» Articles » PMID: 22617817

Vascular Development During Distraction Osteogenesis Proceeds by Sequential Intramuscular Arteriogenesis Followed by Intraosteal Angiogenesis

Overview
Journal Bone
Date 2012 May 24
PMID 22617817
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Vascular formation is intimately associated with bone formation during distraction osteogenesis (DO). While prior studies on this association have focused on vascular formation locally within the regenerate, we hypothesized that this vascular formation, as well as the resulting osteogenesis, relies heavily on the response of the vascular network in surrounding muscular compartments. To test this hypothesis, the spatiotemporal sequence of vascular formation was assessed in both muscular and osseous compartments in a murine model of DO and was compared to the progression of osteogenesis. Micro-computed tomography (μCT) scans were performed sequentially, before and after demineralization, on specimens containing contrast-enhanced vascular casts. Image registration and subtraction procedures were developed to examine the co-related, spatiotemporal patterns of vascular and osseous tissue formation. Immunohistochemistry was used to assess the contributory roles of arteriogenesis (formation of large vessels) and angiogenesis (formation of small vessels) to overall vessel formation. Mean vessel thickness showed an increasing trend during the period of active distraction (p=0.068), whereas vessel volume showed maximal increases during the consolidation period (p=0.009). The volume of mineralized tissue in the regenerate increased over time (p<0.039), was correlated with vessel volume (r=0.59; p=0.025), and occurred primarily during consolidation. Immunohistological data suggested that: 1) the period of active distraction was characterized primarily by arteriogenesis in the surrounding muscle; 2) during consolidation, angiogenesis predominated in the intraosteal region; and 3) vessel formation proceeded from the surrounding muscle into the regenerate. These data show that formation of vascular tissue occurs in both muscular and osseous compartments during DO and that periods of intense osteogenesis are concurrent with those of angiogenesis. The results further suggest the presence of morphogenetic factors that coordinate the development of vascular tissues from the intramuscular compartment into the regions of osseous regeneration.

Citing Articles

An micro-multiphysics agent-based approach for simulating bone regeneration in a mouse femur defect model.

Kendall J, Ledoux C, Marques F, Boaretti D, Schulte F, Morgan E Front Bioeng Biotechnol. 2024; 11:1289127.

PMID: 38164405 PMC: 10757951. DOI: 10.3389/fbioe.2023.1289127.


The accordion technique enhances bone regeneration via angiogenesis factor in a rat distraction osteogenesis model.

Liu K, Wang S, Yalikun A, Ren P, Yusufu A Front Physiol. 2023; 14:1259567.

PMID: 37745241 PMC: 10514895. DOI: 10.3389/fphys.2023.1259567.


Local delivery of hydrogel encapsulated vascular endothelial growth factor for the prevention of medication-related osteonecrosis of the jaw.

Sharma D, Hamlet S, Vaquette C, Petcu E, Ramamurthy P, Ivanovski S Sci Rep. 2021; 11(1):23371.

PMID: 34862395 PMC: 8642483. DOI: 10.1038/s41598-021-02637-w.


Downregulation of microRNA-16-5p accelerates fracture healing by promoting proliferation and inhibiting apoptosis of osteoblasts in patients with traumatic brain injury.

Sun Y, Xiong Y, Yan C, Chen L, Chen D, Mi B Am J Transl Res. 2019; 11(8):4746-4760.

PMID: 31497196 PMC: 6731405.


Mechanical solutions to salvage failed distraction osteogenesis in large bone defect management.

Borzunov D, Shastov A Int Orthop. 2018; 43(5):1051-1059.

PMID: 29934717 DOI: 10.1007/s00264-018-4032-6.


References
1.
Jacoby C, Boring Y, Beck A, Zernecke A, Aurich V, Weber C . Dynamic changes in murine vessel geometry assessed by high-resolution magnetic resonance angiography: a 9.4T study. J Magn Reson Imaging. 2008; 28(3):637-45. DOI: 10.1002/jmri.21482. View

2.
Kinner B, Gerstenfeld L, Einhorn T, Spector M . Expression of smooth muscle actin in connective tissue cells participating in fracture healing in a murine model. Bone. 2002; 30(5):738-45. DOI: 10.1016/s8756-3282(02)00695-6. View

3.
Fei J, Jia F, Peyrin F, Francoise P, Malaval L, Vico L . Imaging and quantitative assessment of long bone vascularization in the adult rat using microcomputed tomography. Anat Rec (Hoboken). 2009; 293(2):215-24. DOI: 10.1002/ar.21054. View

4.
Zelzer E, Mamluk R, Ferrara N, Johnson R, Schipani E, Olsen B . VEGFA is necessary for chondrocyte survival during bone development. Development. 2004; 131(9):2161-71. DOI: 10.1242/dev.01053. View

5.
Frohlich M, Grayson W, Wan L, Marolt D, Drobnic M, Vunjak-Novakovic G . Tissue engineered bone grafts: biological requirements, tissue culture and clinical relevance. Curr Stem Cell Res Ther. 2008; 3(4):254-64. PMC: 2773298. DOI: 10.2174/157488808786733962. View