Computational modeling of light processing in the habenula and dorsal raphe based on laser ablation of functionally-defined cells

Background: The habenula is a major regulator of serotonergic neurons in the dorsal raphe, and thus of brain state. The functional connectivity between these regions is incompletely characterized. Here, we use the ability of changes in irradiance to trigger reproducible changes in activity in the ha...

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Main Authors: Cheng, Ruey-Kuang, Jagannathan, N. Suhas, Kathrada, Ahmad Ismat, Jesuthasan, Suresh, Tucker-Kellogg, Lisa
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2024
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Online Access:https://hdl.handle.net/10356/178842
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Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-178842
record_format dspace
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Medicine, Health and Life Sciences
Neural circuits
Computational modelling
spellingShingle Medicine, Health and Life Sciences
Neural circuits
Computational modelling
Cheng, Ruey-Kuang
Jagannathan, N. Suhas
Kathrada, Ahmad Ismat
Jesuthasan, Suresh
Tucker-Kellogg, Lisa
Computational modeling of light processing in the habenula and dorsal raphe based on laser ablation of functionally-defined cells
description Background: The habenula is a major regulator of serotonergic neurons in the dorsal raphe, and thus of brain state. The functional connectivity between these regions is incompletely characterized. Here, we use the ability of changes in irradiance to trigger reproducible changes in activity in the habenula and dorsal raphe of zebrafish larvae, combined with two-photon laser ablation of specific neurons, to establish causal relationships. Results: Neurons in the habenula can show an excitatory response to the onset or offset of light, while neurons in the anterior dorsal raphe display an inhibitory response to light, as assessed by calcium imaging. The raphe response changed in a complex way following ablations in the dorsal habenula (dHb) and ventral habenula (vHb). After ablation of the ON cells in the vHb (V-ON), the raphe displayed no response to light. After ablation of the OFF cells in the vHb (V-OFF), the raphe displayed an excitatory response to darkness. After ablation of the ON cells in the dHb (D-ON), the raphe displayed an excitatory response to light. We sought to develop in silico models that could recapitulate the response of raphe neurons as a function of the ON and OFF cells of the habenula. Early attempts at mechanistic modeling using ordinary differential equation (ODE) failed to capture observed raphe responses accurately. However, a simple two-layer fully connected neural network (NN) model was successful at recapitulating the diversity of observed phenotypes with root-mean-squared error values ranging from 0.012 to 0.043. The NN model also estimated the raphe response to ablation of D-off cells, which can be verified via future experiments. Conclusion: Lesioning specific cells in different regions of habenula led to qualitatively different responses to light in the dorsal raphe. A simple neural network is capable of mimicking experimental observations. This work illustrates the ability of computational modeling to integrate complex observations into a simple compact formalism for generating testable hypotheses, and for guiding the design of biological experiments.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Cheng, Ruey-Kuang
Jagannathan, N. Suhas
Kathrada, Ahmad Ismat
Jesuthasan, Suresh
Tucker-Kellogg, Lisa
format Article
author Cheng, Ruey-Kuang
Jagannathan, N. Suhas
Kathrada, Ahmad Ismat
Jesuthasan, Suresh
Tucker-Kellogg, Lisa
author_sort Cheng, Ruey-Kuang
title Computational modeling of light processing in the habenula and dorsal raphe based on laser ablation of functionally-defined cells
title_short Computational modeling of light processing in the habenula and dorsal raphe based on laser ablation of functionally-defined cells
title_full Computational modeling of light processing in the habenula and dorsal raphe based on laser ablation of functionally-defined cells
title_fullStr Computational modeling of light processing in the habenula and dorsal raphe based on laser ablation of functionally-defined cells
title_full_unstemmed Computational modeling of light processing in the habenula and dorsal raphe based on laser ablation of functionally-defined cells
title_sort computational modeling of light processing in the habenula and dorsal raphe based on laser ablation of functionally-defined cells
publishDate 2024
url https://hdl.handle.net/10356/178842
_version_ 1814047290501890048
spelling sg-ntu-dr.10356-1788422024-07-14T15:37:38Z Computational modeling of light processing in the habenula and dorsal raphe based on laser ablation of functionally-defined cells Cheng, Ruey-Kuang Jagannathan, N. Suhas Kathrada, Ahmad Ismat Jesuthasan, Suresh Tucker-Kellogg, Lisa Lee Kong Chian School of Medicine (LKCMedicine) Institute of Molecular and Cell Biology, A*STAR Department of Biomedical Engineering, NUS Medicine, Health and Life Sciences Neural circuits Computational modelling Background: The habenula is a major regulator of serotonergic neurons in the dorsal raphe, and thus of brain state. The functional connectivity between these regions is incompletely characterized. Here, we use the ability of changes in irradiance to trigger reproducible changes in activity in the habenula and dorsal raphe of zebrafish larvae, combined with two-photon laser ablation of specific neurons, to establish causal relationships. Results: Neurons in the habenula can show an excitatory response to the onset or offset of light, while neurons in the anterior dorsal raphe display an inhibitory response to light, as assessed by calcium imaging. The raphe response changed in a complex way following ablations in the dorsal habenula (dHb) and ventral habenula (vHb). After ablation of the ON cells in the vHb (V-ON), the raphe displayed no response to light. After ablation of the OFF cells in the vHb (V-OFF), the raphe displayed an excitatory response to darkness. After ablation of the ON cells in the dHb (D-ON), the raphe displayed an excitatory response to light. We sought to develop in silico models that could recapitulate the response of raphe neurons as a function of the ON and OFF cells of the habenula. Early attempts at mechanistic modeling using ordinary differential equation (ODE) failed to capture observed raphe responses accurately. However, a simple two-layer fully connected neural network (NN) model was successful at recapitulating the diversity of observed phenotypes with root-mean-squared error values ranging from 0.012 to 0.043. The NN model also estimated the raphe response to ablation of D-off cells, which can be verified via future experiments. Conclusion: Lesioning specific cells in different regions of habenula led to qualitatively different responses to light in the dorsal raphe. A simple neural network is capable of mimicking experimental observations. This work illustrates the ability of computational modeling to integrate complex observations into a simple compact formalism for generating testable hypotheses, and for guiding the design of biological experiments. Agency for Science, Technology and Research (A*STAR) Nanyang Technological University Published version This research is supported by the Singapore Ministry of Education Academic Research Fund Tier 2 grant MOE2019-T2-1-138 and by Duke-NUS SRP Phase 2 Research Block Grant to LTK; core funding from the Institute of Cell and Molecular Biology to SJ; and an NTU undergraduate student fellowship to AIK. The Duke-NUS block grant paid the publication fees. Any opinions, findings and conclusions or recommendations expressed in this material are those of the author(s) and do not reflect the views of the funders. Funders had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript. 2024-07-09T00:49:52Z 2024-07-09T00:49:52Z 2024 Journal Article Cheng, R., Jagannathan, N. S., Kathrada, A. I., Jesuthasan, S. & Tucker-Kellogg, L. (2024). Computational modeling of light processing in the habenula and dorsal raphe based on laser ablation of functionally-defined cells. BMC Neuroscience, 25(Suppl 1), 22-. https://dx.doi.org/10.1186/s12868-024-00866-z 1471-2202 https://hdl.handle.net/10356/178842 10.1186/s12868-024-00866-z 38627616 2-s2.0-85190478496 Suppl 1 25 22 en BMC Neuroscience © 2024 The Author(s). Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. application/pdf