흰쥐 대뇌세포의 저산소증 모델에서 석창포(石菖蒲 Acori graminei rhizoma. AGR)에 의한 유전자 표현 변화의 microarray 분석
박동준, 정승현, 문일수, Wonchoel Lee, 신길조
Abstract
박동준, 정승현, 문일수, Wonchoel Lee, 신길조
Abstract
Acori graminei Rhizoma (AGR) is a perennial herb which has been used clinically as a traditional oriental medicine against stroke, Alzheimer’s disease, and vascular dementia. We investigated the effect of AGR on the modulation of gene expression profile in a hypoxic model of cultured rat cortical cells. Rat cerebrocortical cells were grown in Neurobasal medium. On DIV12, cells were treated with AGR (10 ㎍/㎖), given a hypoxic shock (2% O₂, 3 hr) on DIV14, and total RNAs were prepared one day after shock. Microarray analyses indicated that the expression levels of most genes were altered within the global M values +0.5 and -0.5, i.e., 40% increase or decrease. There were 750 genes which were upregulated by < global M +0.2, while 700 genes were downregulated by > global M -0.2. The overall profile of gene expression suggests that AGR suppresses apoptosis (upregulation of anti-apopotic genes such as TEGT, TIEG, Dad, p53, and downregulation of pro-apopotic genes such as DAPK, caspase 2, pdcd8), ROS (upregulation of RARα, AhR), and that AGR has neurotrophic effects (upregulation of Akt1, Akt2). These results provide a platform for investigation of the molecular mechanism of the effect of AGR in neuroprotection.
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Acori graminei Rhizoma (AGR) is a perennial herb which has been used clinically as a traditional oriental medicine against stroke, Alzheimer’s disease, and vascular dementia. We investigated the effect of AGR on the modulation of gene expression profile in a hypoxic model of cultured rat cortical cells. Rat cerebrocortical cells were grown in Neurobasal medium. On DIV12, cells were treated with AGR (10 ㎍/㎖), given a hypoxic shock (2% O₂, 3 hr) on DIV14, and total RNAs were prepared one day after shock. Microarray analyses indicated that the expression levels of most genes were altered within the global M values +0.5 and -0.5, i.e., 40% increase or decrease. There were 750 genes which were upregulated by < global M +0.2, while 700 genes were downregulated by > global M -0.2. The overall profile of gene expression suggests that AGR suppresses apoptosis (upregulation of anti-apopotic genes such as TEGT, TIEG, Dad, p53, and downregulation of pro-apopotic genes such as DAPK, caspase 2, pdcd8), ROS (upregulation of RARα, AhR), and that AGR has neurotrophic effects (upregulation of Akt1, Akt2). These results provide a platform for investigation of the molecular mechanism of the effect of AGR in neuroprotection.
Key concepts: Downregulation and upregulation, Microarray analysis techniques, Neuroprotection, Gene, Microarray, Gene expression, Clusterin, Biology