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Fc受体介导的吞噬作用在巨噬细胞中于极低的胞质钙离子浓度水平下发生。

Fc receptor-mediated phagocytosis occurs in macrophages at exceedingly low cytosolic Ca2+ levels.

作者信息

Di Virgilio F, Meyer B C, Greenberg S, Silverstein S C

机构信息

Rover Laboratory of Cellular Physiology, Department of Physiology and Cellular Biophysics, Columbia University College of Physicians and Surgeons, New York 10032.

出版信息

J Cell Biol. 1988 Mar;106(3):657-66. doi: 10.1083/jcb.106.3.657.

Abstract

Cytosolic free Ca2+ ([Ca2+]i) homeostasis was investigated in mouse peritoneal macrophages and in the macrophage-like cell line J774. [Ca2+]i measurements were performed in both cells in suspension and cells in monolayers loaded with either quin2 or fura-2. Resting [Ca2+]i was 110-140 and 85-120 nM for cell suspensions and monolayers, respectively. There were no significant differences in [Ca2+]i between the two macrophage populations whether quin2 or fura-2 were used as Ca2+ indicators. Addition of heat-aggregated IgG, IgG-coated erythrocyte ghosts, or a rat monoclonal antibody (2.4G2) directed against mouse Fc receptor II induced a rise in [Ca2+]i. This [Ca2+]i increase was consistently observed in J774 and peritoneal macrophage suspensions and in J774 macrophage monolayers; in contrast it was observed inconsistently in peritoneal macrophages in monolayer cultures. The increase in [Ca2+]i induced by ligation of Fc receptors was inhibited totally in macrophages in suspension and by 80% in macrophages in monolayers by a short preincubation of macrophages with PMA; however, phagocytosis itself was unaffected. The effect of reducing cytosolic Ca2+ to very low concentrations on Fc receptor-mediated phagocytosis was also investigated. By incubating macrophages with high concentrations of quin2/AM in the absence of extracellular Ca2+, or by loading EGTA into the cytoplasm, the [Ca2+]i was buffered and clamped to 1-10 nM. Despite this, the phagocytosis of IgG-coated erythrocytes proceeded normally. These observations confirm the report of Young et al. (Young, J. D., S. S. Ko, and Z. A. Cohn. 1984. Proc. Natl. Acad. Sci. USA. 81:5430-5434) that ligation of Fc receptors causes Ca2+ mobilization in macrophages. However, these results confirm and extend the findings of McNeil et al. (McNeil, P. L., J. A. Swanson, S. D. Wright, S. C. Silverstein, and D. L. Taylor. 1986. J. Cell Biol. 102:1586-1592) that a rise in [Ca2+]i is not required for Fc receptor-mediated phagocytosis; and they provide direct evidence that Fc receptor-mediated phagocytosis occurs normally even at exceedingly low [Ca2+]i.

摘要

在小鼠腹腔巨噬细胞和巨噬细胞样细胞系J774中研究了胞质游离钙离子([Ca2+]i)的稳态。使用喹啉-2(quin2)或氟罗-2(fura-2)对悬浮细胞和单层细胞中的[Ca2+]i进行了测量。细胞悬浮液和单层细胞的静息[Ca2+]i分别为110 - 140 nM和85 - 120 nM。无论使用quin2还是fura-2作为Ca2+指示剂,两种巨噬细胞群体之间的[Ca2+]i均无显著差异。添加热聚集的IgG、IgG包被的红细胞空壳或针对小鼠Fc受体II的大鼠单克隆抗体(2.4G2)可诱导[Ca2+]i升高。在J774和腹腔巨噬细胞悬浮液以及J774巨噬细胞单层中均一致观察到这种[Ca2+]i的增加;相比之下,在单层培养的腹腔巨噬细胞中观察到的情况并不一致。通过用佛波酯(PMA)对巨噬细胞进行短时间预孵育,Fc受体连接诱导的[Ca2+]i增加在悬浮的巨噬细胞中被完全抑制,在单层巨噬细胞中被抑制80%;然而,吞噬作用本身不受影响。还研究了将胞质Ca2+降低到非常低的浓度对Fc受体介导的吞噬作用的影响。通过在无细胞外Ca2+的情况下用高浓度的quin2/AM孵育巨噬细胞,或将乙二醇双乙醚二胺四乙酸(EGTA)加载到细胞质中,[Ca2+]i被缓冲并钳制在1 - 10 nM。尽管如此,IgG包被的红细胞的吞噬作用仍正常进行。这些观察结果证实了扬等人(Young, J. D., S. S. Ko, and Z. A. Cohn. 1984. Proc. Natl. Acad. Sci. USA. 81:5430 - 5434)的报道,即Fc受体的连接会导致巨噬细胞中的Ca2+动员。然而,这些结果证实并扩展了麦克尼尔等人(McNeil, P. L., J. A. Swanson, S. D. Wright, S. C. Silverstein, and D. L. Taylor. 1986. J. Cell Biol. 102:1586 - 1592)的发现,即Fc受体介导的吞噬作用不需要[Ca2+]i升高;并且它们提供了直接证据,表明即使在极低的[Ca2+]i水平下,Fc受体介导的吞噬作用也能正常发生。

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