4.7 Article

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

Journal

LAB ON A CHIP
Volume 11, Issue 22, Pages 3888-3895

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1lc20549h

Keywords

-

Funding

  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

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available