4.7 Article

Valve-based microfluidic compression platform: single axon injury and regrowth

期刊

LAB ON A CHIP
卷 11, 期 22, 页码 3888-3895

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1lc20549h

关键词

-

资金

  1. Johns Hopkins Institute for Nanobiotechnology
  2. Maryland Technology Development Corporation
  3. US National Institutes of Health [1F31NS066753-01]
  4. NIDA [K08DA22946]
  5. Howard Hughes Medical Institute
  6. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [F31NS066753] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE ON DRUG ABUSE [K08DA022946] Funding Source: NIH RePORTER

向作者/读者索取更多资源

We describe a novel valve-based microfluidic axon injury micro-compression (AIM) platform that enables focal and graded compression of micron-scale segments of single central nervous system (CNS) axons. The device utilizes independently controlled push-down injury pads that descend upon pressure application and contact underlying axonal processes. Regulated compressed gas is input into the AIM system and pressure levels are modulated to specify the level of injury. Finite element modeling (FEM) is used to quantitatively characterize device performance and parameterize the extent of axonal injury by estimating the forces applied between the injury pad and glass substrate. In doing so, injuries are normalized across experiments to overcome small variations in device geometry. The AIM platform permits, for the first time, observation of axon deformation prior to, during, and immediately after focal mechanical injury. Single axons acutely compressed (similar to 5 s) under varying compressive loads (0-250 kPa) were observed through phase time-lapse microscopy for up to 12 h post injury. Under mild injury conditions (< 55 kPa) similar to 73% of axons continued to grow, while at moderate (55-95 kPa) levels of injury, the number of growing axons dramatically reduced to 8%. At severe levels of injury (> 95 kPa), virtually all axons were instantaneously transected and nearly half (similar to 46%) of these axons were able to regrow within the imaging period in the absence of exogenous stimulating factors.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据