Cargando…
Arf6 Can Trigger Wave Regulatory Complex-Dependent Actin Assembly Independent of Arno
The small GTPase ADP-ribosylation factor 6 (Arf6) anchors at the plasma membrane to orchestrate key functions, such as membrane trafficking and regulating cortical actin cytoskeleton rearrangement. A number of studies have identified key players that interact with Arf6 to regulate actin dynamics in...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177560/ https://www.ncbi.nlm.nih.gov/pubmed/32252226 http://dx.doi.org/10.3390/ijms21072457 |
_version_ | 1783525247174049792 |
---|---|
author | Singh, Vikash Davidson, Anthony C. Hume, Peter J. Koronakis, Vassilis |
author_facet | Singh, Vikash Davidson, Anthony C. Hume, Peter J. Koronakis, Vassilis |
author_sort | Singh, Vikash |
collection | PubMed |
description | The small GTPase ADP-ribosylation factor 6 (Arf6) anchors at the plasma membrane to orchestrate key functions, such as membrane trafficking and regulating cortical actin cytoskeleton rearrangement. A number of studies have identified key players that interact with Arf6 to regulate actin dynamics in diverse cell processes, yet it is still unknown whether Arf6 can directly signal to the wave regulatory complex to mediate actin assembly. By reconstituting actin dynamics on supported lipid bilayers, we found that Arf6 in co-ordination with Rac1(Ras-related C3 botulinum toxin substrate 1) can directly trigger actin polymerization by recruiting wave regulatory complex components. Interestingly, we demonstrated that Arf6 triggers actin assembly at the membrane directly without recruiting the Arf guanine nucleotide exchange factor (GEF) ARNO (ARF nucleotide-binding site opener), which is able to activate Arf1 to enable WRC-dependent actin assembly. Furthermore, using labelled E. coli, we demonstrated that actin assembly by Arf6 also contributes towards efficient phagocytosis in THP-1 macrophages. Taken together, this study reveals a mechanism for Arf6-driven actin polymerization. |
format | Online Article Text |
id | pubmed-7177560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71775602020-04-28 Arf6 Can Trigger Wave Regulatory Complex-Dependent Actin Assembly Independent of Arno Singh, Vikash Davidson, Anthony C. Hume, Peter J. Koronakis, Vassilis Int J Mol Sci Article The small GTPase ADP-ribosylation factor 6 (Arf6) anchors at the plasma membrane to orchestrate key functions, such as membrane trafficking and regulating cortical actin cytoskeleton rearrangement. A number of studies have identified key players that interact with Arf6 to regulate actin dynamics in diverse cell processes, yet it is still unknown whether Arf6 can directly signal to the wave regulatory complex to mediate actin assembly. By reconstituting actin dynamics on supported lipid bilayers, we found that Arf6 in co-ordination with Rac1(Ras-related C3 botulinum toxin substrate 1) can directly trigger actin polymerization by recruiting wave regulatory complex components. Interestingly, we demonstrated that Arf6 triggers actin assembly at the membrane directly without recruiting the Arf guanine nucleotide exchange factor (GEF) ARNO (ARF nucleotide-binding site opener), which is able to activate Arf1 to enable WRC-dependent actin assembly. Furthermore, using labelled E. coli, we demonstrated that actin assembly by Arf6 also contributes towards efficient phagocytosis in THP-1 macrophages. Taken together, this study reveals a mechanism for Arf6-driven actin polymerization. MDPI 2020-04-02 /pmc/articles/PMC7177560/ /pubmed/32252226 http://dx.doi.org/10.3390/ijms21072457 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Singh, Vikash Davidson, Anthony C. Hume, Peter J. Koronakis, Vassilis Arf6 Can Trigger Wave Regulatory Complex-Dependent Actin Assembly Independent of Arno |
title | Arf6 Can Trigger Wave Regulatory Complex-Dependent Actin Assembly Independent of Arno |
title_full | Arf6 Can Trigger Wave Regulatory Complex-Dependent Actin Assembly Independent of Arno |
title_fullStr | Arf6 Can Trigger Wave Regulatory Complex-Dependent Actin Assembly Independent of Arno |
title_full_unstemmed | Arf6 Can Trigger Wave Regulatory Complex-Dependent Actin Assembly Independent of Arno |
title_short | Arf6 Can Trigger Wave Regulatory Complex-Dependent Actin Assembly Independent of Arno |
title_sort | arf6 can trigger wave regulatory complex-dependent actin assembly independent of arno |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177560/ https://www.ncbi.nlm.nih.gov/pubmed/32252226 http://dx.doi.org/10.3390/ijms21072457 |
work_keys_str_mv | AT singhvikash arf6cantriggerwaveregulatorycomplexdependentactinassemblyindependentofarno AT davidsonanthonyc arf6cantriggerwaveregulatorycomplexdependentactinassemblyindependentofarno AT humepeterj arf6cantriggerwaveregulatorycomplexdependentactinassemblyindependentofarno AT koronakisvassilis arf6cantriggerwaveregulatorycomplexdependentactinassemblyindependentofarno |