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创伤性脑损伤后大鼠大脑皮层中 p21 激活激酶 6 的上调。

Upregulation of p21-activated Kinase 6 in rat brain cortex after traumatic brain injury.

机构信息

Department of Neurosurgery, Affiliated Hospital of Nantong University, Nantong University, 226001 Nantong, People's Republic of China.

出版信息

J Mol Histol. 2011 Jun;42(3):195-203. doi: 10.1007/s10735-011-9324-8. Epub 2011 May 4.

DOI:10.1007/s10735-011-9324-8
PMID:21541790
Abstract

p21-activated Kinase 6 (PAK6) is a serine/threonine kinase belonging to the p21-activated kinase (PAK) family. PAK kinases are well-known regulators of a wide variety of cellular functions, including regulation of cytoskeleton rearrangement, cell survival, apoptosis and the mitogen-activated protein kinase signaling pathway. To elucidate the expressions and possible functions of PAK6 in central nervous system (CNS) lesion and repair, we performed a traumatic brain injury (TBI) model in adult rats. Western blot analysis revealed that PAK6 level significantly increased at day 3 after damage, and then declined during the following days. Besides, double immunofluorescence staining showed PAK6 was primarily expressed in the neurons and a few of glial cells in the normal group. While after injury, the expression of PAK6 was increased significantly in the astrocytes and neurons, and the astrocytes had largely proliferated. We also examined the expression of proliferating cell nuclear antigen (PCNA) whose change was correlated with the expression of PAK6. Importantly, double immunofluorescence staining revealed that cell proliferation evaluated by PCNA appeared in many PAK6-expressing cells at day 3 after injury. In addition, injury-induced expression of PAK6 was co-labeled by active caspase-3 during neuronal apoptosis after injury. Collectively, we hypothesized PAK6 may play important roles in CNS pathophysiology after TBI and further research is needed to have a good understanding of its function and mechanism.

摘要

p21 激活激酶 6(PAK6)是一种丝氨酸/苏氨酸激酶,属于 p21 激活激酶(PAK)家族。PAK 激酶是广泛的细胞功能的已知调节剂,包括细胞骨架重排、细胞存活、细胞凋亡和丝裂原激活的蛋白激酶信号通路的调节。为了阐明 PAK6 在中枢神经系统(CNS)损伤和修复中的表达和可能的功能,我们在成年大鼠中进行了创伤性脑损伤(TBI)模型。Western blot 分析显示,PAK6 水平在损伤后第 3 天显著增加,随后在接下来的几天内下降。此外,双免疫荧光染色显示 PAK6 主要在正常组的神经元和少数神经胶质细胞中表达。而在损伤后,PAK6 在星形胶质细胞和神经元中的表达显著增加,星形胶质细胞大量增殖。我们还检查了增殖细胞核抗原(PCNA)的表达,其变化与 PAK6 的表达相关。重要的是,双免疫荧光染色显示,损伤后第 3 天,许多表达 PAK6 的细胞中出现了由 PCNA 评估的细胞增殖。此外,在损伤诱导的神经元凋亡中,PAK6 的表达与活性 caspase-3 共标记。总之,我们假设 PAK6 在 TBI 后中枢神经系统病理生理学中可能发挥重要作用,需要进一步研究以更好地了解其功能和机制。

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PAK激酶的结构、生物化学及生物学特性
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The expression of FBP1 after traumatic brain injury and its role in astrocyte proliferation.创伤性脑损伤后 FBP1 的表达及其在星形胶质细胞增殖中的作用。
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SCY1-like 1 binding protein 1 (SCYL1-bp1) interacts with p53-induced RING H2 protein (Pirh2) after traumatic brain injury in rats.SCY1 样蛋白 1 结合蛋白 1(SCYL1-bp1)在大鼠创伤性脑损伤后与 p53 诱导的环指蛋白 2(Pirh2)相互作用。
J Mol Histol. 2013 Jun;44(3):271-83. doi: 10.1007/s10735-013-9488-5. Epub 2013 Mar 12.
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