Fukino Keiko, Suzuki Toru, Saito Yuichiro, Shindo Takayuki, Amaki Toshihiro, Kurabayashi Masahiko, Nagai Ryozo
Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
Biochem Biophys Res Commun. 2002 Apr 26;293(1):332-7. doi: 10.1016/S0006-291X(02)00216-4.
Advanced age is a major risk factor of peripheral artery disease. We examined the effects of the aging-suppressor gene klotho on angiogenesis in response to ischemia by introducing ischemic hindlimb model in mice heterozygously deficient for the klotho gene and in wild type mice. Blood flow recovery as assessed by laser doppler perfusion imaging and angiogenesis as assessed by density of PECAM-1/CD31-positive positive capillaries were markedly impaired in mice heterozygously deficient for the klotho gene (both <0.05). Our findings show that the aging-suppressor gene klotho affects angiogenesis and the possibility that age-related impairment of angiogenesis might be regulated by the klotho gene. Our results present a new possibility of therapeutic angiogenesis for patients of advanced age.
高龄是外周动脉疾病的主要风险因素。我们通过在klotho基因杂合缺陷小鼠和野生型小鼠中建立缺血后肢模型,研究了衰老抑制基因klotho对缺血诱导的血管生成的影响。通过激光多普勒灌注成像评估的血流恢复以及通过PECAM-1/CD31阳性毛细血管密度评估的血管生成在klotho基因杂合缺陷小鼠中均显著受损(两者均P<0.05)。我们的研究结果表明,衰老抑制基因klotho影响血管生成,并且血管生成的年龄相关损伤可能受klotho基因调控。我们的结果为高龄患者治疗性血管生成提供了新的可能性。