Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Sci Rep. 2017 May 16;7(1):1952. doi: 10.1038/s41598-017-02107-2.
Glial scar is a significant barrier to neural implant function. Micromotion between the implant and tissue is suspected to be a key driver of glial scar formation around neural implants. This study explores the ability of soft hydrogel coatings to modulate glial scar formation by reducing local strain. PEG hydrogels with controllable thickness and elastic moduli were formed on the surface of neural probes. These coatings significantly reduced the local strain resulting from micromotion around the implants. Coated implants were found to significantly reduce scarring in vivo, compared to hard implants of identical diameter. Increasing implant diameter was found to significantly increase scarring for glass implants, as well as increase local BBB permeability, increase macrophage activation, and decrease the local neural density. These results highlight the tradeoff in mechanical benefit with the size effects from increasing the overall diameter following the addition of a hydrogel coating. This study emphasizes the importance of both mechanical and geometric factors of neural implants on chronic timescales.
胶质瘢痕是神经植入物功能的重大障碍。植入物和组织之间的微动被怀疑是神经植入物周围胶质瘢痕形成的关键驱动因素。本研究通过降低局部应变来探索软水凝胶涂层调节胶质瘢痕形成的能力。在神经探针表面形成了具有可控厚度和弹性模量的 PEG 水凝胶。这些涂层显著降低了植入物周围微动引起的局部应变。与相同直径的硬植入物相比,涂层植入物在体内显著减少了瘢痕形成。研究发现,对于玻璃植入物,增加植入物直径会显著增加瘢痕形成,同时增加局部 BBB 通透性、增加巨噬细胞激活,并降低局部神经密度。这些结果强调了在添加水凝胶涂层后增加整体直径带来的机械益处与尺寸效应之间的权衡。本研究强调了神经植入物在慢性时间尺度上的机械和几何因素的重要性。