Laboratory of Veterinary Pharmacology, School of Veterinary Medicine, Kitasato University, Towada, Aomori, 034-0828, Japan.
Laboratory of Veterinary Pharmacology, School of Veterinary Medicine, Kitasato University, Towada, Aomori, 034-0828, Japan.
Biochem Biophys Res Commun. 2018 Sep 5;503(2):776-783. doi: 10.1016/j.bbrc.2018.06.075. Epub 2018 Jun 22.
Exosomes, the smallest extracellular vesicle, contain various molecules and mediate cell-cell communication. A number of studies demonstrate exosomes are involved in important physiological and pathological processes. Moreover, microRNA (miRNA) regulating hypertension development through the suppression of certain translation was recently reported. However, roles of exosomes containing various molecules including miRNA on development of essential hypertension have not been examined. We tested the hypothesis that plasma exosomes regulate systemic blood pressure in normotensive and spontaneously hypertensive rats (SHR). Normotensive Wistar Kyoto rats (WKY) and SHR (5-10-week-old) were intraperitoneally administrated with exosomes derived from plasma in WKY or SHR weekly for 6 weeks. Exosomes were isolated by an ultracentrifuge method. SHR-derived exosomes significantly increased systolic blood pressure in WKY, while WKY-derived exosomes decreased it in SHR. In WKY, SHR-derived exosomes induced modest structural changes of thoracic aorta, such as wall thickening and decreased abundance of collagen, which were similar to the changes observed in SHR. On the contrary, WKY-derived exosomes tended to reverse the changes in SHR. WKY-derived exosomes significantly suppressed the increased prostaglandin F-induced contraction of mesenteric arterial smooth muscle in SHR. In addition, wet weight and perivascular fibrosis of left ventricles in WKY were significantly increased by SHR-derived exosomes, while the fibrosis but not ventricular weight was significantly decreased by WKY-derived exosomes in SHR. We for the first time demonstrated that plasma exosomes can modulate systemic blood pressure as well as structure and function of cardiovascular tissues in both normotensive and hypertensive rats.
外泌体是最小的细胞外囊泡,包含各种分子,并介导细胞间通讯。许多研究表明外泌体参与重要的生理和病理过程。此外,最近有研究报道,miRNA 通过抑制某些翻译来调节高血压的发生。然而,包含 miRNA 等各种分子的外泌体在原发性高血压发展中的作用尚未得到检验。我们检验了这样一个假设,即血浆外泌体调节正常血压和自发性高血压大鼠(SHR)的全身血压。正常血压的 Wistar 京都大鼠(WKY)和 SHR(5-10 周龄)每周经腹腔给予来自 WKY 或 SHR 血浆的外泌体,共 6 周。通过超速离心法分离外泌体。SHR 来源的外泌体可显著增加 WKY 的收缩压,而 WKY 来源的外泌体则降低 SHR 的收缩压。在 WKY 中,SHR 来源的外泌体引起胸主动脉的轻微结构变化,如壁增厚和胶原减少,与 SHR 中观察到的变化相似。相反,WKY 来源的外泌体倾向于逆转 SHR 的变化。WKY 来源的外泌体显著抑制了 SHR 肠系膜动脉平滑肌中前列腺素 F 诱导的收缩增加。此外,SHR 来源的外泌体显著增加了 WKY 的左心室湿重和血管周围纤维化,而 WKY 来源的外泌体则显著降低了 SHR 的纤维化但不降低心室重量。我们首次证明,血浆外泌体可以调节正常血压以及正常血压和高血压大鼠的心血管组织的结构和功能。