Comment on ‘Orthogonal lipid sensors identify transbilayer asymmetry of plasma membrane cholesterol’

Author:

Courtney Kevin C1ORCID,Fung Karen YY2,Maxfield Frederick R3ORCID,Fairn Gregory D2,Zha Xiaohui14ORCID

Affiliation:

1. Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ontario, Canada

2. Keenan Research Centre, St. Michael’s Hospital, Toronto, Canada

3. Department of Biochemistry, Weill Cornell Medical College, New York, United States

4. Chronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Canada

Abstract

The plasma membrane in mammalian cells is rich in cholesterol, but how the cholesterol is partitioned between the two leaflets of the plasma membrane remains a matter of debate. Recently, Liu et al. used domain 4 (D4) of perfringolysin O as a cholesterol sensor to argue that cholesterol is mostly in the exofacial leaflet (<xref ref-type="bibr" rid="bib7">Liu et al., 2017</xref>). This conclusion was made by interpreting D4 binding in live cells using in vitro calibrations with liposomes. However, liposomes may be unfaithful in mimicking the plasma membrane, as we demonstrate here. Also, D4 binding is highly sensitive to the presence of cytosolic proteins. In addition, we find that a D4 variant, which requires >35 mol% cholesterol to bind to liposomes in vitro, does in fact bind to the cytoplasmic leaflet of the plasma membrane in a cholesterol-dependent manner. Thus, we believe, based on the current evidence, that it is unlikely that there is a significantly higher proportion of cholesterol in the exofacial leaflet of the plasma membrane compared to the cytosolic leaflet.

Funder

Canadian Institutes of Health Research

Natural Sciences and Engineering Research Council of Canada

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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