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A New in Vitro Model of GDLD by Knocking Out<i>TACSTD2</i>and Its Paralogous Gene<i>EpCAM</i>in Human Corneal Epithelial Cells
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- Peng Xu
- Department of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan
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- Chifune Kai
- Department of Ocular Immunology and Regenerative Medicine, Osaka University Graduate School of Medicine, Osaka, Japan
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- Satoshi Kawasaki
- Department of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan
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- Yuki Kobayashi
- Department of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan
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- Kouji Yamamoto
- Department of Biostatistics, Yokohama City University, School of Medicine, Kanagawa, Japan
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- Motokazu Tsujikawa
- Department of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan
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- Ryuhei Hayashi
- Department of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan
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- Kohji Nishida
- Department of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan
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Description
PURPOSE: Gelatinous drop-like corneal dystrophy (GDLD) is a rare autosomal recessive corneal dystrophy that causes severe vision loss. Because of its poor prognosis, there is a demand for novel treatments for GDLD. Here, we establish a new in vitro disease model of GDLD based on immortalized human corneal epithelial (HCE-T) cells. METHODS: By using transcription activator-like effector nuclease plasmids, tumor-associated calcium signal transducer 2 (TACSTD2) and its paralogous gene, epithelial cell adhesion molecule (EpCAM), were knocked out in HCE-T cells. Fluorescence-activated cell sorting was performed to obtain cells in which both TACSTD2 and EpCAM were knocked out (DKO cells). In DKO cells, the expression levels and subcellular localizations of claudin (CLDN) 1, 4, and 7, and ZO-1 were investigated, along with epithelial barrier function. By using DKO cells, the feasibility of gene therapy for GDLD was also investigated. RESULTS: DKO cells exhibited decreased expression and aberrant subcellular localization of CLDN1 and CLDN7 proteins, as well as decreased epithelial barrier function. Transduction of the TACSTD2 gene into DKO cells nearly normalized expression levels and subcellular localization of CLDN1 and CLDN7 proteins, while significantly increasing epithelial barrier function. CONCLUSIONS: We established an in vitro disease model of GDLD by knocking out TACSTD2 and its paralogous gene, EpCAM, in HCE-T cells. This cell line accurately reflected pathological aspects of GDLD. TRANSLATIONAL RELEVANCE: We expect that the cell line will be useful to elucidate the pathogenesis of GDLD and develop novel treatments for GDLD.
Journal
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- Translational Vision Science & Technology
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Translational Vision Science & Technology 7 (6), 30-, 2018-12-21
Association for Research in Vision and Ophthalmology (ARVO)
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Keywords
Details 詳細情報について
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- CRID
- 1360848661476162944
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- ISSN
- 21642591
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- Article Type
- journal article
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- Data Source
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- Crossref
- KAKEN
- OpenAIRE