Impact and mechanisms of drag-reducing polymers on shear stress regulation in pulmonary hypertension.

Yali Wang, Qing Ye, Yongqi Cui, Yunjiang Wu, Sipei Cao, Feng Hu
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Abstract

Background: Pulmonary hypertension (PH) is a refractory disease characterized by elevated pulmonary artery pressure and resistance. Drag-reducing polymers (DRPs) are blood-soluble macromolecules that reduce vascular resistance by altering the blood dynamics and rheology. Our previous work indicated that polyethylene oxide (PEO) can significantly reduce the medial wall thickness and vascular resistance of the pulmonary arteries, but the specific mechanism is still unclear.

Methods: This study was designed to investigate the role and mechanism of PEO on intracellular calcium [Ca2 +] i and cytoskeletal proteins of endothelial cells (ECs) induced by low shear stress (LSS) in PH. Primary Pulmonary Artery Endothelial Cells (PAECs) were subjected to steady LSS (1 dyn/cm2) or physiological shear stress (SS) (10 dyn/cm2) for 20 h in a BioFlux 200 flow system. Calcium influx assays were conducted to evaluate the mechanisms of PEO on [Ca2 +] i. Subsequently, taking the key protein that induces cytoskeletal remodeling, the regulatory light chain (RLC) phosphorylation, as the breakthrough point, this study focused on the two key pathways of PEO that regulate phosphorylation of RLC: Myosin light chain kinase (MLCK) and Rho-associated kinase (ROCK) pathways.

Results: Our current research revealed that PEO at LSS (1 dyn/cm2) significantly suppressed LSS-induced [Ca2 +] i and the expression level of transient receptor potential channel 1(TRPC1). In addition, ECs convert LSS stimuli into the upregulation of cytoskeletal proteins, including filamentous actin (F-actin), MLCK, ROCK, p-RLC, and pp-RLC. Further experiments using pharmacological inhibitors demonstrated that PEO at the LSS downregulated cytoskeleton-related proteins mainly through the ROCK and MLCK pathways.

Conclusions: This study considered intracellular calcium and cytoskeleton rearrangement as entry points to study the application of PEO in the biomedical field, which has important theoretical significance and practical application value for the treatment of PH.

减阻聚合物对肺动脉高压剪切应力调节的影响和机制。
背景:肺动脉高压(PH)是一种以肺动脉压力和阻力升高为特征的难治性疾病。降阻聚合物(DRP)是一种可溶于血液的大分子,可通过改变血液动力学和流变学来降低血管阻力。我们之前的研究表明,聚环氧乙烷(PEO)能显著降低肺动脉内侧壁厚度和血管阻力,但具体机制仍不清楚:本研究旨在探讨 PEO 对低剪切应力(LSS)诱导的 PH 内皮细胞(ECs)胞内钙[Ca2 +] i 和细胞骨架蛋白的作用和机制。原代肺动脉内皮细胞(PAECs)在 BioFlux 200 流量系统中接受稳定的低剪切应力(1 dyn/cm2)或生理剪切应力(SS)(10 dyn/cm2)20 小时。随后,本研究以诱导细胞骨架重塑的关键蛋白--调节轻链(RLC)磷酸化为突破点,重点研究了PEO调节RLC磷酸化的两个关键途径:肌球蛋白轻链激酶(MLCK)和Rho相关激酶(ROCK)途径:我们目前的研究发现,LSS(1 dyn/cm2)条件下的PEO能显著抑制LSS诱导的[Ca2 +] i和瞬时受体电位通道1(TRPC1)的表达水平。此外,心血管细胞将 LSS 刺激转化为细胞骨架蛋白的上调,包括丝状肌动蛋白(F-actin)、MLCK、ROCK、pp-RLC 和 pp-RLC。使用药理抑制剂进行的进一步实验表明,LSS 处的 PEO 主要通过 ROCK 和 MLCK 途径下调细胞骨架相关蛋白:本研究将细胞内钙离子和细胞骨架重排作为研究PEO在生物医学领域应用的切入点,对PH的治疗具有重要的理论意义和实际应用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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