Interleukin-34-dependent perivascular macrophages promote vascular function in the brain

The development of most macrophages depends on the colony-stimulating factor 1 (CSF-1) receptor, which has two ligands: CSF-1 and interleukin-34 (IL-34). While IL-34 is required for the homeostasis of microglia, the parenchymal macrophages in the central nervous system (CNS), it is unclear whether brain border-associated macrophages (BAMs) also depend on this cytokine. Here, we demonstrated that the embryonic development of murine BAMs in the choroid plexus, leptomeninges, and perivascular spaces required CSF-1, while IL-34 was critical for their maintenance in adulthood. In the brain, Il34 was expressed by mural cells and perivascular fibroblasts, and its transgenic deletion in these cells interrupted BAM maintenance. Il34 deficiency coincided with transcriptional changes in vascular cells, leading to increased flow velocity and vasomotion in pial and penetrating arterioles. Similarly, Mrc1<sup>Cre</sup>Csf1r<sup>fl/fl</sup> mice lacking CD206<sup>+</sup> perivascular BAMs exhibited increased hemodynamics in arterial networks. These findings reveal a crosstalk between vascular cells and CNS macrophages regulating cerebrovascular function.

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Publication Details

Journal
Immunity
Published
2025-05-01
DOI
https://doi.org/10.1016/j.immuni.2025.04.003
Citations
14
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
11.79
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article

Interleukin-34-dependent perivascular macrophages promote vascular function in the brain

Johanna Schaffenrath, Caroline Mussak, Paweł Pelczar, Jeanne Droux et al.
14 citations
Immunity
Neuroinflammation and Neurodegeneration Mechanisms
11.79
article

Interleukin-34-dependent perivascular macrophages promote vascular function in the brain

Johanna Schaffenrath, Caroline Mussak, Paweł Pelczar, Jeanne Droux, Marijne Vermeer, Sarah Mundt, Sheng‐Fu Huang, Bruno Weber, Victor Kreiner, Kenichi Asano, E. Roussel, Melanie Greter, Sònia Tugues, Sebastian A. Stifter, Christian Stockmann, Annika Keller, Sebastian G. Utz, Soline Bourgeois, Ekaterina Petrova, Mohamad El Amki, Zhenyue Chen, Hannah Van Hove, Burkhard Becher, Mitchell Bijnen, Charlotte Calvet, Quanyu Zhou, Upasana Maheshwari, Wiebke Mildenberger, Chaim Glück, Florian Ingelfinger, Iva Lelios, Christian Ashworth, Daniel Razansky, Susanne Wegener, Philipp Häne, J Juang
article en
14 citations

Abstract

The development of most macrophages depends on the colony-stimulating factor 1 (CSF-1) receptor, which has two ligands: CSF-1 and interleukin-34 (IL-34). While IL-34 is required for the homeostasis of microglia, the parenchymal macrophages in the central nervous system (CNS), it is unclear whether brain border-associated macrophages (BAMs) also depend on this cytokine. Here, we demonstrated that the embryonic development of murine BAMs in the choroid plexus, leptomeninges, and perivascular spaces required CSF-1, while IL-34 was critical for their maintenance in adulthood. In the brain, Il34 was expressed by mural cells and perivascular fibroblasts, and its transgenic deletion in these cells interrupted BAM maintenance. Il34 deficiency coincided with transcriptional changes in vascular cells, leading to increased flow velocity and vasomotion in pial and penetrating arterioles. Similarly, Mrc1<sup>Cre</sup>Csf1r<sup>fl/fl</sup> mice lacking CD206<sup>+</sup> perivascular BAMs exhibited increased hemodynamics in arterial networks. These findings reveal a crosstalk between vascular cells and CNS macrophages regulating cerebrovascular function.

ImmunityVol. 58(5)
Tokyo University of Pharmacy and Life Sciences (JP), The University of Texas at San Antonio Health Science Center (US), University of Basel (CH), University of Zurich (CH), Institute for Biomedical Engineering (CH), University Hospital of Zurich (CH), The University of Texas at San Antonio (US)
Zero hunger
Openalex Percentile: Top 1%
Neuroinflammation and Neurodegeneration Mechanisms
11.79
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