| Literature DB >> 33011110 |
Yukiko Nagahara1, Motokazu Tsujikawa2, Ryota Koto3, Koji Uesugi4, Shigeru Sato5, Satoshi Kawasaki1, Kazuichi Maruyama1, Kohji Nishida6.
Abstract
Gelatinous drop-like corneal dystrophy (GDLD) is a severe inherited corneal dystrophy characterized by subepithelial corneal amyloid deposition. We had previously succeeded in identifying the responsible gene, TACSTD2, and subsequently found that the epithelial barrier function is significantly decreased. As with GDLD patients, the knockout mice showed severe loss of tight junction, progressive opacity, and neovascularization in the cornea. We devised an easy method to confirm the loss of the corneal barrier function even before corneal opacity is observed. Furthermore, by using knockout mice, we were able to verify clinical findings, such as the wound healing delay and light-induced acceleration of the disease. This mouse model should prove to be a highly useful tool for investigating the pathology of GDLD and for developing new therapies.Entities:
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Year: 2020 PMID: 33011110 DOI: 10.1016/j.ajpath.2020.08.017
Source DB: PubMed Journal: Am J Pathol ISSN: 0002-9440 Impact factor: 4.307