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Targeted genomic disruption of H-ras and N-ras has no effect on early renal changes after unilateral ureteral ligation

机译:H-ras和N-ras的靶向基因组破坏对单侧输尿管结扎后的早期肾脏变化没有影响

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Purpose To assess the contribution of two different Ras monomeric GTPases isoforms H- and N-Ras in the early changes associated to obstructive nephropathy induced by unilateral ureteral obstruction (UUO). Methods UUO was performed in N-ras (N-ras~(-/-)) and H-ras (H-ras~(-/-)) knock-out mice and control (H-ras~(+/+)/N-ras~(+/+)) mice of C57B1/6 background. Fibronectin, alpha-smooth muscle actin, cleaved caspase-3, ki-67, Ras-GTP, pERK, and pAkt expression was analyzed by western blot and/or immunohis-tochemistry. Ras isoforms activation and caspase activity were determined by both western blot and ELISA. Results Three days after UUO, obstructed (O) kidneys of H-ras~(-/-) N-ras~(-/-) and H-ras~(+/+)/N-ras~(+/+) mice showed no significant differences in activated total ras, pERK1/2, pAkt, total Akt levels, fibronectin, alpha-SMA expression, cell proliferation, and activated caspase-3.
机译:目的评估两种不同的Ras单体GTPases同工型H-和N-Ras在与单侧输尿管梗阻(UUO)诱发的梗阻性肾病相关的早期变化中的作用。方法在N-ras(N-ras〜(-/-))和H-ras(H-ras〜(-/-))基因敲除小鼠和对照组(H-ras〜(+ / +))中进行UUO C57B1 / 6背景的/ N-ras〜(+ / +))小鼠。通过蛋白质印迹和/或免疫组织化学分析了纤连蛋白,α-平滑肌肌动蛋白,裂解的胱天蛋白酶-3,ki-67,Ras-GTP,pERK和pAkt的表达。 Ras亚型的激活和caspase活性通过Western印迹和ELISA测定。结果UUO后三天,H-ras〜(-/-)N-ras〜(-/-)和H-ras〜(+ / +)/ N-ras〜(+ / +)的(O)肾阻塞小鼠在活化的总ras,pERK1 / 2,pAkt,总的Akt水平,纤连蛋白,α-SMA表达,细胞增殖和活化的caspase-3中无显着差异。

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