SUNY Upstate Medical University, Division of Vascular Surgery and Endovascular Services, Syracuse, New York, USA.
Physiol Res. 2019 Dec 30;68(6):893-900. doi: 10.33549/physiolres.934148. Epub 2019 Oct 25.
Thrombospondins (TSPs) are matricellular glycoproteins expressed in response to vascular injury. TSP-1 and TSP-2 are promotors of arterial remodeling while TSP-5 is believed to be protective. The current study assessed the differential effect of TSPs on protein expression in vascular smooth muscle cells (VSMCs). We hypothesized that TSP-1, TSP-2 and TSP-5 would regulate VSMC proteins involved in arterial remodeling. Human VSMCs were exposed to TSP-1, -2, -5 or serum free media (24 hours). Cell lysates were used to assess the targets TSP-1, TSP-2, TSP-5 and CD44), while the culture media was used to detect TGF-ß1, PDGF-BB, ANGPTL-4 and IL-8. Statistical analysis was performed by t-test and p< 0.05 was considered significant. All TSPs increased their own expression and TSP-5 increased TSP-2. TSP-1 and TSP-2 increased production of ANGPTL-4 and PDGF-BB, while TSP-5 only increased ANGPTL-4. TSP-1 increased exclusively TGF-ß1 and CD44 production. TSP-2 increased TSP-1 expression. All TSPs decreased IL-8. The findings suggest that TSP-1 and TSP-2 may promote vascular remodeling, in part, by increasing ANGPTL-4, PDGF-BB and their own expression. TSP-5 did not upregulate the inflammatory mediators TSP-1, PDGF-BB or TGF-ß1, but upregulated its own expression, which could be a protective mechanism against the response to vascular injury.
血栓反应蛋白(TSPs)是一种细胞外基质糖蛋白,在血管损伤时表达增加。TSP-1 和 TSP-2 促进动脉重塑,而 TSP-5 则被认为具有保护作用。本研究评估了 TSPs 对血管平滑肌细胞(VSMCs)中蛋白质表达的差异影响。我们假设 TSP-1、TSP-2 和 TSP-5 将调节参与动脉重塑的 VSMC 蛋白。将人 VSMCs 暴露于 TSP-1、-2、-5 或无血清培养基(24 小时)中。使用细胞裂解物评估 TSP-1、TSP-2、TSP-5 和 CD44 的靶标,而使用培养基检测 TGF-β1、PDGF-BB、ANGPTL-4 和 IL-8。通过 t 检验进行统计分析,p<0.05 被认为具有统计学意义。所有 TSP 都增加了自身的表达,TSP-5 增加了 TSP-2。TSP-1 和 TSP-2 增加了 ANGPTL-4 和 PDGF-BB 的产生,而 TSP-5 仅增加了 ANGPTL-4。TSP-1 仅增加 TGF-β1 和 CD44 的产生。TSP-2 增加了 TSP-1 的表达。所有 TSP 均降低了 IL-8。研究结果表明,TSP-1 和 TSP-2 可能通过增加 ANGPTL-4、PDGF-BB 及其自身表达来促进血管重塑。TSP-5 并未上调炎症介质 TSP-1、PDGF-BB 或 TGF-β1,但上调了自身表达,这可能是一种对血管损伤反应的保护机制。