Bone marrow-derived myeloid progenitors in the leptomeninges of adult mice

Author:

Koeniger Tobias1,Bell Luisa1,Mifka Anika2,Enders Michael2,Hautmann Valentin1,Mekala Subba Rao1,Kirchner Philipp3ORCID,Ekici Arif B.3,Schulz Christian4,Wörsdörfer Philipp1,Mencl Stine5,Kleinschnitz Christoph5,Ergün Süleyman1,Kuerten Stefanie126ORCID

Affiliation:

1. Institute of Anatomy and Cell Biology, Julius Maximilian University of Würzburg, Würzburg, Germany

2. Institute of Anatomy and Cell Biology, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany

3. Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany

4. Medizinische Klinik und Poliklinik I, Ludwig Maximilian University of Munich, Munich, Germany

5. University Hospital Essen, Department of Neurology, University Duisburg-Essen, Essen, Germany

6. Anatomisches Institut, Neuroanatomie, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany

Abstract

Abstract Although the bone marrow contains most hematopoietic activity during adulthood, hematopoietic stem and progenitor cells can be recovered from various extramedullary sites. Cells with hematopoietic progenitor properties have even been reported in the adult brain under steady-state conditions, but their nature and localization remain insufficiently defined. Here, we describe a heterogeneous population of myeloid progenitors in the leptomeninges of adult C57BL/6 mice. This cell pool included common myeloid, granulocyte/macrophage, and megakaryocyte/erythrocyte progenitors. Accordingly, it gave rise to all major myelo-erythroid lineages in clonogenic culture assays. Brain-associated progenitors persisted after tissue perfusion and were partially inaccessible to intravenous antibodies, suggesting their localization behind continuous blood vessel endothelium such as the blood-arachnoid barrier. Flt3Cre lineage tracing and bone marrow transplantation showed that the precursors were derived from adult hematopoietic stem cells and were most likely continuously replaced via cell trafficking. Importantly, their occurrence was tied to the immunologic state of the central nervous system (CNS) and was diminished in the context of neuroinflammation and ischemic stroke. Our findings confirm the presence of myeloid progenitors at the meningeal border of the brain and lay the foundation to unravel their possible functions in CNS surveillance and local immune cell production.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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