Rezende Flavia, Schürmann Christoph, Schütz Susanne, Harenkamp Sabine, Herrmann Eva, Seimetz Michael, Weißmann Norbert, Schröder Katrin
Institute for Cardiovascular Physiology, Goethe-University, Frankfurt, Germany.
Instituts für Biostatistik und Mathematische Modellierung, Goethe-University, Frankfurt, Germany.
Redox Biol. 2017 Apr;11:312-314. doi: 10.1016/j.redox.2016.12.012. Epub 2016 Dec 22.
The free radical theory of aging suggests reactive oxygen species as a main reason for accumulation of damage events eventually leading to aging. Nox4, a member of the family of NADPH oxidases constitutively produces ROS and therefore has the potential to be a main driver of aging. Herein we analyzed the life span of Nox4 deficient mice and found no difference when compared to their wildtype littermates. Accordingly neither Tert expression nor telomere length was different in cells isolated from those animals. In fact, Nox4 mRNA expression in lungs of wildtype mice dropped with age. We conclude that Nox4 has no influence on lifespan of healthy mice.
衰老的自由基理论认为活性氧是损伤事件积累并最终导致衰老的主要原因。Nox4是NADPH氧化酶家族的一员,可组成性地产生活性氧,因此有可能成为衰老的主要驱动因素。在此,我们分析了Nox4基因敲除小鼠的寿命,发现与它们的野生型同窝小鼠相比没有差异。相应地,从这些动物分离的细胞中,端粒酶逆转录酶(Tert)的表达和端粒长度均无差异。事实上,野生型小鼠肺组织中Nox4 mRNA的表达随年龄增长而下降。我们得出结论,Nox4对健康小鼠的寿命没有影响。