Cholesterol Handling in Lysosomes and Beyond
Trends in Cell Biology, ISSN: 0962-8924, Vol: 30, Issue: 6, Page: 452-466
2020
- 124Citations
- 213Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations124
- Citation Indexes123
- 123
- CrossRef12
- Policy Citations1
- Policy Citation1
- Captures213
- Readers213
- 213
Review Description
Lysosomes are of major importance for the regulation of cellular cholesterol homeostasis. Food-derived cholesterol and cholesterol esters contained within lipoproteins are delivered to lysosomes by endocytosis. From the lysosomal lumen, cholesterol is transported to the inner surface of the lysosomal membrane through the glycocalyx; this shuttling requires Niemann–Pick C (NPC) 1 and NPC2 proteins. The lysosomal membrane proteins lysosomal-associated membrane protein (LAMP)-2 and lysosomal integral membrane protein (LIMP)-2/SCARB2 also bind cholesterol. LAMP-2 may serve as a cholesterol reservoir, whereas LIMP-2, like NPC1, is able to transport cholesterol through a transglycocalyx tunnel. Contact sites and fusion events between lysosomes and other organelles mediate the distribution of cholesterol. Lysosomal cholesterol content is sensed thereby regulating mammalian target of rapamycin complex (mTORC)-dependent signaling. This review summarizes our understanding of the major steps in cholesterol handling from the moment it enters the lysosome until it leaves this compartment.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0962892420300520; http://dx.doi.org/10.1016/j.tcb.2020.02.007; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85082409103&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/32413315; https://linkinghub.elsevier.com/retrieve/pii/S0962892420300520; https://dx.doi.org/10.1016/j.tcb.2020.02.007
Elsevier BV
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