Khalyfa Abdelnaby, Sanz-Rubio David
Department of Child Health and the Child Health Research Institute, University of Missouri School of Medicine, Columbia, MO 65201, USA.
Translational Research Unit, Hospital Universitario Miguel Servet, Instituto de Investigación Sanitaria de Aragón (IISAragón), 50009 Zaragoza, Spain.
Int J Mol Sci. 2021 Apr 21;22(9):4301. doi: 10.3390/ijms22094301.
Sleep is very important for overall health and quality of life, while sleep disorder has been associated with several human diseases, namely cardiovascular, metabolic, cognitive, and cancer-related alterations. Obstructive sleep apnea (OSA) is the most common respiratory sleep-disordered breathing, which is caused by the recurrent collapse of the upper airway during sleep. OSA has emerged as a major public health problem and increasing evidence suggests that untreated OSA can lead to the development of various diseases including neurodegenerative diseases. In addition, OSA may lead to decreased blood oxygenation and fragmentation of the sleep cycle. The formation of free radicals or reactive oxygen species (ROS) can emerge and react with nitric oxide (NO) to produce peroxynitrite, thereby diminishing the bioavailability of NO. Hypoxia, the hallmark of OSA, refers to a decline of tissue oxygen saturation and affects several types of cells, playing cell-to-cell communication a vital role in the outcome of this interplay. Red blood cells (RBCs) are considered transporters of oxygen and nutrients to the tissues, and these RBCs are important interorgan communication systems with additional functions, including participation in the control of systemic NO metabolism, redox regulation, blood rheology, and viscosity. RBCs have been shown to induce endothelial dysfunction and increase cardiac injury. The mechanistic links between changes of RBC functional properties and cardiovascular are largely unknown. Extracellular vesicles (EVs) are secreted by most cell types and released in biological fluids both under physiological and pathological conditions. EVs are involved in intercellular communication by transferring complex cargoes including proteins, lipids, and nucleic acids from donor cells to recipient cells. Advancing our knowledge about mechanisms of RBC-EVs formation and their pathophysiological relevance may help to shed light on circulating EVs and to translate their application to clinical practice. We will focus on the potential use of RBC-EVs as valuable diagnostic and prognostic biomarkers and state-specific cargoes, and possibilities as therapeutic vehicles for drug and gene delivery. The use of RBC-EVs as a precision medicine for the diagnosis and treatment of the patient with sleep disorder will improve the prognosis and the quality of life in patients with cardiovascular disease (CVD).
睡眠对整体健康和生活质量非常重要,而睡眠障碍与多种人类疾病相关,即心血管、代谢、认知和癌症相关的改变。阻塞性睡眠呼吸暂停(OSA)是最常见的呼吸性睡眠障碍性呼吸,由睡眠期间上呼吸道反复塌陷引起。OSA已成为一个主要的公共卫生问题,越来越多的证据表明,未经治疗的OSA可导致包括神经退行性疾病在内的各种疾病的发生。此外,OSA可能导致血液氧合降低和睡眠周期碎片化。自由基或活性氧(ROS)的形成会出现并与一氧化氮(NO)反应生成过氧亚硝酸盐,从而降低NO的生物利用度。低氧是OSA的标志,指组织氧饱和度下降,影响多种类型的细胞,在这种相互作用的结果中,细胞间通讯起着至关重要的作用。红细胞(RBCs)被认为是氧气和营养物质向组织的转运体,这些红细胞是重要的器官间通讯系统,具有额外的功能,包括参与全身NO代谢的控制、氧化还原调节、血液流变学和粘度。红细胞已被证明会导致内皮功能障碍并增加心脏损伤。红细胞功能特性变化与心血管之间的机制联系在很大程度上尚不清楚。细胞外囊泡(EVs)由大多数细胞类型分泌,并在生理和病理条件下释放到生物体液中。EVs通过将包括蛋白质、脂质和核酸在内的复杂货物从供体细胞转移到受体细胞来参与细胞间通讯。增进我们对红细胞-EV形成机制及其病理生理相关性的了解,可能有助于阐明循环中的EVs,并将其应用转化为临床实践。我们将专注于红细胞-EV作为有价值的诊断和预后生物标志物以及特定状态货物的潜在用途,以及作为药物和基因递送治疗载体的可能性。将红细胞-EV用作睡眠障碍患者诊断和治疗的精准药物,将改善心血管疾病(CVD)患者的预后和生活质量。