Bosch-Marce Marta, Okuyama Hiroaki, Wesley Jacob B, Sarkar Kakali, Kimura Hideo, Liu Ye V, Zhang Huafeng, Strazza Marianne, Rey Sergio, Savino Lindsey, Zhou Yi Fu, McDonald Karin R, Na Youn, Vandiver Scott, Rabi Alireza, Shaked Yuval, Kerbel Robert, Lavallee Theresa, Semenza Gregg L
Vascular Biology Program, Institute for Cell Engineering, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Circ Res. 2007 Dec 7;101(12):1310-8. doi: 10.1161/CIRCRESAHA.107.153346. Epub 2007 Oct 11.
Ischemia is a stimulus for production of angiogenic cytokines that activate local vascular cells and mobilize angiogenic cells to the circulation. These responses are impaired in elderly patients with peripheral arterial disease. Hypoxia-inducible factor (HIF)-1 mediates adaptive responses to ischemia, including production of angiogenic cytokines. In this study, we demonstrate that aging and HIF-1 loss-of-function impair the expression of multiple angiogenic cytokines, mobilization of angiogenic cells, maintenance of tissue viability, and recovery of limb perfusion following femoral artery ligation. We show that HIF-1 directly activates transcription of the gene encoding stem cell factor and that mice lacking the cognate receptor C-KIT have impaired recovery from ischemia. Administration of AdCA5, an adenovirus encoding a constitutively active form of HIF-1alpha, improved the recovery of perfusion in older mice to levels similar to those in young mice. Injection of AdCA5 into nonischemic limb was sufficient to increase the number of circulating angiogenic cells. These results indicate that HIF-1 activity is necessary and sufficient for the mobilization of angiogenic cells and that HIF-1alpha gene therapy can counteract the pathological effects of aging in a mouse model of limb ischemia.
缺血是促使血管生成细胞因子产生的刺激因素,这些细胞因子可激活局部血管细胞并促使血管生成细胞进入循环系统。在患有外周动脉疾病的老年患者中,这些反应会受到损害。缺氧诱导因子(HIF)-1介导对缺血的适应性反应,包括血管生成细胞因子的产生。在本研究中,我们证明衰老和HIF-1功能丧失会损害多种血管生成细胞因子的表达、血管生成细胞的动员、组织活力的维持以及股动脉结扎后肢体灌注的恢复。我们发现HIF-1直接激活编码干细胞因子的基因转录,并且缺乏同源受体C-KIT的小鼠从缺血中恢复的能力受损。给予AdCA5(一种编码组成型活性形式HIF-1α的腺病毒)可使老年小鼠的灌注恢复水平提高至与年轻小鼠相似的水平。将AdCA5注射到非缺血肢体足以增加循环血管生成细胞的数量。这些结果表明,HIF-1活性对于血管生成细胞的动员是必要且充分的,并且HIF-1α基因治疗可以在肢体缺血小鼠模型中抵消衰老的病理效应。