Sun Xiao-le, Yang Zi, Wang Jia-lue, Wang Wei, Wang Xiao-ye, Wu Shu-ying
Department of Obstetrics & Gynecology, Peking University Third Hospital, Beijing 100191, China.
Department of Obstetrics & Gynecology, Peking University Third Hospital, Beijing 100191, China. Email:
Zhonghua Yi Xue Za Zhi. 2013 Dec 17;93(47):3786-90.
To explore the interaction mechanism and influence between fatty acids oxidation and p38MAPK signal transduction pathway in trophoblast cells stimulated by fatty acids of different chain lengths.
Serum-free trophoblast cells cultured in vitro were divided into 5 groups, i.e. incubation with DMEM/F12 medium without FFA (F-FFA), short-chain fatty acids (SC-FFA), medium-chain fatty acids (MC-FFA), long-chain fatty acids (LC-FFA) and very long-chain fatty acids (VLC-FFA). Then cells in each group were stimulated by DMEM/F12 medium, NADPH oxidase inhibitor (Apocynin) and p38MAPK inhibitor (SB203580) and were subdivided into FFA plus-DMEM group, plus-NADPH-I and plus-p38MAPK-I groups. Expressions of mRNA and protein of LCHAD in trophoblast cells were detected by real-time polymerase chain reaction (PCR) and Western blot.
(1) mRNA expression of LCHAD: the Δct of mRNA of LCHAD in F-FFA+DMED, SC-FFA+DMEM, MC-FFA+DMEM, LC-FFA+DMEM, LC-FFA+NADPH-I, LC-FFA+p38MAPK-I and VLC-FFA+DMEM, VLC-FFA+NADPH-I, VLC-FFA+p38MAPK-I groups were 4.57 ± 0.12, 4.36 ± 0.09, 4.55 ± 0.10, 6.84 ± 0.42, 4.45 ± 0.24, 5.08 ± 0.36, 2.23 ± 0.15, 3.90 ± 0.32, 3.81 ± 0.41. Compared with the F-FFA groups, the relative mRNA expressions of LCHAD significantly decreased in LC-FFA+DMEM/p38MAPK-I groups (P < 0.05) while increased in VLC-FFA groups (P < 0.05). Compared with the LC-FFA+DMEM groups, the relative mRNA expressions of LCHAD increased in LC-FFA+NADPH-I/p38MAPK-I groups (P < 0.05). The relative mRNA expressions of LCHAD in VLC-FFA+NADPH-I/p38MAPK-I groups significantly decreased versus VLC-FFA+DMEM group (P < 0.05). (2) Protein expression of LCHAD: The relative protein expressions of LCHAD in F-FFA+DMED, SC-FFA+DMEM, MC-FFA+DMEM, LC-FFA+DMEM, LC-FFA+NADPH-I, LC-FFA+p38MAPK-I and VLC-FFA+DMEM, VLC-FFA+NADPH-I, VLC-FFA+p38MAPK-I groups were 23.6 ± 13.0, 21.2 ± 10.2, 19.7 ± 1.9, 10.6 ± 2.6, 14.0 ± 1.8, 14.0 ± 2.8, 29.3 ± 1.9, 35.8 ± 3.2 and 35.2 ± 4.5 respectively. Compared with the F-FFA groups, the protein expressions of LCHAD significantly decreased in LC-FFA groups (P < 0.05) while increased in VLC-FFA+NADPH-I/p38MAPK-I groups (P < 0.05).
Free fatty acids affect the gene and protein expressions of mitochondrial β-oxidation enzyme of LCHAD in trophoblastic cells. Fatty acid β-oxidation is impaired in trophoblast cells incubated with long-chain fatty acid. NADPH oxidase and p38MAPK inhibitors may alleviate such an effect. Thus p38MAPK signal transduction pathway may participate in this process. The correlation between very long chain fatty acids and fatty acid β-oxidation is confirmed. But their interactions require further explorations.
探讨不同链长脂肪酸刺激滋养层细胞时,脂肪酸氧化与p38丝裂原活化蛋白激酶(p38MAPK)信号转导通路之间的相互作用机制及影响。
将体外培养的无血清滋养层细胞分为5组,即分别用不含游离脂肪酸(FFA)的DMEM/F12培养基(F-FFA)、短链脂肪酸(SC-FFA)、中链脂肪酸(MC-FFA)、长链脂肪酸(LC-FFA)和极长链脂肪酸(VLC-FFA)孵育。然后用DMEM/F12培养基、NADPH氧化酶抑制剂(阿朴吗啡)和p38MAPK抑制剂(SB203580)刺激每组细胞,并将其细分为FFA加-DMEM组、加-NADPH-I组和加-p38MAPK-I组。采用实时聚合酶链反应(PCR)和蛋白质免疫印迹法检测滋养层细胞中长链3-羟基酰基辅酶A脱氢酶(LCHAD)的mRNA和蛋白表达。
(1)LCHAD的mRNA表达:F-FFA+DMED、SC-FFA+DMEM、MC-FFA+DMEM、LC-FFA+DMEM、LC-FFA+NADPH-I、LC-FFA+p38MAPK-I组以及VLC-FFA+DMEM、VLC-FFA+NADPH-I、VLC-FFA+p38MAPK-I组中LCHAD的mRNA的Δct分别为4.57±0.12、4.36±0.09、4.55±0.10、6.84±0.42、4.45±0.24、5.08±0.36、2.23±0.15、3.90±0.32、3.81±0.41。与F-FFA组相比,LC-FFA+DMEM/p38MAPK-I组中LCHAD的相对mRNA表达显著降低(P<0.05),而VLC-FFA组中则升高(P<0.05)。与LC-FFA+DMEM组相比,LC-FFA+NADPH-I/p38MAPK-I组中LCHAD的相对mRNA表达升高(P<0.05)。VLC-FFA+NADPH-I/p38MAPK-I组中LCHAD的相对mRNA表达与VLC-FFA+DMEM组相比显著降低(P<0.05)。(2)LCHAD的蛋白表达:F-FFA+DMED、SC-FFA+DMEM、MC-FFA+DMEM、LC-FFA+DMEM、LC-FFA+NADPH-I、LC-FFA+p38MAPK-I组以及VLC-FFA+DMEM、VLC-FFA+NADPH-I、VLC-FFA+p38MAPK-I组中LCHAD的相对蛋白表达分别为23.6±13.0、21.2±10.2、19.7±1.9、10.6±2.6、14.0±1.8、14.0±2.8、29.3±1.9、35.8±3.2和35.2±4.5。与F-FFA组相比,LC-FFA组中LCHAD的蛋白表达显著降低(P<0.05),而VLC-FFA+NADPH-I/p38MAPK-I组中则升高(P<0.05)。
游离脂肪酸影响滋养层细胞中LCHAD线粒体β氧化酶的基因和蛋白表达。用长链脂肪酸孵育的滋养层细胞中脂肪酸β氧化受损。NADPH氧化酶和p38MAPK抑制剂可能减轻这种作用。因此,p38MAPK信号转导通路可能参与这一过程。极长链脂肪酸与脂肪酸β氧化之间的相关性得到证实。但其相互作用有待进一步探索。