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首页> 外文期刊>Wound repair and regeneration: official publication of the Wound Healing Society [and] the European Tissue Repair Society >Role of salivary vascular endothelial growth factor (VEGF) in palatal mucosal wound healing
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Role of salivary vascular endothelial growth factor (VEGF) in palatal mucosal wound healing

机译:唾液血管内皮生长的作用伤口愈合因子(VEGF)在腭粘膜

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摘要

The mucosa of alimentary tract heals more rapidly than cutaneous wounds. The underlying mechanisms of this enhanced healing have not been completely elucidated. Constant exposure to salivary growth factors has been shown to play a critical role in mucosal homeostasis and tissue repair. Angiogenesis also has an essential role in successful wound repair. One of the main angiogenic growth factors, vascular endothelial growth factor (VEGF), has a pleiotropic role in tissue repair via neovascularization, reepithelialization, and regulation of extracellular matrix. We have previously reported a critical role for salivary VEGF in bowel adaptation after small bowel resection. We hypothesize that salivary VEGF is an essential stimulus for oral mucosal tissue repair, and use the murine palatal wound model to test our hypothesis. In a loss-of-function experiment, we removed the primary source of VEGF production through selective submandibular gland (SMG) sialoadenectomy in a murine model and observed the effects on wound closure and neovascularization. We then performed a selective loss-of-function experiment using the protein VEGF-Trap to inhibit salivary VEGF. In a gain-of-function experiment, we supplemented oral VEGF following SMG sialoadenectomy. After SMG sialoadenectomy, there was significant reduction in salivary VEGF level, wound closure, and vessel density. Lower levels of salivary VEGF were correlated with impaired neovascularization and reepithelialization. The selective blockade of VEGF using VEGF-Trap resulted in a similar impairment in wound healing and neovascularization. The sole supplementation of oral VEGF after SMG sialoadenectomy rescued the impaired wound healing phenotype and restored neovascularization to normal levels. These data show a novel role for salivary-VEGF in mucosal wound healing, and provide a basis for the development of novel therapeutics aimed at augmenting wound repair of the oral mucosa, as well as wounds at other sites in the alimentary tract.
机译:消化道的黏膜愈合更快比皮肤的伤口。这个增强的治疗尚未完全阐明。因素起到重要的作用粘膜内稳态和组织修复。血管生成也有不可或缺的作用成功的伤口修复。血管生成生长因子,血管内皮生长因子(VEGF)、多效性的作用通过新血管化组织修复,reepithelialization和监管细胞外基质。唾液VEGF在肠道的至关重要的作用适应小肠切除术后。假设唾VEGF是必不可少的刺激口腔粘膜组织修复,和使用鼠腭伤口模型来测试我们的假设。删除VEGF生产的主要来源通过选择性颌下腺(SMG)涎腺切除术在小鼠模型,观察对伤口关闭的影响新生血管形成。使用蛋白质功能丧失的实验VEGF抑制剂抑制唾液VEGF。功能实验,我们补充口服SMG涎腺切除术后VEGF。涎腺切除术,有显著的减少唾液中VEGF水平,伤口闭合,船密度。与新血管形成和受损reepithelialization。使用VEGF抑制剂导致类似的VEGF在伤口愈合和损伤新生血管形成。口服后VEGF SMG涎腺切除术救了伤口愈合的表现型和恢复受损新血管形成到正常水平。在粘膜显示salivary-VEGF小说角色伤口愈合,并提供一个基础治疗针对的新发展增加口腔黏膜的伤口修复伤口在食物的其他网站束。

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