Cargando…

Actin Waves and Dynamic Patterning of the Plasma Membrane

Plasma membrane and underlying actin network are connected to a functional unit that by non-linear interactions is capable of forming patterns. For instance, in cell motility and chemotaxis, cells polarize to form a protruding front and a retracting tail. Here we address dynamic patterns that are fo...

Descripción completa

Detalles Bibliográficos
Autores principales: Gerisch, Guenther, Prassler, Jana, Butterfield, Nelson, Ecke, Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: YJBM 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6747932/
https://www.ncbi.nlm.nih.gov/pubmed/31543704
_version_ 1783452004810489856
author Gerisch, Guenther
Prassler, Jana
Butterfield, Nelson
Ecke, Mary
author_facet Gerisch, Guenther
Prassler, Jana
Butterfield, Nelson
Ecke, Mary
author_sort Gerisch, Guenther
collection PubMed
description Plasma membrane and underlying actin network are connected to a functional unit that by non-linear interactions is capable of forming patterns. For instance, in cell motility and chemotaxis, cells polarize to form a protruding front and a retracting tail. Here we address dynamic patterns that are formed on a planar substrate surface and are therefore easily accessible to optical recording. In these patterns two distinct areas of the membrane and actin cortex are interconverted at the site of circular actin waves. The inner territory circumscribed by a wave is distinguished from the external area by a high PIP3 content and high Ras activity. In contrast, the external area is occupied with the PIP3-degrading phosphatase PTEN. In the underlying cortex, these areas differ in the proteins associated with the actin network. Actin waves can be formed at zones of increasing as well as decreasing Ras activity. Both types of waves are headed by myosin IB. When waves collide, they usually extinguish each other, and their decay is accompanied by the accumulation of coronin. No membrane patterns have been observed after efficient depolymerization of actin, suggesting that residual actin filaments are necessary for the pattern generating system to work. Where appropriate, we relate the experimental data obtained with Dictyostelium to human normal and malignant cell behavior, in particular to the role of Ras-GAP as an enhancer of macropinocytosis, to mutations in the tumor suppressor PTEN, to frustrated phagocytosis, and to the role of coronin in immune cells and neurons.
format Online
Article
Text
id pubmed-6747932
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher YJBM
record_format MEDLINE/PubMed
spelling pubmed-67479322019-09-20 Actin Waves and Dynamic Patterning of the Plasma Membrane Gerisch, Guenther Prassler, Jana Butterfield, Nelson Ecke, Mary Yale J Biol Med Original Contribution Plasma membrane and underlying actin network are connected to a functional unit that by non-linear interactions is capable of forming patterns. For instance, in cell motility and chemotaxis, cells polarize to form a protruding front and a retracting tail. Here we address dynamic patterns that are formed on a planar substrate surface and are therefore easily accessible to optical recording. In these patterns two distinct areas of the membrane and actin cortex are interconverted at the site of circular actin waves. The inner territory circumscribed by a wave is distinguished from the external area by a high PIP3 content and high Ras activity. In contrast, the external area is occupied with the PIP3-degrading phosphatase PTEN. In the underlying cortex, these areas differ in the proteins associated with the actin network. Actin waves can be formed at zones of increasing as well as decreasing Ras activity. Both types of waves are headed by myosin IB. When waves collide, they usually extinguish each other, and their decay is accompanied by the accumulation of coronin. No membrane patterns have been observed after efficient depolymerization of actin, suggesting that residual actin filaments are necessary for the pattern generating system to work. Where appropriate, we relate the experimental data obtained with Dictyostelium to human normal and malignant cell behavior, in particular to the role of Ras-GAP as an enhancer of macropinocytosis, to mutations in the tumor suppressor PTEN, to frustrated phagocytosis, and to the role of coronin in immune cells and neurons. YJBM 2019-09-20 /pmc/articles/PMC6747932/ /pubmed/31543704 Text en Copyright ©2019, Yale Journal of Biology and Medicine https://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons CC BY-NC license, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use the material for commercial purposes.
spellingShingle Original Contribution
Gerisch, Guenther
Prassler, Jana
Butterfield, Nelson
Ecke, Mary
Actin Waves and Dynamic Patterning of the Plasma Membrane
title Actin Waves and Dynamic Patterning of the Plasma Membrane
title_full Actin Waves and Dynamic Patterning of the Plasma Membrane
title_fullStr Actin Waves and Dynamic Patterning of the Plasma Membrane
title_full_unstemmed Actin Waves and Dynamic Patterning of the Plasma Membrane
title_short Actin Waves and Dynamic Patterning of the Plasma Membrane
title_sort actin waves and dynamic patterning of the plasma membrane
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6747932/
https://www.ncbi.nlm.nih.gov/pubmed/31543704
work_keys_str_mv AT gerischguenther actinwavesanddynamicpatterningoftheplasmamembrane
AT prasslerjana actinwavesanddynamicpatterningoftheplasmamembrane
AT butterfieldnelson actinwavesanddynamicpatterningoftheplasmamembrane
AT eckemary actinwavesanddynamicpatterningoftheplasmamembrane