Department of Medicine, Division of Cardiovascular, Respiratory and Neurology, Asahikawa Medical University, Asahikawa, Japan.
Department of Cardiovascular Regeneration and Innovation, Asahikawa Medical University, Asahikawa, Japan.
Biochem Biophys Res Commun. 2014 Jan 3;443(1):150-5. doi: 10.1016/j.bbrc.2013.11.070. Epub 2013 Dec 2.
An immature vasa vasorum in the adventitia of arteries has been implicated in induction of the formation of unstable atherosclerotic plaques. Normalization/maturation of the vasa vasorum may be an attractive therapeutic approach for arteriosclerotic diseases. Nerve growth factor (NGF) is a pleotropic molecule with angiogenic activity in addition to neural growth effects. However, whether NGF affects the formation of microvessels in addition to innervation during pathological angiogenesis is unclear. In the present study, we show a new role for NGF in neovessels around injured arterial walls using a novel in vivo angiogenesis assay. The vasa vasorum around arterial walls was induced to grow using wire-mediated mouse femoral arterial injury. When collagen-coated tube (CCT) was placed beside the injured artery for 7-14 days, microvessels grew two-dimensionally in a thin layer on the CCT (CCT-membrane) in accordance with the development of the vasa vasorum. The perivascular nerve was found at not only arterioles but also capillaries in the CCT-membrane. Biodegradable hydrogels containing VEGF and NGF were applied around the injured artery/CCT. VEGF significantly increased the total length and instability of microvessels within the CCT-membrane. In contrast, NGF induced regeneration of the peripheral nerve around the microvessels and induced the maturation and stabilization of microvessels. In an ex vivo nerve-free angiogenesis assay, although NGF potentially stimulated vascular sprouting from aorta tissues, no effects of NGF on vascular maturation were observed. These data demonstrated that NGF had potent angiogenic effects on the microvessels around the injured artery, and especially induced the maturation/stabilization of microvessels in accordance with the regeneration of perivascular nerves.
血管外膜中的不成熟血管周细胞被认为参与了不稳定粥样斑块的形成。血管周细胞的正常化/成熟可能是动脉粥样硬化疾病的一种有吸引力的治疗方法。神经生长因子(NGF)是一种多效分子,除了具有神经生长作用外,还有血管生成活性。然而,NGF 是否除了在病理性血管生成中的神经支配外还影响微血管的形成尚不清楚。在本研究中,我们使用一种新的体内血管生成测定法,在受伤的动脉壁周围的新血管中显示了 NGF 的一个新作用。使用线介导的小鼠股动脉损伤诱导动脉壁周围的血管周细胞生长。当将涂有胶原蛋白的管(CCT)放置在受伤的动脉旁边 7-14 天时,微脉管系统在 CCT(CCT 膜)上二维生长,与血管周细胞的发育一致。在 CCT 膜中的毛细血管中,发现了血管周神经不仅位于小动脉中。将含有 VEGF 和 NGF 的可生物降解水凝胶应用于受伤的动脉/CCT 周围。VEGF 显著增加了 CCT 膜内微血管的总长度和不稳定性。相比之下,NGF 诱导了微血管周围外周神经的再生,并诱导了微血管的成熟和稳定。在体外无神经血管生成测定中,尽管 NGF 可能刺激了来自主动脉组织的血管发芽,但未观察到 NGF 对血管成熟的影响。这些数据表明,NGF 对受伤动脉周围的微血管具有强大的血管生成作用,并且特别诱导了与血管周神经再生一致的微血管的成熟/稳定。