4.1 Review

Dying under pressure: cellular characterisation and in vivo functions of cell death induced by compaction

Journal

BIOLOGY OF THE CELL
Volume 111, Issue 3, Pages 51-66

Publisher

WILEY
DOI: 10.1111/boc.201800075

Keywords

Apoptosis; Cell death; Development; Intercellular communication

Categories

Funding

  1. Societe de Biologie Cellulaire Francaise (SBCF)
  2. FRM (Fondation pour la Recherche Medicale) [ARF20170938651]
  3. Marie Sklodowska-Curie Fellowship
  4. Institut Pasteur (G5 starting package)
  5. ERC starting grant CoSpaDD (Competition for Space in Development and Disease) [758457]
  6. European Research Council (ERC) [758457] Funding Source: European Research Council (ERC)

Ask authors/readers for more resources

Cells and tissues are exposed to multiple mechanical stresses during development, tissue homoeostasis and diseases. While we start to have an extensive understanding of the influence of mechanics on cell differentiation and proliferation, how excessive mechanical stresses can also lead to cell death and may be associated with pathologies has been much less explored so far. Recently, the development of new perturbative approaches allowing modulation of pressure and deformation of tissues has demonstrated that compaction (the reduction of tissue size or volume) can lead to cell elimination. Here, we discuss the relevant type of stress and the parameters that could be causal to cell death from single cell to multicellular systems. We then compare the pathways and mechanisms that have been proposed to influence cell survival upon compaction. We eventually describe the relevance of compaction-induced death in vivo, and its functions in morphogenesis, tissue size regulation, tissue homoeostasis and cancer progression.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.1
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available