Aging in rat causes hepatic hyperresposiveness to interleukin-1β which is mediated by neutral sphingomyelinase-2


  • 2Rutkute K, Asmis R,. Nikolova-Karakashian MN. Decline in liver GSH during aging regulates NSMase-2 activity and cellular response to IL-1β stimulation (Submitted, 2006; J Lipid Res)

  • Potential conflict of interest: Nothing to report.


The process of aging has recently been shown to substantially affect the ability of cells to respond to inflammatory challenges. We demonstrate that aging leads to hepatic hyperresponsiveness to interleukin 1β (IL-1β), and we examine the factors that could be responsible for this phenomenon. IL-1β-induced phosphorylation of c-jun N-terminal kinase (JNK) in hepatocytes isolated from aged rats was 3 times more potent than that in hepatocytes from young rats. Moreover, JNK was activated by substantially lower doses of IL-1β. These age-related changes in JNK phosphorylation correlated with diminished IL-1β–induced degradation of interleukin-1 receptor–associated kinase-1 (IRAK-1). Expression levels of IL1β receptor I, total JNK, IRAK-1, and transforming growth factor-β–activated kinase-1 (TAK-1) were not affected by aging. However, increased neutral sphingomyelinase activity was observed in hepatocytes from old animals, which we show is caused by induction of the plasma membrane localized neutral sphingomyelinase-2 (NSMase-2). We provide evidence that NSMase-2 is both required and sufficient for the onset of IL-1β hyperresponsiveness during aging. Overexpression of NSMase-2 in hepatocytes from young rats leads both to a reduction in IRAK-1 degradation and potentiation of JNK phosphorylation, mimicking that seen in hepatocytes from old animals. More importantly, inhibition of NSMase activity in hepatocytes from aged rats using either scyphostatin or short interfering ribonucleic acid (siRNA) leads to reversion to the “young” phenotype of IL-1β response. Conclusion: These results show that the process of aging causes increased basal NSMase-2 activity in hepatocytes, which in turn leads to IRAK-1 stabilization, JNK potentiation, and ultimately IL-1β hyperresponsiveness. (HEPATOLOGY 2007.)