Brain-derived neurotrophic factor prevents the endothelial barrier dysfunction induced by interleukin-1 beta and tumor necrosis factor-alpha

作者：Matsuda S^*; Fujita T; Kajiya M; Kashiwai K; Takeda K; Shiba H; Kurihara H

来源：Journal of Periodontal Research, 2015, 50(4): 444-451.

DOI：10.1111/jre.12226

• brain-derived neurotrophic factor
• endothelial cell permeability
• inflammatory cytokine
• periodontal tissue regeneration

Background and ObjectiveBrain-derived neurotrophic factor (BDNF) promotes the regeneration of periodontal tissue. Although a local inflammatory step is required to initiate the subsequent process of tissue regeneration, excessive inflammation may inhibit or delay tissue regeneration. Therefore, the regulation of inflammation is essential for periodontal tissue regeneration. In the present study, we examined the influence of BDNF on the human microvascular endothelial cell (HMVEC) barrier dysfunction induced by interleukin (IL)-1 or tumor necrosis factor (TNF)- to determine the effects of BDNF on the regulation of local inflammation in periodontal tissue regeneration.
Material and MethodsEndothelial permeability was analyzed using a Dextran transport assay with transwell plates. The expression of vascular endothelial (VE)-cadherin was assessed by immunoblotting and immunofluorescence microscopy.
ResultsBDNF (25ng/mL) inhibited increase induced in endothelial permeability by IL-1 and TNF-. IL-1 and TNF- decreased VE-cadherin protein levels, while BDNF recovered the reduction in HMVECs. BDNF protected the increase induced in endothelial permeability by IL-1 and TNF- through TrkB. The single addition of BDNF into the culture increased the expression of VE-cadherin in HMVECs.
ConclusionBDNF played an important role in inhibiting endothelial barrier dysfunction, which suggests that it may assist in enhancing periodontal tissue regeneration.

• 出版日期2015-8