# Scaffold-Free Bone Regeneration Through Collaboration Between Type IV Collagen and FBXL14

**Authors:** Mari Akiyama

PMC · DOI: 10.3390/jcm14207160 · Journal of Clinical Medicine · 2025-10-11

## TL;DR

This study explores how type IV collagen and FBXL14 work together to regenerate bone without a scaffold, using cells from bovine periosteum.

## Contribution

The study reveals a novel collaboration between type IV collagen and FBXL14 in scaffold-free bone regeneration.

## Key findings

- Type IV collagen and FBXL14 were expressed in Volkmann’s and Haversian canals in bone and periosteum.
- After 5 weeks, these proteins surrounded calcified crystals containing osteocalcin and formed periosteum-derived cells.
- Von Kossa and osteocalcin staining confirmed the presence of calcified substances in the crystals.

## Abstract

Background: The periosteum and periosteum-derived cells have attracted considerable attention for their potential use in clinical applications for treating bone defects. Bovine periosteum-derived cells have been investigated because of their capability for scaffold-free bone regeneration. Previous mass spectrometry (MS) and immunohistochemistry studies have shown the presence of F-box/leucine-rich repeat protein 14 (FBXL14) in bovine periosteum and periosteum-derived cells. Recently, studies using ESI-Q-Orbitrap MS suggested the presence of type IV collagen in the periosteum. The aim of the present study was to clarify the relationship between type IV collagen and FBXL14 in the formation of periosteum-derived cells. Methods: Bovine periosteum-derived cells were obtained from Japanese Black Cattle’s legs in Medium 199 with ascorbic acid and 10% fetal bovine serum. Immunohistochemistry for type IV collagen and FBXL14 was performed using bovine bone with periosteum and periosteum alone for explant culture. Results: Both type IV collagen and FBXL14 were expressed in Volkmann’s canals and the Haversian canals in bone and periosteum. After 5 weeks, type IV collagen and FBXL14 surrounded crystals containing osteocalcin and had formed periosteum-derived cells. Von Kossa staining and immunostaining of osteocalcin revealed that the crystals contained calcified substances and osteocalcin. Conclusions: Clinically, understanding osteocalcin-interacting proteins will help promote bone regeneration. Interactions between type IV collagen and FBXL14 may contribute to scaffold-free bone regeneration.

## Linked entities

- **Genes:** FBXL14 (F-box and leucine rich repeat protein 14) [NCBI Gene 144699]
- **Proteins:** FBXL14 (F-box and leucine rich repeat protein 14), bglap2 (bone gamma-carboxyglutamate (gla) protein (osteocalcin) 2)
- **Chemicals:** ascorbic acid (PubChem CID 9888239)
- **Species:** Bos taurus (taxon 9913), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 281646] {aka BGP}, FBXL14 (F-box and leucine rich repeat protein 14) [NCBI Gene 531211]
- **Diseases:** bone defects (MESH:D001847)
- **Chemicals:** ascorbic acid (MESH:D001205), Medium 199 (-)
- **Species:** Bos taurus (bovine, species) [taxon 9913]

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12565019/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12565019/full.md

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Source: https://tomesphere.com/paper/PMC12565019