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Dynamic balance between vesicle transport and microtubule growth enables neurite outgrowth

Whole cell responses involve multiple subcellular processes (SCPs). To understand how balance between SCPs controls the dynamics of whole cell responses we studied neurite outgrowth in rat primary cortical neurons in culture. We used a combination of dynamical models and experiments to understand th...

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Autores principales: Yadaw, Arjun Singh, Siddiq, Mustafa M., Rabinovich, Vera, Tolentino, Rosa, Hansen, Jens, Iyengar, Ravi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546251/
https://www.ncbi.nlm.nih.gov/pubmed/31042702
http://dx.doi.org/10.1371/journal.pcbi.1006877
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author Yadaw, Arjun Singh
Siddiq, Mustafa M.
Rabinovich, Vera
Tolentino, Rosa
Hansen, Jens
Iyengar, Ravi
author_facet Yadaw, Arjun Singh
Siddiq, Mustafa M.
Rabinovich, Vera
Tolentino, Rosa
Hansen, Jens
Iyengar, Ravi
author_sort Yadaw, Arjun Singh
collection PubMed
description Whole cell responses involve multiple subcellular processes (SCPs). To understand how balance between SCPs controls the dynamics of whole cell responses we studied neurite outgrowth in rat primary cortical neurons in culture. We used a combination of dynamical models and experiments to understand the conditions that permitted growth at a specified velocity and when aberrant growth could lead to the formation of dystrophic bulbs. We hypothesized that dystrophic bulb formation is due to quantitative imbalances between SCPs. Simulations predict redundancies between lower level sibling SCPs within each type of high level SCP. In contrast, higher level SCPs, such as vesicle transport and exocytosis or microtubule growth characteristic of each type need to be strictly coordinated with each other and imbalances result in stalling of neurite outgrowth. From these simulations, we predicted the effect of changing the activities of SCPs involved in vesicle exocytosis or microtubule growth could lead to formation of dystrophic bulbs. siRNA ablation experiments verified these predictions. We conclude that whole cell dynamics requires balance between the higher-level SCPs involved and imbalances can terminate whole cell responses such as neurite outgrowth.
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spelling pubmed-65462512019-06-17 Dynamic balance between vesicle transport and microtubule growth enables neurite outgrowth Yadaw, Arjun Singh Siddiq, Mustafa M. Rabinovich, Vera Tolentino, Rosa Hansen, Jens Iyengar, Ravi PLoS Comput Biol Research Article Whole cell responses involve multiple subcellular processes (SCPs). To understand how balance between SCPs controls the dynamics of whole cell responses we studied neurite outgrowth in rat primary cortical neurons in culture. We used a combination of dynamical models and experiments to understand the conditions that permitted growth at a specified velocity and when aberrant growth could lead to the formation of dystrophic bulbs. We hypothesized that dystrophic bulb formation is due to quantitative imbalances between SCPs. Simulations predict redundancies between lower level sibling SCPs within each type of high level SCP. In contrast, higher level SCPs, such as vesicle transport and exocytosis or microtubule growth characteristic of each type need to be strictly coordinated with each other and imbalances result in stalling of neurite outgrowth. From these simulations, we predicted the effect of changing the activities of SCPs involved in vesicle exocytosis or microtubule growth could lead to formation of dystrophic bulbs. siRNA ablation experiments verified these predictions. We conclude that whole cell dynamics requires balance between the higher-level SCPs involved and imbalances can terminate whole cell responses such as neurite outgrowth. Public Library of Science 2019-05-01 /pmc/articles/PMC6546251/ /pubmed/31042702 http://dx.doi.org/10.1371/journal.pcbi.1006877 Text en © 2019 Yadaw et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yadaw, Arjun Singh
Siddiq, Mustafa M.
Rabinovich, Vera
Tolentino, Rosa
Hansen, Jens
Iyengar, Ravi
Dynamic balance between vesicle transport and microtubule growth enables neurite outgrowth
title Dynamic balance between vesicle transport and microtubule growth enables neurite outgrowth
title_full Dynamic balance between vesicle transport and microtubule growth enables neurite outgrowth
title_fullStr Dynamic balance between vesicle transport and microtubule growth enables neurite outgrowth
title_full_unstemmed Dynamic balance between vesicle transport and microtubule growth enables neurite outgrowth
title_short Dynamic balance between vesicle transport and microtubule growth enables neurite outgrowth
title_sort dynamic balance between vesicle transport and microtubule growth enables neurite outgrowth
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546251/
https://www.ncbi.nlm.nih.gov/pubmed/31042702
http://dx.doi.org/10.1371/journal.pcbi.1006877
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