首页> 外文期刊>Journal of neurotrauma >Effects of injury severity on regional and temporal mRNA expression levels of calpains and caspases after traumatic brain injury in rats.
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Effects of injury severity on regional and temporal mRNA expression levels of calpains and caspases after traumatic brain injury in rats.

机译:损伤严重程度对大鼠脑外伤后钙蛋白酶和胱天蛋白酶区域和时间mRNA表达水平的影响。

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摘要

Despite a preponderance of studies demonstrating gene expression and/or enzymatic activation of calpain and caspase proteases after traumatic brain injury (TBI), no studies have examined the effects of injury magnitude on expression levels of these cell death effectors after TBI. Determination of the degree to which injury severity affects specific expression profiles is critical to understanding the relevant pathways contributing to post-trauma pathology and for developing targeted therapeutics. This investigation tested the hypothesis that different injury magnitudes (1.0, 1.2, and 1.6 mm) cause alterations in the regional and temporal patterns of mRNA expression of calpain-related (calpain-1 and -2, calpastatin) and caspase-related (caspases -3, -8, -9, BID) gene products after cortical impact in rats. Quantitative RT-PCR was used to compare effects of injury severity on mRNA levels in ipsilateral (injured) cortex and hippocampus, 6 h to 5 days post-injury. TBI caused increases in mRNA expression ofall proteins examined, with the highest expression detected in the cortex. Generally, injury magnitude and levels of gene expression were positively correlated. High levels of gene induction were observed with BID, caspase-3, and -8, while caspase-9 mRNA had the lowest level of induction. Interestingly, although calpains are activated within minutes of TBI, calpain mRNA expression was highest 72 h to 5 days post-TBI. This study is the first analysis of the regional and temporal expression of calpains and caspases after TBI. These data provide insight into the inter-relationship of these two protease families and on the distinct but overlapping cascades of cell death after TBI.
机译:尽管有大量研究表明创伤性脑损伤(TBI)后钙蛋白酶和caspase蛋白酶的基因表达和/或酶活化,但尚无研究检查过损伤程度对TBI后这些细胞死亡效应子表达水平的影响。确定损伤严重程度影响特定表达谱的程度对于了解有助于创伤后病理的相关途径以及开发靶向治疗剂至关重要。这项研究检验了以下假设:不同的损伤程度(1.0、1.2和1.6 mm)会导致钙蛋白酶相关(calpain-1和-2,钙蛋白酶抑制素)和caspase相关(caspases- 3,-8,-9,BID)基因产物在大鼠皮层受到冲击后产生。定量RT-PCR用于比较损伤严重程度对受伤后6 h至5天同侧(受伤)皮层和海马中mRNA水平的影响。 TBI导致所检查的所有蛋白质的mRNA表达增加,在皮质中检测到最高的表达。通常,损伤程度和基因表达水平呈正相关。 BID,caspase-3和-8观察到高水平的基因诱导,而caspase-9 mRNA的诱导水平最低。有趣的是,尽管钙蛋白酶在TBI的几分钟内被激活,但钙蛋白酶mRNA的表达在TBI后72小时至5天最高。这项研究是首次分析TBI后钙蛋白酶和胱天蛋白酶的区域和时间表达。这些数据提供了对这两个蛋白酶家族的相互关系以及TBI后细胞死亡的独特但重叠的级联的见解。

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