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oai:null:10339/930582026-09-02T11:53:01Zcom_10339_14934col_10339_38132

Bashore, Alexander Cusa 2019-01-11T09:35:19Z 2024-01-10T09:30:06Z 2018 https://wakespace.lib.wfu.edu/handle/10339/93058 Hepatic ATP binding cassette transporter A1 (ABCA1) and apolipoprotein M (apoM) both have been shown to influence high density lipoprotein (HDL) metabolism. Hepatic ABCA1, a plasma membrane protein, functions to transport free cholesterol (FC) and phospholipids across the plasma membrane to apolipoproteins, forming nascent HDL particles. Hepatic ABCA1 is essential in HDL particle formation and maintenance of plasma HDL cholesterol (HDL-C) levels. However, its role in trafficking of hepatic FC into plasma versus bile for reverse cholesterol transport (RCT) is poorly understood. We found that hepatocyte specific ABCA1 knockout (HSKO) mice have increased plasma HDL cholesteryl ester (CE) clearance, selective uptake, and fecal excretion compared to control mice and these increases are mediated by increased hepatic LDLr expression. ABCA1 deletion also resulted in diminished recycling of HDL-C taken up by the liver back into plasma. Hepatocyte ABCA1 deletion unmasks a novel and selective FC trafficking pathway in which increased LDLr expression accelerates plasma HDL selective CE uptake by the liver and promotes HDL RCT into feces, consequently reducing HDL-derived hepatic FC recycling into plasma. en Wake Forest University Apolipoprotein Cholesterol High Density Lipoprotein Lipids Metabolism THE ROLE OF HEPATOCYTE ATP-BINDING CASSETTE TRANSPORTER A1 (ABCA1) AND APOLIPOPROTEIN M (APOM) IN HIGH DENSITY LIPOPROTEIN (HDL) METABOLISM Dissertation Parks, John S Tallant, Elisabeth A Kavanagh, Kylie Liu, Mingxia Zhu, Xuewei Physiology and Pharmacology 2024-01-10 open.access