کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3069669 1580692 2011 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Elevation of p-NR2AS1232 by Cdk5/p35 contributes to retinal ganglion cell apoptosis in a rat experimental glaucoma model
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی عصب شناسی
پیش نمایش صفحه اول مقاله
Elevation of p-NR2AS1232 by Cdk5/p35 contributes to retinal ganglion cell apoptosis in a rat experimental glaucoma model
چکیده انگلیسی

Glaucoma, mainly caused by high intraocular pressure (IOP), is characterized by apoptotic death of retinal ganglion cells (RGCs). We investigated the possible involvement of cyclin-dependent kinase 5 (Cdk5) and its activator p35, which have been implicated in a variety of neurological disorders, in RGC apoptosis in a rat experimental glaucoma model reproduced by blocking episcleral veins. Cholera toxin B subunit (CTB) retrogradely labeled RGCs displayed a dramatic reduction in number both in the central and peripheral retina on day 14 (D14) (P < 0.05 vs control), D21 (P < 0.01 vs control) and D28 (P < 0.001 vs control) after operation. Terminal dUTP nick end labeling (TUNEL)-positive cells were detected on D14 both in the central and peripheral regions, and numerous TUNEL-positive cells were found on D21 and D28 in both the regions (P all < 0.001 vs control). As compared with the control eyes, the expression level of Cdk5 was significantly increased on D21 (P < 0.001), whereas that of p35 displayed a marked increase on D14 (P < 0.01) and D21 (P < 0.001). Meanwhile, both NR2A and p-NR2AS1232 increased from D14 onwards (P < 0.01 to 0.001). Co-immunoprecipitation indicated a direct interaction between Cdk5 and p-NR2AS1232. Intraperitoneal injection of the Cdk5 inhibitor roscovitine remarkably inhibited RGC apoptosis (P < 0.001 vs vehicle group) and increased the number of CTB-labeled RGCs (P < 0.05 to 0.01 vs vehicle group) in whole flat-mounted retinas, which was accompanied by a significant decrease in expression levels of p35 and p-NR2AS1232 (P all < 0.01 vs vehicle group). Our results suggest that elevation of p-NR2AS1232 by Cdk5/p35 contributes to RGC apoptotic death in experimental glaucoma rats, which could be effectively ameliorated by inhibiting Cdk5/p35.

Research highlights
► Cdk5/p35 in the retina is activated by elevated IOP in a rat glaucoma model.
► Elevation of p-NR2AS1232 by activated Cdk5/p35 contributes to RGC apoptosis.
► Roscovitine ameliorates RGC apoptosis by inhibiting the activity of Cdk5/p35.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neurobiology of Disease - Volume 43, Issue 2, August 2011, Pages 455–464
نویسندگان
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