Glycotherapeutics Group, Institute of Medical Biology, Agency for Science, Technology and Research, Singapore.
The Ferrier Research Institute, Victoria University of Wellington, Lower Hutt, New Zealand.
Biomaterials. 2014 Aug;35(25):6776-86. doi: 10.1016/j.biomaterials.2014.04.084. Epub 2014 May 20.
The therapeutic use of VEGF165 to stimulate blood vessel formation for the treatment of peripheral arterial disease or cardiovascular-related disease has met with limited success. Here we describe an affinity-isolated heparan sulfate glycotherapeutic (HS7(+ve)) that binds to, and enhances the bioactivity of, VEGF165. Application of HS7(+ve) complexed with VEGF165 results in enhanced VEGF165-VEGFR2 interaction, prolonged downstream pErk1/2 signalling, and increased cell proliferation and tube formation in HUVECs, compared with VEGF165 alone. The pro-angiogenic potential of HS7(+ve) was further assessed in vivo using the chick embryo chorioallantoic membrane (CAM) assay. Exogenous dosing with HS7(+ve) alone significantly enhanced the formation of new blood vessels with potencies comparable to VEGF165. These results demonstrate the potential for vascular therapy of glycotherapeutic agents targeted at augmenting the bioactivity of VEGF165.
VEGF165 的治疗用途在于刺激血管形成,以治疗外周动脉疾病或心血管相关疾病,但收效甚微。在此,我们描述了一种亲和分离的肝素硫酸盐糖治疗剂(HS7(+ve)),它可以与 VEGF165 结合并增强其生物活性。与单独使用 VEGF165 相比,将 HS7(+ve)与 VEGF165 复合应用可增强 VEGF165-VEGFR2 相互作用,延长下游 pErk1/2 信号传导,并增加 HUVEC 中的细胞增殖和管形成。我们还通过鸡胚尿囊膜(CAM)实验在体内进一步评估了 HS7(+ve) 的促血管生成潜能。单独给予外源性 HS7(+ve) 可显著增强新血管的形成,其效力与 VEGF165 相当。这些结果表明,靶向增强 VEGF165 生物活性的糖治疗剂在血管治疗方面具有潜力。