Cao Renhai, Bråkenhielm Ebba, Pawliuk Robert, Wariaro David, Post Mark J, Wahlberg Eric, Leboulch Philippe, Cao Yihai
Laboratory of Angiogenesis Research, Microbiology and Tumor Biology Center, Karolinska Institutet, Stockholm, Sweden.
Nat Med. 2003 May;9(5):604-13. doi: 10.1038/nm848. Epub 2003 Mar 31.
The establishment of functional and stable vascular networks is essential for angiogenic therapy. Here we report that a combination of two angiogenic factors, platelet-derived growth factor (PDGF)-BB and fibroblast growth factor (FGF)-2, synergistically induces vascular networks, which remain stable for more than a year even after depletion of angiogenic factors. In both rat and rabbit ischemic hind limb models, PDGF-BB and FGF-2 together markedly stimulated collateral arteriogenesis after ligation of the femoral artery, with a significant increase in vascularization and improvement in paw blood flow. A possible mechanism of angiogenic synergism between PDGF-BB and FGF-2 involves upregulation of the expression of PDGF receptor (PDGFR)-alpha and PDGFR-beta by FGF-2 in newly formed blood vessels. Our data show that a specific combination of angiogenic factors establishes functional and stable vascular networks, and provides guidance for the ongoing clinical trials of angiogenic factors for the treatment of ischemic diseases.
建立功能性和稳定的血管网络对于血管生成治疗至关重要。在此,我们报告两种血管生成因子,血小板衍生生长因子(PDGF)-BB和成纤维细胞生长因子(FGF)-2的组合可协同诱导血管网络,即使在血管生成因子耗尽后,该血管网络仍可稳定存在一年以上。在大鼠和兔缺血后肢模型中,PDGF-BB和FGF-2共同显著刺激股动脉结扎后的侧支动脉生成,血管化显著增加,爪部血流改善。PDGF-BB和FGF-2之间血管生成协同作用的一种可能机制涉及FGF-2在新形成血管中上调血小板衍生生长因子受体(PDGFR)-α和PDGFR-β的表达。我们的数据表明,血管生成因子的特定组合可建立功能性和稳定的血管网络,并为目前正在进行的血管生成因子治疗缺血性疾病的临床试验提供指导。