Marasco W A, Becker E L, Oliver J M
Am J Pathol. 1980 Mar;98(3):749-68.
The behavior of cells undergoing chemotaxis may be analyzed in terms of their orientation, a static characteristic, and of their locomotion. We have examined the extracellular divalent cation requirements for orientation and locomotion of rabbit polymorphonuclear leukocytes (neutrophils) in a gradient of the chemotactic peptide N-formyl-methionyl-leu-cyl-phenylalanine (F-Met-Leu-Phe) using the chemotaxis chamber recently developed by Zigmond. This chamber allows direct observation of cells attached to glass coverslips as they move up a gradient of chemotactic agent established across a 1-mm bridge. The orientation of neutrophils in the direction of the gradient was equally efficient whether cells and F-Met-Leu-Phe were suspended in merium supplemented with both Ca2+ and Mg2+ (complete medium), with Mg2+ but not Ca2+ (by simple omission of Ca2+ or by addition of EGTA), or with nonsupplemented medium (by omission of Ca2+ and Mg2+ or by addition of EDTA). These data confirm and extend Zigmond's earlier observation that exogenous divalent cations are not required for polymorphonuclear leukocyte orientation toward the chemotactic peptide. In contrast, cell locomotion, determined by linking the chemotaxis chamber to a time-lapse videocassette recorder and TV monitor, is markedly affected by the medium's content of divalent cations. Cells suspended in medium supplemented with Mg2+ but not calcium (by omission or chelation) or in nonsupplemented medium moved on the average 25% more rapidly than cells in complete Ca2+ and Mg2+ medium. Although the simple omission of Mg2+ does not prevent chemotaxis, chelation of Mg2+ in the medium completely abolishes leukocyte locomotion. Addition of varying concentrations of Mg2+ to the buffer in the presence of EDTA established that cell movement is fully restored by Mg2+ concentrations in the range of 3 X 10(-9) M, concentrations easily attained in the absence of added Mg2+. It was concluded that neither Ca2+ nor Mg2+ is needed for orientation in response to F-Met-Leu-Phe. However, low levels of exogenous Mg2+ but not Ca2+ are required for effective locomotion of neutrophils in the Zigmond changer. This result contrasts with data obtained in the Boyden chamber, where exogenous Ca2+ is considered essential for maximum chemotactic response.
可以根据细胞的定向(一种静态特征)及其移动来分析经历趋化作用的细胞行为。我们使用齐格蒙德最近开发的趋化作用室,研究了兔多形核白细胞(中性粒细胞)在趋化肽N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸(F-Met-Leu-Phe)梯度中定向和移动所需的细胞外二价阳离子。该趋化作用室允许直接观察附着在玻璃盖玻片上的细胞,当它们沿着横跨1毫米桥建立的趋化剂梯度向上移动时。无论细胞和F-Met-Leu-Phe是悬浮在补充有Ca2+和Mg2+的培养基(完全培养基)中、仅补充有Mg2+而无Ca2+的培养基中(通过简单省略Ca2+或添加乙二醇双四乙酸),还是悬浮在未补充培养基中(通过省略Ca2+和Mg2+或添加乙二胺四乙酸),中性粒细胞在梯度方向上的定向效率是相同的。这些数据证实并扩展了齐格蒙德早期的观察结果,即多形核白细胞向趋化肽定向不需要外源性二价阳离子。相比之下,通过将趋化作用室连接到延时录像带录像机和电视监视器来确定的细胞移动,明显受到培养基中二价阳离子含量的影响。悬浮在补充有Mg2+但无钙的培养基中(通过省略或螯合)或未补充培养基中的细胞,平均移动速度比在含有完整Ca2+和Mg2+的培养基中的细胞快25%。虽然简单省略Mg2+并不阻止趋化作用,但培养基中Mg2+的螯合完全消除了白细胞的移动。在存在乙二胺四乙酸的情况下,向缓冲液中添加不同浓度的Mg2+表明,Mg2+浓度在3×10(-9)M范围内可完全恢复细胞移动,在不添加Mg2+的情况下很容易达到该浓度。得出的结论是,响应F-Met-Leu-Phe进行定向时,Ca2+和Mg2+都不需要。然而,在齐格蒙德趋化作用室中,中性粒细胞有效移动需要低水平的外源性Mg2+而不是Ca2+。这一结果与在博伊登小室中获得的数据形成对比,在博伊登小室中,外源性Ca2+被认为对最大趋化反应至关重要。