Gamma-aminobutyric acid A receptor gamma 2 subunit following Mg-free-induced seizures in cultured developing neurons
Jian Li
Dingan Mao
Tao Bo
Xingfang Li
Lu Yi
Zhuwen Yi
摘要:BACKGROUND: Studies have demonstrated that in vitro cultured cortical neurons from embryonic rats can produce spontaneous recurrent epileptiform discharges following transient Mg2+-free extraceUular solution culture. OBJECTIVE: To explore gamma-aminobutyric acid A receptor (GABAAR) γ2 subunit expression following Mg2+-free-induced seizures in cultured developing neurons. DESIGN, TIME AND SETTING: Cellular and molecular biology. The in vitro experiment was performed at the Department of Pediatrics, Second Xiangya Hospital of Central Southern University between January 2007 and February 2008. MATERIALS: Cortical neurons of Wistar rats on gestational days 16-17 were used. Normal extracellular solution (pH 7.3) consisted of NaCl 145 mmol/L, KCl 2.5 mmol/L, HEPES 10 mmol/L, MgCl2 1 mmol/L, CaCl2 2 mmol/L, glucose 10 mmol/L, and glycine 0.01 mmol/L. In addition, there was no MgCl2 in the Mg2+-free extraccllular solution. METHODS: Cortical neurons cultured for 6 days were exposed to normal extracellular solution (control group) and Mg2+-free media (Mg2+-free group) respectively for 3 hours, followed by continuous culture in DMEM solution. MAIN OUTCOME MEASURES: On days 1,7 and 12 after Mg2+-free treatment, real-time RT-PCR, immunochemistry, and flow cytometry were used to detect GABAAR γ2 subunit expression. RESULTS: Compared with the control group, GABAAR γ2-positive cells decreased significantly on days 1 and 7 after Mg2+-free treatment (P < 0.01), but significantly increased on day 12 (P < 0.01). GABAAR γ2 subunit mRNA expression decreased significantly at 7 days Mg2+-free treatment when measured by real-time RT-PCR compared with the control group (P < 0.05). CONCLUSION: GABAAR γ2 subunit expression is modified following Mg-free-induced seizures in cultured developing neurons. This indicates the possibility that abnormal GABAA receptor expression might play an important role in development of neuronal injury.
机标关键词:continuous culturemolecular biologysolution culturein vitroneuronal injurymRNA expressionflow cytometryWistar rats
资助基金:(No. 30400483)
论文发表日期:2008-01-01
在线出版日期:2025-08-15(本平台首次上网日期,不代表文献的发表时间)
页数:5( 1187-1191 )
英文信息
