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Parabiosis in Mice: A Detailed Protocol
Published on: October 6, 2013
Cross-circulation and cell distribution kinetics in parabiotic mice
Barry C Gibney1, Kenji Chamoto, Grace S Lee
1Laboratory of Adaptive and Regenerative Biology, Brigham & Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Journal of Cellular Physiology
|April 20, 2011
Summary
Blood-borne nucleated cells are crucial for tissue repair. This study used parabiosis to track cell circulation, revealing no barriers and identifying distinct distribution kinetics in lymphoid organs for different cell types.
Area of Science:
- Immunology
- Cell Biology
- Regenerative Medicine
Background:
- Blood-borne nucleated cells play roles in inflammation, tissue repair, and regeneration.
- The circulation kinetics and tissue distribution of progenitor and stem cells in blood are poorly understood due to their low concentration.
Purpose of the Study:
- To investigate the cross-circulation and cell distribution kinetics of blood cells using a parabiosis model.
- To determine the equilibrium and residence times of various peripheral blood cell subpopulations in lymphoid organs.
Main Methods:
- Utilized C57/B6 GFP(+)/wild-type parabionts for cross-circulation studies.
- Employed flow cytometry to analyze peripheral blood and lymphoid organ cell subpopulations.
- Quantified cell exchange flow rates and distribution kinetics over 28 days.
Main Results:
- No "parabiotic barrier" was observed; all peripheral blood cell subpopulations reached equilibrium within 14 days.
- The mean blood exchange flow rate between parabionts was 16 µl/h (0.66% of circulating volume per hour).
- Differential distribution kinetics were observed in lymphoid organs: CD8(+) and CD11c(+) cells equilibrated within 28 days, while B220(+) and CD4(+) cells had not reached equilibrium.
Conclusions:
- Parabiosis is a valuable model for studying blood cell circulation kinetics and tissue distribution.
- Residence times and recirculating pools of specific lymphocyte subpopulations vary significantly.
- Fluorochrome markers combined with parabiosis offer insights into cell lineage tracking and tissue homing.

