Department of Surgery University of Wisconsin-Madison Madison WI.
Department of Biomedical Engineering University of Wisconsin-Madison Madison WI.
J Am Heart Assoc. 2023 Feb 7;12(3):e028121. doi: 10.1161/JAHA.122.028121. Epub 2023 Feb 3.
Combined pre-/postcapillary pulmonary hypertension (Cpc-PH), a complication of left heart failure, is associated with higher mortality rates than isolated postcapillary pulmonary hypertension alone. Currently, knowledge gaps persist on the mechanisms responsible for the progression of isolated postcapillary pulmonary hypertension (Ipc-PH) to Cpc-PH. Here, we review the biomechanical and mechanobiological impact of left heart failure on pulmonary circulation, including mechanotransduction of these pathological forces, which lead to altered biological signaling and detrimental remodeling, driving the progression to Cpc-PH. We focus on pathologically increased cyclic stretch and decreased wall shear stress; mechanotransduction by endothelial cells, smooth muscle cells, and pulmonary arterial fibroblasts; and signaling-stimulated remodeling of the pulmonary veins, capillaries, and arteries that propel the transition from Ipc-PH to Cpc-PH. Identifying biomechanical and mechanobiological mechanisms of Cpc-PH progression may highlight potential pharmacologic avenues to prevent right heart failure and subsequent mortality.
左心衰竭引起的混合性毛细血管前/后肺动脉高压(Cpc-PH)比单纯性毛细血管后肺动脉高压(Ipc-PH)的死亡率更高。目前,对于孤立性毛细血管后肺动脉高压(Ipc-PH)进展为 Cpc-PH 的机制仍存在知识空白。在这里,我们回顾了左心衰竭对肺循环的生物力学和力学生物学影响,包括这些病理力的力学转导,导致改变的生物学信号和有害重塑,从而推动向 Cpc-PH 的进展。我们重点关注病理性增加的循环拉伸和减少的壁面切应力;内皮细胞、平滑肌细胞和肺动脉成纤维细胞的力学转导;以及信号刺激的肺静脉、毛细血管和动脉重塑,推动从 Ipc-PH 向 Cpc-PH 的转变。确定 Cpc-PH 进展的生物力学和力学生物学机制可能突出潜在的药理学途径,以预防右心衰竭和随后的死亡率。