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蛋白激酶C、蛋白激酶B和细胞外信号调节激酶1/2介导的聚(ADP-核糖)聚合酶1、核因子κB和PEA15活性调节对癫痫持续状态后区域特异性星形胶质细胞反应有明显调控作用。

PKC, AKT and ERK1/2-Mediated Modulations of PARP1, NF-κB and PEA15 Activities Distinctly Regulate Regional Specific Astroglial Responses Following Status Epilepticus.

作者信息

Kim Ji-Eun, Kang Tae-Cheon

机构信息

Department of Anatomy and Neurobiology, Institute of Epilepsy Research, College of Medicine, Hallym University, Chuncheon, South Korea.

出版信息

Front Mol Neurosci. 2019 Jul 24;12:180. doi: 10.3389/fnmol.2019.00180. eCollection 2019.

Abstract

Status epilepticus (SE, a prolonged seizure activity) leads to reactive astrogliosis and astroglial apoptosis in the regional specific manners, independent of hemodynamics. Poly(ADP-ribose) polymerase-1 (PARP1) activity is relevant to these distinct astroglial responses. Since various regulatory signaling molecules beyond PARP1 activity may be involved in the distinct astroglial response to SE, it is noteworthy to explore the roles of protein kinases in PARP1-mediated reactive astrogliosis and astroglial apoptosis following SE, albeit at a lesser extent. In the present study, inhibitions of protein kinase C (PKC), AKT and extracellular signal-related kinases 1/2 (ERK1/2), but not calcium/calmodulin-dependent protein kinase II (CaMKII), attenuated CA1 reactive astrogliosis accompanied by reducing PARP1 activity following SE, respectively. However, inhibition of AKT and ERK1/2 deteriorated SE-induced dentate astroglial loss concomitant with the diminished PARP1 activity. Following SE, PKC- and AKT inhibitors diminished phosphoprotein enriched in astrocytes of 15 kDa (PEA15)-S104 and -S116 phosphorylations in CA1 astrocytes, but not in dentate astrocytes, respectively. Inhibitors of PKC, AKT and ERK1/2 also abrogated SE-induced nuclear factor-κB (NF-κB)-S311 and -S468 phosphorylations in CA1 astrocytes. In contrast, both AKT and ERK1/2 inhibitors enhanced NF-κB-S468 phosphorylation in dentate astrocytes. Furthermore, PARP1 inhibitor aggravated dentate astroglial loss following SE. AKT inhibition deteriorated dentate astroglial loss and led to CA1 astroglial apoptosis following SE, which were ameliorated by AKT activation. These findings suggest that activities of PARP1, PEA15 and NF-κB may be distinctly regulated by PKC, AKT and ERK1/2, which may be involved in regional specific astroglial responses following SE.

摘要

癫痫持续状态(SE,一种长时间的癫痫发作活动)会以区域特异性方式导致反应性星形胶质细胞增生和星形胶质细胞凋亡,且与血流动力学无关。聚(ADP-核糖)聚合酶-1(PARP1)的活性与这些不同的星形胶质细胞反应相关。由于PARP1活性之外的各种调节信号分子可能参与了对SE的不同星形胶质细胞反应,因此尽管程度较轻,但探索蛋白激酶在SE后PARP1介导的反应性星形胶质细胞增生和星形胶质细胞凋亡中的作用仍值得关注。在本研究中,蛋白激酶C(PKC)、AKT和细胞外信号调节激酶1/2(ERK1/2)的抑制,而非钙/钙调蛋白依赖性蛋白激酶II(CaMKII)的抑制,分别减轻了SE后CA1区的反应性星形胶质细胞增生,同时降低了PARP1活性。然而,抑制AKT和ERK1/2会加剧SE诱导的齿状回星形胶质细胞丢失,同时PARP1活性降低。SE后,PKC和AKT抑制剂分别减少了CA1区星形胶质细胞中15 kDa富含磷蛋白(PEA15)的S104和S116磷酸化,但未减少齿状回星形胶质细胞中的磷酸化。PKC、AKT和ERK1/2的抑制剂也消除了SE诱导的CA1区星形胶质细胞中核因子-κB(NF-κB)的S311和S468磷酸化。相反,AKT和ERK1/2抑制剂均增强了齿状回星形胶质细胞中NF-κB的S468磷酸化。此外,PARP1抑制剂加重了SE后的齿状回星形胶质细胞丢失。AKT抑制加剧了SE后的齿状回星形胶质细胞丢失,并导致CA1区星形胶质细胞凋亡,而AKT激活可改善这些情况。这些发现表明,PARP1、PEA15和NF-κB的活性可能受到PKC、AKT和ERK1/2的不同调节,这可能参与了SE后的区域特异性星形胶质细胞反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dbd/6667551/1a3de0e2e1bc/fnmol-12-00180-g0001.jpg

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