Erianin alleviates diabetic retinopathy by reducing retinal inflammation initiated by microglial cells via inhibiting hyperglycemia‐mediated ERK1/2–NF‐κB signaling pathway. Issue 11 (31st July 2019)
- Record Type:
- Journal Article
- Title:
- Erianin alleviates diabetic retinopathy by reducing retinal inflammation initiated by microglial cells via inhibiting hyperglycemia‐mediated ERK1/2–NF‐κB signaling pathway. Issue 11 (31st July 2019)
- Main Title:
- Erianin alleviates diabetic retinopathy by reducing retinal inflammation initiated by microglial cells via inhibiting hyperglycemia‐mediated ERK1/2–NF‐κB signaling pathway
- Authors:
- Zhang, Tianyu
Ouyang, Hao
Mei, Xiyu
Lu, Bin
Yu, Zengyang
Chen, Kaixian
Wang, Zhengtao
Ji, Lili - Abstract:
- Abstract : Blood‐retinal barrier (BRB) breakdown is a typical event in the early stage of diabetic retinopathy (DR). This study aims to elucidate the protection of erianin, a natural compound isolated from Dendrobium chrysotoxum Lindl, against DR development. Erianin alleviated BRB breakdown and rescued the reduced claudin1 and occludin expression in retinas from streptozotocin‐induced diabetic mice. Erianin reduced microglial activation, ERK1/2 phosphorylation, NF‐κB transcriptional activation, and the elevated TNF‐α expression both in vitro and in vivo. ERK1/2 inhibitor U0126 abrogated NF‐κB activation in D‐glucose‐treated BV2 cells. Erianin reduced cellular glucose uptake, and molecular docking analysis indicated the potential interaction of erianin with glucose transporter (GLUT)1. GLUT1 inhibitor (STF31) reduced the activation of the ERK1/2‐NF‐κB signaling pathway. Coculture with D‐glucose‐stimulated microglial BV2 cells and with TNF‐α stimulation both induced inner BRB and outer BRB damage in human retinal endothelial cells and APRE19 cells, but erianin improved all these damages. In summary, erianin attenuated BRB breakdown during DR development by inhibiting microglia‐triggered retinal inflammation via reducing cellular glucose uptake and abrogating the subsequent activation of the downstream ERK1/2‐NF‐κB pathway. Moreover, erianin also alleviated BRB damage induced by TNF‐α released from the activated microglia.—Zhang, T., Ouyang, H., Mei, X., Lu, B., Yu, Z., Chen,Abstract : Blood‐retinal barrier (BRB) breakdown is a typical event in the early stage of diabetic retinopathy (DR). This study aims to elucidate the protection of erianin, a natural compound isolated from Dendrobium chrysotoxum Lindl, against DR development. Erianin alleviated BRB breakdown and rescued the reduced claudin1 and occludin expression in retinas from streptozotocin‐induced diabetic mice. Erianin reduced microglial activation, ERK1/2 phosphorylation, NF‐κB transcriptional activation, and the elevated TNF‐α expression both in vitro and in vivo. ERK1/2 inhibitor U0126 abrogated NF‐κB activation in D‐glucose‐treated BV2 cells. Erianin reduced cellular glucose uptake, and molecular docking analysis indicated the potential interaction of erianin with glucose transporter (GLUT)1. GLUT1 inhibitor (STF31) reduced the activation of the ERK1/2‐NF‐κB signaling pathway. Coculture with D‐glucose‐stimulated microglial BV2 cells and with TNF‐α stimulation both induced inner BRB and outer BRB damage in human retinal endothelial cells and APRE19 cells, but erianin improved all these damages. In summary, erianin attenuated BRB breakdown during DR development by inhibiting microglia‐triggered retinal inflammation via reducing cellular glucose uptake and abrogating the subsequent activation of the downstream ERK1/2‐NF‐κB pathway. Moreover, erianin also alleviated BRB damage induced by TNF‐α released from the activated microglia.—Zhang, T., Ouyang, H., Mei, X., Lu, B., Yu, Z., Chen, K., Wang, Z., Ji, L. Erianin alleviates diabetic retinopathy by reducing retinal inflammation initiated by microglial cells via inhibiting hyperglycemia‐mediated ERK1/2‐NF‐κB signaling pathway. FASEB J. 33, 11776‐11790 (2019). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 33:Issue 11(2019)
- Journal:
- FASEB journal
- Issue:
- Volume 33:Issue 11(2019)
- Issue Display:
- Volume 33, Issue 11 (2019)
- Year:
- 2019
- Volume:
- 33
- Issue:
- 11
- Issue Sort Value:
- 2019-0033-0011-0000
- Page Start:
- 11776
- Page End:
- 11790
- Publication Date:
- 2019-07-31
- Subjects:
- BRB breakdown -- GLUT1 -- TNF‐α -- tight junctions -- molecular docking analysis
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201802614RRR ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23879.xml