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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
YJBM
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6747932/ https://www.ncbi.nlm.nih.gov/pubmed/31543704 |
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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 |
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