The Use of Spinning-Disk Confocal Microscopy for the Intravital Analysis of Platelet Dynamics in Response to Systemic and Local Inflammation
2011

Studying Platelet Dynamics in Inflammation

publication 10 minutes Evidence: high

Author Information

Author(s): Jenne Craig N., Wong Connie H. Y., Petri Björn, Kubes Paul

Primary Institution: University of Calgary

Hypothesis

Can new methods for visualizing platelets in vivo improve our understanding of their role in inflammation?

Conclusion

The study successfully demonstrates new techniques for visualizing platelet dynamics in response to inflammation, revealing their interactions with neutrophils and other cells.

Supporting Evidence

  • Platelets were observed to form large aggregates in response to LPS-induced inflammation.
  • New methods allowed for real-time visualization of platelet interactions with neutrophils.
  • CD49b was identified as a suitable marker for in vivo platelet labeling without affecting their function.

Takeaway

Researchers found new ways to see how platelets behave during inflammation, showing that they interact a lot with other immune cells.

Methodology

The study used spinning-disk confocal microscopy to visualize platelets in live mice, employing anti-CD49b antibodies for labeling.

Potential Biases

Potential bias in interpreting platelet behavior due to the use of specific labeling techniques.

Limitations

The study primarily focused on mouse models, which may not fully represent human physiology.

Participant Demographics

Mice aged 7-10 weeks, weighing 20-30 g.

Statistical Information

P-Value

p<0.001

Statistical Significance

p<0.001

Digital Object Identifier (DOI)

10.1371/journal.pone.0025109

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication