Biglycan potentially regulates angiogenesis during fracture repair by altering expression and function of endostatin

• Published in: Matrix biology Vol. 52-54; pp. 141 - 150
• Main Authors: Myren, Maja, Kirby, David J., Noonan, Megan L., Maeda, Azusa, Owens, Rick T., Ricard-Blum, Sylvie, Kram, Vardit, Kilts, Tina M., Young, Marian F.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.05.2016; Elsevier
• Subjects: Angiogenesis; Animals; Biglycan; Biglycan - genetics; Biglycan - metabolism; Biochemistry; Biochemistry, Molecular Biology; Computed Tomography Angiography; Down-Regulation; Endostatin; Endostatins - metabolism; Endothelial Cells - cytology; Endothelial Cells - metabolism; Fracture Healing; Gene Knockout Techniques; Life Sciences; Mice; Neovascularization, Physiologic; X-Ray Microtomography; Angiogenesis; Biglycan; Fracture healing; Endostatin
• ISSN: 0945-053X; 1569-1802
• DOI: 10.1016/j.matbio.2016.03.008

The small proteoglycan biglycan (Bgn) is highly expressed in the organic matrix of bone and plays a role in bone formation. Previous work implicated Bgn in vessel growth during bone healing [1]. By infusing barium sulfate (BaSO4) into WT and Bgn-deficient mice we discovered the positive effect of Bgn in modulating angiogenesis during fracture healing. Using micro-computed tomography angiography we found significant differences in the vessel size and volume among other parameters. To further understand the mechanistic basis for this, we explored the relationship between Bgn and the anti-angiogenic protein endostatin. Immunohistochemistry (IHC) showed co-localization of Bgn and endostatin in regions of bone formation, with increased endostatin staining in Bgn-KO compared to WT at 14days post-fracture. To further elucidate the relationship between Bgn and endostatin, an endothelial cell tube formation assay was used. This study showed that endothelial cells treated with endostatin had significantly decreased vessel length and vessel branches compared to untreated cells, while cells treated with endostatin and Bgn at a 1:1M ratio had vessel length and vessel branches comparable to untreated cells. This indicated that Bgn was able to mitigate the inhibitory effect of endostatin on endothelial cell growth. In summary, these results suggest that Bgn is needed for proper blood vessel formation during fracture healing, and one mechanism by which Bgn impacts angiogenesis is through inhibition of endostatin. •Biglycan deficient mice have reduced angiogenesis during fracture healing.•Biglycan co-localizes with endostatin at sites of new bone formation.•Endostatin mRNA and protein are up-regulated in the Bgn-deficient callus.•Bgn counteracts the anti-angiogenic effects of endostatin in vessel growth.