TY - JOUR
T1 - Control of neurite growth and guidance by an inhibitory cell-body signal
AU - Bicknell, Brendan A.
AU - Pujic, Zac
AU - Dayan, Peter
AU - Goodhill, Geoffrey J.
N1 - Funding Information:
This work was supported by an Australian Postgraduate Award (BAB), the National Health and Medical Research Council Project Grants 1083707 and 1107986 (GJG), and the Gatsby Charitable Foundation (PD). PD is on a leave of absence from UCL at Uber Technologies. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
© 2018 Bicknell et al. http://creativecommons.org/licenses/by/4.0/
PY - 2018/6
Y1 - 2018/6
N2 - The development of a functional nervous system requires tight control of neurite growth and guidance by extracellular chemical cues. Neurite growth is astonishingly sensitive to shallow concentration gradients, but a widely observed feature of both growth and guidance regulation, with important consequences for development and regeneration, is that both are only elicited over the same relatively narrow range of concentrations. Here we show that all these phenomena can be explained within one theoretical framework. We first test long-standing explanations for the suppression of the trophic effects of nerve growth factor at high concentrations, and find they are contradicted by experiment. Instead we propose a new hypothesis involving inhibitory signalling among the cell bodies, and then extend this hypothesis to show how both growth and guidance can be understood in terms of a common underlying signalling mechanism. This new model for the first time unifies several key features of neurite growth regulation, quantitatively explains many aspects of experimental data, and makes new predictions about unknown details of developmental signalling.
AB - The development of a functional nervous system requires tight control of neurite growth and guidance by extracellular chemical cues. Neurite growth is astonishingly sensitive to shallow concentration gradients, but a widely observed feature of both growth and guidance regulation, with important consequences for development and regeneration, is that both are only elicited over the same relatively narrow range of concentrations. Here we show that all these phenomena can be explained within one theoretical framework. We first test long-standing explanations for the suppression of the trophic effects of nerve growth factor at high concentrations, and find they are contradicted by experiment. Instead we propose a new hypothesis involving inhibitory signalling among the cell bodies, and then extend this hypothesis to show how both growth and guidance can be understood in terms of a common underlying signalling mechanism. This new model for the first time unifies several key features of neurite growth regulation, quantitatively explains many aspects of experimental data, and makes new predictions about unknown details of developmental signalling.
UR - http://www.scopus.com/inward/record.url?scp=85049364711&partnerID=8YFLogxK
U2 - 10.1371/journal.pcbi.1006218
DO - 10.1371/journal.pcbi.1006218
M3 - Article
C2 - 29927943
AN - SCOPUS:85049364711
VL - 14
JO - PLoS Computational Biology
JF - PLoS Computational Biology
SN - 1553-734X
IS - 6
M1 - e1006218
ER -