Jin K, Mao X O, Eshoo M W, del Rio G, Rao R, Chen D, Simon R P, Greenberg D A
Buck Institute for Age Research, Novato, CA 94945, USA.
Neurochem Res. 2002 Oct;27(10):1105-12. doi: 10.1023/a:1020913123054.
We used cDNA microarray gene expression profiling to characterize the transcriptional response to exposure of cultured mouse cerebral cortical neurons to hypoxia for 24 hr. Of 11,200 genes examined, 1,405 (12.5%) were induced or repressed at least 1.5-fold, whereas 26 known genes were induced and 20 known genes were repressed at least 2.5-fold. The most strongly induced genes included genes coding for endoplasmic reticulum proteins (Ero1L/Giig11, Sac1p, Ddit3/Gadd153), proteins involved in ubiquitination (Arih2, P4hb), proteins induced by hypoxia in non-neuronal systems (Gpi1, Aldo1, Anxa2, Hig1), and proteins that might promote cell death (Gas5, Egr1, Ndr1, Vdac2). These findings reinforce the importance of endoplasmic reticulum-based mechanisms and of protein-ubiquitination pathways in the neuronal response to hypoxia.
我们使用cDNA微阵列基因表达谱来表征培养的小鼠大脑皮质神经元暴露于缺氧环境24小时后的转录反应。在检测的11200个基因中,有1405个(12.5%)基因的表达被诱导或抑制了至少1.5倍,而有26个已知基因的表达被诱导且有20个已知基因的表达被抑制了至少2.5倍。诱导最强的基因包括编码内质网蛋白的基因(Ero1L/Giig11、Sac1p、Ddit3/Gadd153)、参与泛素化的蛋白(Arih2、P4hb)、在非神经元系统中由缺氧诱导的蛋白(Gpi1、Aldo1、Anxa2、Hig1)以及可能促进细胞死亡的蛋白(Gas5、Egr1、Ndr1、Vdac2)。这些发现强化了基于内质网的机制和蛋白质泛素化途径在神经元对缺氧反应中的重要性。