Shah D, Shen W C
Department of Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles 90033.
J Drug Target. 1994;2(2):93-9. doi: 10.3109/10611869409015897.
The effect of enterocyte-like differentiation on the transferrin receptor (TfR) polarity in filter-grown Caco-2 cells was studied. The ratio of apical to basolateral TfRs which was found to be approximately 1:1 on the first day after the cells had reached confluence, changed to 1:40 eight days after reaching confluence. The transepithelial electrical resistance (TEER), transport of horseradish peroxidase (HRP) across the monolayer, and total cellular TfR number remained constant over this period. However, the activity of brush border membrane-associated alkaline phosphatase, an established marker for enterocyte differentiation, increased over this 8-day period concurrent with a decrease in apical TfR number. These results suggest that enterocyte-like differentiation rather than tight junction formation is most likely responsible for the polarized distribution of TfRs in Caco-2 cells. The effects of the fungal metabolite brefeldin A (BFA) on TfR distribution and TfR-mediated transcytosis in Caco-2 cells were also studied. BFA caused a marked decrease in the number of basolateral TfRs along with a slight increase in the number of apical TfR. BFA enhanced the TfR-mediated transcytosis of both 125I-Tf and the horseradish peroxidase-Tf conjugate across Caco-2 cells in both apical-to-basolateral and basolateral-to-apical directions. These findings imply a potential application of BFA as an enhancer for TfR-mediated delivery of protein drugs across the intestinal epithelium.
研究了肠上皮样分化对滤膜培养的Caco-2细胞中转铁蛋白受体(TfR)极性的影响。细胞汇合后第一天,顶端与基底外侧TfR的比例约为1:1,汇合后八天该比例变为1:40。在此期间,跨上皮电阻(TEER)、辣根过氧化物酶(HRP)跨单层的转运以及细胞总TfR数量保持不变。然而,作为肠上皮细胞分化既定标志物的刷状缘膜相关碱性磷酸酶的活性在此8天期间增加,同时顶端TfR数量减少。这些结果表明,肠上皮样分化而非紧密连接的形成最有可能是Caco-2细胞中TfR极化分布的原因。还研究了真菌代谢产物布雷菲德菌素A(BFA)对Caco-2细胞中TfR分布和TfR介导的转胞吞作用的影响。BFA导致基底外侧TfR数量显著减少,同时顶端TfR数量略有增加。BFA增强了125I-Tf和辣根过氧化物酶-Tf偶联物在顶端到基底外侧和基底外侧到顶端方向跨Caco-2细胞的TfR介导的转胞吞作用。这些发现暗示BFA作为TfR介导的蛋白质药物跨肠上皮递送增强剂的潜在应用。