Carrizzo Albino, Procaccini Claudio, Lenzi Paola, Fusco Clorinda, Villa Francesco, Migliarino Serena, De Lucia Massimiliano, Fornai Francesco, Matarese Giuseppe, Puca Annibale A, Vecchione Carmine
1Vascular Pathophysiology Unit, IRCCS Neuromed, 86077 Pozzilli, IS Italy.
2Laboratorio di Immunologia, Istituto di Endocrinologia e Oncologia Sperimentale, Consiglio Nazionale delle Ricerche (IEOS-CNR), Naples, Italy.
Immun Ageing. 2019 Feb 2;16:4. doi: 10.1186/s12979-019-0144-0. eCollection 2019.
Pentraxin 3 (PTX3), an acute-phase inflammation protein produced by several cell types, has long been described as a possible biomarker for age-related cardiovascular and cerebrovascular diseases. Although several mechanisms of action have been identified to date in the vascular and immune systems, the direct effects of PTX3 on isolated endothelial cells at morphological and metabolic levels remain unknown.
PTX3 induced cytoplasmic vacuolization and dilution of mitochondrial matrix in isolated, human endothelial cells. Moreover, metabolic assays revealed that PTX3 increases respiratory capacity in support of mitochondrial function, and partially sustains the glycolytic pathway.
PTX3 has, per se a direct action on ultrastructural and bioenergetic parameters of isolated endothelial cells. This finding can be associated with our previous demonstration of a deleterious effect of PTX3 on the endothelial layer. More studies are needed to clearly demonstrate any direct correlation between these ultrastructural and bioenergetic changes with endothelial dysfunction, especially with regard to age-related cerebro- and cardio-vascular diseases.
五聚体3(PTX3)是一种由多种细胞类型产生的急性期炎症蛋白,长期以来一直被认为可能是与年龄相关的心血管和脑血管疾病的生物标志物。尽管迄今为止已在血管和免疫系统中确定了几种作用机制,但PTX3对分离的内皮细胞在形态和代谢水平上的直接影响仍不清楚。
PTX3在分离的人内皮细胞中诱导细胞质空泡化和线粒体基质稀释。此外,代谢分析表明,PTX3增加呼吸能力以支持线粒体功能,并部分维持糖酵解途径。
PTX3本身对分离的内皮细胞的超微结构和生物能量参数有直接作用。这一发现可能与我们之前证明的PTX3对内皮细胞层的有害作用有关。需要更多的研究来明确证明这些超微结构和生物能量变化与内皮功能障碍之间的任何直接相关性,特别是在与年龄相关的脑血管和心血管疾病方面。