Chen M, Yang Y, Braunstein E, Georgeson K E, Harmon C M
Department of Surgery, University of Alabama at Birmingham, 35233, USA.
Am J Physiol Endocrinol Metab. 2001 Nov;281(5):E916-23. doi: 10.1152/ajpendo.2001.281.5.E916.
Fatty acid translocase (FAT)/CD36 is one of several putative plasma membrane long-chain fatty acid (LCFA) transport proteins; however, its role in intestinal absorption of LCFA is unknown. We hypothesized that FAT/CD36 would be differentially expressed along the longitudinal axis of the gut and during intestinal development, suggesting specificity of function. We found that intestinal mucosal FAT/CD36 mRNA levels varied by anatomic location along the longitudinal gut axis: stomach 45 +/- 7, duodenum 173 +/- 29, jejunum 238 +/- 17, ileum 117 +/- 14, and colon 9 +/- 1% (means +/- SE with 18S mRNA as control). FAT/CD36 protein levels were also higher in proximal compared with distal intestinal mucosa. Mucosal FAT/CD36 mRNA was also regulated during intestinal maturation, with a fourfold increase from neonatal to adult animals. In addition, FAT/CD36 mRNA levels and enterocyte LCFA uptake were rapidly downregulated by intraduodenal oleate infusion. These findings suggest that FAT/CD36 plays a role in the uptake of LCFA by small intestinal enterocytes. This may have important implications in understanding fatty acid absorption in human physiological and pathophysiological conditions.
脂肪酸转位酶(FAT)/CD36是几种假定的质膜长链脂肪酸(LCFA)转运蛋白之一;然而,其在肠道LCFA吸收中的作用尚不清楚。我们推测FAT/CD36会在肠道的纵轴上以及肠道发育过程中差异表达,这表明其功能具有特异性。我们发现,肠道黏膜FAT/CD36 mRNA水平沿肠道纵轴的解剖位置而变化:胃为45±7,十二指肠为173±29,空肠为238±17,回肠为117±14,结肠为9±1%(以18S mRNA为对照的均值±标准误)。与远端肠道黏膜相比,近端肠道黏膜的FAT/CD36蛋白水平也更高。黏膜FAT/CD36 mRNA在肠道成熟过程中也受到调控,从新生动物到成年动物增加了四倍。此外,十二指肠内注入油酸可使FAT/CD36 mRNA水平和肠上皮细胞LCFA摄取迅速下调。这些发现表明FAT/CD36在小肠肠上皮细胞摄取LCFA中发挥作用。这对于理解人类生理和病理生理条件下的脂肪酸吸收可能具有重要意义。