Rice Kevin M, Desai Devashish H, Preston Deborah L, Wehner Paulette S, Blough Eric R
Department of Biological Sciences, Marshall University, Huntington, WV 25755-1090, USA.
Exp Physiol. 2007 Sep;92(5):963-70. doi: 10.1113/expphysiol.2007.037275. Epub 2007 May 25.
The effects of ageing on the cardiovascular system contribute to substantial alterations in cellular morphology and function. The variables regulating these changes are unknown; however, one set of signalling molecules that may be of particular importance in mediating numerous cellular responses, including control of cell growth, differentiation and adaptation, are the proteins associated with the mitogen-activated protein kinase (MAPK) signalling systems. The MAPKs, in conjunction with the p70 S6k signalling cascade, have emerged as critical components for regulating numerous mechanotransduction-related cellular responses. Here we investigate the ability of uniaxial stretch to activate the MAPK and p70 S6k pathways in adult (6-month-old), aged (30-month-old) and very aged (36-month-old) Fischer 344/NNiaHSd x Brown Norway/BiNia (FBN) rats. Western blotting of the MAPK family proteins extracellular signal-regulated kinase (Erk) 1/2, p38- and c-Jun NH(2)-terminal kinase (Jnk)-MAPKs showed differential expression and activation between these proteins with age. An acute 15 min interval of 20% uniaxial stretch using an ex vivo aortic preparation demonstrated similar regulation of Erk1/2, p38- and Jnk-MAPK. However, ageing altered uniaxial induced p70 S6k pathway signalling. These observations confirm previous data demonstrating that MAPK proteins are mechanically regulated and also suggest that p70 S6k signalling expression and activation are controlled differently with ageing. Taken together, these data may help to explain, in part, the age-related changes in vascular morphology, function and response to injury.
衰老对心血管系统的影响会导致细胞形态和功能发生显著改变。调节这些变化的变量尚不清楚;然而,一组在介导众多细胞反应(包括细胞生长、分化和适应的控制)中可能特别重要的信号分子是与丝裂原活化蛋白激酶(MAPK)信号系统相关的蛋白质。MAPK与p70 S6k信号级联一起,已成为调节众多机械转导相关细胞反应的关键成分。在这里,我们研究了单轴拉伸激活成年(6个月大)、老年(30个月大)和非常老年(36个月大)的Fischer 344/NNiaHSd×Brown Norway/BiNia(FBN)大鼠中MAPK和p70 S6k通路的能力。对MAPK家族蛋白细胞外信号调节激酶(Erk)1/2、p38和c-Jun NH(2)-末端激酶(Jnk)-MAPK进行蛋白质免疫印迹分析,结果显示这些蛋白质随年龄的增长存在差异表达和激活。使用离体主动脉制剂进行20%单轴拉伸15分钟的急性处理,结果表明对Erk1/2、p38和Jnk-MAPK的调节相似。然而,衰老改变了单轴诱导的p70 S6k通路信号传导。这些观察结果证实了先前的数据,即MAPK蛋白受机械调节,同时也表明p70 S6k信号的表达和激活在衰老过程中受到不同的控制。综上所述,这些数据可能有助于部分解释与年龄相关的血管形态、功能和损伤反应的变化。