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

Compr Physiol. 2018 Mar 26;8(2):493-507. doi: 10.1002/cphy.c170026.

Abstract

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. © 2018 American Physiological Society. Compr Physiol 8:493-507, 2018.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biological Transport / physiology
  • CD36 Antigens / physiology*
  • Chylomicrons / biosynthesis
  • Digestive System / metabolism
  • Enterocytes / metabolism
  • Fatty Acids / metabolism
  • Homeostasis / physiology
  • Humans
  • Intestinal Absorption / physiology*
  • Lipid Metabolism / physiology*
  • Phospholipids / metabolism

Substances

  • CD36 Antigens
  • Chylomicrons
  • Fatty Acids
  • Phospholipids