The W. M. Keck Dynamic Image Analysis Facility, Department of Biology, The University of Iowa, Iowa City, IA 52242, USA.
J Cell Sci. 2010 Nov 1;123(Pt 21):3756-67. doi: 10.1242/jcs.068619. Epub 2010 Oct 12.
Using a newly developed microfluidic chamber, we have demonstrated in vitro that Ca(2+) functions as a chemoattractant of aggregation-competent Dictyostelium discoideum amoebae, that parallel spatial gradients of cAMP and Ca(2+) are more effective than either alone, and that cAMP functions as a stronger chemoattractant than Ca(2+). Effective Ca(2+) gradients are extremely steep compared with effective cAMP gradients. This presents a paradox because there is no indication to date that steep Ca(2+) gradients are generated in aggregation territories. However, given that Ca(2+) chemotaxis is co-acquired with cAMP chemotaxis during development, we speculate on the role that Ca(2+) chemotaxis might have and the possibility that steep, transient Ca(2+) gradients are generated during natural aggregation in the interstitial regions between cells.
利用新开发的微流控室,我们在体外证明了 Ca(2+) 是聚集能力强的盘基网柄菌变形虫的趋化因子,cAMP 和 Ca(2+) 的平行空间梯度比单独一种更有效,并且 cAMP 是比 Ca(2+) 更强的趋化因子。与有效的 cAMP 梯度相比,有效的 Ca(2+) 梯度非常陡峭。这是一个悖论,因为目前没有迹象表明在聚集区域会产生陡峭的 Ca(2+) 梯度。然而,鉴于在发育过程中 Ca(2+) 趋化性与 cAMP 趋化性同时获得,我们推测 Ca(2+) 趋化性可能具有的作用,以及在细胞间的间质区域中自然聚集过程中产生陡峭、短暂的 Ca(2+) 梯度的可能性。