Cell migration directionality and speed are independently regulated by RasG and Gβ in Dictyostelium cells in electrotaxis

Motile cells manifest increased migration speed and directionality in gradients of stimuli, including chemoattractants, electrical potential and substratum stiffness. Here, we demonstrate that Dictyostelium cells move directionally in response to an electric field (EF) with specific acceleration/dec...

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Main Authors: Taeck J. Jeon, Runchi Gao, Hyeseon Kim, Ara Lee, Pyeonghwa Jeon, Peter N. Devreotes, Min Zhao
Format: Article
Language:English
Published: The Company of Biologists 2019-07-01
Series:Biology Open
Subjects:
Online Access:http://bio.biologists.org/content/8/7/bio042457
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spelling doaj-4ac0c5ca2ba54fa593b4f15eef1be74e2021-06-02T12:13:21ZengThe Company of BiologistsBiology Open2046-63902019-07-018710.1242/bio.042457042457Cell migration directionality and speed are independently regulated by RasG and Gβ in Dictyostelium cells in electrotaxisTaeck J. Jeon0Runchi Gao1Hyeseon Kim2Ara Lee3Pyeonghwa Jeon4Peter N. Devreotes5Min Zhao6 Department of Biology & BK21-Plus Research Team for Bioactive Control Technology, College of Natural Sciences, Chosun University, Gwangju 61452, Republic of Korea School of life science, Yunnan Normal University, Kunming, Yunnan 650500, China Department of Biology & BK21-Plus Research Team for Bioactive Control Technology, College of Natural Sciences, Chosun University, Gwangju 61452, Republic of Korea Department of Biology & BK21-Plus Research Team for Bioactive Control Technology, College of Natural Sciences, Chosun University, Gwangju 61452, Republic of Korea Department of Biology & BK21-Plus Research Team for Bioactive Control Technology, College of Natural Sciences, Chosun University, Gwangju 61452, Republic of Korea Department of Cell Biology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA Departments of Dermatology and Ophthalmology, Institute for Regenerative Cures, School of Medicine, University of California at Davis, CA 95817, USA Motile cells manifest increased migration speed and directionality in gradients of stimuli, including chemoattractants, electrical potential and substratum stiffness. Here, we demonstrate that Dictyostelium cells move directionally in response to an electric field (EF) with specific acceleration/deceleration kinetics of directionality and migration speed. Detailed analyses of the migration kinetics suggest that migration speed and directionality are separately regulated by Gβ and RasG, respectively, in EF-directed cell migration. Cells lacking Gβ, which is essential for all chemotactic responses in Dictyostelium, showed EF-directed cell migration with the same increase in directionality in an EF as wild-type cells. However, these cells failed to show induction of the migration speed upon EF stimulation as much as wild-type cells. Loss of RasG, a key regulator of chemoattractant-directed cell migration, resulted in almost complete loss of directionality, but similar acceleration/deceleration kinetics of migration speed as wild-type cells. These results indicate that Gβ and RasG are required for the induction of migration speed and directionality, respectively, in response to an EF, suggesting separation of migration speed and directionality even with intact feedback loops between mechanical and signaling networks.http://bio.biologists.org/content/8/7/bio042457DirectionalityMigration speedMotilityElectrotaxisDictyostelium
collection DOAJ
language English
format Article
sources DOAJ
author Taeck J. Jeon
Runchi Gao
Hyeseon Kim
Ara Lee
Pyeonghwa Jeon
Peter N. Devreotes
Min Zhao
spellingShingle Taeck J. Jeon
Runchi Gao
Hyeseon Kim
Ara Lee
Pyeonghwa Jeon
Peter N. Devreotes
Min Zhao
Cell migration directionality and speed are independently regulated by RasG and Gβ in Dictyostelium cells in electrotaxis
Biology Open
Directionality
Migration speed
Motility
Electrotaxis
Dictyostelium
author_facet Taeck J. Jeon
Runchi Gao
Hyeseon Kim
Ara Lee
Pyeonghwa Jeon
Peter N. Devreotes
Min Zhao
author_sort Taeck J. Jeon
title Cell migration directionality and speed are independently regulated by RasG and Gβ in Dictyostelium cells in electrotaxis
title_short Cell migration directionality and speed are independently regulated by RasG and Gβ in Dictyostelium cells in electrotaxis
title_full Cell migration directionality and speed are independently regulated by RasG and Gβ in Dictyostelium cells in electrotaxis
title_fullStr Cell migration directionality and speed are independently regulated by RasG and Gβ in Dictyostelium cells in electrotaxis
title_full_unstemmed Cell migration directionality and speed are independently regulated by RasG and Gβ in Dictyostelium cells in electrotaxis
title_sort cell migration directionality and speed are independently regulated by rasg and gβ in dictyostelium cells in electrotaxis
publisher The Company of Biologists
series Biology Open
issn 2046-6390
publishDate 2019-07-01
description Motile cells manifest increased migration speed and directionality in gradients of stimuli, including chemoattractants, electrical potential and substratum stiffness. Here, we demonstrate that Dictyostelium cells move directionally in response to an electric field (EF) with specific acceleration/deceleration kinetics of directionality and migration speed. Detailed analyses of the migration kinetics suggest that migration speed and directionality are separately regulated by Gβ and RasG, respectively, in EF-directed cell migration. Cells lacking Gβ, which is essential for all chemotactic responses in Dictyostelium, showed EF-directed cell migration with the same increase in directionality in an EF as wild-type cells. However, these cells failed to show induction of the migration speed upon EF stimulation as much as wild-type cells. Loss of RasG, a key regulator of chemoattractant-directed cell migration, resulted in almost complete loss of directionality, but similar acceleration/deceleration kinetics of migration speed as wild-type cells. These results indicate that Gβ and RasG are required for the induction of migration speed and directionality, respectively, in response to an EF, suggesting separation of migration speed and directionality even with intact feedback loops between mechanical and signaling networks.
topic Directionality
Migration speed
Motility
Electrotaxis
Dictyostelium
url http://bio.biologists.org/content/8/7/bio042457
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