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在补充血清和无血清培养基中分化的亲代和克隆人肠Caco-2细胞系的通透性特征。

Permeability characteristics of parental and clonal human intestinal Caco-2 cell lines differentiated in serum-supplemented and serum-free media.

作者信息

Ranaldi Giulia, Consalvo Rosa, Sambuy Yula, Scarino Maria Laura

机构信息

INRAN, Via Ardeatina 546, 00178 Rome, Italy.

出版信息

Toxicol In Vitro. 2003 Oct-Dec;17(5-6):761-7. doi: 10.1016/s0887-2333(03)00095-x.

Abstract

The aim of this study was to define the permeability characteristics of the parental Caco-2/ATCC cell line and of three clonal lines (Caco-2/TC7, Caco-2/AQ, Caco-2/15) differentiated in serum-supplemented or in serum-free defined medium. The Caco-2 cells were grown in DMEM supplemented with either 10% foetal calf serum or insulin-transferrin-selenium and lipids (cholesterol, palmitic acid, oleic acid) for up to 24 days after seeding on polyethylene terephthalate filter inserts (1 microm pore diameter). The permeability of the cell monolayer was assessed by measuring trans-epithelial electrical resistance (TEER) and the apparent permeability (Papp) of the extracellular marker mannitol during differentiation from day 6 until day 24. In all lines TEER values increased during differentiation reaching a plateau value around day 15 after seeding, while the Papp for mannitol decreased sharply around day 8 and levelled off thereafter. Substantial differences were observed in the maximal TEER values achieved during differentiation in the four lines examined (Caco-2/TC7 <Caco-2/ATCC<Caco-2/AQ<Caco-2/15), while the Papp for mannitol, upon differentiation, was not significantly different in all four lines. Media composition (serum-supplemented vs. defined medium) did not generally affect the TEER (with the exception of the Caco-2/ATCC). Conversely, the presence of serum in the medium consistently lowered and stabilised Papp values as compared with defined medium.

摘要

本研究的目的是确定亲代Caco-2/ATCC细胞系以及在补充血清或无血清限定培养基中分化的三个克隆系(Caco-2/TC7、Caco-2/AQ、Caco-2/15)的通透性特征。将Caco-2细胞接种于聚对苯二甲酸乙二醇酯滤膜(孔径1微米)上,在添加10%胎牛血清或胰岛素-转铁蛋白-硒及脂质(胆固醇、棕榈酸、油酸)的DMEM中培养长达24天。通过测量跨上皮电阻(TEER)以及在分化第6天至第24天期间细胞单层对细胞外标记物甘露醇的表观通透性(Papp)来评估细胞单层的通透性。在所有细胞系中,TEER值在分化过程中均增加,在接种后约第15天达到平台值,而甘露醇的Papp在第8天左右急剧下降,此后趋于平稳。在所检测的四个细胞系(Caco-2/TC7 <Caco-2/ATCC<Caco-2/AQ<Caco-2/15)中,分化过程中达到的最大TEER值存在显著差异,而分化后所有四个细胞系中甘露醇的Papp无显著差异。培养基组成(补充血清与限定培养基)一般不影响TEER(Caco-2/ATCC除外)。相反,与限定培养基相比,培养基中血清的存在持续降低并稳定了Papp值。

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