骨科祛痰逐瘀方经MAPK/ERK通路诱导血管内皮细胞迁移与血管管腔形成
Orthopedic Qutan Zhuyu Decoction induces vascular endothelial cell migration and lumen formation via MAPK/ERK pathway
  
DOI:10.3969/j.issn.1006-7108.2019.06.004
中文关键词:  中医中药  祛痰逐瘀方  血管内皮细胞  管腔形成  MARK/ERK  周细胞
英文关键词:Chinese traditional medicine  Qutan Zhuyu Decoction  vascular endothelial cells  lumen formation  MARK/ERK  pericyte
基金项目:国家自然科学基金面上项目(81573996,81473697,81873327)
作者单位
陈镇秋1,2 洪郭驹2,3 韩晓蕊4 何伟1,2 张庆文1,2 魏秋实1,2* 1.广州中医药大学第一附属医院关节骨科广东 广州 510405 2.广州中医药大学岭南医学中心国家重点学科中医骨伤科学实验室广东 广州 510405 3.加拿大阿尔伯塔省埃德蒙顿阿尔伯塔大学医学院外科部T6G 2R3 4.广州市第一人民医院/华南理工大学第二附属医院放射科广东 广州 510006 
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中文摘要:
      目的 探究祛痰逐瘀方(Qutan Zhuyu Decoction,QZD)经MAPK/ERK通路诱导血管内皮细胞迁徙与血管管腔形成的作用,明确QZD在骨血管化重建中的机制。方法 对大鼠进行QZD灌胃,并采集和分离获得含药血清;培养SVEC和10T1/2细胞,分别将二者分为空白组、bFGF组(阳性对照组)、QZD中药组(实验组),其中实验组为将QZD含药血清加入细胞培养基中。对干预后的SVEC进行迁徙实验,另外对SVEC进行管腔形成实验,对10T1/2进行免疫荧光染色观察中药促管腔形成效果,运用Western blot检测ERK1/2、p38等蛋白表达,研究QZD对SVEC的作用机制。结果 (1)QZD含药血清较空白组促进SVEC细胞的迁徙(P<0.05);(2)QZD含药血清较空白组可促进SVEC血管管腔形成,包括管腔面积(P<0.05)和管腔腔周长度(P<0.05);(3)荧光染色实验提示,QZD含药血清较空白组促进10T1/2细胞呈规律性聚集,并形成管腔状状态;(4)Western blot实验提示,QZD含药血清可促进SVEC中ERK1/2和p38 的磷酸化(P<0.05)。结论 QZD经MARK/ERK通路调控和诱导血管内皮细胞的迁徙和血管官腔的形成,提示其可运用于骨血管化重建中。
英文摘要:
      Objective Qutan Zhuyu Decoction (QZD) is an important prescription for the treatment of orthopedic diseases. The purpose of our study is to investigate the role of QZD in inducing vascular endothelial cell migration and vascular lumen formation via MAPK/ERK pathway, and to clarify the mechanism of QZD in bone vascularization. Methods QZD was administered to rats, and serum containing QZD was collected and isolated. SVEC and 10T1/2 cells were cultured and divided into blank group, bFGF group (positive control group) and QZD group (test group). QZD containing serum was added into the cell culture medium of the test group. The migration experiment was carried out on the SVEC after intervention; the SVEC was subjected to lumen formation experiment; the immunofluorescence staining of 10T1/2 was used to observe the effect of QZD on lumen formation; the expression of ERK1/2, p38 was detected by Western blot for measuring its mechanism. Results (1) QZD containing serum promoted the migration of SVEC cells compared with the blank group (P<0.05); (2) QZD-containing serum could promote the formation of SVEC vascular lumen, including lumen area (P<0.05) and length of cavity (P<0.05); (3) Fluorescence staining experiment suggested that QZD-containing serum promotes regular aggregation of 10T1/2 cells and forms a luminal state compared with the blank group; (4) Western blot test suggested that QZD containing serum promoted phosphorylation of ERK1/2 and p38 in SVEC (P<0.05). Conclusion QZD regulates and induces vascular endothelial cell migration and lumen formation via MARK/ERK pathway, indicating that it can be used in bone vascular remodeling.
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