A Clockwork Bleb: cytoskeleton, calcium, and cytoplasmic fluidity

Published on Oct 14, 2021in FEBS Journal5.542
路 DOI :10.1111/FEBS.16220
Junichi Ikenouchi21
Estimated H-index: 21
(Kyushu University),
Kana Aoki4
Estimated H-index: 4
(Kyushu University)
Sources
Abstract
When the plasma membrane (PM) detaches from the underlying actin cortex, the PM expands according to intracellular pressure and a spherical membrane protrusion called a bleb is formed. This bleb retracts when the actin cortex is reassembled underneath the PM. Whereas this phenomenon seems simple at first glance, there are many interesting, unresolved cell biological questions in each process. For example, what is the membrane source to enlarge the surface area of the PM during rapid bleb expansion? What signals induce actin reassembly for bleb retraction, and how is cytoplasmic fluidity regulated to allow rapid membrane deformation during bleb expansion? Furthermore, emerging evidence indicates that cancer cells use blebs for invasion, but little is known about how molecules that are involved in bleb formation, expansion, and retraction are coordinated for directional amoeboid migration. In this review, we discuss the molecular mechanisms involved in the regulation of blebs, which have been revealed by various experimental systems.
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