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Kwon, Hyug Moo
Immunometabolism and Cancer Lab
Research Interests
  • TonEBP, Obesity, Cancer, Chronic inflammatory diseases, Brain disorder, Kidney disorder, Genomic instability


Tonicity response element binding protein associated with neuronal cell death in the experimental diabetic retinopathy

DC Field Value Language Kim, Seong-Jae ko Kim, Hwajin ko Park, Jeongsook ko Chung, Inyoung ko Kwon, H. Moo ko Choi, Wan-Sung ko Yoo, Ji-Myong ko 2015-01-22T00:01:12Z - 2015-01-20 ko 2014-12 ko
dc.identifier.citation INTERNATIONAL JOURNAL OF OPHTHALMOLOGY , v.7, no.6, pp.935 - 940 ko
dc.identifier.issn 2222-3959 ko
dc.identifier.uri -
dc.description.abstract AIM: To study the contribution of tonicity response element binding protein (TonEBP) in retinal ganglion cell (RGC) death of diabetic retinopathy (DR). METHODS: Diabetes was induced in C57BL/6 mice by five consecutive intraperitoneal injections of 55 mg/kg streptozotocin (STZ). Control mice received vehicle (phosphate -buffered saline). All mice were killed 2mo after injections, and the extent of cell death and the protein expression levels of TonEBP and aldose reductase (AR) were examined. RESULTS: The TonEBP and AR protein levels and the death of RGC were significantly increased in the retinas of diabetic mice compared with controls 2mo after the induction of diabetes. Terminal deoxynucleotidyl transferase (TdT) -mediated dUTP nick end labeling (TUNEL) -positive signals co -localized with TonEBP immunoreactive RGC. These changes were increased in the diabetic retinas compared with controls. CONCLUSION: The present data show that AR and TonEBP are upregulated in the DR and TonEBP may contribute to apoptosis of RGC in the DR. ko
dc.description.statementofresponsibility close -
dc.language 영어 ko
dc.publisher IJO PRESS ko
dc.title Tonicity response element binding protein associated with neuronal cell death in the experimental diabetic retinopathy ko
dc.type ARTICLE ko
dc.identifier.scopusid 2-s2.0-84925452356 ko
dc.identifier.wosid 000346551300004 ko
dc.type.rims ART ko
dc.description.wostc 2 *
dc.description.scopustc 2 * 2015-12-28 * 2015-11-04 *
dc.identifier.doi 10.3980/j.issn.2222-3959.2014.06.04 ko
dc.identifier.url ko
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