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The density difference between tissue and neural probes is a key factor for glial scarring

机译:组织和神经探针之间的密度差异是神经胶质瘢痕形成的关键因素

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A key to successful chronic neural interfacing is to achieve minimal glial scarring surrounding the implants, as the astrocytes and microglia may functionally insulate the interface. A possible explanation for the development of these reactions is mechanical forces arising between the implants and the brain. Here, we show that the difference between the density of neural probes and that of the tissue, and the resulting inertial forces, are key factors for the development of the glial scar. Two probes of similar size, shape, surface structure and elastic modulus but differing greatly in density were implanted into the rat brain. After six weeks, significantly lower astrocytic and microglial reactions were found surrounding the low-density probes, approaching no reaction at all. This provides a major key to design fully biocompatible neural interfaces and a new platform for in vivo assays of tissue reactions to probes with differing materials, surface structures, and shapes.
机译:成功的慢性神经接口的关键是使星形胶质细胞和小胶质细胞在功能上隔离界面,从而使植入物周围的神经胶质瘢痕最少。这些反应发展的可能解释是在植入物和大脑之间产生的机械力。在这里,我们表明神经探针和组织的密度之间的差异以及所产生的惯性力是神经胶质瘢痕发展的关键因素。将两种大小,形状,表面结构和弹性模量相似但密度相差很大的探针植入大鼠脑中。六周后,发现低密度探针周围的星形胶质细胞和小胶质细胞反应明显降低,根本没有反应。这提供了设计完全生物相容性神经接口的主要钥匙,以及用于体内分析组织反应到具有不同材料,表面结构和形状的探针的新平台。

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