首页> 美国卫生研究院文献>Immunology >The inhibition of T-lymphocyte proliferation by fatty acids is via an eicosanoid-independent mechanism.
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The inhibition of T-lymphocyte proliferation by fatty acids is via an eicosanoid-independent mechanism.

机译:脂肪酸对T淋巴细胞增殖的抑制作用是通过类二十烷酸非依赖性机制实现的。

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摘要

Eicosanoids, in particular prostaglandin E2 (PGE2), are potent inhibitors of a number of immune responses, including lymphocyte proliferation. We have previously shown that fatty acids, especially polyunsaturated fatty acids (PUFA), inhibit mitogen-stimulated proliferation of lymphocytes. One mechanism by which fatty acids could exert their inhibitory effect is via modulation of eicosanoid synthesis. This possibility was investigated in the present study. PGE2 concentrations in the medium taken from lymphocytes cultured in the presence of a range of different fatty acids did not correlate with the inhibitory effects of the fatty acids upon lymphocyte proliferation. Although PGE2 at concentrations above 10 nM caused inhibition of lymphocyte proliferation, PGE2 at the concentration measured in lymphocyte culture medium (0.3-4 nM) was not inhibitory. PGE3 did not inhibit lymphocyte proliferation, except at high concentrations (greater than 250 nM). The maximal inhibition of proliferation caused by PGE2 or PGE3 was less than the inhibition caused by each of the fatty acids except myristic or palmitic acids. Inclusion of inhibitors of phospholipase A2, cyclo-oxygenase or lipoxygenase in the culture medium did not prevent the fatty acids from exerting their inhibitory effect on lymphocyte proliferation. The eicosanoids present in lymph node cell cultures originate from macrophages rather than lymphocytes. Depletion of macrophages from the cell preparation by adherence did not prevent fatty acids from inhibiting proliferation. Proliferation of thoracic duct lymphocytes, which are devoid of macrophages, is inhibited by fatty acids to a similar extent as proliferation of lymph node lymphocytes. These observations provide convincing evidence that the inhibition of lymphocyte proliferation by fatty acids is independent of the production of eicosanoids. Therefore, other mechanisms must be investigated if the effect of fatty acids upon lymphocyte proliferation is to be understood at a biochemical level.
机译:类花生酸,特别是前列腺素E2(PGE2),是许多免疫反应(包括淋巴细胞增殖)的有效抑制剂。先前我们已经表明,脂肪酸,尤其是多不饱和脂肪酸(PUFA)抑制有丝分裂原刺激的淋巴细胞增殖。脂肪酸发挥抑制作用的一种机制是通过调节类花生酸合成。在本研究中研究了这种可能性。取自在一系列不同脂肪酸存在下培养的淋巴细胞的培养基中的PGE2浓度与脂肪酸对淋巴细胞增殖的抑制作用无关。尽管浓度高于10 nM的PGE2抑制了淋巴细胞的增殖,但以淋巴细胞培养基中测量的浓度(0.3-4 nM)的PGE2却没有抑制作用。除高浓度(大于250 nM)外,PGE3不抑制淋巴细胞增殖。 PGE2或PGE3引起的最大增殖抑制作用小于肉豆蔻酸或棕榈酸以外的每种脂肪酸引起的抑制作用。在培养基中包含磷脂酶A2,环氧化酶或脂氧化酶抑制剂并不能阻止脂肪酸对淋巴细胞增殖产生抑制作用。存在于淋巴结细胞培养物中的类花生酸来源于巨噬细胞而不是淋巴细胞。通过粘附从细胞制剂中消耗巨噬细胞不能防止脂肪酸抑制增殖。不含巨噬细胞的胸导管淋巴细胞的增殖受脂肪酸的抑制程度与淋巴结淋巴细胞的增殖相似。这些观察结果提供了令人信服的证据,表明脂肪酸对淋巴细胞增殖的抑制作用与类花生酸的产生无关。因此,如果要从生化水平理解脂肪酸对淋巴细胞增殖的作用,则必须研究其他机制。

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