Kishida Etsu, Tajiri Michiko, Masuzawa Yasuo
Department of Life and Health Science, Hyogo University of Teacher Education, Yashiro, Hyogo 673-1494, Japan.
Biochim Biophys Acta. 2006 Apr;1761(4):454-62. doi: 10.1016/j.bbalip.2006.03.023. Epub 2006 Apr 1.
We previously reported that docosahexaenoic acid (DHA) attenuated tumor necrosis factor (TNF)-induced apoptosis in human monocytic U937 cells (J. Nutr. 130: 1095-1101, 2000). In the present study, we examined the effects of DHA and other polyunsaturated fatty acids (PUFA) on TNF-induced necrosis, another mode of cell death, using L929 murine fibrosarcoma cells. After preincubation with PUFA conjugated with BSA for 24 h, cells were treated with TNF or TNF+actinomycin D (Act D). Preincubation of cells with DHA enriched this polyunsaturated acid in the phospholipids and attenuated cell death induced by either TNF or TNF+Act D. When cells were treated with TNF alone, DNA laddering was not detected, and cells were coincidently stained with both annexin V-FITC and propidium iodide, indicating that the death mode was necrotic. TNF+Act D predominantly induced necrosis, although concurrent apoptotic cell death was also observed in this case. Preincubation with oleic acid, linoleic acid or 20:3(n-3) did not affect TNF-induced necrosis. Conversely, supplementation with n-3 docosapentaenoic acid (DPAn-3) or eicosapentaenoic acid (EPA) reduced necrotic cell death, but to a lesser extent in comparison with DHA. Unlike the case of U937 cell apoptosis, arachidonic acid (AA) significantly attenuated L929 cell necrosis, and 20:3(n-6) or 22:4(n-6) showed similar or less activity, respectively. Statistical evaluation indicated that the order of effective PUFA activity was DHA>DPAn-3> or =EPA>AA approximately 20:3(n-6)> or =22:4(n-6). One step desaturation, C2 elongation or C2 cleavage within the n-6 or n-3 fatty acid group was probably very active in L929 cells, because AA, synthesized from 20:3(n-6) or 22:4(n-6), and C22 fatty acids, synthesized from AA or EPA, were preferentially retained in cellular phospholipids. These observations suggested that attenuation of TNF-induced necrosis by the supplementation of various C20 or C22 polyunsaturated fatty acids is mainly attributable to the enrichment of three kinds of polyunsaturated fatty acids, i.e., DHA, DPAn-3 or AA, in phospholipids. Among these fatty acids, DHA was the most effective in the reduction of L929 necrosis as observed in the case of U937 apoptosis. This suggests that DHA-enriched membranes can protect cell against TNF irrespective of death modes and that membranous DHA may abrogate the death signaling common to necrosis and apoptosis.
我们先前报道过,二十二碳六烯酸(DHA)可减轻肿瘤坏死因子(TNF)诱导的人单核细胞U937细胞凋亡(《营养学杂志》130: 1095 - 1101, 2000)。在本研究中,我们使用L929小鼠纤维肉瘤细胞,研究了DHA和其他多不饱和脂肪酸(PUFA)对TNF诱导的坏死(另一种细胞死亡模式)的影响。在用与牛血清白蛋白(BSA)结合的PUFA预孵育24小时后,细胞用TNF或TNF +放线菌素D(Act D)处理。用DHA预孵育细胞可使这种多不饱和酸在磷脂中富集,并减轻由TNF或TNF + Act D诱导的细胞死亡。当细胞单独用TNF处理时,未检测到DNA梯状条带,并且细胞同时被膜联蛋白V - FITC和碘化丙啶染色,表明死亡模式为坏死。TNF + Act D主要诱导坏死,尽管在这种情况下也观察到了同时发生的凋亡性细胞死亡。用油酸、亚油酸或20:3(n - 3)预孵育不影响TNF诱导的坏死。相反,补充n - 3二十二碳五烯酸(DPAn - 3)或二十碳五烯酸(EPA)可减少坏死性细胞死亡,但与DHA相比程度较小。与U937细胞凋亡的情况不同,花生四烯酸(AA)显著减轻L929细胞坏死,并且20:3(n - 6)或22:4(n - 6)分别显示出相似或更低的活性。统计评估表明,有效PUFA活性的顺序为DHA > DPAn - 3≥EPA > AA≈20:3(n - 6)≥22:4(n - 6)。n - 6或n - 3脂肪酸组内的一步去饱和、C2延长或C2裂解在L929细胞中可能非常活跃,因为由20:3(n - 6)或22:4(n - 6)合成的AA以及由AA或EPA合成的C22脂肪酸优先保留在细胞磷脂中。这些观察结果表明,补充各种C20或C22多不饱和脂肪酸减轻TNF诱导的坏死主要归因于三种多不饱和脂肪酸,即DHA、DPAn - 3或AA在磷脂中的富集。在这些脂肪酸中,如在U937细胞凋亡的情况中所观察到的,DHA在减少L929细胞坏死方面最有效。这表明富含DHA的膜可以保护细胞免受TNF的影响,而与死亡模式无关,并且膜性DHA可能消除坏死和凋亡共有的死亡信号。