Caco-2 Cell Sheet Partially Laminated with HT29-MTX Cells as a Novel In Vitro Model of Gut Epithelium Drug Permeability

Author:

Cheng Yi1,Watanabe Chie12,Ando Yusuke2,Kitaoka Satoshi3,Egawa Yuya3,Takashima Tomoya1,Matsumoto Akihiro1,Murakami Masahiro1ORCID

Affiliation:

1. Laboratory of Pharmaceutics, Faculty of Pharmacy, Osaka Ohtani University, 3-11-1 Nishikori-kita, Tondabayashi 584-0854, Osaka, Japan

2. Laboratory of Clinical Pathology, Faculty of Pharmacy and Pharmaceutical Sciences, School of Pharmacy, Josai University, 1-1, Keyakidai, Sakado 350-0295, Saitama, Japan

3. Laboratory of Physical Pharmacy, Faculty of Pharmacy and Pharmaceutical Sciences, School of Pharmacy, Josai University, 1-1, Keyakidai, Sakado 350-0295, Saitama, Japan

Abstract

The intestinal epithelial Caco-2 cell monolayer is a well-established in vitro model useful for predicting intestinal drug absorption in humans. Coculture models of Caco-2 and goblet-cell-like HT29-MTX cells have been developed to overcome the lack of a mucus layer; however, those models are much leakier compared to the intestinal epithelium. Here, we developed a partially laminated culture model where HT29-MTX cells were superimposed onto a Caco-2 monolayer to overcome this issue. A morphological study showed that the piled HT29-MTX cells were voluntarily incorporated into the Caco-2 monolayer, and mucus production was confirmed via periodic acid-Schiff and mucin protein 2 staining. Permeability was evaluated in terms of transepithelial electrical resistance (TEER) and the apparent permeability of paracellular markers with different molecular sizes. The partially laminated model maintained the high barrier function of the Caco-2 monolayer, whose permeability appeared adjustable according to the HT29-MTX/Caco-2 cell ratio. In contrast, the coculture models showed abnormally high permeability of those markers, correlated with low TEER. Thus, the partially laminated model enabled in vitro recapitulation of effective mucosal barrier function. Consequently, this novel model may be useful as an in vitro high-throughput evaluation system for enteral mucosal permeability and mucus-penetrating efficiency of drugs and nanocarriers.

Funder

JST, CREST

Publisher

MDPI AG

Subject

Pharmaceutical Science

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