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线粒体钙摄取对于替代型巨噬细胞极化和吞噬活性至关重要。

Mitochondrial Calcium Uptake Is Instrumental to Alternative Macrophage Polarization and Phagocytic Activity.

机构信息

Department of Medicine, University of Padova, Via Giustiniani 2, 35128 Padova, Italy.

Veneto Institute of Molecular Medicine, Via G. Orus 2, 35129 Padova, Italy.

出版信息

Int J Mol Sci. 2019 Oct 8;20(19):4966. doi: 10.3390/ijms20194966.

Abstract

Macrophages are highly plastic and dynamic cells that exert much of their function through phagocytosis. Phagocytosis depends on a coordinated, finely tuned, and compartmentalized regulation of calcium concentrations. We examined the role of mitochondrial calcium uptake and mitochondrial calcium uniporter (MCU) in macrophage polarization and function. In primary cultures of human monocyte-derived macrophages, calcium uptake in mitochondria was instrumental for alternative (M2) macrophage polarization. Mitochondrial calcium uniporter inhibition with KB-R7943 or MCU knockdown, which prevented mitochondrial calcium uptake, reduced M2 polarization, while not affecting classical (M1) polarization. Challenging macrophages with fragments induced spikes of mitochondrial calcium concentrations, which were prevented by MCU inhibition or silencing. In addition, mitochondria remodelled in M2 macrophages during phagocytosis, especially close to sites of internalization. Remarkably, inhibition or knockdown of MCU significantly reduced the phagocytic capacity of M2 macrophages. KB-R7943, which also inhibits the membrane sodium/calcium exchanger and Complex I, reduced mitochondria energization and cellular ATP levels, but such effects were not observed with MCU silencing. Therefore, phagocytosis inhibition by MCU knockdown depended on the impaired mitochondrial calcium buffering rather than changes in mitochondrial and cellular energy status. These data uncover a new role for MCU in alternative macrophage polarization and phagocytic activity.

摘要

巨噬细胞是高度可塑性和动态的细胞,其主要功能通过吞噬作用发挥。吞噬作用依赖于钙浓度的协调、精细调节和区室化调节。我们研究了线粒体钙摄取和线粒体钙单向转运体(MCU)在巨噬细胞极化和功能中的作用。在人单核细胞来源的巨噬细胞的原代培养中,线粒体中的钙摄取对于替代(M2)巨噬细胞极化至关重要。用 KB-R7943 或 MCU 敲低抑制线粒体钙摄取,可减少 M2 极化,而不影响经典(M1)极化。用 片段刺激巨噬细胞,引起线粒体钙浓度的尖峰,MCU 抑制或沉默可阻止这种尖峰。此外,在吞噬过程中,M2 巨噬细胞中的线粒体发生重塑,尤其是在内化部位附近。值得注意的是,MCU 的抑制或敲低显著降低了 M2 巨噬细胞的吞噬能力。KB-R7943 还抑制质膜钠/钙交换体和复合物 I,降低线粒体的能量状态和细胞内的 ATP 水平,但 MCU 沉默则没有观察到这些效应。因此,MCU 敲低对吞噬作用的抑制依赖于受损的线粒体钙缓冲作用,而不是线粒体和细胞能量状态的变化。这些数据揭示了 MCU 在替代巨噬细胞极化和吞噬活性中的新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a3f/6801659/91b726b5d982/ijms-20-04966-g001.jpg

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