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作者

Geru Tao Hao Wang Yishi Shen Lei Zhai Boyan Liu Bingxiang Wang Wei Chen Sijie Xing Yuan Chen Hong-Mei Gu Shucun Qin Da-Wei Zhang

作者单位

Affiliations ¹ School of Basic Medical Sciences, The Second Affiliated Hospital of Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, China (G.T., H.W., L.Z., B.L., B.W., W.C., S.X., Y.C., S.Q.). ² Institute of Atherosclerosis in Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, China (G.T., H.W., L.Z., B.L., B.W., W.C., S.X., Y.C., S.Q.). ³ Department of Pediatrics and Group on the Molecular and Cell Biology of Lipids, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada (H.-M.G., D.-W.Z.).

刊名

Arteriosclerosis, thrombosis, and vascular biology

年份

2023

ISSN

1524-4636

关键词

chylomicrons enterocytes infarction liver thoracic duct.

摘要

Background: Postprandial dyslipidemia is a causative risk factor for cardiovascular disease. The majority of absorbed dietary lipids are packaged into chylomicron and then delivered to circulation. Previous studies showed that Surf4 mediates very low-density lipoprotein secretion from hepatocytes. Silencing hepatic Surf4 markedly reduces the development of atherosclerosis in different mouse models of atherosclerosis without causing hepatic steatosis. However, the role of Surf4 in chylomicron se...更多

Background: Postprandial dyslipidemia is a causative risk factor for cardiovascular disease. The majority of absorbed dietary lipids are packaged into chylomicron and then delivered to circulation. Previous studies showed that Surf4 mediates very low-density lipoprotein secretion from hepatocytes. Silencing hepatic Surf4 markedly reduces the development of atherosclerosis in different mouse models of atherosclerosis without causing hepatic steatosis. However, the role of Surf4 in chylomicron secretion is unknown. Methods: We developed inducible intestinal-specific Surf4 knockdown mice using Vil1Cre-ER and Surf4 mice. Metabolic cages were used to monitor mouse metabolism. Enzymatic kits were employed to measure serum and tissue lipid levels. The expression of target genes was detected by qRT-PCR and Western Blot. Transmission electron microscopy and radiolabeled oleic acid were used to assess the structure of enterocytes and intestinal lipid absorption and secretion, respectively. Proteomics was performed to determine changes in protein expression in serum and jejunum. Results: Surf4 mice, especially male Surf4 mice, displayed significant body weight loss, increased mortality, and reduced metabolism. Surf4 mice exhibited lipid accumulation in enterocytes and impaired fat absorption and secretion. Lipid droplets and small lipid vacuoles were accumulated in the cytosol and the endoplasmic reticulum lumen of the enterocytes of Surf4 mice, respectively. Surf4 colocalized with apoB and co-immunoprecipitated with apoB48 in differentiated Caco-2 cells. Intestinal Surf4 deficiency also significantly reduced serum triglyceride, cholesterol, and free fatty acid levels in mice. Proteomics data revealed that diverse pathways were altered in Surf4 mice. In addition, Surf4 mice had mild liver damage, decreased liver size and weight, and reduced hepatic triglyceride levels. Conclusions: Our findings demonstrate that intestinal Surf4 plays an essential role in lipid absorption and chylomicron secretion and suggest that the therapeutic use of Surf4 inhibition requires highly cell/tissue-specific targeting.收起

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