Ikemoto A, Kobayashi T, Emoto K, Umeda M, Watanabe S, Okuyama H
Faculty of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabedori, Nagoya, Mizuhoku, 467-8603, Japan.
Arch Biochem Biophys. 1999 Apr 1;364(1):67-74. doi: 10.1006/abbi.1999.1110.
We have shown previously that docosahexaenoic acid (DHA) promotes and arachidonic acid (AA) suppresses neurite outgrowth of PC12 cells induced by nerve growth factor (NGF) and that incorporation of [3H]ethanolamine into phosphatidylethanolamine (PE) is suppressed in PC12 cells by AA while DHA has no effect. In the present study, the effects of these fatty acids on PE synthesis via decarboxylation of phosphatidylserine (PS), another pathway of PE synthesis, and distribution of aminophospholipids were examined. Incorporation of [3H]serine into PS and PE was elevated in the course of NGF-induced differentiation and was further stimulated significantly by DHA, but not by AA. [3H]Ethanolamine uptake by PC12 cells was significantly suppressed by AA but not by DHA while these fatty acids did not affect [3H]serine uptake, indicating that the suppression by AA of [3H]ethanolamine incorporation into phosphatidylethanolamine is attributable, at least in part, to a reduction in [3H]ethanolamine uptake. The distribution of PE in the outer leaflet of plasma membrane decreased during differentiation, which is known to be accompanied by an increase in the surface area of plasma membrane. Supplementation of PC12 cells with DHA or AA did not affect the distribution of aminophospholipids. Thus, DHA and AA affected aminophospholipid synthesis and neurite outgrowth differently, but not the transport and distribution of aminophospholipids, while the PE concentration in the outer leaflet of the plasma membrane decreased in association with morphological changes in PC12 cells induced by NGF.
我们之前已经表明,二十二碳六烯酸(DHA)可促进神经生长因子(NGF)诱导的PC12细胞神经突生长,而花生四烯酸(AA)则抑制该生长;并且,AA可抑制PC12细胞中[3H]乙醇胺掺入磷脂酰乙醇胺(PE),而DHA则无此作用。在本研究中,我们检测了这些脂肪酸对磷脂酰丝氨酸(PS)脱羧合成PE这一PE合成的另一途径以及氨基磷脂分布的影响。在NGF诱导分化过程中,[3H]丝氨酸掺入PS和PE的量增加,且DHA可进一步显著刺激这一过程,但AA无此作用。AA可显著抑制PC12细胞对[3H]乙醇胺的摄取,但DHA无此作用,而这些脂肪酸不影响[3H]丝氨酸的摄取,这表明AA对[3H]乙醇胺掺入磷脂酰乙醇胺的抑制作用至少部分归因于[3H]乙醇胺摄取的减少。在分化过程中,质膜外小叶中PE的分布减少,已知这伴随着质膜表面积的增加。用DHA或AA处理PC12细胞不影响氨基磷脂的分布。因此,DHA和AA对氨基磷脂合成和神经突生长的影响不同,但不影响氨基磷脂的转运和分布,而质膜外小叶中的PE浓度随着NGF诱导的PC12细胞形态变化而降低。