Naccache P H, Molski T F, Volpi M, Mackin W M, Becker E L, Sha'afi R I
J Cell Physiol. 1983 Jun;115(3):243-8. doi: 10.1002/jcp.1041150305.
Arachidonic acid when added simultaneously with the chemotactic peptide formyl-methionyl-leucyl-phenylalanine (f-Met-Leu-Phe) inhibits the ability of the latter to initiate several but not all of its effects on rabbit peritoneal neutrophils. Stimulated neutrophil aggregation, calcium uptake, and increases in the steady state level of exchangeable calcium are all inhibited by 1-10 microM arachidonic acid. The binding of f-Met-Leu-Phe and the parameters of intracellular calcium redistribution (calcium efflux and changes in the steady state level of exchangeable calcium in the absence of extracellular calcium) and of stimulated sodium uptake are, on the other hand, unaffected by the same concentrations of arachidonic acid. Arachidonic acid, the saturated analog of arachidonic acid, was found not to inhibit f-Met-Leu-Phe-stimulated aggregation and calcium uptake. Arachidonic acid, therefore, in addition to its well-described agonist properties, also possesses antagonist activities toward rabbit neutrophils. These results add a new level of complexity to the study of the role of arachidonic acid in cell activation.
花生四烯酸与趋化肽甲酰甲硫氨酰亮氨酰苯丙氨酸(f-Met-Leu-Phe)同时添加时,会抑制后者对兔腹膜中性粒细胞引发多种(但并非全部)效应的能力。1-10微摩尔的花生四烯酸会抑制受刺激的中性粒细胞聚集、钙摄取以及可交换钙稳态水平的升高。另一方面,f-Met-Leu-Phe的结合以及细胞内钙再分布参数(细胞外无钙时的钙外流和可交换钙稳态水平的变化)和受刺激的钠摄取不受相同浓度花生四烯酸的影响。花生四烯酸的饱和类似物被发现不会抑制f-Met-Leu-Phe刺激的聚集和钙摄取。因此,花生四烯酸除了具有其已被充分描述的激动剂特性外,对兔中性粒细胞还具有拮抗活性。这些结果为花生四烯酸在细胞激活中作用的研究增添了新的复杂层面。