Microphase separation of living cells
A. Carrère,
J. d’Alessandro,
O. Cochet-Escartin,
J. Hesnard,
N. Ghazi,
C. Rivière,
C. Anjard,
F. Detcheverry () and
J.-P. Rieu ()
Additional contact information
A. Carrère: University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière
J. d’Alessandro: University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière
O. Cochet-Escartin: University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière
J. Hesnard: University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière
N. Ghazi: University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière
C. Rivière: University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière
C. Anjard: University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière
F. Detcheverry: University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière
J.-P. Rieu: University of Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière
Nature Communications, 2023, vol. 14, issue 1, 1-11
Abstract:
Abstract Self-organization of cells is central to a variety of biological systems and physical concepts of condensed matter have proven instrumental in deciphering some of their properties. Here we show that microphase separation, long studied in polymeric materials and other inert systems, has a natural counterpart in living cells. When placed below a millimetric film of liquid nutritive medium, a quasi two-dimensional, high-density population of Dictyostelium discoideum cells spontaneously assembles into compact domains. Their typical size of 100 μm is governed by a balance between competing interactions: an adhesion acting as a short-range attraction and promoting aggregation, and an effective long-range repulsion stemming from aerotaxis in near anoxic condition. Experimental data, a simple model and cell-based simulations all support this scenario. Our findings establish a generic mechanism for self-organization of living cells and highlight oxygen regulation as an emergent organizing principle for biological matter.
Date: 2023
References: View references in EconPapers View complete reference list from CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/s41467-023-36395-2 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36395-2
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-023-36395-2
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().