Tiwari Kirti Kumar, Moorthy Bhagavatula, Lingappan Krithika
Department of Pediatrics, Section of Neonatology, Texas Children's Hospital, Baylor College of Medicine, 1102 Bates Avenue, MC: FC530.01, Houston, TX 77030, USA.
Department of Pediatrics, Section of Neonatology, Texas Children's Hospital, Baylor College of Medicine, 1102 Bates Avenue, MC: FC530.01, Houston, TX 77030, USA.
Toxicol In Vitro. 2015 Oct;29(7):1369-76. doi: 10.1016/j.tiv.2015.05.008. Epub 2015 May 21.
GDF15 (growth and differentiation factor 15) is a secreted cytokine, a direct target of p53 and plays a role in cell proliferation and apoptosis. It is induced by oxidative stress and has anti-apoptotic effects. The role of GDF15 in hyperoxic lung injury is unknown. We tested the hypothesis that GDF15 will be induced in vitro, in a model of pulmonary oxygen toxicity, and will play a critical role in decreasing cell death and oxidative stress. BEAS-2B (human bronchial epithelial cells) and human pulmonary vascular endothelial cells (HPMEC) were exposed to hyperoxia, and expression of GDF15 and effect of GDF15 disruption on cell viability and oxidative stress was determined. Furthermore, we studied the effect of p53 knockdown on GDF15 expression. In vitro, both BEAS-2B and HPMEC cells showed a significant increase in GDF15 expression upon exposure to hyperoxia. After GDF15 knockdown, there was a significant decrease in cell viability and increase in oxidative stress compared to control cells transfected with siRNA with a scrambled sequence. Knockdown of p53 significantly decreased the induction of GDF15 by hyperoxia. In conclusion, we show that GDF15 has a pro-survival and anti-oxidant role in hyperoxia and that p53 plays a key role in its induction.
生长分化因子15(GDF15)是一种分泌型细胞因子,是p53的直接靶点,在细胞增殖和凋亡中发挥作用。它由氧化应激诱导产生,具有抗凋亡作用。GDF15在高氧肺损伤中的作用尚不清楚。我们检验了以下假设:在肺氧中毒模型中,GDF15在体外会被诱导产生,并且在减少细胞死亡和氧化应激方面发挥关键作用。将人支气管上皮细胞(BEAS-2B)和人肺血管内皮细胞(HPMEC)暴露于高氧环境中,测定GDF15的表达以及GDF15缺失对细胞活力和氧化应激的影响。此外,我们研究了p53基因敲低对GDF15表达的影响。在体外,BEAS-2B细胞和HPMEC细胞在暴露于高氧环境后,GDF15表达均显著增加。与转染了乱序序列小干扰RNA(siRNA)的对照细胞相比,GDF15基因敲低后,细胞活力显著降低,氧化应激增加。p53基因敲低显著降低了高氧对GDF15的诱导作用。总之,我们表明GDF15在高氧环境中具有促生存和抗氧化作用,并且p53在其诱导过程中起关键作用。