Andrisic Luka, Collinson Emma J, Tehlivets Oksana, Perak Eleonora, Zarkovic Tomislav, Dawes Ian W, Zarkovic Neven, Cipak Gasparovic Ana
Rudjer Boskovic Institute, Bijenicka 54, 10000, Zagreb, Croatia.
Mol Cell Biochem. 2015 Jan;399(1-2):27-37. doi: 10.1007/s11010-014-2229-6. Epub 2014 Oct 4.
Pathophysiology of polyunsaturated fatty acids (PUFAs) is associated with aberrant lipid and oxygen metabolism. In particular, under oxidative stress, PUFAs are prone to autocatalytic degradation via peroxidation, leading to formation of reactive aldehydes with numerous potentially harmful effects. However, the pathological and compensatory mechanisms induced by lipid peroxidation are very complex and not sufficiently understood. In our study, we have used yeast capable of endogenous PUFA synthesis in order to understand the effects triggered by PUFA accumulation on cellular physiology of a eukaryotic organism. The mechanisms induced by PUFA accumulation in S. cerevisiae expressing Hevea brasiliensis Δ12-fatty acid desaturase include down-regulation of components of electron transport chain in mitochondria as well as up-regulation of pentose-phosphate pathway and fatty acid β-oxidation at the transcriptional level. Interestingly, while no changes were observed at the transcriptional level, activities of two important enzymatic antioxidants, catalase and glutathione-S-transferase, were altered in response to PUFA accumulation. Increased intracellular glutathione levels further suggest an endogenous oxidative stress and activation of antioxidative defense mechanisms under conditions of PUFA accumulation. Finally, our data suggest that PUFA in cell membrane causes metabolic changes which in turn lead to adaptation to endogenous oxidative stress.
多不饱和脂肪酸(PUFAs)的病理生理学与异常的脂质和氧代谢相关。特别是在氧化应激下,PUFAs易于通过过氧化作用发生自催化降解,导致形成具有众多潜在有害影响的反应性醛类。然而,脂质过氧化所诱导的病理和代偿机制非常复杂,尚未得到充分理解。在我们的研究中,我们使用了能够内源性合成PUFAs的酵母,以了解PUFA积累对真核生物细胞生理学所引发的影响。在表达巴西橡胶树Δ12-脂肪酸去饱和酶的酿酒酵母中,PUFA积累所诱导的机制包括线粒体中电子传递链组分的下调以及转录水平上磷酸戊糖途径和脂肪酸β-氧化的上调。有趣的是,虽然在转录水平未观察到变化,但两种重要的酶促抗氧化剂过氧化氢酶和谷胱甘肽-S-转移酶的活性因PUFA积累而发生改变。细胞内谷胱甘肽水平的升高进一步表明在PUFA积累条件下存在内源性氧化应激和抗氧化防御机制的激活。最后,我们的数据表明细胞膜中的PUFA会引起代谢变化,进而导致对内源性氧化应激的适应。