-------------------------------------------------------- 2014/06/20 咦, 有PubPeer alert呦... Christos Chinopoulos | Jun 20 2014 05:48 EST
Could it be that LPS-induced succinate over-production is due to itaconate formation? LPS induces Irg1, a gene coding for cis-aconitate decarboxylase, specifically expressed in cells of macrophage lineage Proc Natl Acad Sci U S A. 2013 May 7;110(19):7820-5. doi: 10.1073/pnas.1218599110, yielding itaconate. Itaconate is preferentially used by succinyl CoA ligase forming itaconyl CoA, thus generating an accumulation of succinate when the ligase operates towards succinyl CoA formation ADLER J, WANG SF, & Lardy HA (1957) The metabolism of itaconic acid by liver mitochondria. J. Biol. Chem, 229, 865-879, and WANG SF, ADLER J, & Lardy HA (1961) The pathway of itaconate metabolism by liver mitochondria. J. Biol. Chem, 236, 26-30. http://www.ncbi.nlm.nih.gov/pubmed/23535595#cm23535595_4939
因此,剩下的唯一可能應是使用diethylsuccinate(DS)和butylmalonate(BM)所造成的差異。例如,BM除了induce HIF1A stabilization以外,還有stabilize其它IL1B之上游分子,而那些因子在DS那一組並未出現。如此便可解釋為何HIF1A和IL1B在兩種藥處理下,蛋白量並未成正相關。 How do you like this idea, Yi-Hong? 😀