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Staurosporine induces different cell death forms in cultured rat astrocytes

机译:星形孢菌素在培养的大鼠星形胶质细胞中诱导不同的细胞死亡形式

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摘要

Background. Astroglial cells are frequently involved in malignant transformation. Besides apoptosis, necroptosis, a different form of regulated cell death, seems to be related with glioblastoma genesis, proliferation, angiogenesis and invasion. In the present work we elucidated mechanisms of necroptosis in cultured astrocytes, and compared them with apoptosis, caused by staurosporine. Materials and methods. Cultured rat cortical astrocytes wereused for a cell death studies. Cell death was induced by different concentrations of staurosporine, and modified by inhibitors of apoptosis (z-vad-fmk) and necroptosis (nec-1). Different forms of a cell death were detected using flow cytometry.Results. We showed that staurosporine, dependingon concentration, induces both, apoptosis as well as necroptosis.Treatment with 10-7 M staurosporine increased apoptosis of astrocytes after the regeneration in a staurosporine free medium. When caspases were inhibited, apoptosis was attenuated, while necroptosis was slightly increased. Treatment with 10-6 M staurosporine induced necroptosis that occurred after the regeneration of astrocytes in a staurosporine free medium, as well as without regeneration period. Necroptosis was significantly attenuated by nec-1 which inhibits RIP1 kinase. On the other hand, the inhibition of caspases had no effect on necroptosis. Furthermore, staurosporine activated RIP1 kinase increased the production of reactive oxygen species, while an antioxidant BHA significantly attenuated necroptosis.Conclusion. Staurosporine can induce apoptosis and/or necroptosis in cultured astrocytes via different signalling pathways. Distinction between different forms of cell death is crucial in the studies of therapy-induced necroptosis.
机译:背景。星形胶质细胞经常参与恶性转化。除凋亡外,坏死病是一种不同形式的调节性细胞死亡,似乎与胶质母细胞瘤的发生,增殖,血管生成和侵袭有关。在目前的工作中,我们阐明了培养的星形胶质细胞坏死性坏死的机制,并将它们与星形孢菌素引起的细胞凋亡进行了比较。材料和方法。将培养的大鼠皮质星形胶质细胞用于细胞死亡研究。细胞死亡是由不同浓度的星形孢菌素诱导的,并由凋亡抑制剂(z-vad-fmk)和坏死病(nec-1)抑制。使用流式细胞仪检测到不同形式的细胞死亡。我们表明星形孢菌素,取决于浓度,诱导凋亡和坏死病。用10-7 M星形孢菌素治疗可在无星形孢菌素的培养基中再生后增加星形胶质细胞的凋亡。当胱天蛋白酶被抑制时,细胞凋亡减弱,而坏死病则略有增加。在无星形孢菌素的培养基中星形胶质细胞再生后以及没有再生期的情况下,用10-6 M星形孢菌素处理可诱发坏死。 nec-1可抑制RIP1激酶,从而明显减轻尸检病。另一方面,抑制胱天蛋白酶对坏死病没有影响。此外,星形孢菌素激活的RIP1激酶可增加活性氧的产生,而抗氧化剂BHA可显着减轻坏死性肾病。星形孢菌素可通过不同的信号传导途径诱导培养的星形胶质细胞凋亡和/或坏死。在治疗诱发的坏死病研究中,区分不同形式的细胞死亡至关重要。

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