4.7 Article

Circular compartmentalized microfluidic platform: Study of axon-glia interactions

Journal

LAB ON A CHIP
Volume 10, Issue 6, Pages 741-747

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b918640a

Keywords

-

Funding

  1. Johns Hopkins Institute for Nanobiotechnology
  2. Maryland Technology Development Corporation [104307]
  3. National Institutes of Health [1F31NS066753-01]
  4. NIDA [K08DA22946]
  5. NIMH [5P30MH075673]
  6. Howard Hughes Medical Institute Early Career Physician-Scientist
  7. NATIONAL INSTITUTE OF MENTAL HEALTH [P30MH075673] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [F31NS066753] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE ON DRUG ABUSE [K08DA022946] Funding Source: NIH RePORTER

Ask authors/readers for more resources

We describe a compartmentalized circular microfluidic platform that enables directed cell placement within defined microenvironments for the study of axon-glia interactions. The multi-compartment platform consists of independent units of radial microchannel arrays that fluidically isolate somal from axonal compartments. Fluidic access ports punched near the microchannels allow for direct pipetting of cells into the device. Adjacent somal or axonal compartments can be readily merged so that independent groups of neurons or axons can be maintained in either separate or uniform microenvironments. We demonstrate three distinct modes of directed cell placement in this device, to suit varying experimental needs for the study of axon-glia interactions: (1) centrifugation of the circular platform can result in a two-fold increase in axonal throughput in microchannels and provides a new technique to establish axon-glia interactions; (2) microstencils can be utilized to directly place glial cells within areas of interest; and (3) intimate axon-glia co-culture can be attained via standard pipetting techniques. We take advantage of this microfluidic platform to demonstrate a two-fold preferential accumulation of microglia specifically near injured CNS axons, an event implicated in the maintenance and progression of a number of chronic neuroinflammatory and neurodegenerative diseases.

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