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Hypoxia-Inducible Factor-1α Target Genes Contribute to Retinal Neuroprotection.

作者信息

Cheng Lin, Yu Honghua, Yan Naihong, Lai Kunbei, Xiang Mengqing

机构信息

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University Guangzhou, China.

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen UniversityGuangzhou, China; Department of Ophthalmology, General Hospital of Guangzhou Military Command of PLAGuangzhou, China.

出版信息

Front Cell Neurosci. 2017 Feb 27;11:20. doi: 10.3389/fncel.2017.00020. eCollection 2017.


DOI:10.3389/fncel.2017.00020
PMID:28289375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5326762/
Abstract

Hypoxia-inducible factor (HIF) is a transcription factor that facilitates cellular adaptation to hypoxia and ischemia. Long-standing evidence suggests that one isotype of HIF, HIF-1α, is involved in the pathogenesis of various solid tumors and cardiac diseases. However, the role of HIF-1α in retina remains poorly understood. HIF-1α has been recognized as neuroprotective in cerebral ischemia in the past two decades. Additionally, an increasing number of studies has shown that HIF-1α and its target genes contribute to retinal neuroprotection. This review will focus on recent advances in the studies of HIF-1α and its target genes that contribute to retinal neuroprotection. A thorough understanding of the function of HIF-1α and its target genes may lead to identification of novel therapeutic targets for treating degenerative retinal diseases including glaucoma, age-related macular degeneration, diabetic retinopathy, and retinal vein occlusions.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09b5/5326762/9e83db666f64/fncel-11-00020-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09b5/5326762/a87b5e55cc81/fncel-11-00020-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09b5/5326762/9e83db666f64/fncel-11-00020-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09b5/5326762/a87b5e55cc81/fncel-11-00020-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09b5/5326762/9e83db666f64/fncel-11-00020-g0002.jpg

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本文引用的文献

[1]
Nrf2 activators modulate oxidative stress responses and bioenergetic profiles of human retinal epithelial cells cultured in normal or high glucose conditions.

Pharmacol Res. 2015-9

[2]
Pathophysiological roles of adrenomedullin-RAMP2 system in acute and chronic cerebral ischemia.

Peptides. 2014-12

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PLoS One. 2014-8-29

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PLoS One. 2014-8-13

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PLoS One. 2014-7-11

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Mol Vis. 2014-6-2

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Curr Eye Res. 2015-1

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Critical neuroprotective roles of heme oxygenase-1 induction against axonal injury-induced retinal ganglion cell death.

J Neurosci Res. 2014-9

[9]
Protective effects of remote ischemic conditioning against ischemia/reperfusion-induced retinal injury in rats.

Vis Neurosci. 2014-5

[10]
Neuronal cell death in the inner retina and the influence of vascular endothelial growth factor inhibition in a diabetic rat model.

Am J Pathol. 2014-4-5

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