Protective Effect of Raf-1 Kinase Inhibitory Protein on Diabetic Retinal Neurodegeneration through P38-MAPK Pathway

This study aimed to investigate the effect of Raf-1 kinase inhibitory protein (RKIP) on diabetic retinal neurodegeneration in streptozotocin-treated rat model and high glucose-treated rat Müller cells. Control and streptozotocin-treated rats were intravitreally injected with saline, RKIP gene overex...

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Vydané v:Current eye research Ročník 47; číslo 1; s. 135 - 142
Hlavní autori: Wu, Chuanling, Xu, Kai, Liu, Wenqiang, Liu, Anqi, Liang, Huimin, Li, Qunwang, Feng, Zhen, Yang, Yang, Ding, Jiayuan, Zhang, Tianyi, Liu, Yingxue, Liu, Xuezheng, Zuo, Zhongfu
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: England Taylor & Francis 02.01.2022
Predmet:
Animals
Apoptosis
Diabetes Mellitus, Experimental
diabetic retinal neurodegeneration
diabetic retinopathy
Diabetic Retinopathy - diagnosis
Diabetic Retinopathy - genetics
Diabetic Retinopathy - metabolism
Disease Models, Animal
Ependymoglial Cells - pathology
Gene Expression Regulation
intravitreal injection
MAP Kinase Signaling System - genetics
Müller cells
p38 mitogen-activated protein kinase
Proto-Oncogene Proteins c-raf - biosynthesis
Proto-Oncogene Proteins c-raf - genetics
Raf-1 kinase inhibitory protein
Rats
Rats, Sprague-Dawley
Raf-1 kinase inhibitory protein
diabetic retinal neurodegeneration
Müller cells
intravitreal injection
p38 mitogen-activated protein kinase
diabetic retinopathy
ISSN:0271-3683, 1460-2202, 1460-2202
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Shrnutí:This study aimed to investigate the effect of Raf-1 kinase inhibitory protein (RKIP) on diabetic retinal neurodegeneration in streptozotocin-treated rat model and high glucose-treated rat Müller cells. Control and streptozotocin-treated rats were intravitreally injected with saline, RKIP gene overexpression lentivirus (oeRKIP) or negative control lentivirus (RKIP-vector). Normal or high glucose-treated Müller cells were transfected with saline, RKIP gene overexpression lentivirus or negative control lentivirus. Western blotting and immunofluorescence assay were utilized to evaluate the function of RKIP on the expression of RKIP, p38 mitogen-activated protein kinase (p38-MAPK), glutamate/aspartate transporter (GLAST), glutamine synthetase (GS), glial fibrillar acidic protein (GFAP) and cysteine-aspartic acid protease-3 (caspase-3). A glutamate assay kit was adopted to detect glutamate level in retina samples. Apoptosis of Müller cells was determined by Annexin-V/PI staining and flow cytometry. High glucose-treated Müller cells exhibited promoted apoptosis, while RKIP overexpression in high glucose-treated Müller cells down-regulated the enhanced apoptosis. Compared with rats injected with saline, streptozotocin-treated hyperglycemic rats displayed enhancement in the immunoreactivities of p38-MAPK and GFAP as well as in the protein expression of p38-MAPK and caspase-3. Strikingly, intravitreal injection of RKIP gene overexpression lentivirus in the hyperglycemic rats reversed the augmented immunoreactivities and protein expression mentioned above. Meanwhile, RKIP overexpression in the hyperglycemic rats improved the immunoreactivities and protein expression of RKIP, GS and GLAST. Besides, RKIP down-regulated the increased level of retinal glutamate in the hyperglycemic rats. Intravitreal injection of RKIP gene overexpression lentivirus functioned in preventing diabetic retinal neurodegeneration in a rat model of diabetes presumably by inhibiting p38-MAPK pathway.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0271-3683
1460-2202
1460-2202
DOI:10.1080/02713683.2021.1944644