# Isolation of Human Osteal Macrophages

**Authors:** Juliana Franziska Bousch, Stefanie Lichtenberg, Matthis Schnitker, Jenny Schlösser, Christoph Viktor Suschek, Uwe Maus, Christoph Beyersdorf

PMC · DOI: 10.3390/life16030376 · 2026-02-27

## TL;DR

This paper introduces a new method to isolate human osteal macrophages, which are important for bone formation and could help study bone diseases like osteoporosis.

## Contribution

The paper presents a standardized protocol for isolating human osteal macrophages from femoral head specimens.

## Key findings

- Osteomacs can be reliably isolated using CD14-based MACS or CD14/CD45/ALP-based FACS after bone marrow removal.
- Isolated osteomacs show markers of M1-like and M2-like macrophage activation states.
- The isolated cells are morphologically heterogeneous and can be cultured in vitro.

## Abstract

Osteal macrophages (“osteomacs”) are resident bone macrophages that support osteoblast differentiation and bone formation. Despite their importance in bone homeostasis, their function in human bone metabolism and osteoporosis remains poorly understood, largely due to the lack of a standardized isolation protocol. Here, we present a protocol for isolating primary human osteomacs from femoral head specimens obtained during arthroplasty. After the removal of bone marrow to minimize contamination with marrow-derived macrophages, bone fragments were enzymatically digested and osteomacs were isolated using CD14-based MACS® or CD14/CD45/ALP-based FACS. Immunofluorescence confirmed macrophage identity and revealed expression of markers associated with both M1-like and M2-like activation states. Isolated cells displayed heterogeneous morphology and could be maintained in culture. This protocol enables reproducible isolation of human osteomacs and provides a foundation for translational studies investigating osteoimmune interactions in bone disease and osteoporosis.

## Linked entities

- **Proteins:** CD14 (CD14 molecule), PTPRC (protein tyrosine phosphatase receptor type C), ALPP (alkaline phosphatase, placental)
- **Diseases:** osteoporosis (MONDO:0005298)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CD14 (CD14 molecule) [NCBI Gene 929], ATHS (atherosclerosis susceptibility (lipoprotein associated)) [NCBI Gene 470] {aka ALP}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}
- **Diseases:** osteoporosis (MESH:D010024), bone disease (MESH:D001847)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027567/full.md

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Source: https://tomesphere.com/paper/PMC13027567