Pons Vincent, Rivest Serge
Neuroscience Laboratory, Centre Hospitalier Universitaire (CHU) de Québec Research Center and Department of Molecular Medicine, Faculty of Medicine, Laval University, Quebec, QC, Canada.
Front Cell Neurosci. 2018 Dec 20;12:499. doi: 10.3389/fncel.2018.00499. eCollection 2018.
Macrophage colony-stimulating factor (mCSF) is a cytokine known to promote the recruitment of macrophages inducing the release of CCL2, a chemokine mobilizing monocytes to sites of inflammation. Additionally, it induces microglia/macrophage proliferation and the polarization of these cells towards a M2-like phenotype, impairing their ability to release pro-inflammatory factors and toxic mediators, while favoring the release of mediators promoting tissue repair. Another important player is the mCSF receptor CSFR1, which is highly expressed in monocytes, macrophages and microglia. Here, we discuss the new interesting therapeutic avenue of the mCSF/CSFR1 axis on brain diseases. More specifically, mCSF cascade might stimulate the survival/proliferation of oligodendrocytes, enhance the immune response as well as modulate the release of growth factors and the phagocytic activity of immune cells to remove myelin debris and toxic proteins from the brain.
巨噬细胞集落刺激因子(mCSF)是一种细胞因子,已知其可促进巨噬细胞的募集,诱导趋化因子CCL2的释放,CCL2可将单核细胞动员至炎症部位。此外,它还能诱导小胶质细胞/巨噬细胞增殖,并使这些细胞向M2样表型极化,削弱它们释放促炎因子和毒性介质的能力,同时有利于促进组织修复的介质的释放。另一个重要因素是mCSF受体CSFR1,它在单核细胞、巨噬细胞和小胶质细胞中高度表达。在此,我们讨论mCSF/CSFR1轴在脑部疾病方面新的有趣治疗途径。更具体地说,mCSF级联反应可能刺激少突胶质细胞的存活/增殖,增强免疫反应,并调节生长因子的释放以及免疫细胞的吞噬活性,以清除大脑中的髓鞘碎片和毒性蛋白。