Related Experiment Video
Updated: Oct 23, 2025

08:41
Calvarial Model of Bone Augmentation in Rabbit for Assessment of Bone Growth and Neovascularization in Bone Substitution Materials
Published on: August 13, 2019
8.5K
Combining Bone Collagen Matrix with hUC-MSCs for Application to Alveolar Process Cleft in a Rabbit Model
Xue-Cheng Sun1,2, Hu Wang1,3, Dan Zhang1,3
1Reproductive and Genetic Center of National Research Institute for Family Planning, Beijing, 100081, China.
Stem Cell Reviews and Reports
|August 22, 2021
Summary
Combining bone collagen matrix with human umbilical cord mesenchymal stem cells (hUC-MSCs) significantly enhanced bone regeneration in a rabbit alveolar cleft model. This approach shows promise for treating severe bone defects.
Area of Science:
- Regenerative Medicine
- Biomaterials Science
- Orthopedic Surgery
Background:
- Current bone defect treatments have limited efficacy due to poor osteoinduction.
- Human umbilical cord mesenchymal stem cells (hUC-MSCs) show potential for bone regeneration.
- The mechanism of combining hUC-MSCs with bone collagen matrix for alveolar cleft repair is not fully understood.
Purpose of the Study:
- To investigate the efficacy of combining a bone collagen matrix with hUC-MSCs for alveolar process cleft repair in a rabbit model.
- To elucidate the underlying mechanisms of enhanced bone regeneration.
Main Methods:
- A rabbit alveolar process cleft model was created.
- Bone defects were treated with either bone collagen matrix alone or combined with hUC-MSCs.
- Assessment of new bone formation and cellular activity using X-ray, micro-CT, histochemistry, and TUNEL assays at 3 and 6 months.
Main Results:
- The hUC-MSC combination group showed significantly higher bone formation rates compared to controls at both 3 and 6 months.
- Apoptosis rates in the hUC-MSC group were elevated at 3 months but reduced at 6 months post-surgery.
Conclusions:
- Combining bone collagen matrix with hUC-MSCs effectively promotes new bone regeneration in alveolar process cleft defects.
- The mechanism involves enhanced osteoblast formation, chondrocyte growth, type I collagen production, and BMP-2 generation.

