Tension, Free Space, and Cell Damage in a Microfluidic Wound Healing Assay
2011

Cell Movement in Wound Healing Assay

publication Evidence: moderate

Author Information

Author(s): Michael Murrell, Roger Kamm, Paul Matsudaira

Primary Institution: Massachusetts Institute of Technology

Hypothesis

Is the initial driving force for leading edge migration due to the creation of free space or the induction of signaling from cell damage?

Conclusion

Free space alone is sufficient to induce movement, but this movement is predominantly limited to the leading edge.

Supporting Evidence

  • Cells at the leading edge can migrate into free space created by enzymatic denudation.
  • Submarginal cells move slowly and are less persistent compared to those in classical scratch assays.
  • Reactive oxygen species did not restore motility in the presence of free space.

Takeaway

When cells are injured, the ones at the edge can move into the empty space, but the ones further back have a harder time moving.

Methodology

A microfluidic technique was used to enzymatically denude cells and study their migration dynamics in response to free space and chemical factors.

Limitations

The study may not fully replicate the complex environment of natural wound healing due to the controlled conditions of the microfluidic assay.

Digital Object Identifier (DOI)

10.1371/journal.pone.0024283

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