Schaloske Ralph H, Blaesius Dagmar, Schlatterer Christina, Lusche Daniel F
Department of Chemistry and Biochemistry, University of California at San Diego,9500 Gilman Drive, La Jolla, CA 92093-0601, USA.
J Biosci. 2007 Dec;32(7):1281-9. doi: 10.1007/s12038-007-0137-6.
Cyclic AMP (cAMP)is a natural chemoattractant of the social amoeba Dictyostelium discoideum. It is detected by cell surface cAMP receptors. Besides a signalling cascade involving phosphatidylinositol 3,4,5-trisphosphate (PIP3), Ca2+ signalling has been shown to have a major role in chemotaxis. Previously, we have shown that arachidonic acid (AA) induces an increase in the cytosolic Ca2+ concentration by causing the release of Ca2+ from intracellular stores and activating influx of extracellular Ca2+. Here we report that AA is a chemoattractant for D. discoideum cells differentiated for 8-9 h. Motility towards a glass capillary filled with an AA solution was dose-dependent and qualitatively comparable to cAMP-induced chemotaxis. Ca2+ played an important role in AA chemotaxis of wild-type Ax2 as ethyleneglycol-bis(b-aminoethyl)-N,N,N',N'-tetraacetic acid (EGTA) added to the extracellular buffer strongly inhibited motility. In the HM1049 mutant whose iplA gene encoding a putative Ins(1,4,5)P3 -receptor had been knocked out, chemotaxis was only slightly affected by EGTA. Chemotaxis in the presence of extracellular Ca2+ was similar in both strains. Unlike cAMP, addition of AA to a cell suspension did not change cAMP or cGMP levels. A model for AA chemotaxis based on the findings in this and previous work is presented.
环磷酸腺苷(cAMP)是社会性变形虫盘基网柄菌的一种天然趋化因子。它由细胞表面的cAMP受体检测。除了涉及磷脂酰肌醇3,4,5 - 三磷酸(PIP3)的信号级联反应外,Ca2+信号传导已被证明在趋化作用中起主要作用。此前,我们已经表明,花生四烯酸(AA)通过引起细胞内钙库释放Ca2+并激活细胞外Ca2+内流,从而诱导胞质Ca2+浓度升高。在此我们报告,AA是诱导分化8 - 9小时的盘基网柄菌细胞的趋化因子。朝向装有AA溶液的玻璃毛细管的运动具有剂量依赖性,并且在性质上与cAMP诱导的趋化作用相当。Ca2+在野生型Ax2的AA趋化作用中起重要作用,因为添加到细胞外缓冲液中的乙二醇双(β - 氨基乙基)-N,N,N',N'-四乙酸(EGTA)强烈抑制运动。在编码假定的肌醇-1,4,5 - 三磷酸(Ins(1,4,5)P3)受体的iplA基因被敲除的HM1049突变体中,趋化作用仅受到EGTA的轻微影响。在两种菌株中,细胞外Ca2+存在时的趋化作用相似。与cAMP不同,向细胞悬液中添加AA不会改变cAMP或cGMP水平。基于本研究及之前工作的发现,我们提出了一个AA趋化作用的模型。