کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2493377 1556638 2013 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
TGF-beta superfamily member activin A acts with BDNF and erythropoietin to improve survival of spiral ganglion neurons in vitro
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب رفتاری
پیش نمایش صفحه اول مقاله
TGF-beta superfamily member activin A acts with BDNF and erythropoietin to improve survival of spiral ganglion neurons in vitro
چکیده انگلیسی


• For the first time, activin type-I receptors were demonstrated in SGN.
• An increased survival of SGN through activin A was shown for the first time.
• Combined application of activin, BDNF and EPO led to an increased neuroprotection.
• The increase in neuronal survival was blocked by the addition of EPO-inhibitors.

Activins are regulators of embryogenesis, osteogenesis, hormones and neuronal survival. Even though activin receptor type II has been detected in spiral ganglion neurons (SGN), little is known about the role of activins in the inner ear. An activin-mediated neuroprotection is of considerable clinical interest since SGN are targets of electrical stimulation with cochlear implants in hearing impaired patients. Thus, the presence of activin type-I and type-II receptors was demonstrated immunocytochemically and the individual and combined effects of activin A, erythropoietin (EPO) and brain-derived neurotrophic factor (BDNF) on SGN were examined in vitro.SGN isolated from neonatal rats (P 3–5) were cultured in serum-free medium supplemented with activin A, BDNF and EPO. Compared to the negative control, survival rates of SGN were significantly improved when cultivated individually with activin A (p < 0.001) and in combination with BDNF (p < 0.001). Neither neurite outgrowth nor neuronal survival was influenced by the addition of EPO to activin A-treated neurons. However, when all three factors were added, a significantly (p < 0.001) improved neuronal survival was observed (61.2 ± 3.6%) compared to activin A (25.4 ± 2.1%), BDNF (22.8 ± 3.3%) and BDNF + EPO (19.2 ± 1.5%). Under the influence of the EPO-inhibitors, this increase in neuronal survival was blocked. Acting with BDNF and EPO to promote neuronal survival in vitro, activin A presents an interesting factor for pharmacological intervention in the inner ear. The present study demonstrates a synergetic effect of a combined therapy with several trophic factors.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuropharmacology - Volume 75, December 2013, Pages 416–425
نویسندگان
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