The Anti-Angiogenic Effect of Microbotox on Rosacea Is Due to the Suppressed Secretion of VEGF by Mast Cells Resulting From Internalization of the MRGPRX2 Receptor.

IF 1.3
Jing Wan, Yue Le, Meng-Meng Geng, Bing-Qi Dong, Zhi-Kai Liao, Lin-Xia Liu, Tie-Chi Lei
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Abstract

Background: Intradermal microdroplet injections of botulinum toxin type-A (BoNT/A) effectively ameliorate rosacea-related angiogenesis, but the mechanism remains unclear.

Objective: To explore the anti-angiogenesis of BoNT/A in the rosacea-like mouse model and to measure the secretion of vascular endothelial growth factor (VEGF) by mast cells.

Methods: A rosacea-like mouse model was induced by LL37 in both Mas-related G-protein-coupled receptor B2 conditional knockout (MrgprB2-/-) mice and wild-type (WT) mice, then treated with BoNT/A and/or Apatinib. The abundance of endothelial cells and mast cells in mouse skin was determined using dual immunofluorescence staining. The VEGF levels in supernatants and cell lysates of laboratory of allergic disease 2 (LAD2) mast cells were assessed using reverse transcription quantitative polymerase chain reaction, western blots, and enzyme-linked immunosorbent assay. The effect of conditioned medium (CM) collected from LAD2 on human umbilical vein endothelial cells (HUVECs) was determined using tube formation assays. The number of proliferative cells was confirmed using the 5-ethynyl-2'-deoxyuridine incorporation assays. The effect of BoNT/A on the internalization of Mas-related G-protein-coupled receptor X2 (MRGPRX2) was detected using flow cytometry and immunofluorescence staining.

Results: LL37-induced rosacea-like skin manifestations were significantly alleviated in MrgprB2-/- mice compared to WT controls. BoNT/A mitigated the LL37-induced secretion of VEGF by LAD2. The CM from BoNT/A-treated LAD2 inhibited HUVEC proliferation and tube formation. The LAD2 cells co-treated with LL37 and BoNT/A exhibited dramatically enhanced MRGPRX2 internalization.

Conclusion: BoNT/A enhances LL37-mediated MRGPRX2 internalization in mast cells, thereby reducing VEGF secretion and neovascularization and improving facial flushing symptom in rosacea.

微肉毒杆菌毒素对酒糟鼻的抗血管生成作用是由于MRGPRX2受体内化抑制肥大细胞分泌VEGF。
背景:皮内微滴注射A型肉毒毒素(BoNT/A)可有效改善酒渣鼻相关血管生成,但其机制尚不清楚。目的:探讨BoNT/A在酒糟样小鼠模型中的抗血管生成作用,并检测肥大细胞对血管内皮生长因子(VEGF)的分泌。方法:将mas相关g蛋白偶联受体B2条件敲除(MrgprB2-/-)小鼠和野生型(WT)小鼠分别用LL37诱导酒糟样小鼠模型,然后用BoNT/A和/或阿帕替尼处理。采用双免疫荧光染色法测定小鼠皮肤内皮细胞和肥大细胞的丰度。采用逆转录定量聚合酶链反应、western blots和酶联免疫吸附法检测过敏性疾病2 (LAD2)肥大细胞上清液和细胞裂解液中VEGF水平。采用试管成形法测定从LAD2收集的条件培养基(CM)对人脐静脉内皮细胞(HUVECs)的影响。增殖细胞的数量用5-乙基-2'-脱氧尿苷掺入法确定。采用流式细胞术和免疫荧光染色检测BoNT/A对mas相关g蛋白偶联受体X2 (MRGPRX2)内化的影响。结果:与WT对照组相比,MrgprB2-/-小鼠ll37诱导的酒渣鼻样皮肤表现明显减轻。BoNT/A可减轻ll37诱导的LAD2对VEGF的分泌。BoNT/ a处理LAD2的CM抑制HUVEC增殖和管状形成。与LL37和BoNT/A共处理的LAD2细胞表现出显著增强的MRGPRX2内化。结论:BoNT/A增强ll37介导的肥大细胞MRGPRX2内化,从而减少VEGF分泌和新生血管形成,改善酒糟面部潮红症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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