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Effect of different dose rates of ionizing radiation on ciliogenesis in hTERT-RPEl cells

机译:不同剂量率的电离辐射对HTERT-RPEL细胞纤西发生的影响

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Ionizing radiation (IR) induces genome instability and chromosome aberration in mammalian cells. IR exposure generates DNA damage, which is repaired by several DNA repair pathways. Meanwhile, IR also induces ciliogenesis and centrosome overduplication associated with cell cycle checkpoint mechanism. Centrosome number is strictly regulated, since overduplicated centrosomes cause aneuploidy, leading to tumorigenesis. Primary cilia play a sensory role in several signaling pathways during development and cellular homeostasis. In this study, to address how IR affects ciliogenesis, we irradiated telomerase reverse transcriptase-immortalized retina pigmentation epithelial cell, hTERT-RPEl, with γ-ray at different dose rates, that is 2 mGy/s (low dose rate) and 100 mGy/s (high dose rate). Centrosome and primary cilia were detected by immunofluorescence using y-tubulin and acetylated-a-tubulin antibodies, respectively. After IR exposure, we saw an increase in cells with primary cilia and the combined treatment of IR exposure with serum starvation stimulation showed an additive effect. This study provides a new insight into radiation effect on the extracellular response.
机译:电离辐射(IR)在哺乳动物细胞中诱导基因组不稳定性和染色体畸变。 IR暴露产生DNA损伤,由几种DNA修复途径修复。同时,IR还诱导与细胞周期检查点机制相关的纤毛生成和中心过度补充。由于过量多重的中心引起非整倍性,导致肿瘤内酯,因此严格调节中心数量。原发性纤毛在发育和细胞稳态期间在几种信号通路中发挥感官作用。在本研究中,为了解决IR的影响,我们如何用不同剂量率的γ射线照射端粒酶逆转录酶 - 永生型视网膜色素沉积上皮细胞,HTERT-RPEL,即2毫率/ s(低剂量率)和100米/ s(高剂量率)。通过使用Y-管蛋白和乙酰化 - a-微管蛋白抗体分别通过免疫荧光检测中心纤毛。 IR暴露后,我们看到具有原发性纤毛细胞的细胞增加,并且用血清饥饿刺激的IR暴露的组合治疗表现出添加剂效应。本研究为辐射对细胞外应答的影响提供了新的洞察。

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