Optimization of Caco-2 and HT29 co-culture in vitro cell models for permeability studies

被引:105
作者
Pan, Fengguang [1 ]
Han, Lu [1 ]
Zhang, Yan [1 ]
Yu, Yiding [1 ]
Liu, Jingbo [1 ]
机构
[1] Jilin Univ, Lab Nutr & Funct Food, Changchun 130062, Jilin, Peoples R China
关键词
Cell seeding ratio; co-culture; gene expression; monolayer; optimization; INTESTINAL BARRIER FUNCTION; CACO-2/HT29-MTX COCULTURES; ORAL ABSORPTION; MESSENGER-RNA; TRANSPORT; MONOLAYERS; PEPTIDES; LINE; EXPRESSION; PREDICTION;
D O I
10.3109/09637486.2015.1077792
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The purpose of this study was to investigate the appropriate proportion of Caco-2 and HT29 co-culture in vitro cell models for permeability studies. The results showed that the transepithelial electrical resistance values of 9: 1 and 1: 0 groups (263 +/- 3.61 and 300 +/- 7.55) after 21-day culture were >250 Omega cm(2), which were suitable for further experiments. The confocal laser microscopy showed that the group of 9: 1 (Caco-2: HT29) had the highest integrity, whereas the group of 0: 1 (Caco-2: HT29) exhibited the lowest. The staining study confirmed that mucus was successfully produced by HT29 cells, and it was also produced in co-cultures with Caco-2 cells model, but the Caco-2 monocultures did not have any blue staining, which made us affirm that mucus is only produced in the presence of HT29 cells. The real-time PCR results showed that the total highest expression level of ALPi and MUC5AC was the ratio of 9: 1 (Caco-2: HT29) and lowest is 1: 1 (Caco-2: HT29). So we concluded that 9: 1 (Caco-2: HT29) is the optimal Caco-2 to HT29 ratio in the in vitro model co-culture for permeability studies.
引用
收藏
页码:680 / 685
页数:6
相关论文
共 39 条
[1]   Functional characterization of peptide transporters in MDCKII-MDR1 cell line as a model for oral absorption studies [J].
Agarwal, Sheetal ;
Jain, Ritesh ;
Pal, Dhananjay ;
Mitra, Ashim K. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 332 (1-2) :147-152
[2]   Models to Predict Intestinal Absorption of Therapeutic Peptides and Proteins [J].
Antunes, Filipa ;
Andrade, Fernanda ;
Ferreira, Domingos ;
Nielsen, Hanne Morck ;
Sarmento, Bruno .
CURRENT DRUG METABOLISM, 2013, 14 (01) :4-20
[3]   Towards the characterization of an in vitro triple co-culture intestine cell model for permeability studies [J].
Araujo, Francisca ;
Sarmento, Bruno .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 458 (01) :128-134
[4]   Caco-2 monolayers in experimental and theoretical predictions of drug transport [J].
Artursson, Per ;
Palm, Katrin ;
Luthman, Kristina .
ADVANCED DRUG DELIVERY REVIEWS, 2012, 64 :280-289
[5]   Cell culture-based models for intestinal permeability: a critique [J].
Balimane, PV ;
Chong, S .
DRUG DISCOVERY TODAY, 2005, 10 (05) :335-343
[6]   Intestinal barrier function [J].
Baumgart, DC ;
Dignass, AU .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2002, 5 (06) :685-694
[7]   A tunable Caco-2/HT29-MTX co-culture model mimicking variable permeabilities of the human intestine obtained by an original seeding procedure [J].
Beduneau, Arnaud ;
Tempesta, Camille ;
Fimbel, Stephane ;
Pellequer, Yann ;
Jannin, Vincent ;
Demarne, Frederic ;
Lamprecht, Alf .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2014, 87 (02) :290-298
[8]   Transport of lipophilic drug molecules in a new mucus-secreting cell culture model based on HT29-MTX cells [J].
Behrens, I ;
Stenberg, P ;
Artursson, P ;
Kissel, T .
PHARMACEUTICAL RESEARCH, 2001, 18 (08) :1138-1145
[9]   In Vitro Study of Intestinal Transport of Inorganic and Methylated Arsenic Species by Caco-2/HT29-MTX Cocultures [J].
Calatayud, Marta ;
Vazquez, Marta ;
Devesa, Vicenta ;
Velez, Dinoraz .
CHEMICAL RESEARCH IN TOXICOLOGY, 2012, 25 (12) :2654-2662
[10]   Assessment of poly(methacrylic acid-co-N-vinyl pyrrolidone) as a carrier for the oral delivery of therapeutic proteins using Caco-2 and HT29-MTX cell lines [J].
Carr, Daniel A. ;
Peppas, Nicholas A. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2010, 92A (02) :504-512