Guo Min, Jiang Wei, Hou Nali, et al. All-trans retinoic acid(ATRA) inhibits apoptosis of primary neurons induced by oxygen and glucose-deprivation via retinoic acid receptor alpha. [J]. Journal of Chongqing Medical University 41(1):8-13(2016)
Guo Min, Jiang Wei, Hou Nali, et al. All-trans retinoic acid(ATRA) inhibits apoptosis of primary neurons induced by oxygen and glucose-deprivation via retinoic acid receptor alpha. [J]. Journal of Chongqing Medical University 41(1):8-13(2016) DOI: 10.13406/j.cnki.cyxb.000623.
All-trans retinoic acid(ATRA) inhibits apoptosis of primary neurons induced by oxygen and glucose-deprivation via retinoic acid receptor alpha
OGD+ATRA组(1.08±0.49)与OGD组(1.00±0.15)Caspase-3 m RNA表达水平无明显差异(P=0.148)。结论 :ATRA可以激活其受体RARα进而下调TGF-β
抑制凋亡因子Caspase-3的表达
最终抑制OGD损伤引起的原代神经元凋亡。
Abstract
Objective:To investigate whether all-trans retinoic acid(ATRA)can inhibit apoptosis effects on primary neurons caused by oxygen and glucose-deprivation(OGD). Methods:Primary neurons were isolated and cultured in vitro
and were determined for neuron-specific enolase(NSE) by immunofluorescence technique. Primary neurons were divided into three groups:control group
OGD group and OGD+ATRA group. Cell morphology before and after OGD injury was observed by inverted microscopy. Apoptosis rate of primary neurons after OGD injury was measured by flow cytometry. The gene transcription levels of retinoic acid receptor alpha(RARα)
transforming growth factor-β1(TGF-β1)
transforming growth factor-β2(TGF-β2)
cysteinyl aspartate specific proteinase(Caspase-3)were examined via real-time PCR
while the protein expressions of RARα
TGF-β
Caspase-3 were determined by Western blot. Results:Successfully cultured primary neurons
neuron-specific enolase was observed in primary neurons obviously. After OGD injury
the cell death of OGD group was more obvious than OGD+ATRA group. Flow cytometry suggested that the apoptosis rate of OGD+ATRA group(26.11±2.96)% significantly decreased when compared with that of OGD group(52.14±5.23)%(P=0.025). The m RNA and protein levels of RARα in OGD+ATRA group(1.52±0.43
0.22±0.02)were significantly higher than those in OGD group(0.49±013
0.10±0.02)(P=0.006
P=0.005). The m RNA transcription levels of TGF-β1
TGF-β2 were significantly lower in OGD+ATRA group(0.45±0.10
0.41±0.08)than in OGD group(0.81±0.15
0.98±0.15)(P=0.034
P=0.018). The protein expressions of TGF-β
Caspase-3 were significantly lower in OGD+ATRA group(0.22±0.04
0.18±0.03)than in OGD group(0.39±0.05
0.47±0.06)(P=0.016
P=0.002). And the m RNA transcription of Caspase-3 in OGD +ATRA group(1.08 ±0.49) and OGD group(1.00 ±0.15) were not significantly different(P =0.148).Conclusion:ATRA inhibits the apoptosis of primary neurons induced by OGD injury via activating its receptor RARα and then turning down TGF-β and Caspase-3 expressions.
关键词
全反式视黄酸缺氧缺糖损伤原代神经元转录生长因子β含半胱氨酸的天冬氨酸蛋白水解酶-3
Keywords
all-trans retinoic acidoxygen and glucose-deprivationprimary neuronstransforming growth factor-βcysteinyl aspartate specific proteinase