Literature DB >> 23872712

Vitrigel-eye irritancy test method using HCE-T cells.

Hiroyuki Yamaguchi1, Hajime Kojima, Toshiaki Takezawa.   

Abstract

We previously reported that the time-dependent relative changes of transepithelial electrical resistance (TEER) after exposing four different chemicals to a human corneal epithelium (HCE) model were well correlated to the potential of ocular irritancy. Meanwhile, we recently developed a collagen vitrigel membrane (CVM) chamber possessing a scaffold composed of high-density collagen fibrils equivalent to connective tissues in vivo as a three-dimensional culture tool. The CVM chamber is useful for biomedical assays and immunohistology using cryosections that are inappropriate to be performed using the conventional Millicell chamber with a polyethylene terephthalate membrane. In this study, we aimed to develop a new eye irritancy test (EIT) method called "Vitrigel-EIT method" that can facilitate to briefly and accurately estimate the widespread irritancy of test chemicals by applying the TEER assay system to a HCE model fabricated in the CVM chamber. HCE-T cells (a HCE-derived cell strain) were cultured in the CVM chamber for 6 days, and consequently, the Vitrigel-HCE model possessing the following characteristics of HCE in vivo was formed: six cell layers with specific protein expressions and their barrier function. Time-dependent profiles of TEER values after exposing 30 test chemicals to the HCE model were converted into the scores of three indexes (time lag, intensity, and plateau level), and each chemical was successfully classified into irritant or nonirritant category by utilizing the criteria for the indexes, resulting in the excellent correlation with Globally Harmonized System of Classification and Labelling of Chemicals (GHS) classification (sensitivity: 100%, specificity: 75%, accuracy: 90%). These data suggest that the widespread eye irritancy of chemicals can be predicted without false negatives by the Vitrigel-EIT method. Interestingly, the disruption of tight junctions was immunohistologically observed after exposing not only irritants but also three compounds classified as nonirritant by GHS but found positive in our Vitrigel-EIT method confirming a possible mild irritant property.

Entities:  

Keywords:  HCE-T cells.; collagen vitrigel membrane; corneal epithelium; eye irritation test; transepithelial electrical resistance

Mesh:

Substances:

Year:  2013        PMID: 23872712     DOI: 10.1093/toxsci/kft159

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  6 in total

1.  Fluid dwell impact induces peritoneal fibrosis in the peritoneal cavity reconstructed in vitro.

Authors:  Shigehisa Aoki; Mitsuru Noguchi; Toshiaki Takezawa; Satoshi Ikeda; Kazuyoshi Uchihashi; Hiroyuki Kuroyama; Tomoyuki Chimuro; Shuji Toda
Journal:  J Artif Organs       Date:  2015-08-30       Impact factor: 1.731

Review 2.  In vitro reconstructed 3D corneal tissue models for ocular toxicology and ophthalmic drug development.

Authors:  Yulia Kaluzhny; Mitchell Klausner
Journal:  In Vitro Cell Dev Biol Anim       Date:  2021-02-05       Impact factor: 2.416

3.  Predictive performance of the Vitrigel-eye irritancy test method using 118 chemicals.

Authors:  Hiroyuki Yamaguchi; Hajime Kojima; Toshiaki Takezawa
Journal:  J Appl Toxicol       Date:  2015-10-15       Impact factor: 3.446

4.  Collagen vitrigel promotes hepatocytic differentiation of induced pluripotent stem cells into functional hepatocyte-like cells.

Authors:  Shun Nakai; Ima Shibata; Takahiro Shitamichi; Hiroyuki Yamaguchi; Nobuyuki Takagi; Tomoaki Inoue; Toshito Nakagawa; Jumpei Kiyokawa; Satoshi Wakabayashi; Tomoya Miyoshi; Eriko Higashi; Seiichi Ishida; Nobuaki Shiraki; Shoen Kume
Journal:  Biol Open       Date:  2019-07-02       Impact factor: 2.422

Review 5.  Research and Development of Microphysiological Systems in Japan Supported by the AMED-MPS Project.

Authors:  Seiichi Ishida
Journal:  Front Toxicol       Date:  2021-04-29

6.  Development of an oxygenation culture method for activating the liver-specific functions of HepG2 cells utilizing a collagen vitrigel membrane chamber.

Authors:  Ayumi Oshikata-Miyazaki; Toshiaki Takezawa
Journal:  Cytotechnology       Date:  2015-12-09       Impact factor: 2.058

  6 in total

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