Němcová-Fürstová Vlasta, James Roger F L, Kovář Jan
Department of Cell and Molecular Biology & Center for Research of Diabetes, Metabolism and Nutrition, Third Faculty of Medicine, Charles University, Ruská 87, Prague, Czech Republic.
Cell Physiol Biochem. 2011;27(5):525-38. doi: 10.1159/000329954. Epub 2011 Jun 15.
In this study we have tested the effect of unsaturated fatty acids on the proapoptotic effects of saturated fatty acids in the human pancreatic β-cells NES2Y.
We found that unsaturated palmitoleic and oleic acid at a concentration of 0.2 mM and higher are able to completely inhibit the proapoptotic effect of their counterpart saturated palmitic and stearic acid at a concentration of 1 mM. Apoptosis induced by stearic acid was associated with significant activation of caspase-6, -7, -9, -2 and -8, but not with significant activation of caspase-3. The activation of caspases was blocked by coincubation with oleic acid. Stearic acid treatment was not associated with a significant change in mitochondrial membrane potential, reactive oxygen species level and with cytochrome c release from mitochondria. Furthermore, stearic acid treatment was not associated with changes in p21(WAF1/CIP1), PIDD, Fas receptor and Fas ligand expression. However, we detected endoplasmic reticulum (ER) stress markers, i. e. a significant upregulation of BiP and CHOP expression as well as XBP1 mRNA splicing. These changes were inhibited by coincubation with oleic acid.
Presented data indicate that oleic acid inhibits apoptosis induction by stearic acid in NES2Y cells upstream of caspase activation and ER stress induction. It does not involve an interference with the mitochondrial pathway of apoptosis induction, with p53 activation and PIDD expression as well as with Fas receptor and Fas ligand expression.
在本研究中,我们测试了不饱和脂肪酸对人胰腺β细胞NES2Y中饱和脂肪酸促凋亡作用的影响。
我们发现,浓度为0.2 mM及更高的不饱和棕榈油酸和油酸能够完全抑制浓度为1 mM的相应饱和棕榈酸和硬脂酸的促凋亡作用。硬脂酸诱导的细胞凋亡与caspase-6、-7、-9、-2和-8的显著激活有关,但与caspase-3的显著激活无关。与油酸共同孵育可阻断半胱天冬酶的激活。硬脂酸处理与线粒体膜电位、活性氧水平的显著变化以及细胞色素c从线粒体的释放无关。此外,硬脂酸处理与p21(WAF1/CIP1)、PIDD、Fas受体和Fas配体表达的变化无关。然而,我们检测到内质网(ER)应激标志物,即BiP和CHOP表达的显著上调以及XBP1 mRNA剪接。与油酸共同孵育可抑制这些变化。
现有数据表明,油酸在半胱天冬酶激活和内质网应激诱导的上游抑制NES2Y细胞中硬脂酸诱导的细胞凋亡。它不涉及对细胞凋亡诱导的线粒体途径、p53激活和PIDD表达以及Fas受体和Fas配体表达的干扰。