Cellular Localization and Trafficking of the Human ABCG1 Transporter

Edward B Neufeld; Katherine O'Brien; Avram D Walts; John A Stonik; Steven J Demosky; Daniela Malide; Christian A Combs; Alan T Remaley

doi:10.3390/biology3040781

Cellular Localization and Trafficking of the Human ABCG1 Transporter

Biology (Basel). 2014 Nov 14;3(4):781-800. doi: 10.3390/biology3040781.

Authors

Edward B Neufeld¹, Katherine O'Brien², Avram D Walts³, John A Stonik⁴, Steven J Demosky⁵, Daniela Malide⁶, Christian A Combs⁷, Alan T Remaley⁸

Affiliations

¹ Lipoprotein Metabolism Section, Cardiovascular and Pulmonary Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA. neufelde@mail.nih.gov.
² Lipid Trafficking Core, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA. obrienk@nhlbi.nih.gov.
³ Lipid Trafficking Core, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA. awalts@yahoo.com.
⁴ Lipoprotein Metabolism Section, Cardiovascular and Pulmonary Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA. jstonik@verizon.net.
⁵ Lipoprotein Metabolism Section, Cardiovascular and Pulmonary Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA. sjdjr@nhlbi.nih.gov.
⁶ NHLBI Light Microscopy Core Facility, National Institutes of Health, Bethesda, MD 20892, USA. dmalide@mail.nih.gov.
⁷ NHLBI Light Microscopy Core Facility, National Institutes of Health, Bethesda, MD 20892, USA. combsc@nih.gov.
⁸ Lipoprotein Metabolism Section, Cardiovascular and Pulmonary Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA. Alan.Remaley@nih.gov.

Abstract

We have developed a suitable heterologous cell expression system to study the localization, trafficking, and site(s) of function of the human ABCG1 transporter. Increased plasma membrane (PM) and late endosomal (LE) cholesterol generated by ABCG1 was removed by lipoproteins and liposomes, but not apoA-I. Delivery of ABCG1 to the PM and LE was required for ABCG1-mediated cellular cholesterol efflux. ABCG1 LEs frequently contacted the PM, providing a collisional mechanism for transfer of ABCG1-mobilized cholesterol, similar to ABCG1-mediated PM cholesterol efflux to lipoproteins. ABCG1-mobilized LE cholesterol also trafficked to the PM by a non-vesicular pathway. Transfer of ABCG1-mobilized cholesterol from the cytoplasmic face of LEs to the PM and concomitant removal of cholesterol from the outer leaflet of the PM bilayer by extracellular acceptors suggests that ABCG1 mobilizes cholesterol on both sides of the lipid bilayer for removal by acceptors. ABCG1 increased uptake of HDL into LEs, consistent with a potential ABCG1-mediated cholesterol efflux pathway involving HDL resecretion. Thus, ABCG1 at the PM mobilizes PM cholesterol and ABCG1 in LE/LYS generates mobile pools of cholesterol that can traffic by both vesicular and non-vesicular pathways to the PM where it can also be transferred to extracellular acceptors with a lipid surface.