# In Vitro and In Ovo CAM Model Evaluation of Periosteum-Derived Micrografts

**Authors:** Rawan Almujaydil, Conor J. McCann, Linh Nguyen, Francesco D’Aiuto

PMC · DOI: 10.3390/jfb17030148 · 2026-03-18

## TL;DR

This study explores how periosteum-derived micrografts combined with bone substitutes can improve tissue regeneration by enhancing blood vessel growth.

## Contribution

The novel contribution is demonstrating that periosteum-derived micrografts significantly enhance angiogenesis when combined with bone substitutes in a CAM model.

## Key findings

- Periosteum-derived micrografts combined with bone substitutes significantly increased vascularization in the CAM model.
- Histological analysis confirmed enhanced vascularization with positive SMA staining in micrograft groups.
- Micrografts improved total vessel area, length, and branching points compared to controls.

## Abstract

Despite advances in periodontal regenerative therapies, consistent tissue regeneration remains challenging, with cells playing an essential role in successful repair. Therefore, this study tested different dental bone substitutes embedded in the chorioallantoic membrane (CAM) combined with periosteum-derived micrografts obtained using a chair-side device (Rigenera HBW system). Cell populations within the micrografts were identified and characterised via immunofluorescence and flow cytometry (CD31, CD105, CD34, CD90, CD73, and CD45). A CAM model was employed to examine the angiogenic potential of micrografts combined with bone substitutes, which were analysed through quantitative blood vessel/vascularisation assessments using the Ikosa software (2025), along with histological and immunohistochemical evaluations such as smooth muscle actin (SMA), H&E, and Masson’s trichrome staining. Statistical analysis was performed using GraphPad Prism 10. The addition of periosteum-derived micrografts resulted in angiogenic enhancement compared to the controls. Notable enhancement of total vessel area, total length, and branching points were obtained when Fisiograft® (p = 0.0007, p = 0.0002, and p < 0.0001, respectively), New Shore® (p = 0.0006, p = 0.0149, and p = 0.0083, respectively), and Bio-Oss® (p = 0.0038 and p = 0.0010, respectively) were combined with micrografts, compared to the positive controls. The histological and immunohistochemical analyses confirmed increased vascularisation (positive staining for SMA) in the micrograft groups. Periosteum-derived micrografts represent a promising adjunct to conventional bone-grafting materials, promoting vascularisation and potentially enhancing tissue regeneration and healing outcomes.

## Full-text entities

- **Genes:** NT5E (5'-nucleotidase ecto) [NCBI Gene 4907] {aka CALJA, CD73, E5NT, NT, NT5, NTE}, SMN1 (survival of motor neuron 1, telomeric) [NCBI Gene 6606] {aka BCD541, GEMIN1, SMA, SMA1, SMA2, SMA3}, Thy1 (thymus cell antigen 1, theta) [NCBI Gene 21838] {aka CD90, T25, Thy-1, Thy-1.2, Thy1.1, Thy1.2}, THY1 (Thy-1 cell surface antigen) [NCBI Gene 7070] {aka CD90, CDw90}, Apc (APC, WNT signaling pathway regulator) [NCBI Gene 11789] {aka CC1, Min, mAPC}, Eng (endoglin) [NCBI Gene 13805] {aka CD105, Endo, S-endoglin}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}, Nt5e (5' nucleotidase, ecto) [NCBI Gene 23959] {aka 2210401F01Rik, 5'-NT, CD73, NT, Nt5, eNT}, CD34 (CD34 molecule) [NCBI Gene 947], PECAM1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 5175] {aka CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM}, Pecam1 (platelet/endothelial cell adhesion molecule 1) [NCBI Gene 18613] {aka Cd31, PECAM-1, Pecam}, Cd34 (CD34 antigen) [NCBI Gene 12490], Ptprc (protein tyrosine phosphatase receptor type C) [NCBI Gene 19264] {aka B220, CD45R, Cd45, L-CA, Ly-5, Lyt-4}
- **Diseases:** injury to (MESH:D014947), CAM (MESH:D015433), bone defect (MESH:D001847), maxillofacial and alveolar bone defects (MESH:D008446), Periodontitis (MESH:D010518), immunodeficient (MESH:D007153), inflammatory disease (MESH:D007249)
- **Chemicals:** paraffin (MESH:D010232), BC (-), penicillin (MESH:D010406), BO (MESH:C077540), H&amp;E (MESH:D006371), PBS (MESH:D007854), alpha-MEM (MESH:C420642), DAPI (MESH:C007293), paraformaldehyde (MESH:C003043), PLGA (MESH:D000077182), CO2 (MESH:D002245), EDTA (MESH:D004492), NaCl (MESH:D012965)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Gallus gallus (bantam, species) [taxon 9031]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027172/full.md

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Source: https://tomesphere.com/paper/PMC13027172