Cargando…

Different modes of state transitions determine pattern in the Phosphatidylinositide-Actin system

BACKGROUND: In a motile polarized cell the actin system is differentiated to allow protrusion at the front and retraction at the tail. This differentiation is linked to the phosphoinositide pattern in the plasma membrane. In the highly motile Dictyostelium cells studied here, the front is dominated...

Descripción completa

Detalles Bibliográficos
Autores principales: Gerisch, Günther, Ecke, Mary, Wischnewski, Dirk, Schroth-Diez, Britta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199247/
https://www.ncbi.nlm.nih.gov/pubmed/21982379
http://dx.doi.org/10.1186/1471-2121-12-42
_version_ 1782214548529348608
author Gerisch, Günther
Ecke, Mary
Wischnewski, Dirk
Schroth-Diez, Britta
author_facet Gerisch, Günther
Ecke, Mary
Wischnewski, Dirk
Schroth-Diez, Britta
author_sort Gerisch, Günther
collection PubMed
description BACKGROUND: In a motile polarized cell the actin system is differentiated to allow protrusion at the front and retraction at the tail. This differentiation is linked to the phosphoinositide pattern in the plasma membrane. In the highly motile Dictyostelium cells studied here, the front is dominated by PI3-kinases producing PI(3,4,5)tris-phosphate (PIP3), the tail by the PI3-phosphatase PTEN that hydrolyses PIP3 to PI(4,5)bis-phosphate. To study de-novo cell polarization, we first depolymerized actin and subsequently recorded the spontaneous reorganization of actin patterns in relation to PTEN. RESULTS: In a transient stage of recovery from depolymerization, symmetric actin patterns alternate periodically with asymmetric ones. The switches to asymmetry coincide with the unilateral membrane-binding of PTEN. The modes of state transitions in the actin and PTEN systems differ. Transitions in the actin system propagate as waves that are initiated at single sites by the amplification of spontaneous fluctuations. In PTEN-null cells, these waves still propagate with normal speed but loose their regular periodicity. Membrane-binding of PTEN is induced at the border of a coherent PTEN-rich area in the form of expanding and regressing gradients. CONCLUSIONS: The state transitions in actin organization and the reversible transition from cytoplasmic to membrane-bound PTEN are synchronized but their patterns differ. The transitions in actin organization are independent of PTEN, but when PTEN is present, they are coupled to periodic changes in the membrane-binding of this PIP3-degrading phosphatase. The PTEN oscillations are related to motility patterns of chemotaxing cells.
format Online
Article
Text
id pubmed-3199247
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-31992472011-10-24 Different modes of state transitions determine pattern in the Phosphatidylinositide-Actin system Gerisch, Günther Ecke, Mary Wischnewski, Dirk Schroth-Diez, Britta BMC Cell Biol Research Article BACKGROUND: In a motile polarized cell the actin system is differentiated to allow protrusion at the front and retraction at the tail. This differentiation is linked to the phosphoinositide pattern in the plasma membrane. In the highly motile Dictyostelium cells studied here, the front is dominated by PI3-kinases producing PI(3,4,5)tris-phosphate (PIP3), the tail by the PI3-phosphatase PTEN that hydrolyses PIP3 to PI(4,5)bis-phosphate. To study de-novo cell polarization, we first depolymerized actin and subsequently recorded the spontaneous reorganization of actin patterns in relation to PTEN. RESULTS: In a transient stage of recovery from depolymerization, symmetric actin patterns alternate periodically with asymmetric ones. The switches to asymmetry coincide with the unilateral membrane-binding of PTEN. The modes of state transitions in the actin and PTEN systems differ. Transitions in the actin system propagate as waves that are initiated at single sites by the amplification of spontaneous fluctuations. In PTEN-null cells, these waves still propagate with normal speed but loose their regular periodicity. Membrane-binding of PTEN is induced at the border of a coherent PTEN-rich area in the form of expanding and regressing gradients. CONCLUSIONS: The state transitions in actin organization and the reversible transition from cytoplasmic to membrane-bound PTEN are synchronized but their patterns differ. The transitions in actin organization are independent of PTEN, but when PTEN is present, they are coupled to periodic changes in the membrane-binding of this PIP3-degrading phosphatase. The PTEN oscillations are related to motility patterns of chemotaxing cells. BioMed Central 2011-10-07 /pmc/articles/PMC3199247/ /pubmed/21982379 http://dx.doi.org/10.1186/1471-2121-12-42 Text en Copyright ©2011 Gerisch et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gerisch, Günther
Ecke, Mary
Wischnewski, Dirk
Schroth-Diez, Britta
Different modes of state transitions determine pattern in the Phosphatidylinositide-Actin system
title Different modes of state transitions determine pattern in the Phosphatidylinositide-Actin system
title_full Different modes of state transitions determine pattern in the Phosphatidylinositide-Actin system
title_fullStr Different modes of state transitions determine pattern in the Phosphatidylinositide-Actin system
title_full_unstemmed Different modes of state transitions determine pattern in the Phosphatidylinositide-Actin system
title_short Different modes of state transitions determine pattern in the Phosphatidylinositide-Actin system
title_sort different modes of state transitions determine pattern in the phosphatidylinositide-actin system
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199247/
https://www.ncbi.nlm.nih.gov/pubmed/21982379
http://dx.doi.org/10.1186/1471-2121-12-42
work_keys_str_mv AT gerischgunther differentmodesofstatetransitionsdeterminepatterninthephosphatidylinositideactinsystem
AT eckemary differentmodesofstatetransitionsdeterminepatterninthephosphatidylinositideactinsystem
AT wischnewskidirk differentmodesofstatetransitionsdeterminepatterninthephosphatidylinositideactinsystem
AT schrothdiezbritta differentmodesofstatetransitionsdeterminepatterninthephosphatidylinositideactinsystem