Loading…
Long-range ordered vorticity patterns in living tissue induced by cell division
In healthy blood vessels with a laminar blood flow, the endothelial cell division rate is low, only sufficient to replace apoptotic cells. The division rate significantly increases during embryonic development and under halted or turbulent flow. Cells in barrier tissue are connected and their motili...
Saved in:
Published in: | Nature communications 2014-12, Vol.5 (1), p.5720-5720, Article 5720 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | In healthy blood vessels with a laminar blood flow, the endothelial cell division rate is low, only sufficient to replace apoptotic cells. The division rate significantly increases during embryonic development and under halted or turbulent flow. Cells in barrier tissue are connected and their motility is highly correlated. Here we investigate the long-range dynamics induced by cell division in an endothelial monolayer under non-flow conditions, mimicking the conditions during vessel formation or around blood clots. Cell divisions induce long-range, well-ordered vortex patterns extending several cell diameters away from the division site, in spite of the system’s low Reynolds number. Our experimental results are reproduced by a hydrodynamic continuum model simulating division as a local pressure increase corresponding to a local tension decrease. Such long-range physical communication may be crucial for embryonic development and for healing tissue, for instance around blood clots.
Endothelial cell division is highly sensitive to fluid conditions and essential for blood vessel healing. Here Rossen
et al.
demonstrate how cell division triggers the emergence of long-range votex patterns in endothelial tissue under conditions that mimic blood vessel formation and blood clots. |
---|---|
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms6720 |