# Influence of Unidirectional Vacuum Application on Bone Healing in Maxillofacial Surgery

**Authors:** Tom Alexander Schröder, Athanasios Karasavvas, Maximilian Bauckloh, Matthias C. Schulz, Günter Lauer, Lysann Michaela Kroschwald

PMC · DOI: 10.3390/cells14100751 · Cells · 2025-05-21

## TL;DR

This study shows that applying vacuum pressure can speed up bone healing in the face and mouth area, which could help patients recover faster from injuries.

## Contribution

The study introduces evidence that unidirectional vacuum application accelerates bone regeneration in maxillofacial surgery.

## Key findings

- Vacuum pressure at 530 mbar significantly increased bone tissue regeneration by up to 30%.
- Osteoblasts showed up to 400% upregulation of osteogenic marker genes like Col1, BMP4, OCN, and RUNX2.
- The RANKL/OPG ratio in osteoblasts decreased to 41%, indicating enhanced osteogenesis.

## Abstract

Negative-pressure wound therapy (NPWT) using vacuum-assisted closure (VAC) is a well known tissue defect bridging method that applies a vacuum pump to sterile, open-cell foam dressings via suction tubes. Although it has mostly been described for soft tissue use, there are also a few studies concerning its use on hard tissue. However, as oral and maxillofacial surgery has to deal with both soft and hard tissue, which lie next to each other in these regions, there is a particular need to assess the influence of negative pressure on bone. Therefore, the effects of different negative pressure levels (530 mbar and 725 mbar) and atmospheric pressure (1013 mbar) on bone tissue cultures and osteoblast cell cultures were investigated over periods of 1, 3, and 6 weeks. During the culture period, osteoblast growth and the tissue regeneration of bone defects were studied in vitro using tissue cultures that were histologically supplemented by cytological investigations and quantitative RNA expression studies. In the bone defect model, there was a faster defect reduction using NPWT; the effect was especially strong for 530 mbar. Compared to the control group, up to 30% more newly generated bone tissue was detected. This effect on the mineralization capacity was assessed by the mRNA expression of osteogenic marker genes, as well as the receptor activator of nuclear factor κB ligand (RANKL) and osteoprotegerin (OPG), two multifaceted cytokines that regulate bone metabolism. The influence of negative pressure consequently resulted in a decreased RANKL/OPG ratio in osteoblasts. Associated with the upregulation of marker genes to up to 400%, including Col1, BMP4, OCN, and RUNX2, the decrease in the RANKL/OPG ratio to 41% indicates the stimulation of osteogenesis. Since VAC has been shown to be a safe and effective method to close wounds in general, these data suggest that patients suffering from compound bone and soft tissue defects in the maxillofacial area may benefit from an adapted therapy approach accelerating both soft and hard tissue regeneration.

## Linked entities

- **Genes:** TNFSF11 (TNF superfamily member 11) [NCBI Gene 8600], BTF3P11 (basic transcription factor 3 pseudogene 11) [NCBI Gene 690], COL1 (CONSTANS-like 1) [NCBI Gene 831442], BMP4 (bone morphogenetic protein 4) [NCBI Gene 652], BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632], RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860]

## Full-text entities

- **Genes:** BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632] {aka BGP, OC, OCN}, RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860] {aka AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD}, TNFSF11 (TNF superfamily member 11) [NCBI Gene 8600] {aka CD254, ODF, OPGL, OPTB2, RANKL, TNLG6B}, BMP4 (bone morphogenetic protein 4) [NCBI Gene 652] {aka BMP2B, BMP2B1, MCOPS6, OFC11, ZYME}, TNFRSF11B (TNF receptor superfamily member 11b) [NCBI Gene 4982] {aka OCIF, OPG, PDB5, TR1}
- **Diseases:** bone and (MESH:D001847), tissue defects (MESH:D017695)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12110666/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12110666/full.md

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Source: https://tomesphere.com/paper/PMC12110666