# Csf1r⁻ macrophages govern the second wave of neutrophils for bone repair

**Authors:** Yasuhiro Kobayashi, Zhifeng He, Linan Shi, Yuko Nakamichi, Kohei Murakami, Toshide Mizoguchi, Yuki Matsushita, Hirotaka Matsumoto, Shinichirou Ito, Shunsuke Uehara, Rina Iwamoto, Takumi Takahashi, Zizhao Tian, Toru Hiraga Hiraga, Ruoxuan Li, Masataka Kasahara, Kazuo Okamoto, Hiroshi Takayanagi, Martin Matzuk, Nobuyuki Udagawa

PMC · DOI: 10.21203/rs.3.rs-6695752/v1 · Research Square · 2025-05-22

## TL;DR

A specific type of macrophage helps repair bone by recruiting neutrophils and promoting cell growth through Wnt and activin signaling.

## Contribution

Discovery of osteodirective macrophages (OdMacs) and their role in recruiting preneutrophils to enhance bone regeneration.

## Key findings

- OdMacs recruit activin A-expressing preneutrophils to bone injury sites.
- Wnt signaling in bone marrow stromal cells and activin A from preneutrophils are critical for bone regeneration.
- OdMacs form regenerative niches that could be targeted for regenerative therapies.

## Abstract

Macrophages play a pivotal role in tissue regeneration, including bone healing; however, the mechanisms and cell types through which they establish regenerative niches are not yet fully understood. Here, we identified a distinct subset of osteodirective macrophages (OdMacs), characterized by the expression profile F4/80⁺ Csf1r⁻ Cx3cr1hi Ccr2hi, which contribute to the formation of bone regenerative niches following injury. Histological analysis and FACS analysis, combined with transcriptomic profiling (RNA-seq and scRNA-seq), revealed that OdMacs facilitate the recruitment of activin A-expressing preneutrophils (preNeu) to sites of bone injury. This recruitment enhances the proliferation and osteogenic differentiation of LepR⁺ bone marrow stromal cells (BMSCs), thereby promoting bone regeneration. Furthermore, genetic studies using Axin2-Cre; tdTomato, Inhba, and Wls conditional knockout mice underscored the essential roles of Wnt signaling in BMSCs and preNeu-derived activin A in orchestrating this regenerative process. The OdMac-regulated regenerative niche represents a promising therapeutic target for regenerative medicine.

## Linked entities

- **Genes:** AXIN2 (axin 2) [NCBI Gene 8313], INHBA (inhibin subunit beta A) [NCBI Gene 3624], WLS (Wnt ligand secretion mediator) [NCBI Gene 79971]
- **Proteins:** Wnt (protein Wnt-2)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Adgre1 (adhesion G protein-coupled receptor E1) [NCBI Gene 13733] {aka DD7A5-7, EGF-TM7, Emr1, F4/80, Gpf480, Ly71}, Axin2 (axin 2) [NCBI Gene 12006] {aka Axi1, Axil, Conductin}, Wls (wntless WNT ligand secretion mediator) [NCBI Gene 68151] {aka 5031439A09Rik, EVI, Gpr177}, Csf1r (colony stimulating factor 1 receptor) [NCBI Gene 12978] {aka CD115, CSF-1R, Csfmr, Fim-2, Fim2, Fms}, Lepr (leptin receptor) [NCBI Gene 16847] {aka B219, LEP-R, LEPROT, Leprb, Modb1, OB-RGRP}
- **Diseases:** bone injury (MESH:D001847)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

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Source: https://tomesphere.com/paper/PMC12136757