Institute of Cardiovascular Research, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Cardiovascular Department, First People's Hospital of Chong Qing Liang Jiang New Zone, Chongqing, 401120, China.
Stem Cell Res Ther. 2017 Oct 24;8(1):237. doi: 10.1186/s13287-017-0684-1.
Endothelial progenitor cell (EPC) differentiation is considered crucial for vascular repair. Vascular endothelial growth factor (VEGF) induces EPC differentiation, but the underlying mechanism of this phenomenon remains unclear. Connexin 43 (Cx43) is reported to be involved in the regulation of stem cell differentiation. Therefore, we sought to determine whether Cx43 is involved in VEGF-induced EPC differentiation and vascular repair.
Rat spleen-derived EPCs were cultured and treated with various concentrations of VEGF (0, 10, or 50 ng/mL), and the relationship between EPC differentiation and Cx43 expression was evaluated. Thereafter, fluorescence redistribution after photobleaching was performed to assess the relationship between adjacent EPC differentiation and Cx43-induced gap junction intercellular communication (GJIC). After carotid artery injury, EPCs pretreated with VEGF were injected into the tail veins, and the effects of Cx43 on vascular repair were evaluated.
EPCs cultured with VEGF exhibited accelerated differentiation and increased expression of Cx43. However, inhibition of Cx43 expression using short interfering RNA (siRNA) attenuated EPC GJIC and consequent EPC differentiation. VEGF-pretreated EPC transplantation promoted EPC homing and reendothelialization, and inhibited neointimal formation. These effects were attenuated by siRNA inhibition of Cx43.
Our results from in vivo and in vitro experiments indicated that VEGF promotes EPC differentiation and vascular repair through Cx43.
内皮祖细胞 (EPC) 的分化被认为对血管修复至关重要。血管内皮生长因子 (VEGF) 可诱导 EPC 分化,但这一现象的潜在机制尚不清楚。间隙连接蛋白 43 (Cx43) 据报道参与了干细胞分化的调节。因此,我们试图确定 Cx43 是否参与 VEGF 诱导的 EPC 分化和血管修复。
培养大鼠脾源性 EPC 并给予不同浓度的 VEGF(0、10 或 50ng/mL)处理,评估 EPC 分化与 Cx43 表达之间的关系。随后,通过荧光漂白后再分布技术评估相邻 EPC 分化与 Cx43 诱导的缝隙连接细胞间通讯 (GJIC) 之间的关系。颈动脉损伤后,将经 VEGF 预处理的 EPC 注入尾静脉,评估 Cx43 对血管修复的影响。
用 VEGF 培养的 EPC 表现出加速分化和 Cx43 表达增加。然而,使用小干扰 RNA (siRNA) 抑制 Cx43 表达减弱了 EPC 的 GJIC 和随后的 EPC 分化。VEGF 预处理的 EPC 移植促进 EPC 归巢和再内皮化,并抑制新生内膜形成。Cx43 的 siRNA 抑制减弱了这些作用。
我们的体内和体外实验结果表明,VEGF 通过 Cx43 促进 EPC 分化和血管修复。