4.4 Article

Intestinal CD36 and Other Key Proteins of Lipid Utilization: Role in Absorption and Gut Homeostasis

期刊

COMPREHENSIVE PHYSIOLOGY
卷 8, 期 2, 页码 493-507

出版社

WILEY
DOI: 10.1002/cphy.c170026

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资金

  1. National Institutes of Health [T32HL007275]
  2. Nutrition and Obesity Research Center (NORC) Pilot and Feasibility grant [P30 DK-056341, R01 DK033301, R01 DK060022]
  3. Adipocyte Biology and Molecular Nutrition Core of the NORC
  4. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [T32HL007275] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK060022, P30DK056341, R01DK033301, R01DK111175] Funding Source: NIH RePORTER

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Several proteins have been implicated in fatty acid (FA) transport by enterocytes including the scavenger receptor CD36 (SR-B2), the scavenger receptor B1 (SR-B1) a member of the CD36 family and the FA transport protein 4 (FATP4). Here, we review the regulation of enterocyte FA uptake and its function in lipid absorption including prechylomicron formation, assembly and transport. Emphasis is given to CD36, which is abundantly expressed along the digestive tract of rodents and humans and has been the most studied. We also address the pleiotropic functions of CD36 that go beyond lipid absorption and metabolism to include recent evidence of its impact on intestinal homeostasis and barrier maintenance. Areas of progress involving contribution of membrane phospholipid remodeling and of cytosolic FA-binding proteins, FABP1 and FABP2 to fat absorption will be covered. (c) 2018 American Physiological Society.

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