Effects of neurotrophin-3 and nerve growth factor on the morphology, proliferation, and cell death of C6 glioma cells
PHARMACOLOGY, CLINICAL PHARMACOLOGY
Abstract
Introduction. Due to the ineffectiveness of standard chemotherapy and radiotherapy for glioblastoma, there is a need to find new drugs that selectively and effectively target tumor cells while sparing healthy tissue cells. The aim of the study was the effects of neurotrophin-3 (NT-3) and β-form of nerve growth factor (β-NGF) for 3 and 7 days on the morphology, proliferation and death of rat C6 glioma cells. Materials and methods. C6 glioma cells were cultured in Petri dishes (250,000 cells/dish) in Eagle’s medium supplemented with 10% fetal bovine serum (FBS) at 37 °C and 5% CO2 for 7 days. Cells were treated with NT-3 (10 and 20 ng/ml) and β-NGF (100 and 200 ng/ml). Cell size and area, number, length, and ferning of processes were assessed using intravital digital microscopy with IM1000 and Image J (version 1.38r). The proliferation index and cell death rate (%) were also determined.
Results. β-NGF (100 and 200 ng/ml) exhibited pronounced cytostatic activity. This was demonstrated by a more than fourfold suppression of the proliferation index, a decrease in the degree of outgrowth ferning, and stimulation of cell death at both observation times. In contrast, the effect of NT-3 was demonstrated by a 2-3-fold increase in proliferation (days 3 and 7) and a sharp decrease in ferning and cell death. Conclusions. The results demonstrate the opposing effects of NT-3 and NGF on the morpho-functional profile of C6 cells.
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