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脑皮质内植入物周围的脑膜炎症反应和纤维组织重塑:体内双光子成像研究。

Meningeal inflammatory response and fibrous tissue remodeling around intracortical implants: An in vivo two-photon imaging study.

机构信息

Bioengineering, University of Pittsburgh, United States; Center for the Neural Basis of Cognition, University of Pittsburgh and Carnegie Mellon University, United States.

Bioengineering, University of Pittsburgh, United States; Center for the Neural Basis of Cognition, University of Pittsburgh and Carnegie Mellon University, United States; Radiology, University of Pittsburgh, United States.

出版信息

Biomaterials. 2019 Mar;195:111-123. doi: 10.1016/j.biomaterials.2018.12.031. Epub 2018 Dec 31.

Abstract

Meningeal inflammation and encapsulation of neural electrode arrays is a leading cause of device failure, yet little is known about how it develops over time or what triggers it. This work characterizes the dynamic changes of meningeal inflammatory cells and collagen-I in order to understand the meningeal tissue response to neural electrode implantation. We use in vivo two-photon microscopy of CX3CR1-GFP mice over the first month after electrode implantation to quantify changes in inflammatory cell behavior as well as meningeal collagen-I remodeling. We define a migratory window during the first day after electrode implantation hallmarked by robust inflammatory cell migration along electrodes in the meninges as well as cell trafficking through meningeal venules. This migratory window attenuates by 2 days post-implant, but over the next month, the meningeal collagen-I remodels to conform to the surface of the electrode and thickens. This work shows that there are distinct time courses for initial meningeal inflammatory cell infiltration and meningeal collagen-I remodeling. This may indicate a therapeutic window early after implantation for modulation and mitigation of meningeal inflammation.

摘要

脑膜炎症和神经电极阵列的包裹是导致设备故障的主要原因,但对于其随时间如何发展以及是什么引发了这种情况,人们知之甚少。本研究旨在描述脑膜炎症细胞和 I 型胶原的动态变化,以了解脑膜组织对神经电极植入的反应。我们在植入电极后的第一个月内,使用 CX3CR1-GFP 小鼠的活体双光子显微镜来量化炎症细胞行为以及脑膜 I 型胶原重塑的变化。我们定义了一个迁移窗口,即在电极植入后的第一天,炎症细胞沿着脑膜中的电极强烈迁移,并通过脑膜小静脉进行细胞迁移。这个迁移窗口在植入后 2 天减弱,但在接下来的一个月里,脑膜 I 型胶原重塑以适应电极的表面并变厚。这项工作表明,脑膜炎症细胞浸润和脑膜 I 型胶原重塑存在明显的时间进程。这可能表明在植入后的早期存在治疗窗口,可用于调节和减轻脑膜炎症。

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