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细胞培养条件是否会影响Caco-2细胞单层中肽的载体介导转运?

Do cell culture conditions influence the carrier-mediated transport of peptides in Caco-2 cell monolayers?

作者信息

Behrens Isabel, Kissel Thomas

机构信息

Department of Pharmaceutics and Biopharmacy, University of Marburg, Philipps-University, Ketzerbach 63, D-35032, Marburg/Lahn, Germany.

出版信息

Eur J Pharm Sci. 2003 Aug;19(5):433-42. doi: 10.1016/s0928-0987(03)00146-5.

Abstract

Despite the fact that different laboratories have reported large differences in permeability for actively transported substrates, Caco-2 cell monolayers are widely used as in vitro model to study small intestinal drug transport. Therefore, we investigated the effect of cell culture conditions, such as time in culture, membrane support, seeding density and supplements to the medium, on the morphology, the formation of tight junctions, as well as the expression of two peptide transporters (PepT1, HPT1) and the efflux pump, P-glycoprotein (Pgp), in Caco-2 cell monolayers. Tight junction formation was assessed by transepithelial electrical resistance measurements; multi-cell layer formation by confocal laser scanning microscopy, the expression of transporters by RT-PCR and the permeability of the PepT1 substrate, cephradine. Both morphology and the expression of carrier-mediated transporters, varied strongly as a function of culture conditions. An increase of differentiation, as documented by tight, homogeneous cell monolayer formation displaying a strong expression of all carrier-mediated transporters, was found up to 3 weeks post seeding. One week later, multi-layer structures were observed and the expression of Pgp decreased. Polyester and polyethylene terephthalate membrane supports decreased the paracellular transport rates substantially, while collagen-coating of PC inserts showed no influence on the morphology and even increased carrier-mediated transporter expression. An average seeding density of 6x10(4) cells/cm(2) seemed to be most favorable, since lower seeding densities led to thin monolayers with altered tight junctions and higher seeding densities to the formation of multilayers. In summary, the expression of carrier-mediated transporters was strongly affected by the culture conditions. The full differentiation was reached after 21 days on collagen-coated polycarbonate inserts at an initial seeding density of 6x10(4) cells/cm(2).

摘要

尽管不同实验室报告了主动转运底物的渗透性存在很大差异,但Caco-2细胞单层仍被广泛用作体外模型来研究小肠药物转运。因此,我们研究了细胞培养条件,如培养时间、膜支持物、接种密度和培养基添加物,对Caco-2细胞单层的形态、紧密连接的形成以及两种肽转运体(PepT1、HPT1)和外排泵P-糖蛋白(Pgp)表达的影响。通过跨上皮电阻测量评估紧密连接的形成;通过共聚焦激光扫描显微镜评估多层细胞层的形成,通过RT-PCR评估转运体的表达以及PepT1底物头孢拉定的渗透性。形态和载体介导转运体的表达均随培养条件的变化而有很大差异。接种后长达3周,可观察到细胞紧密、均匀单层的形成,所有载体介导转运体均有强烈表达,表明分化增加。1周后,观察到多层结构,且Pgp的表达下降。聚酯和聚对苯二甲酸乙二酯膜支持物显著降低了细胞旁转运速率,而PC插入物的胶原包被对形态无影响,甚至增加了载体介导转运体的表达。平均接种密度为6×10⁴个细胞/cm²似乎最为适宜,因为较低的接种密度会导致紧密连接改变的薄单层,而较高的接种密度会导致多层形成。总之,载体介导转运体的表达受培养条件的强烈影响。在胶原包被的聚碳酸酯插入物上,初始接种密度为6×10⁴个细胞/cm²,21天后可实现完全分化。

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