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通过大鼠脊髓微阵列分析鉴定的缺血预处理介质

Mediators of ischemic preconditioning identified by microarray analysis of rat spinal cord.

作者信息

Carmel Jason B, Kakinohana Osamu, Mestril Ruben, Young Wise, Marsala Martin, Hart Ronald P

机构信息

WM Keck Center for Collaborative Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.

出版信息

Exp Neurol. 2004 Jan;185(1):81-96. doi: 10.1016/j.expneurol.2003.09.007.

Abstract

Spinal ischemia is a frequent cause of paralysis. Here we explore the biological basis of ischemic preconditioning (IPC), the phenomenon in which a brief period of ischemia can confer protection against subsequent longer and normally injurious ischemia, to identify mediators of endogenous neuroprotection. Using microarrays, we examined gene expression changes induced by brief spinal ischemia using a rat balloon occlusion model. Among the nearly 5000 genes assayed, relatively few showed two-fold changes, and three groups stood out prominently. The first group codes for heat shock protein 70, which is induced selectively and robustly at 30 min after brief ischemia, with increases up to 100-fold. A second group encodes metallothioneins 1 and 2. These mRNAs are increased at 6 and 12 h after ischemia, up to 12-fold. The third group codes for a group of immediate-early genes not previously associated with spinal ischemia: B-cell translocation gene 2 (BTG2), the transcription factors early growth response 1 (egr-1) and nerve growth factor inducible B (NGFI-B), and a mitogen-activated protein kinase phosphatase, ptpn16, an important cell signaling regulator. These mRNAs peak at 30 min and return to baseline or are decreased 6 h after ischemia. Several other potentially protective genes cluster with these induced mRNAs, including small heat shock proteins, and many have not been previously associated with IPC. These results provide both putative mediators of IPC and molecular targets for testing preconditioning therapies.

摘要

脊髓缺血是导致瘫痪的常见原因。在此,我们探讨缺血预处理(IPC)的生物学基础,即短暂缺血可对随后更长时间且通常具有损伤性的缺血产生保护作用的现象,以确定内源性神经保护的介质。我们使用微阵列,通过大鼠球囊闭塞模型研究短暂脊髓缺血诱导的基因表达变化。在所检测的近5000个基因中,相对较少的基因显示出两倍的变化,有三组基因尤为突出。第一组编码热休克蛋白70,在短暂缺血后30分钟选择性且强烈诱导,增加高达100倍。第二组编码金属硫蛋白1和2。这些mRNA在缺血后6小时和12小时增加,高达12倍。第三组编码一组以前未与脊髓缺血相关的即早基因:B细胞易位基因2(BTG2)、转录因子早期生长反应1(egr-1)和神经生长因子诱导B(NGFI-B),以及丝裂原活化蛋白激酶磷酸酶ptpn16,一种重要的细胞信号调节剂。这些mRNA在30分钟达到峰值,在缺血后6小时恢复到基线或下降。其他几个潜在的保护基因与这些诱导的mRNA聚集在一起,包括小热休克蛋白,许多基因以前未与IPC相关联。这些结果既提供了IPC的假定介质,也提供了用于测试预处理疗法的分子靶点。

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