University of Colorado Denver - Pediatric Critical Care, Aurora, Colorado, USA.
Compr Physiol. 2011 Jan;1(1):141-61. doi: 10.1002/cphy.c090017.
A rapidly emerging concept is that the vascular adventitia acts as a biological processing center for the retrieval, integration, storage, and release of key regulators of vessel wall function. It is the most complex compartment of the vessel wall and comprises a variety of cells including fibroblasts, immunomodulatory cells, resident progenitor cells, vasa vasorum endothelial cells, and adrenergic nerves. In response to vascular stress or injury, resident adventitial cells are often the first to be activated and reprogrammed to then influence tone and structure of the vessel wall. Experimental data indicate that the adventitial fibroblast, the most abundant cellular constituent of adventitia, is a critical regulator of vascular wall function. In response to vascular stresses such as overdistension, hypoxia, or infection, the adventitial fibroblast is activated and undergoes phenotypic changes that include proliferation, differentiation, and production of extracellular matrix proteins and adhesion molecules, release of reactive oxygen species, chemokines, cytokines, growth factors, and metalloproteinases that, collectively, affect medial smooth muscle cell tone and growth directly and that stimulate recruitment and retention of circulating inflammatory and progenitor cells to the vessel wall. Resident dendritic cells also participate in "sensing" vascular stress and actively communicate with fibroblasts and progenitor cells to simulate repair processes that involve expansion of the vasa vasorum, which acts as a conduit for further delivery of inflammatory/progenitor cells. This review presents the current evidence demonstrating that the adventitia acts as a key regulator of pulmonary vascular wall function and structure from the "outside in."
一个迅速兴起的概念是血管外膜作为血管壁功能关键调节因子的提取、整合、储存和释放的生物处理中心。它是血管壁最复杂的部分,包含多种细胞,包括成纤维细胞、免疫调节细胞、固有祖细胞、血管周围腔内皮细胞和肾上腺素能神经。在血管应激或损伤时,固有外膜细胞通常是最早被激活和重新编程的细胞,从而影响血管壁的张力和结构。实验数据表明,外膜成纤维细胞是外膜中最丰富的细胞成分,是血管壁功能的关键调节因子。对外膜成纤维细胞的刺激包括过度膨胀、缺氧或感染等血管应激,导致其激活并发生表型变化,包括增殖、分化和细胞外基质蛋白和黏附分子的产生、活性氧物质、趋化因子、细胞因子、生长因子和金属蛋白酶的释放,这些物质共同直接影响中膜平滑肌细胞的张力和生长,并刺激循环炎症细胞和祖细胞向血管壁募集和保留。固有树突状细胞也参与“感知”血管应激,并与成纤维细胞和祖细胞积极交流,模拟修复过程,包括血管周围腔的扩张,作为进一步输送炎症/祖细胞的通道。这篇综述提出了目前的证据,证明外膜作为一个“从外到内”的关键调节因子,调节肺血管壁的功能和结构。