Lassiter Kentu, Dridi Sami, Piekarski Alissa, Greene Elizabeth, Hargis Billy, Kong Byung-Whi, Bottje Walter
Department of Poultry Science, University of Arkansas, Fayetteville, AR 72701, USA.
Department of Poultry Science, University of Arkansas, Fayetteville, AR 72701, USA.
Comp Biochem Physiol A Mol Integr Physiol. 2014 Sep;175:115-23. doi: 10.1016/j.cbpa.2014.06.003. Epub 2014 Jun 14.
A spontaneously immortalized chicken embryo fibroblast (CEF) cell line (DF-1) is known to exhibit faster growth rate and greater sensitivity to oxidative stress compared to the primary parent CEF (pCEF1°) cells. Thus, major objectives of this study were to assess cell bioenergetics in pCEF1° and DF-1 cells under control conditions and in response to 4-hydroxy 2-nonenal (4-HNE) induced oxidative challenge. Cell bioenergetics were assessed by flux analysis of oxygen consumption rate (OCR). Under control conditions, DF-1 cells had higher OCR associated with ATP synthase activity and mitochondrial oxygen reserve capacity as well as lower OCR due to proton leak and non-mitochondrial cytochrome c oxidase activity. In response to 4-HNE (0 to 30 μM), DF-1 cells were more sensitive to oxidant challenge than both young (passage 8) and senescent (passage 19) pCEF1° cells. Both passages 8 and 19 pCEF1° cells exhibited higher proton leak in response to 4-HNE, but this was not observed in DF-1 cells. Inducible proton leak occurs by 4-HNE stimulated activation of uncoupling protein (UCP) and adenine nucleotide translocase (ANT). From mRNA expression data indicated that ANT and avian UCP were down-regulated and up-regulated, respectively, in DF-1 compared to pCEF1° cells. Thus, we hypothesize that DF-1 cells are unable to increase proton leak due to lower expression of ANT, but not avian UCP, and this inability to increase proton leak contributes to greater susceptibility to oxidative stress of DF-1 cells compared to pCEF1° cells.
已知一种自发永生化的鸡胚成纤维细胞(CEF)系(DF-1)与原代亲代CEF(pCEF1°)细胞相比,具有更快的生长速度和对氧化应激更高的敏感性。因此,本研究的主要目的是评估在对照条件下以及对4-羟基-2-壬烯醛(4-HNE)诱导的氧化应激反应中,pCEF1°和DF-1细胞的细胞生物能量学。通过氧消耗率(OCR)的通量分析来评估细胞生物能量学。在对照条件下,DF-1细胞具有与ATP合酶活性和线粒体氧储备能力相关的较高OCR,以及由于质子泄漏和非线粒体细胞色素c氧化酶活性导致的较低OCR。响应4-HNE(0至30 μM)时,DF-1细胞比年轻(第8代)和衰老(第19代)的pCEF1°细胞对氧化应激更敏感。第8代和第19代pCEF1°细胞在响应4-HNE时均表现出较高的质子泄漏,但在DF-1细胞中未观察到这种情况。诱导性质子泄漏是由4-HNE刺激的解偶联蛋白(UCP)和腺嘌呤核苷酸转位酶(ANT)的激活引起的。从mRNA表达数据表明,与pCEF1°细胞相比,DF-1细胞中ANT和禽类UCP分别下调和上调。因此,我们假设DF-1细胞由于ANT表达较低而无法增加质子泄漏,但禽类UCP并非如此,并且这种无法增加质子泄漏导致DF-1细胞比pCEF1°细胞对氧化应激更敏感。