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本文引用的文献

1
Transplantation of hypoxia preconditioned bone marrow mesenchymal stem cells enhances angiogenesis and neurogenesis after cerebral ischemia in rats.缺氧预处理骨髓间充质干细胞移植增强大鼠脑缺血后血管生成和神经发生。
Neurobiol Dis. 2012 Jun;46(3):635-45. doi: 10.1016/j.nbd.2012.03.002. Epub 2012 Mar 9.
2
Various types of stem cells, including a population of very small embryonic-like stem cells, are mobilized into peripheral blood in patients with Crohn's disease.各种类型的干细胞,包括一小群非常类似于胚胎的干细胞,在克罗恩病患者中动员到外周血中。
Inflamm Bowel Dis. 2012 Sep;18(9):1711-22. doi: 10.1002/ibd.22875. Epub 2012 Jan 11.
3
Oxidative stress inflammation and endothelial dysfunction in obstructive sleep apnea.阻塞性睡眠呼吸暂停中的氧化应激、炎症与内皮功能障碍
Front Biosci (Elite Ed). 2012 Jan 1;4(4):1391-403. doi: 10.2741/469.
4
Cardiac stem cells in patients with ischaemic cardiomyopathy (SCIPIO): initial results of a randomised phase 1 trial.缺血性心肌病患者的心脏干细胞(SCIPIO):一项随机 1 期试验的初步结果。
Lancet. 2011 Nov 26;378(9806):1847-57. doi: 10.1016/S0140-6736(11)61590-0. Epub 2011 Nov 14.
5
Early and mid-term effects of obstructive apneas in myocardial injury and inflammation.阻塞性睡眠呼吸暂停对心肌损伤和炎症的早中期影响。
Sleep Med. 2011 Dec;12(10):1037-40. doi: 10.1016/j.sleep.2011.07.009. Epub 2011 Oct 26.
6
Endothelial dysfunction in adults with obstructive sleep apnea.阻塞性睡眠呼吸暂停成年患者的内皮功能障碍
Adv Cardiol. 2011;46:139-170. doi: 10.1159/000325108. Epub 2011 Oct 13.
7
Mesenchymal stem cells: biology, pathophysiology, translational findings, and therapeutic implications for cardiac disease.间质干细胞:生物学、病理生理学、转化研究结果以及在心脏疾病中的治疗意义。
Circ Res. 2011 Sep 30;109(8):923-40. doi: 10.1161/CIRCRESAHA.111.243147.
8
The great migration of bone marrow-derived stem cells toward the ischemic brain: therapeutic implications for stroke and other neurological disorders.骨髓源性干细胞向缺血性脑的巨大迁移:对中风和其他神经障碍的治疗意义。
Prog Neurobiol. 2011 Oct;95(2):213-28. doi: 10.1016/j.pneurobio.2011.08.005. Epub 2011 Aug 30.
9
Endothelial progenitor cells in cardiovascular disease and hypoxia--potential implications to obstructive sleep apnea.心血管疾病和低氧中的内皮祖细胞——对阻塞性睡眠呼吸暂停的潜在影响。
Transl Res. 2011 Jul;158(1):1-13. doi: 10.1016/j.trsl.2010.12.008. Epub 2011 Jan 14.
10
Effect of CPAP on oxidative stress and circulating progenitor cell levels in sleep patients with apnea-hypopnea syndrome.CPAP 对睡眠呼吸暂停低通气综合征患者氧化应激和循环祖细胞水平的影响。
Respir Care. 2011 Nov;56(11):1830-6. doi: 10.4187/respcare.01081. Epub 2011 May 20.

成体干细胞在阻塞性睡眠呼吸暂停中的潜在作用。

Potential role of adult stem cells in obstructive sleep apnea.

作者信息

Almendros Isaac, Carreras Alba, Montserrat Josep M, Gozal David, Navajas Daniel, Farre Ramon

机构信息

CIBER Enfermedades Respiratorias Bunyola, Spain.

出版信息

Front Neurol. 2012 Jul 11;3:112. doi: 10.3389/fneur.2012.00112. eCollection 2012.

DOI:10.3389/fneur.2012.00112
PMID:22807922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3394100/
Abstract

Adult stem cells are undifferentiated cells that can be mobilized from the bone marrow or other organs, home into injured tissues, and differentiate into different cell phenotypes to serve in a repairing capacity. Furthermore, these cells can respond to inflammation and oxidative stress by exhibiting immunomodulatory properties. The protective and reparative roles of mesenchymal stem cells (MSCs), very small embryonic-like stem cells (VSELs), and endothelial progenitor cells (EPCs) have primarily been examined and characterized in auto-immune and cardiovascular diseases. Obstructive sleep apnea (OSA) is a very prevalent disease (4-5% of adult population and 2-3% of children) characterized by an abnormal increase in upper airway collapsibility. Recurrent airway obstructions elicit arterial oxygen desaturations, increased inspiratory efforts, and sleep fragmentation, which have been associated with important long-term neurocognitive, metabolic, and cardiovascular consequences. Since inflammation, oxidative stress and endothelial dysfunction are key factors in the development of the morbid consequences of OSA, bone marrow-derived stem cells could be important modulators of the morbid phenotype by affording a protective role. This mini-review is focused on the recent data available on EPCs, VSELs, and MSCs in both animal models and patients with OSA.

摘要

成体干细胞是未分化的细胞,可从骨髓或其他器官动员出来,归巢至受损组织,并分化为不同的细胞表型以发挥修复功能。此外,这些细胞可通过表现出免疫调节特性来应对炎症和氧化应激。间充质干细胞(MSCs)、极小型胚胎样干细胞(VSELs)和内皮祖细胞(EPCs)的保护和修复作用主要在自身免疫性疾病和心血管疾病中得到研究和表征。阻塞性睡眠呼吸暂停(OSA)是一种非常普遍的疾病(成年人口的4-5%,儿童的2-3%),其特征是上气道可塌陷性异常增加。反复的气道阻塞会引发动脉血氧饱和度下降、吸气努力增加和睡眠碎片化,这些都与重要的长期神经认知、代谢和心血管后果有关。由于炎症、氧化应激和内皮功能障碍是OSA发病后果发展的关键因素,骨髓源性干细胞可能通过发挥保护作用而成为病态表型的重要调节因子。本综述聚焦于动物模型和OSA患者中有关EPCs、VSELs和MSCs的最新数据。