首页> 美国卫生研究院文献>Journal of Cerebral Blood Flow Metabolism >Novel method to study pericyte contractility and responses to ischaemia in vitro using electrical impedance
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Novel method to study pericyte contractility and responses to ischaemia in vitro using electrical impedance

机译:利用电阻抗研究体外周细胞收缩力和对缺血的反应的新方法

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摘要

Pericytes are contractile vascular mural cells overlying capillary endothelium, and they have been implicated in a variety of functions including regulation of cerebral blood flow. Recent work has suggested that both in vivo and ex vivo, ischaemia causes pericytes to constrict and die, which has implications for microvascular reperfusion. Assessing pericyte contractility in tissue slices and in vivo is technically challenging, while in vitro techniques remain unreliable. Here, we used isolated cultures of human brain vascular pericytes to examine their contractile potential in vitro using the iCelligence electrical impedance system. Contraction was induced using the vasoactive peptide endothelin-1, and relaxation was demonstrated using adenosine and sodium nitroprusside. Endothelin-1 treatment also resulted in increased proliferation, which we were able to monitor in the same cell population from which we recorded contractile responses. Finally, the observation of pericyte contraction in stroke was reproduced using chemical ischaemia, which caused a profound and irreversible contraction clearly preceding cell death. These data demonstrate that isolated pericytes retain a contractile phenotype in vitro, and that it is possible to quantify this contraction using real-time electrical impedance recordings, providing a significant new platform for assessing the effects of vasoactive and vasculoprotective compounds on pericyte contractility.
机译:周细胞是覆盖在毛细血管内皮上的收缩性血管壁细胞,它们与多种功能有关,包括调节脑血流量。最近的研究表明,在体内和体外,局部缺血都会导致周细胞收缩和死亡,这对微血管再灌注具有影响。评估组织切片和体内周细胞的收缩力在技术上具有挑战性,而体外技术仍然不可靠。在这里,我们使用iCelligence电阻抗系统在人脑血管周细胞的分离培养物中检查了它们的体外收缩潜能。使用血管活性肽内皮素-1诱导收缩,并使用腺苷和硝普钠证明松弛。内皮素-1处理也导致增殖增加,我们能够在记录收缩反应的相同细胞群中进行监测。最后,中风时周细胞收缩的观察结果是用化学缺血法重现的,它在细胞死亡之前就引起了深刻而不可逆的收缩。这些数据表明分离的周细胞在体外保留了收缩表型,并且可以使用实时电阻抗记录来量化该收缩,为评估血管活性和血管保护性化合物对周细胞收缩性的影响提供了重要的新平台。

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