Department of Human Biology, NUTRIM School for Nutrition, Toxicology and Metabolism, Maastricht University Medical Centre+, Maastricht, The Netherlands.
PLoS One. 2010 Apr 29;5(4):e10380. doi: 10.1371/journal.pone.0010380.
Protein distribution profiles along the human intestinal tract of transporters involved in the absorption of cholesterol and long-chain fatty acids (LCFA) have been scarcely evaluated.
METHODOLOGY/PRINCIPAL FINDINGS: In post-mortem samples from 11 subjects, intestinal transporter distribution profiles were determined via Western Blot. Differences in transporter protein levels were statistically tested using ANOVA and Tukey's Post Hoc comparisons. Levels in all segments were expressed relative to those in duodenum. Except for ABCG5 and FATP4, levels (mean+/-SEM) were the highest in the ileum. For ABCA1, ileal levels (1.80+/-0.26) differed significantly from those in duodenum (P = 0.049) and proximal colon (0.92+/-0.14; P = 0.029). ABCG8 levels in ileum (1.91+/-0.30) differed from those in duodenum (P = 0.041) and distal colon (0.84+/-0.22; P = 0.010) and jejunum (1.64+/-0.26) tended to be higher than distal colon (0.84+/-0.22; P = 0.087). Ileal NPC1L1 levels (2.56+/-0.51) differed from duodenum levels (P = 0.019) and from distal colon (1.09+/-0.22; P = 0.030). There was also a trend (P = 0.098) for higher jejunal (2.23+/-0.37) than duodenal NPC1L1 levels. The levels of ABCG5 did not correlate with those of ABCG8. FAT/CD36 levels in ileum (2.03+/-0.42) differed from those in duodenum (P = 0.017), and proximal and distal colon (0.89+/-0.13 and 0.97+/-0.15 respectively; P = 0.011 and P = 0.014). FABPpm levels in ileum (1.04+/-0.13) differed from proximal (0.64+/-0.07; P = 0.026) and distal colon (0.66+/-0.09; P = 0.037).
CONCLUSIONS/SIGNIFICANCE: The distribution profiles showed a bell-shape pattern along the GI-tract with the highest levels in ileum for ABCA1, ABCG8, NPC1L1, FATCD36 and FABPm, suggesting a prominent role for ileum in transporter-mediated uptake of cholesterol and LCFAs.
人们对涉及胆固醇和长链脂肪酸(LCFA)吸收的肠道转运蛋白在人体肠道中的分布情况知之甚少。
方法/主要发现:在 11 名受试者的尸检样本中,通过 Western Blot 测定肠道转运蛋白的分布情况。使用方差分析和 Tukey 事后检验比较来对转运蛋白的水平差异进行统计学检验。所有肠段的水平均相对于十二指肠的水平进行表达。除 ABCG5 和 FATP4 外,回肠中的蛋白水平最高。ABCA1 的回肠水平(1.80±0.26)与十二指肠(P=0.049)和近端结肠(0.92±0.14;P=0.029)的水平差异有统计学意义。回肠 ABCG8 水平(1.91±0.30)与十二指肠(P=0.041)和远端结肠(0.84±0.22;P=0.010)和空肠(1.64±0.26)的水平差异有统计学意义,且空肠的水平有高于远端结肠的趋势(0.84±0.22;P=0.087)。回肠 NPC1L1 水平(2.56±0.51)与十二指肠(P=0.019)和远端结肠(1.09±0.22;P=0.030)的水平差异有统计学意义。空肠 NPC1L1 水平(P=0.098)也有高于十二指肠的趋势。ABCG5 的水平与 ABCG8 不相关。回肠的 FAT/CD36 水平(2.03±0.42)与十二指肠(P=0.017)和近端结肠(0.89±0.13)和远端结肠(0.97±0.15)的水平差异有统计学意义;与近端结肠(P=0.011)和远端结肠(P=0.014)的水平差异有统计学意义。回肠 FABPpm 水平(1.04±0.13)与空肠(0.64±0.07;P=0.026)和远端结肠(0.66±0.09;P=0.037)的水平差异有统计学意义。
结论/意义:分布曲线显示出沿胃肠道呈钟形模式,ABCA1、ABCG8、NPC1L1、FAT/CD36 和 FABPm 在回肠中的水平最高,这表明回肠在胆固醇和长链脂肪酸的转运体介导吸收中起着重要作用。