Skip to main content
Top
Published in: Journal of Neuroinflammation 1/2024

Open Access 01-12-2024 | Research

CSF1R antagonism results in increased supraspinal infiltration in EAE

Authors: Marilyn Wang, Sofia E. Caryotakis, Glendalyn G. Smith, Alan V. Nguyen, David E. Pleasure, Athena M. Soulika

Published in: Journal of Neuroinflammation | Issue 1/2024

Login to get access

Abstract

Background

Colony stimulating factor 1 receptor (CSF1R) signaling is crucial for the maintenance and function of various myeloid subsets. CSF1R antagonism was previously shown to mitigate clinical severity in experimental autoimmune encephalomyelitis (EAE). The associated mechanisms are still not well delineated.

Methods

To assess the effect of CSF1R signaling, we employed the CSF1R antagonist PLX5622 formulated in chow (PLX5622 diet, PD) and its control chow (control diet, CD). We examined the effect of PD in steady state and EAE by analyzing cells isolated from peripheral immune organs and from the CNS via flow cytometry. We determined CNS infiltration sites and assessed the extent of demyelination using immunohistochemistry of cerebella and spinal cords. Transcripts of genes associated with neuroinflammation were also analyzed in these tissues.

Results

In addition to microglial depletion, PD treatment reduced dendritic cells and macrophages in peripheral immune organs, both during steady state and during EAE. Furthermore, CSF1R antagonism modulated numbers and relative frequencies of T effector cells both in the periphery and in the CNS during the early stages of the disease. Classical neurological symptoms were milder in PD compared to CD mice. Interestingly, a subset of PD mice developed atypical EAE symptoms. Unlike previous studies, we observed that the CNS of PD mice was infiltrated by increased numbers of peripheral immune cells compared to that of CD mice. Immunohistochemical analysis showed that CNS infiltrates in PD mice were mainly localized in the cerebellum while in CD mice infiltrates were primarily localized in the spinal cords during the onset of neurological deficits. Accordingly, during the same timepoint, cerebella of PD but not of CD mice had extensive demyelinating lesions, while spinal cords of CD but not of PD mice were heavily demyelinated.

Conclusions

Our findings suggest that CSF1R activity modulates the cellular composition of immune cells both in the periphery and within the CNS, and affects lesion localization during the early EAE stages.
Appendix
Available only for authorised users
Literature
1.
go back to reference Stanley ER, Chitu V. CSF-1 receptor signaling in myeloid cells. Cold Spring Harb Perspect Biol, 2014. 6(6). Stanley ER, Chitu V. CSF-1 receptor signaling in myeloid cells. Cold Spring Harb Perspect Biol, 2014. 6(6).
2.
go back to reference Grabert K, et al. A transgenic line that reports CSF1R protein expression provides a definitive marker for the mouse mononuclear Phagocyte System. J Immunol. 2020;205(11):3154–66.PubMedCrossRef Grabert K, et al. A transgenic line that reports CSF1R protein expression provides a definitive marker for the mouse mononuclear Phagocyte System. J Immunol. 2020;205(11):3154–66.PubMedCrossRef
3.
go back to reference Chihara T, et al. IL-34 and M-CSF share the receptor fms but are not identical in biological activity and signal activation. Cell Death Differ. 2010;17(12):1917–27.PubMedCrossRef Chihara T, et al. IL-34 and M-CSF share the receptor fms but are not identical in biological activity and signal activation. Cell Death Differ. 2010;17(12):1917–27.PubMedCrossRef
4.
6.
go back to reference Lin W, et al. Function of CSF1 and IL34 in macrophage homeostasis, inflammation, and Cancer. Front Immunol. 2019;10:p2019.CrossRef Lin W, et al. Function of CSF1 and IL34 in macrophage homeostasis, inflammation, and Cancer. Front Immunol. 2019;10:p2019.CrossRef
7.
go back to reference Guilbert LJ, Stanley ER. Specific interaction of murine colony-stimulating factor with mononuclear phagocytic cells. J Cell Biol. 1980;85(1):153–9.PubMedCrossRef Guilbert LJ, Stanley ER. Specific interaction of murine colony-stimulating factor with mononuclear phagocytic cells. J Cell Biol. 1980;85(1):153–9.PubMedCrossRef
8.
go back to reference Nandi S, et al. The CSF-1 receptor ligands IL-34 and CSF-1 exhibit distinct developmental brain expression patterns and regulate neural progenitor cell maintenance and maturation. Dev Biol. 2012;367(2):100–13.PubMedPubMedCentralCrossRef Nandi S, et al. The CSF-1 receptor ligands IL-34 and CSF-1 exhibit distinct developmental brain expression patterns and regulate neural progenitor cell maintenance and maturation. Dev Biol. 2012;367(2):100–13.PubMedPubMedCentralCrossRef
9.
go back to reference Elmore MR, et al. Colony-stimulating factor 1 receptor signaling is necessary for microglia viability, unmasking a microglia progenitor cell in the adult brain. Neuron. 2014;82(2):380–97.PubMedPubMedCentralCrossRef Elmore MR, et al. Colony-stimulating factor 1 receptor signaling is necessary for microglia viability, unmasking a microglia progenitor cell in the adult brain. Neuron. 2014;82(2):380–97.PubMedPubMedCentralCrossRef
10.
go back to reference Quintana E, et al. DNGR-1(+) dendritic cells are located in meningeal membrane and choroid plexus of the noninjured brain. Glia. 2015;63(12):2231–48.PubMedCrossRef Quintana E, et al. DNGR-1(+) dendritic cells are located in meningeal membrane and choroid plexus of the noninjured brain. Glia. 2015;63(12):2231–48.PubMedCrossRef
11.
go back to reference Chinnery HR, Ruitenberg MJ, McMenamin PG. Novel characterization of monocyte-derived cell populations in the meninges and choroid plexus and their rates of replenishment in bone marrow chimeric mice. J Neuropathol Exp Neurol. 2010;69(9):896–909.PubMedCrossRef Chinnery HR, Ruitenberg MJ, McMenamin PG. Novel characterization of monocyte-derived cell populations in the meninges and choroid plexus and their rates of replenishment in bone marrow chimeric mice. J Neuropathol Exp Neurol. 2010;69(9):896–909.PubMedCrossRef
12.
go back to reference Mrdjen D, et al. High-dimensional single-cell mapping of Central Nervous System Immune cells reveals distinct myeloid subsets in Health, Aging, and Disease. Immunity. 2018;48(3):599.PubMedCrossRef Mrdjen D, et al. High-dimensional single-cell mapping of Central Nervous System Immune cells reveals distinct myeloid subsets in Health, Aging, and Disease. Immunity. 2018;48(3):599.PubMedCrossRef
13.
go back to reference Wang Y, Berezovska O, Fedoroff S. Expression of colony stimulating factor-1 receptor (CSF-1R) by CNS neurons in mice. J Neurosci Res. 1999;57(5):616–32.PubMedCrossRef Wang Y, Berezovska O, Fedoroff S. Expression of colony stimulating factor-1 receptor (CSF-1R) by CNS neurons in mice. J Neurosci Res. 1999;57(5):616–32.PubMedCrossRef
14.
go back to reference Luo J, et al. Colony-stimulating factor 1 receptor (CSF1R) signaling in injured neurons facilitates protection and survival. J Exp Med. 2013;210(1):157–72.PubMedPubMedCentralCrossRef Luo J, et al. Colony-stimulating factor 1 receptor (CSF1R) signaling in injured neurons facilitates protection and survival. J Exp Med. 2013;210(1):157–72.PubMedPubMedCentralCrossRef
15.
go back to reference Chitu V, Stanley ER. Regulation of embryonic and postnatal development by the CSF-1 receptor. Curr Top Dev Biol. 2017;123:229–75.PubMedCrossRef Chitu V, Stanley ER. Regulation of embryonic and postnatal development by the CSF-1 receptor. Curr Top Dev Biol. 2017;123:229–75.PubMedCrossRef
16.
17.
go back to reference Hwang D, et al. CSF-1 maintains pathogenic but not homeostatic myeloid cells in the central nervous system during autoimmune neuroinflammation. Proc Natl Acad Sci U S A. 2022;119(14):e2111804119.PubMedPubMedCentralCrossRef Hwang D, et al. CSF-1 maintains pathogenic but not homeostatic myeloid cells in the central nervous system during autoimmune neuroinflammation. Proc Natl Acad Sci U S A. 2022;119(14):e2111804119.PubMedPubMedCentralCrossRef
18.
go back to reference Lei F, et al. CSF1R inhibition by a small-molecule inhibitor is not microglia specific; affecting hematopoiesis and the function of macrophages. Proc Natl Acad Sci U S A. 2020;117(38):23336–8.PubMedPubMedCentralCrossRef Lei F, et al. CSF1R inhibition by a small-molecule inhibitor is not microglia specific; affecting hematopoiesis and the function of macrophages. Proc Natl Acad Sci U S A. 2020;117(38):23336–8.PubMedPubMedCentralCrossRef
19.
go back to reference Funk KE, Klein RS. CSF1R antagonism limits local restimulation of antiviral CD8(+) T cells during viral encephalitis. J Neuroinflammation. 2019;16(1):22.PubMedPubMedCentralCrossRef Funk KE, Klein RS. CSF1R antagonism limits local restimulation of antiviral CD8(+) T cells during viral encephalitis. J Neuroinflammation. 2019;16(1):22.PubMedPubMedCentralCrossRef
20.
go back to reference Spiteri AG, et al. PLX5622 reduces Disease Severity in Lethal CNS infection by off-target inhibition of Peripheral Inflammatory Monocyte production. Front Immunol. 2022;13:851556.PubMedPubMedCentralCrossRef Spiteri AG, et al. PLX5622 reduces Disease Severity in Lethal CNS infection by off-target inhibition of Peripheral Inflammatory Monocyte production. Front Immunol. 2022;13:851556.PubMedPubMedCentralCrossRef
21.
go back to reference Mok S, et al. Inhibition of CSF-1 receptor improves the antitumor efficacy of adoptive cell transfer immunotherapy. Cancer Res. 2014;74(1):153–61.PubMedCrossRef Mok S, et al. Inhibition of CSF-1 receptor improves the antitumor efficacy of adoptive cell transfer immunotherapy. Cancer Res. 2014;74(1):153–61.PubMedCrossRef
22.
go back to reference Ngiow SF, et al. Co-inhibition of colony stimulating factor-1 receptor and BRAF oncogene in mouse models of BRAF(V600E) melanoma. Oncoimmunology. 2016;5(3):e1089381.PubMedCrossRef Ngiow SF, et al. Co-inhibition of colony stimulating factor-1 receptor and BRAF oncogene in mouse models of BRAF(V600E) melanoma. Oncoimmunology. 2016;5(3):e1089381.PubMedCrossRef
23.
go back to reference Spangenberg E, et al. Sustained microglial depletion with CSF1R inhibitor impairs parenchymal plaque development in an Alzheimer’s disease model. Nat Commun. 2019;10(1):3758.PubMedPubMedCentralCrossRef Spangenberg E, et al. Sustained microglial depletion with CSF1R inhibitor impairs parenchymal plaque development in an Alzheimer’s disease model. Nat Commun. 2019;10(1):3758.PubMedPubMedCentralCrossRef
24.
25.
go back to reference Gratuze M et al. Activated microglia mitigate Abeta-associated tau seeding and spreading. J Exp Med, 2021; 218(8). Gratuze M et al. Activated microglia mitigate Abeta-associated tau seeding and spreading. J Exp Med, 2021; 218(8).
26.
go back to reference Zhang D, et al. Microglial activation contributes to cognitive impairments in rotenone-induced mouse Parkinson’s disease model. J Neuroinflammation. 2021;18(1):4.PubMedPubMedCentralCrossRef Zhang D, et al. Microglial activation contributes to cognitive impairments in rotenone-induced mouse Parkinson’s disease model. J Neuroinflammation. 2021;18(1):4.PubMedPubMedCentralCrossRef
27.
go back to reference Cannarile MA et al. Colony-stimulating factor 1 receptor (CSF1R) inhibitors in cancer therapy. J Immunother Cancer, 2017; 5(1): p. 53. Cannarile MA et al. Colony-stimulating factor 1 receptor (CSF1R) inhibitors in cancer therapy. J Immunother Cancer, 2017; 5(1): p. 53.
28.
go back to reference Tan IL, et al. CSF1R inhibition depletes tumor-associated macrophages and attenuates tumor progression in a mouse sonic hedgehog-medulloblastoma model. Oncogene. 2021;40(2):396–407.PubMedCrossRef Tan IL, et al. CSF1R inhibition depletes tumor-associated macrophages and attenuates tumor progression in a mouse sonic hedgehog-medulloblastoma model. Oncogene. 2021;40(2):396–407.PubMedCrossRef
29.
go back to reference Tap WD, et al. Pexidartinib versus placebo for advanced tenosynovial giant cell tumour (ENLIVEN): a randomised phase 3 trial. Lancet. 2019;394(10197):478–87.PubMedPubMedCentralCrossRef Tap WD, et al. Pexidartinib versus placebo for advanced tenosynovial giant cell tumour (ENLIVEN): a randomised phase 3 trial. Lancet. 2019;394(10197):478–87.PubMedPubMedCentralCrossRef
31.
go back to reference Smith CC, et al. Characterizing and overriding the structural mechanism of the Quizartinib-resistant FLT3 gatekeeper F691L mutation with PLX3397. Cancer Discov. 2015;5(6):668–79.PubMedPubMedCentralCrossRef Smith CC, et al. Characterizing and overriding the structural mechanism of the Quizartinib-resistant FLT3 gatekeeper F691L mutation with PLX3397. Cancer Discov. 2015;5(6):668–79.PubMedPubMedCentralCrossRef
33.
go back to reference Feng R, et al. Self-renewing macrophages in dorsal root ganglia contribute to promote nerve regeneration. Proc Natl Acad Sci U S A. 2023;120(7):e2215906120.PubMedPubMedCentralCrossRef Feng R, et al. Self-renewing macrophages in dorsal root ganglia contribute to promote nerve regeneration. Proc Natl Acad Sci U S A. 2023;120(7):e2215906120.PubMedPubMedCentralCrossRef
35.
go back to reference Montilla A, et al. Microglia and meningeal macrophages depletion delays the onset of experimental autoimmune encephalomyelitis. Cell Death Dis. 2023;14(1):16.PubMedPubMedCentralCrossRef Montilla A, et al. Microglia and meningeal macrophages depletion delays the onset of experimental autoimmune encephalomyelitis. Cell Death Dis. 2023;14(1):16.PubMedPubMedCentralCrossRef
36.
go back to reference Lin H, et al. Discovery of a cytokine and its receptor by functional screening of the extracellular proteome. Science. 2008;320(5877):807–11.PubMedCrossRef Lin H, et al. Discovery of a cytokine and its receptor by functional screening of the extracellular proteome. Science. 2008;320(5877):807–11.PubMedCrossRef
37.
go back to reference Hume DA, MacDonald KP. Therapeutic applications of macrophage colony-stimulating factor-1 (CSF-1) and antagonists of CSF-1 receptor (CSF-1R) signaling. Blood. 2012;119(8):1810–20.PubMedCrossRef Hume DA, MacDonald KP. Therapeutic applications of macrophage colony-stimulating factor-1 (CSF-1) and antagonists of CSF-1 receptor (CSF-1R) signaling. Blood. 2012;119(8):1810–20.PubMedCrossRef
38.
go back to reference Sehgal A, Irvine KM, Hume DA. Functions of macrophage colony-stimulating factor (CSF1) in development, homeostasis, and tissue repair. Semin Immunol. 2021;54:101509.PubMedCrossRef Sehgal A, Irvine KM, Hume DA. Functions of macrophage colony-stimulating factor (CSF1) in development, homeostasis, and tissue repair. Semin Immunol. 2021;54:101509.PubMedCrossRef
39.
go back to reference Delaney C, et al. Attenuated CSF-1R signalling drives cerebrovascular pathology. EMBO Mol Med. 2021;13(2):e12889.PubMedCrossRef Delaney C, et al. Attenuated CSF-1R signalling drives cerebrovascular pathology. EMBO Mol Med. 2021;13(2):e12889.PubMedCrossRef
40.
go back to reference Lee E, et al. IFN-gamma signaling in the central nervous system controls the course of experimental autoimmune encephalomyelitis independently of the localization and composition of inflammatory foci. J Neuroinflammation. 2012;9:7.PubMedPubMedCentralCrossRef Lee E, et al. IFN-gamma signaling in the central nervous system controls the course of experimental autoimmune encephalomyelitis independently of the localization and composition of inflammatory foci. J Neuroinflammation. 2012;9:7.PubMedPubMedCentralCrossRef
41.
go back to reference Mills Ko E, et al. Deletion of astroglial CXCL10 delays clinical onset but does not affect progressive axon loss in a murine autoimmune multiple sclerosis model. J Neuroinflammation. 2014;11:105.PubMedPubMedCentralCrossRef Mills Ko E, et al. Deletion of astroglial CXCL10 delays clinical onset but does not affect progressive axon loss in a murine autoimmune multiple sclerosis model. J Neuroinflammation. 2014;11:105.PubMedPubMedCentralCrossRef
42.
go back to reference Moreno M, et al. Conditional ablation of astroglial CCL2 suppresses CNS accumulation of M1 macrophages and preserves axons in mice with MOG peptide EAE. J Neurosci. 2014;34(24):8175–85.PubMedPubMedCentralCrossRef Moreno M, et al. Conditional ablation of astroglial CCL2 suppresses CNS accumulation of M1 macrophages and preserves axons in mice with MOG peptide EAE. J Neurosci. 2014;34(24):8175–85.PubMedPubMedCentralCrossRef
43.
44.
go back to reference Nguyen AV, et al. Montelukast, an antagonist of Cysteinyl Leukotriene Signaling, impairs burn Wound Healing. Plast Reconstr Surg. 2022;150(1):e92–104.CrossRef Nguyen AV, et al. Montelukast, an antagonist of Cysteinyl Leukotriene Signaling, impairs burn Wound Healing. Plast Reconstr Surg. 2022;150(1):e92–104.CrossRef
45.
go back to reference Nguyen AV, et al. Skin-Resident beta2AR Signaling delays burn Wound Healing. J Invest Dermatol. 2021;141(8):2098–101. e4.PubMedCrossRef Nguyen AV, et al. Skin-Resident beta2AR Signaling delays burn Wound Healing. J Invest Dermatol. 2021;141(8):2098–101. e4.PubMedCrossRef
47.
go back to reference Mildner A, et al. Ly-6G + CCR2- myeloid cells rather than Ly-6ChighCCR2 + monocytes are required for the control of bacterial infection in the central nervous system. J Immunol. 2008;181(4):2713–22.PubMedCrossRef Mildner A, et al. Ly-6G + CCR2- myeloid cells rather than Ly-6ChighCCR2 + monocytes are required for the control of bacterial infection in the central nervous system. J Immunol. 2008;181(4):2713–22.PubMedCrossRef
48.
go back to reference Filiano AJ, Gadani SP, Kipnis J. How and why do T cells and their derived cytokines affect the injured and healthy brain? Nat Rev Neurosci. 2017;18(6):375–84.PubMedPubMedCentralCrossRef Filiano AJ, Gadani SP, Kipnis J. How and why do T cells and their derived cytokines affect the injured and healthy brain? Nat Rev Neurosci. 2017;18(6):375–84.PubMedPubMedCentralCrossRef
49.
go back to reference Cugurra A et al. Skull and vertebral bone marrow are myeloid cell reservoirs for the meninges and CNS parenchyma. Science, 2021. 373(6553). Cugurra A et al. Skull and vertebral bone marrow are myeloid cell reservoirs for the meninges and CNS parenchyma. Science, 2021. 373(6553).
50.
go back to reference Wang Y, et al. IL-34 is a tissue-restricted ligand of CSF1R required for the development of Langerhans cells and microglia. Nat Immunol. 2012;13(8):753–60.PubMedPubMedCentralCrossRef Wang Y, et al. IL-34 is a tissue-restricted ligand of CSF1R required for the development of Langerhans cells and microglia. Nat Immunol. 2012;13(8):753–60.PubMedPubMedCentralCrossRef
51.
go back to reference Lonardi S, et al. CSF1R is required for differentiation and Migration of Langerhans Cells and Langerhans Cell histiocytosis. Cancer Immunol Res. 2020;8(6):829–41.PubMedCrossRef Lonardi S, et al. CSF1R is required for differentiation and Migration of Langerhans Cells and Langerhans Cell histiocytosis. Cancer Immunol Res. 2020;8(6):829–41.PubMedCrossRef
52.
go back to reference Merad M, Ginhoux F, Collin M. Origin, homeostasis and function of Langerhans cells and other langerin-expressing dendritic cells. Nat Rev Immunol. 2008;8(12):935–47.PubMedCrossRef Merad M, Ginhoux F, Collin M. Origin, homeostasis and function of Langerhans cells and other langerin-expressing dendritic cells. Nat Rev Immunol. 2008;8(12):935–47.PubMedCrossRef
53.
go back to reference Church KA, et al. Models of microglia depletion and replenishment elicit protective effects to alleviate vascular and neuronal damage in the diabetic murine retina. J Neuroinflammation. 2022;19(1):300.PubMedPubMedCentralCrossRef Church KA, et al. Models of microglia depletion and replenishment elicit protective effects to alleviate vascular and neuronal damage in the diabetic murine retina. J Neuroinflammation. 2022;19(1):300.PubMedPubMedCentralCrossRef
54.
go back to reference King IL, Dickendesher TL, Segal BM. Circulating Ly-6 C + myeloid precursors migrate to the CNS and play a pathogenic role during autoimmune demyelinating disease. Blood. 2009;113(14):3190–7.PubMedPubMedCentralCrossRef King IL, Dickendesher TL, Segal BM. Circulating Ly-6 C + myeloid precursors migrate to the CNS and play a pathogenic role during autoimmune demyelinating disease. Blood. 2009;113(14):3190–7.PubMedPubMedCentralCrossRef
55.
go back to reference Jonas RA, et al. The spider effect: morphological and orienting classification of microglia in response to stimuli in vivo. PLoS ONE. 2012;7(2):e30763.PubMedPubMedCentralCrossRef Jonas RA, et al. The spider effect: morphological and orienting classification of microglia in response to stimuli in vivo. PLoS ONE. 2012;7(2):e30763.PubMedPubMedCentralCrossRef
56.
go back to reference Chiu IM, et al. A neurodegeneration-specific gene-expression signature of acutely isolated microglia from an amyotrophic lateral sclerosis mouse model. Cell Rep. 2013;4(2):385–401.PubMedPubMedCentralCrossRef Chiu IM, et al. A neurodegeneration-specific gene-expression signature of acutely isolated microglia from an amyotrophic lateral sclerosis mouse model. Cell Rep. 2013;4(2):385–401.PubMedPubMedCentralCrossRef
58.
go back to reference Pulido-Salgado M, et al. RNA-Seq transcriptomic profiling of primary murine microglia treated with LPS or LPS + IFNgamma. Sci Rep. 2018;8(1):16096.PubMedPubMedCentralCrossRef Pulido-Salgado M, et al. RNA-Seq transcriptomic profiling of primary murine microglia treated with LPS or LPS + IFNgamma. Sci Rep. 2018;8(1):16096.PubMedPubMedCentralCrossRef
59.
go back to reference Zhang Y, et al. An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex. J Neurosci. 2014;34(36):11929–47.PubMedPubMedCentralCrossRef Zhang Y, et al. An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex. J Neurosci. 2014;34(36):11929–47.PubMedPubMedCentralCrossRef
60.
go back to reference Cecchini MG, et al. Role of colony stimulating factor-1 in the establishment and regulation of tissue macrophages during postnatal development of the mouse. Development. 1994;120(6):1357–72.PubMedCrossRef Cecchini MG, et al. Role of colony stimulating factor-1 in the establishment and regulation of tissue macrophages during postnatal development of the mouse. Development. 1994;120(6):1357–72.PubMedCrossRef
61.
go back to reference Dai XM, et al. Targeted disruption of the mouse colony-stimulating factor 1 receptor gene results in osteopetrosis, mononuclear phagocyte deficiency, increased primitive progenitor cell frequencies, and reproductive defects. Blood. 2002;99(1):111–20.PubMedCrossRef Dai XM, et al. Targeted disruption of the mouse colony-stimulating factor 1 receptor gene results in osteopetrosis, mononuclear phagocyte deficiency, increased primitive progenitor cell frequencies, and reproductive defects. Blood. 2002;99(1):111–20.PubMedCrossRef
62.
go back to reference Sasmono RT, et al. Mouse neutrophilic granulocytes express mRNA encoding the macrophage colony-stimulating factor receptor (CSF-1R) as well as many other macrophage-specific transcripts and can transdifferentiate into macrophages in vitro in response to CSF-1. J Leukoc Biol. 2007;82(1):111–23.PubMedCrossRef Sasmono RT, et al. Mouse neutrophilic granulocytes express mRNA encoding the macrophage colony-stimulating factor receptor (CSF-1R) as well as many other macrophage-specific transcripts and can transdifferentiate into macrophages in vitro in response to CSF-1. J Leukoc Biol. 2007;82(1):111–23.PubMedCrossRef
63.
go back to reference Imitola J, Chitnis T, Khoury SJ. Cytokines in multiple sclerosis: from bench to bedside. Pharmacol Ther. 2005;106(2):163–77.PubMedCrossRef Imitola J, Chitnis T, Khoury SJ. Cytokines in multiple sclerosis: from bench to bedside. Pharmacol Ther. 2005;106(2):163–77.PubMedCrossRef
64.
go back to reference Wang K, et al. The properties of cytokines in multiple sclerosis: pros and cons. Am J Med Sci. 2018;356(6):552–60.PubMedCrossRef Wang K, et al. The properties of cytokines in multiple sclerosis: pros and cons. Am J Med Sci. 2018;356(6):552–60.PubMedCrossRef
66.
go back to reference Basu S, et al. Evaluation of role of G-CSF in the production, survival, and release of neutrophils from bone marrow into circulation. Blood. 2002;100(3):854–61.PubMedCrossRef Basu S, et al. Evaluation of role of G-CSF in the production, survival, and release of neutrophils from bone marrow into circulation. Blood. 2002;100(3):854–61.PubMedCrossRef
67.
go back to reference Hu J, et al. C-C motif chemokine ligand 20 regulates neuroinflammation following spinal cord injury via Th17 cell recruitment. J Neuroinflammation. 2016;13(1):162.PubMedPubMedCentralCrossRef Hu J, et al. C-C motif chemokine ligand 20 regulates neuroinflammation following spinal cord injury via Th17 cell recruitment. J Neuroinflammation. 2016;13(1):162.PubMedPubMedCentralCrossRef
68.
go back to reference Liao F, et al. CC-chemokine receptor 6 is expressed on diverse memory subsets of T cells and determines responsiveness to macrophage inflammatory protein 3 alpha. J Immunol. 1999;162(1):186–94.PubMedCrossRef Liao F, et al. CC-chemokine receptor 6 is expressed on diverse memory subsets of T cells and determines responsiveness to macrophage inflammatory protein 3 alpha. J Immunol. 1999;162(1):186–94.PubMedCrossRef
69.
go back to reference Yamazaki T, et al. CCR6 regulates the migration of inflammatory and regulatory T cells. J Immunol. 2008;181(12):8391–401.PubMedCrossRef Yamazaki T, et al. CCR6 regulates the migration of inflammatory and regulatory T cells. J Immunol. 2008;181(12):8391–401.PubMedCrossRef
70.
go back to reference Abadier M, et al. Cell surface levels of endothelial ICAM-1 influence the transcellular or paracellular T-cell diapedesis across the blood-brain barrier. Eur J Immunol. 2015;45(4):1043–58.PubMedCrossRef Abadier M, et al. Cell surface levels of endothelial ICAM-1 influence the transcellular or paracellular T-cell diapedesis across the blood-brain barrier. Eur J Immunol. 2015;45(4):1043–58.PubMedCrossRef
71.
go back to reference Steiner O, et al. Differential roles for endothelial ICAM-1, ICAM-2, and VCAM-1 in shear-resistant T cell arrest, polarization, and directed crawling on blood-brain barrier endothelium. J Immunol. 2010;185(8):4846–55.PubMedCrossRef Steiner O, et al. Differential roles for endothelial ICAM-1, ICAM-2, and VCAM-1 in shear-resistant T cell arrest, polarization, and directed crawling on blood-brain barrier endothelium. J Immunol. 2010;185(8):4846–55.PubMedCrossRef
72.
go back to reference Felix R, et al. Role of colony-stimulating factor-1 in bone metabolism. J Cell Biochem. 1994;55(3):340–9.PubMedCrossRef Felix R, et al. Role of colony-stimulating factor-1 in bone metabolism. J Cell Biochem. 1994;55(3):340–9.PubMedCrossRef
73.
go back to reference Haghayegh Jahromi N, et al. Intercellular adhesion Molecule-1 (ICAM-1) and ICAM-2 differentially contribute to Peripheral activation and CNS entry of Autoaggressive Th1 and Th17 cells in experimental autoimmune encephalomyelitis. Front Immunol. 2019;10:3056.PubMedCrossRef Haghayegh Jahromi N, et al. Intercellular adhesion Molecule-1 (ICAM-1) and ICAM-2 differentially contribute to Peripheral activation and CNS entry of Autoaggressive Th1 and Th17 cells in experimental autoimmune encephalomyelitis. Front Immunol. 2019;10:3056.PubMedCrossRef
75.
go back to reference DeNardo DG, et al. Leukocyte complexity predicts breast cancer survival and functionally regulates response to chemotherapy. Cancer Discov. 2011;1(1):54–67.PubMedPubMedCentralCrossRef DeNardo DG, et al. Leukocyte complexity predicts breast cancer survival and functionally regulates response to chemotherapy. Cancer Discov. 2011;1(1):54–67.PubMedPubMedCentralCrossRef
76.
go back to reference Ries CH, et al. Targeting tumor-associated macrophages with anti-CSF-1R antibody reveals a strategy for cancer therapy. Cancer Cell. 2014;25(6):846–59.PubMedCrossRef Ries CH, et al. Targeting tumor-associated macrophages with anti-CSF-1R antibody reveals a strategy for cancer therapy. Cancer Cell. 2014;25(6):846–59.PubMedCrossRef
77.
go back to reference Yan D, et al. Inhibition of colony stimulating factor-1 receptor abrogates microenvironment-mediated therapeutic resistance in gliomas. Oncogene. 2017;36(43):6049–58.PubMedPubMedCentralCrossRef Yan D, et al. Inhibition of colony stimulating factor-1 receptor abrogates microenvironment-mediated therapeutic resistance in gliomas. Oncogene. 2017;36(43):6049–58.PubMedPubMedCentralCrossRef
78.
go back to reference Wujek JR, et al. Axon loss in the spinal cord determines permanent neurological disability in an animal model of multiple sclerosis. J Neuropathol Exp Neurol. 2002;61(1):23–32.PubMedCrossRef Wujek JR, et al. Axon loss in the spinal cord determines permanent neurological disability in an animal model of multiple sclerosis. J Neuropathol Exp Neurol. 2002;61(1):23–32.PubMedCrossRef
80.
go back to reference Sacchetti B, Sacco T, Strata P. Reversible inactivation of amygdala and cerebellum but not perirhinal cortex impairs reactivated fear memories. Eur J Neurosci. 2007;25(9):2875–84.PubMedCrossRef Sacchetti B, Sacco T, Strata P. Reversible inactivation of amygdala and cerebellum but not perirhinal cortex impairs reactivated fear memories. Eur J Neurosci. 2007;25(9):2875–84.PubMedCrossRef
82.
go back to reference Wolpert DM, Ghahramani Z, Jordan MI. An internal model for sensorimotor integration. Science. 1995;269(5232):1880–2.PubMedCrossRef Wolpert DM, Ghahramani Z, Jordan MI. An internal model for sensorimotor integration. Science. 1995;269(5232):1880–2.PubMedCrossRef
83.
go back to reference Wolpert DM, Miall RC, Kawato M. Internal models in the cerebellum. Trends Cogn Sci. 1998;2(9):338–47.PubMedCrossRef Wolpert DM, Miall RC, Kawato M. Internal models in the cerebellum. Trends Cogn Sci. 1998;2(9):338–47.PubMedCrossRef
85.
go back to reference Dagher NN, et al. Colony-stimulating factor 1 receptor inhibition prevents microglial plaque association and improves cognition in 3xTg-AD mice. J Neuroinflammation. 2015;12:139.PubMedPubMedCentralCrossRef Dagher NN, et al. Colony-stimulating factor 1 receptor inhibition prevents microglial plaque association and improves cognition in 3xTg-AD mice. J Neuroinflammation. 2015;12:139.PubMedPubMedCentralCrossRef
87.
go back to reference van der Wildt B, et al. BLZ945 derivatives for PET imaging of colony stimulating factor-1 receptors in the brain. Nucl Med Biol. 2021;100–101:44–51.PubMedCrossRef van der Wildt B, et al. BLZ945 derivatives for PET imaging of colony stimulating factor-1 receptors in the brain. Nucl Med Biol. 2021;100–101:44–51.PubMedCrossRef
88.
go back to reference Huang Y, et al. Repopulated microglia are solely derived from the proliferation of residual microglia after acute depletion. Nat Neurosci. 2018;21(4):530–40.PubMedCrossRef Huang Y, et al. Repopulated microglia are solely derived from the proliferation of residual microglia after acute depletion. Nat Neurosci. 2018;21(4):530–40.PubMedCrossRef
89.
go back to reference Getts DR, et al. Ly6c+ inflammatory monocytes are microglial precursors recruited in a pathogenic manner in West Nile virus encephalitis. J Exp Med. 2008;205(10):2319–37.PubMedPubMedCentralCrossRef Getts DR, et al. Ly6c+ inflammatory monocytes are microglial precursors recruited in a pathogenic manner in West Nile virus encephalitis. J Exp Med. 2008;205(10):2319–37.PubMedPubMedCentralCrossRef
90.
go back to reference Ajami B, et al. Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool. Nat Neurosci. 2011;14(9):1142–9.PubMedCrossRef Ajami B, et al. Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool. Nat Neurosci. 2011;14(9):1142–9.PubMedCrossRef
91.
go back to reference Lund H, et al. Competitive repopulation of an empty microglial niche yields functionally distinct subsets of microglia-like cells. Nat Commun. 2018;9(1):4845.PubMedPubMedCentralCrossRef Lund H, et al. Competitive repopulation of an empty microglial niche yields functionally distinct subsets of microglia-like cells. Nat Commun. 2018;9(1):4845.PubMedPubMedCentralCrossRef
92.
go back to reference Liu Y, et al. Preferential Recruitment of Neutrophils into the Cerebellum and Brainstem contributes to the atypical experimental autoimmune encephalomyelitis phenotype. J Immunol. 2015;195(3):841–52.PubMedPubMedCentralCrossRef Liu Y, et al. Preferential Recruitment of Neutrophils into the Cerebellum and Brainstem contributes to the atypical experimental autoimmune encephalomyelitis phenotype. J Immunol. 2015;195(3):841–52.PubMedPubMedCentralCrossRef
94.
go back to reference Yan Z et al. Deficiency of Socs3 leads to brain-targeted EAE via enhanced neutrophil activation and ROS production. JCI Insight. 2019: 5(9). Yan Z et al. Deficiency of Socs3 leads to brain-targeted EAE via enhanced neutrophil activation and ROS production. JCI Insight. 2019: 5(9).
95.
go back to reference Swierczak A, et al. The promotion of breast cancer metastasis caused by inhibition of CSF-1R/CSF-1 signaling is blocked by targeting the G-CSF receptor. Cancer Immunol Res. 2014;2(8):765–76.PubMedCrossRef Swierczak A, et al. The promotion of breast cancer metastasis caused by inhibition of CSF-1R/CSF-1 signaling is blocked by targeting the G-CSF receptor. Cancer Immunol Res. 2014;2(8):765–76.PubMedCrossRef
96.
go back to reference Martin KR, et al. G-CSF - A double edge sword in neutrophil mediated immunity. Semin Immunol. 2021;54:101516.PubMedCrossRef Martin KR, et al. G-CSF - A double edge sword in neutrophil mediated immunity. Semin Immunol. 2021;54:101516.PubMedCrossRef
98.
go back to reference Zhou J, et al. Neutrophils promote mononuclear cell infiltration during viral-induced encephalitis. J Immunol. 2003;170(6):3331–6.PubMedCrossRef Zhou J, et al. Neutrophils promote mononuclear cell infiltration during viral-induced encephalitis. J Immunol. 2003;170(6):3331–6.PubMedCrossRef
99.
100.
go back to reference Leon B, Lopez-Bravo M, Ardavin C. Monocyte-derived dendritic cells formed at the infection site control the induction of protective T helper 1 responses against Leishmania. Immunity. 2007;26(4):519–31.PubMedCrossRef Leon B, Lopez-Bravo M, Ardavin C. Monocyte-derived dendritic cells formed at the infection site control the induction of protective T helper 1 responses against Leishmania. Immunity. 2007;26(4):519–31.PubMedCrossRef
101.
go back to reference Sanarico N, et al. Human monocyte-derived dendritic cells differentiated in the presence of IL-2 produce proinflammatory cytokines and prime Th1 immune response. J Leukoc Biol. 2006;80(3):555–62.PubMedCrossRef Sanarico N, et al. Human monocyte-derived dendritic cells differentiated in the presence of IL-2 produce proinflammatory cytokines and prime Th1 immune response. J Leukoc Biol. 2006;80(3):555–62.PubMedCrossRef
102.
go back to reference Tanaka H, et al. Human monocyte-derived dendritic cells induce naive T cell differentiation into T helper cell type 2 (Th2) or Th1/Th2 effectors. Role of stimulator/responder ratio. J Exp Med. 2000;192(3):405–12.PubMedPubMedCentralCrossRef Tanaka H, et al. Human monocyte-derived dendritic cells induce naive T cell differentiation into T helper cell type 2 (Th2) or Th1/Th2 effectors. Role of stimulator/responder ratio. J Exp Med. 2000;192(3):405–12.PubMedPubMedCentralCrossRef
103.
go back to reference Zou W, et al. Macrophage-derived dendritic cells have strong Th1-Polarizing potential mediated by β-Chemokines Rather Than IL-12. J Immunol. 2000;165(8):4388–96.PubMedCrossRef Zou W, et al. Macrophage-derived dendritic cells have strong Th1-Polarizing potential mediated by β-Chemokines Rather Than IL-12. J Immunol. 2000;165(8):4388–96.PubMedCrossRef
104.
go back to reference King IL, Kroenke MA, Segal BM. GM-CSF-dependent, CD103 + dermal dendritic cells play a critical role in Th effector cell differentiation after subcutaneous immunization. J Exp Med. 2010;207(5):953–61.PubMedPubMedCentralCrossRef King IL, Kroenke MA, Segal BM. GM-CSF-dependent, CD103 + dermal dendritic cells play a critical role in Th effector cell differentiation after subcutaneous immunization. J Exp Med. 2010;207(5):953–61.PubMedPubMedCentralCrossRef
Metadata
Title
CSF1R antagonism results in increased supraspinal infiltration in EAE
Authors
Marilyn Wang
Sofia E. Caryotakis
Glendalyn G. Smith
Alan V. Nguyen
David E. Pleasure
Athena M. Soulika
Publication date
01-12-2024
Publisher
BioMed Central
Published in
Journal of Neuroinflammation / Issue 1/2024
Electronic ISSN: 1742-2094
DOI
https://doi.org/10.1186/s12974-024-03063-1

Other articles of this Issue 1/2024

Journal of Neuroinflammation 1/2024 Go to the issue