School of Bioscience and Biotechnology, Tokyo University of Technology.
Biol Pharm Bull. 2019;42(6):989-995. doi: 10.1248/bpb.b19-00011.
An Intact form of lactoferrin (LF) is known to be absorbed from the small intestine and transported into the blood circulation. We reevaluated the cellular uptake and release of LF using an enterocyte model of human small intestinal cells derived from the Caco-2 cell line. In contrast to a previous report, we observed that intact bovine LF was taken up into seven and 21 d-cultured Caco-2 cells and successfully released back into the culture medium, even though the human intestinal LF receptor, intelectin-1, was not immunochemically detectable. Similar observations were made for human LF and its derivatives (the N-terminal half of LF designated N-lobe and Fc fusions). These observations regarding the uptake and release of intact LF in Caco-2 cells were consistent with in vivo observations. Therefore, we propose that the uptake and release of intact LF by Caco-2 cells should be assessed as a potential in vitro model of in vivo LF absorption in human intestines.
已知完整的乳铁蛋白(LF)可被小肠吸收并运输到血液循环中。我们使用源自 Caco-2 细胞系的人小肠细胞的肠细胞模型重新评估了 LF 的细胞摄取和释放。与之前的报道相反,我们观察到完整的牛 LF 被摄取到培养 7 天和 21 天的 Caco-2 细胞中,并成功释放回培养基中,尽管人肠道 LF 受体,内凝集素-1,无法用免疫化学方法检测到。对人 LF 及其衍生物(LF 的 N 端半部分命名为 N- lobe 和 Fc 融合物)也观察到了类似的结果。在 Caco-2 细胞中观察到完整 LF 的摄取和释放与体内观察结果一致。因此,我们提出 Caco-2 细胞摄取和释放完整 LF 应被评估为人体肠道中 LF 吸收的潜在体外模型。