Chevalier Jacqueline, Yin Hao, Arpino John-Michael, O'Neil Caroline, Nong Zengxuan, Gilmore Kevin J, Lee Jason J, Prescott Emma, Hewak Matthew, Rice Charles L, Dubois Luc, Power Adam H, Hamilton Douglas W, Pickering J Geoffrey
Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada; Department of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, Canada.
Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Canada.
iScience. 2020 Jun 26;23(6):101251. doi: 10.1016/j.isci.2020.101251. Epub 2020 Jun 6.
Critical limb ischemia (CLI) is a hazardous manifestation of atherosclerosis and treatment failure is common. Abnormalities in the arterioles might underlie this failure but the cellular pathobiology of microvessels in CLI is poorly understood. We analyzed 349 intramuscular arterioles in lower limb specimens from individuals with and without CLI. Arteriolar densities were 1.8-fold higher in CLI muscles. However, 33% of small (<20 μm) arterioles were stenotic and 9% were completely occluded. The lumens were closed by bulky, re-oriented endothelial cells expressing abundant N-cadherin that uniquely localized between adjacent and opposing endothelial cells. S100A4 and SNAIL1 were also expressed, supporting an endothelial-to-mesenchymal transition. SMAD2/3 was activated in occlusive endothelial cells and TGFβ1 was increased in the adjacent mural cells. These findings identify a microvascular closure process based on mesenchymal transitions in a hyper-TGFß environment that may, in part, explain the limited success of peripheral artery revascularization procedures.
严重肢体缺血(CLI)是动脉粥样硬化的一种危险表现,治疗失败很常见。小动脉异常可能是治疗失败的原因,但CLI中微血管的细胞病理生物学仍知之甚少。我们分析了有或无CLI个体下肢标本中的349条肌内小动脉。CLI肌肉中的小动脉密度高1.8倍。然而,33%的小(<20μm)动脉出现狭窄,9%完全闭塞。管腔被大量重新定向的内皮细胞封闭,这些内皮细胞表达丰富的N-钙黏蛋白,独特地定位于相邻和相对的内皮细胞之间。还表达了S100A4和SNAIL1,支持内皮向间充质转化。SMAD2/3在闭塞性内皮细胞中被激活,TGFβ1在相邻的壁细胞中增加。这些发现确定了一种基于高TGFβ环境中间充质转化的微血管闭合过程,这可能部分解释了外周动脉血运重建手术成功率有限的原因。