Thompson Matthew J, Patel Gaurangkumar, Isaacs Jonathan, McMurtry John, Richards Nathan, Daner William
a Division of Hand Surgery, Department of Orthopaedic Surgery , Virginia Commonwealth University Medical Center , Richmond , VA , USA.
Neurol Res. 2017 Mar;39(3):189-197. doi: 10.1080/01616412.2017.1282336. Epub 2017 Jan 23.
Processing necessary to remove immunogenic components of nerve allograft renders it acellular. Seeding with supportive cells may improve axon regeneration. We aim to identify the method associated with implantation of the greatest volume and most even distribution of cells.
Hypodermic needle injection was compared to soaking in solution under both normal and pressurized conditions after micropuncture of the allograft. Distribution within the allograft was measured using an in vitro model of fluorescent beads, as well as cultured Schwann cells.
Injection treatment resulted in larger volumes and a more uniform cross-sectional distribution of implanted cells. Beads and cells behaved similarly relative to the measured outcomes.
Injection instills more cells in a more uniform distribution. In vivo testing may evaluate whether these techniques vary relative to cell survival, cell migration, and clinical outcomes. Size- and concentration-matched fluorescent beads may represent a viable model for analyzing cell implantation.
去除神经同种异体移植物免疫原性成分所需的处理使其成为无细胞状态。接种支持细胞可能会改善轴突再生。我们旨在确定与植入最大体积且分布最均匀的细胞相关的方法。
在对同种异体移植物进行微穿刺后,将皮下注射针注射与在正常和加压条件下浸泡于溶液中进行比较。使用荧光珠体外模型以及培养的雪旺细胞测量同种异体移植物内的分布情况。
注射处理导致植入细胞的体积更大且横截面分布更均匀。相对于测量结果,珠子和细胞的表现相似。
注射能以更均匀的分布注入更多细胞。体内测试可评估这些技术在细胞存活、细胞迁移和临床结果方面是否存在差异。尺寸和浓度匹配的荧光珠可能是分析细胞植入的可行模型。