VEGFR-2 reduces while combined VEGFR-2 and -3 signaling increases inflammation in apical periodontitis

• Published in: Journal of oral microbiology 2016-01, Vol.8 (1), p.32433-11
• Main Authors: Virtej, Anca, Papadakou, Panagiota, Sasaki, Hajime, Bletsa, Athanasia, Berggreen, Ellen
• Format: Article
• Language: English
• Subjects: Angiogenesis; angiogenesis and lymphangiogenesis; Antibodies; Biocompatibility; Biomedical materials; Blocking antibodies; bone resorption; Cytokines; Endothelial cells; Exposure; Granulocytes; Growth factors; Gum disease; immune cells; Immune system; Immunoglobulin G; Inflammation; Inflammatory response; Kinases; Lesions; Leukocytes (neutrophilic); Ligands; Lymph nodes; Lymphatic system; Mice; Molars; Multiple myeloma; Neutrophils; Original; Osteoclasts; Periodontitis; Receptors; Rheumatoid arthritis; Signaling; Teeth; TNF inhibitors; Tumor necrosis factor-TNF; Vascular endothelial growth factor; Vascular endothelial growth factor receptors
• ISSN: 2000-2297; 2000-2297
• DOI: 10.3402/jom.v8.32433

In apical periodontitis, oral pathogens provoke an inflammatory response in the apical area that induces bone resorptive lesions. In inflammation, angio- and lymphangiogenesis take place. Vascular endothelial growth factors (VEGFs) and their receptors (VEGFRs) are key players in these processes and are expressed in immune cells and endothelial cells in the lesions. We aimed at testing the role of VEGFR-2 and -3 in periapical lesion development and investigated their role in lymphangiogenesis in the draining lymph nodes. We induced lesions by pulp exposure in the lower first molars of C57BL/6 mice. The mice received IgG injections or blocking antibodies against VEGFR-2 (anti-R2), VEGFR-3 (anti-R3), or combined VEGFR-2 and -3, starting on day 0 until day 10 or 21 post-exposure. Lesions developed faster in the anti-R2 and anti-R3 group than in the control and anti-R2/R3 groups. In the anti-R2 group, a strong inflammatory response was found expressed as increased number of neutrophils and osteoclasts. A decreased level of pro-inflammatory cytokines was found in the anti-R2/R3 group. Lymphangiogenesis in the draining lymph nodes was inhibited after blocking of VEGFR-2 and/or -3, while the largest lymph node size was seen after anti-R2 treatment. We demonstrate an anti-inflammatory effect of VEGFR-2 signaling in periapical lesions which seems to involve neutrophil regulation and is independent of angiogenesis. Combined signaling of VEGFR-2 and -3 has a pro-inflammatory effect. Lymph node lymphangiogenesis is promoted through activation of VEGFR-2 and/or VEGFR-3.