cargo uptake into cells mediated by the receptor Mincle. We found that the receptor Mincle, previously shown to be a pattern recognition receptor of the innate immune system, tightly binds a range of self-lipids. Moreover, we revealed the minimal molecular motif in lipids that is sufficient for Mincle recognition. Superresolution microscopy showed that Mincle forms vesicles in cytoplasm and colocalizes with added fluorescent lipids in endothelial cells but does not colocalize with either clathrin or caveolin-1, and the added lipids were predominantly incorporated in vesicles that expressed Mincle. Using a model of ganglioside GM3 uptake in brain vessel endothelial cells, we show that the knockout of Mincle led to a dramatic decrease in lipid endocytosis. Taken together, our results have revealed a fundamental lipid endocytosis pathway, which we call Mincle-mediated endocytosis (MiME), and indicate a prospective target for the treatment of disorders of lipid metabolism, which are rapidly increasing in prevalence.
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Lectins, C-Type
/
Endocytosis
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Lipid Metabolism
/
Membrane Proteins
Type of study:
Risk_factors_studies
Limits:
Animals
Language:
En
Year:
2022
Type:
Article