Second Harmonic Generation Imaging of Collagen in Chronically Implantable Electrodes in Brain Tissue

被引:24
作者
Esquibel, Corinne R. [1 ]
Wendt, Kristy D. [1 ]
Lee, Heui C. [2 ,3 ]
Gaire, Janak [4 ]
Shoffstall, Andrew [5 ,6 ]
Urdaneta, Morgan E. [4 ]
Chacko, Jenu, V [1 ]
Brodnick, Sarah K. [1 ]
Otto, Kevin J. [3 ,4 ]
Capadona, Jeffrey R. [5 ,6 ]
Williams, Justin C. [1 ]
Eliceiri, K. W. [1 ,7 ,8 ]
机构
[1] Univ Wisconsin, Dept Biomed Engn, Lab Opt & Computat Instrumentat, Madison, WI 53706 USA
[2] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
[3] Univ Florida, J Crayton Pruitt Family Dept Biomed Engn, Gainesville, FL USA
[4] Univ Florida, Dept Neurosci, Gainesville, FL 32610 USA
[5] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[6] Louis Stokes Cleveland Dept Vet Affairs Med Ctr, Adv Platform Technol Ctr, Cleveland, OH USA
[7] Morgridge Inst Res, Madison, WI 53715 USA
[8] Univ Wisconsin, Dept Med Phys, 1530 Med Sci Ctr, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
second harmonic generation; collagen; glial scar; imaging; implantable device; EXTRACELLULAR-MATRIX; GLIAL SCARS; LONG-TERM; IN-VIVO; REGENERATION; ASTROCYTES; MICROSCOPY; INJURY; CELLS; RAT;
D O I
10.3389/fnins.2020.00095
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Advances in neural engineering have brought about a number of implantable devices for improved brain stimulation and recording. Unfortunately, many of these micro-implants have not been adopted due to issues of signal loss, deterioration, and host response to the device. While glial scar characterization is critical to better understand the mechanisms that affect device functionality or tissue viability, analysis is frequently hindered by immunohistochemical tissue processing methods that result in device shattering and tissue tearing artifacts. Devices are commonly removed prior to sectioning, which can itself disturb the quality of the study. In this methods implementation study, we use the label free, optical sectioning method of second harmonic generation (SHG) to examine brain slices of various implanted intracortical electrodes and demonstrate collagen fiber distribution not found in normal brain tissue. SHG can easily be used in conjunction with multiphoton microscopy to allow direct intrinsic visualization of collagen-containing glial scars on the surface of cortically implanted electrode probes without imposing the physical strain of tissue sectioning methods required for other high resolution light microscopy modalities. Identification and future measurements of these collagen fibers may be useful in predicting host immune response and device signal fidelity.
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页数:8
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