Activation of Master Autophagy Regulator TFEB During Systemic LPS Administration in the Cornea

被引:12
作者
Uchida, Kyoko [1 ]
Unuma, Kana [1 ]
Funakoshi, Takeshi [1 ]
Aki, Toshihiko [1 ]
Uemura, Koichi [1 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch Med, Grad Dent Sci, Tokyo 1138519, Japan
基金
日本学术振兴会;
关键词
cornea; LPS; TFEB; autophagy; lysosome; GENE-TRANSFER; LYSOSOMAL BIOGENESIS; ALPHA-SYNUCLEIN; DISEASE; INFLAMMATION; ENDOTHELIUM; CLEARANCE; MOLECULES; NETWORK; MODELS;
D O I
10.1293/tox.2014-0004
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The involvement of autophagy in the cornea during the systemic inflammatory response elicited by intravenous administration of lipopolysaccharide (LPS) was investigated. Eight-week-old male Sprague-Dawley rats were injected i.v. with 15 mg/kg body weight LPS. RC4 rabbit corneal keratocytes were also used and treated with 100 ng/mL of tumor necrosis factor alpha (TNF alpha) and/or cycloheximide (CHX). The nuclear translocation of transcription factor EB (TFEB), the master transcriptional regulator for autophagy, was observed after LPS administration in the corneal epithelium. Induction of autophagy-related proteins was observed in the cornea after LPS administration, as well as in RC4 cells after treatment with TNF alpha. Administration of trehalose, an inducer of TFEB, mitigated RC4 cell death caused by TNF alpha/CHX. These results demonstrate the importance of TFEB activation in cellular defense against the systemic inflammatory response in the cornea.
引用
收藏
页码:153 / 158
页数:6
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