Colgate University, Biology Department, 13 Oak Drive, Hamilton, NY 13346, USA
Colgate University, Biology Department, 13 Oak Drive, Hamilton, NY 13346, USA.
J Exp Biol. 2020 Jun 22;223(Pt 12):jeb221804. doi: 10.1242/jeb.221804.
There is ample evidence that cell membrane architecture contributes to metabolism and aging in animals; however, the aspects of this architecture that determine the rate of metabolism and longevity are still being debated. The 'membrane pacemaker' hypothesis of metabolism and of aging, respectively, suggest that increased lipid unsaturation and large amounts of polyunsaturated fatty acids (PUFAs) in cell membranes increase the cellular metabolic rate as well as the vulnerability of the cell to oxidative damage, thus increasing organismal metabolic rate and decreasing longevity. Here, we tested these hypotheses by experimentally altering the membrane fatty acid composition of fibroblast cells derived from small and large breed dogs by incubating them in a medium enriched in the monounsaturated fatty acid (MUFA) oleic acid (OA, 18:1) to decrease the total saturation. We then measured cellular metabolic parameters and correlated these parameters with membrane fatty acid composition and oxidative stress. We found that cells from small dogs and OA-incubated cells had lower maximal oxygen consumption and basal oxygen consumption rates, respectively, which are traits associated with longer lifespans. Furthermore, although we did not find differences in oxidative stress, cells from small dogs and OA-treated cells exhibited reduced ATP coupling efficiency, suggesting that these cells are less prone to producing reactive oxygen species. Membrane fatty acid composition did not differ between cells from large and small dogs, but cells incubated with OA had more monounsaturated fatty acids and a higher number of double bonds overall despite a decrease in PUFAs. Our results suggest that increasing the monounsaturation of dog cell membranes may alter some metabolic parameters linked to increases in longevity.
有充分的证据表明,细胞膜结构有助于动物的新陈代谢和衰老;然而,决定新陈代谢和寿命的细胞膜结构方面仍存在争议。新陈代谢和衰老的“膜起搏器”假说分别表明,细胞膜中增加的脂质不饱和程度和大量多不饱和脂肪酸(PUFAs)会增加细胞的代谢率以及细胞对氧化损伤的脆弱性,从而增加机体的代谢率并降低寿命。在这里,我们通过实验改变从小型和大型犬种的成纤维细胞中提取的细胞膜脂肪酸组成来测试这些假设,方法是将细胞在富含单不饱和脂肪酸(MUFA)油酸(OA,18:1)的培养基中孵育,以降低总饱和度。然后,我们测量了细胞的代谢参数,并将这些参数与膜脂肪酸组成和氧化应激相关联。我们发现,小型犬的细胞和 OA 孵育的细胞的最大耗氧量和基础耗氧量分别较低,这些都是与寿命较长相关的特征。此外,尽管我们没有发现氧化应激的差异,但小型犬的细胞和 OA 处理的细胞表现出降低的 ATP 偶联效率,这表明这些细胞不太容易产生活性氧。尽管大型犬和小型犬的细胞之间的膜脂肪酸组成没有差异,但与对照组相比,OA 孵育的细胞中具有更多的单不饱和脂肪酸和更高数量的双键,尽管 PUFAs 减少了。我们的结果表明,增加犬细胞膜的单不饱和程度可能会改变一些与寿命延长相关的代谢参数。