Pith. sign in

REVIEW

L\'evy distributed fluctuations in the living cell cortex

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2309.06226 v2 pith:MXBQJ5R4 submitted 2023-09-12 physics.bio-ph cond-mat.softq-bio.SC

L\'evy distributed fluctuations in the living cell cortex

classification physics.bio-ph cond-mat.softq-bio.SC
keywords fluctuationscellcortexcytoquakesactivedisplacementsdistributionflexible
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
0 comments
read the original abstract

The actomyosin cortex is an active material that provides animal cells with a strong but flexible exterior, whose mechanics, including non-Gaussian fluctuations and occasional large displacements or cytoquakes, have defied explanation. We study the active fluctuations of the cortex using nanoscale tracking of arrays of flexible microposts adhered to multiple cultured cell types. When the confounding effects of static heterogeneity and tracking error are removed, the fluctuations are found to be heavy-tailed and well-described by a truncated L\'evy alpha-stable distribution over a wide range of timescales, in multiple cell types. The largest random displacements closely resemble the earlier-reported cytoquakes, but notably, we find these cytoquakes are not due to earthquake-like cooperative rearrangement of many cytoskeletal elements. Rather, they are indistinguishable from chance large excursions of a super-diffusive random process driven by heavy-tailed noise. The non-cooperative microscopic events driving these fluctuations need not be larger than the expected elastic energy of single tensed cortical actin filaments, and the implied distribution of microscopic event energies will need to be accounted for by future models of the cytoskeleton.

discussion (0)

Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.