کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6263265 1613852 2014 15 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Research ReportSustained effect of bone marrow mononuclear cell therapy in axonal regeneration in a model of optic nerve crush
ترجمه فارسی عنوان
گزارش تحقیق اثربخشی درمان سلول هسته ای هسته ای مغز استخوان در بازسازی آکنه در یک مدل تحریک عصب بینایی
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
چکیده انگلیسی


- BMMCs transplantation increases axonal outgrowth 28 days after optic nerve crush.
- 28 days after injury, there was no increase in neuronal survival after treatment.
- FGF-2 levels were increased 1 day after crush and treatment but not after 28 days.
- BMMCs have a short-term persistence in the eye.
- A second injection of BMMCs does not increase their persistence or RGC survival.

In adult mammals, the regeneration of the optic nerve is very limited and at the moment there are several groups trying different approaches to increase retinal ganglion cell (RGC) survival and axonal outgrowth. One promising approach is cell therapy. In previous work, we performed intravitreal transplantation of bone-marrow mononuclear cells (BMMCs) after optic nerve crush in adult rats and we demonstrated an increase in RGC survival and axon outgrowth 14 days after injury. In the present work, we investigated if these results could be sustained for a longer period of time. Optic nerve crush was performed in Lister-hooded adult rats and BMMC or saline injections were performed shortly after injury. Neuronal survival and regeneration were evaluated in rats׳ retina and optic nerve after 28 days. We demonstrated an increase of 5.2 fold in the axon outgrowth 28 days after lesion, but the BMMCs had no effect on RGC survival. In an attempt to prolong RGC survival, we established a new protocol with two BMMC injections, the second one 7 days after the injury. Untreated animals received two injections of saline. We observed that although the axonal outgrowth was still increased after the second BMMC injection, the RGC survival was not significantly different from untreated animals. These results demonstrate that BMMCs transplantation promotes neuroregeneration at least until 28 days after injury. However, the effects on RGC survival previously observed by us at 14 days were not sustained at 28 days and could not be prolonged with a second dose of BMMC.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain Research - Volume 1587, 31 October 2014, Pages 54-68
نویسندگان
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