Investigating mechanisms of biophysical diversity between phasic and tonic motor neurons

Thesis: M. Eng., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, May, 2020 === Cataloged from student-submitted PDF of thesis. === Includes bibliographical references (pages 65-67). === Neurons exhibit striking diversity in core neuronal properties (...

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Main Author: Siahpoosh, Yasmin(Yasmin H.)
Other Authors: Troy Littleton.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2021
Subjects:
Online Access:https://hdl.handle.net/1721.1/130197
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spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-1301972021-03-24T05:10:07Z Investigating mechanisms of biophysical diversity between phasic and tonic motor neurons Siahpoosh, Yasmin(Yasmin H.) Troy Littleton. Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science. Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science Electrical Engineering and Computer Science. Thesis: M. Eng., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, May, 2020 Cataloged from student-submitted PDF of thesis. Includes bibliographical references (pages 65-67). Neurons exhibit striking diversity in core neuronal properties (intrinsic biophysical and synaptic properties), which are the building blocks of brain function and computation. Despite the central role of these properties in brain function, the underlying molecular and biophysical mechanisms which generate this diversity remain incompletely understood. In the Drosophila larval motor system, phasic (1s) and tonic (1b) motor neurons (MNs) differ in their intrinsic biophysical properties, providing an ideal system to examine electrophysiological diversity across neuronal populations. To address this question, we combined in vivo whole-cell patch-clamp physiology with biophysical modeling. First, we characterized biophysical diversity between 1s and 1b MNs. To explore molecular mechanisms underlying such diversity, single-neuron PatchSeq RNA profiling experiments were carried out to correlate biophysical properties with differences in ion channel gene expression profiles. These experiments suggest that cyclic nucleotide- gated like (CNGL) ion channels are upregulated in 1b MNs several folds, which indicates that CNGL could be a candidate ion channel that might specify diversity in electrical properties . To test this hypothesis, we misoverexpress CNGL in 1s MNs so that we could investigate how this ion channel contributes to the diversity between them. We developed an analysis toolset in MATLAB that can be used to analyze whole-cell patch-clamp physiology data and obtain excitability properties. Using the Izhikevich model, we were able to quantify and predict the spiking properties of 1s and 1b MNs. Using a ball and stick model, we were able to reproduce the tonic firing pattern of 1b neurons and tested tonic firing patterns in different compartments of 1b neurons. Taken together, this thesis work laid the foundation to begin characterizing biophysical mechanisms of intrinsic diversity of Drosophila neurons by combining experimental data with modeling. by Yasmin Siahpoosh. M. Eng. M.Eng. Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science 2021-03-22T17:14:47Z 2021-03-22T17:14:47Z 2020 2020 Thesis https://hdl.handle.net/1721.1/130197 1241187714 eng MIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided. http://dspace.mit.edu/handle/1721.1/7582 67 pages application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Electrical Engineering and Computer Science.
spellingShingle Electrical Engineering and Computer Science.
Siahpoosh, Yasmin(Yasmin H.)
Investigating mechanisms of biophysical diversity between phasic and tonic motor neurons
description Thesis: M. Eng., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, May, 2020 === Cataloged from student-submitted PDF of thesis. === Includes bibliographical references (pages 65-67). === Neurons exhibit striking diversity in core neuronal properties (intrinsic biophysical and synaptic properties), which are the building blocks of brain function and computation. Despite the central role of these properties in brain function, the underlying molecular and biophysical mechanisms which generate this diversity remain incompletely understood. In the Drosophila larval motor system, phasic (1s) and tonic (1b) motor neurons (MNs) differ in their intrinsic biophysical properties, providing an ideal system to examine electrophysiological diversity across neuronal populations. To address this question, we combined in vivo whole-cell patch-clamp physiology with biophysical modeling. First, we characterized biophysical diversity between 1s and 1b MNs. To explore molecular mechanisms underlying such diversity, single-neuron PatchSeq RNA profiling experiments were carried out to correlate biophysical properties with differences in ion channel gene expression profiles. These experiments suggest that cyclic nucleotide- gated like (CNGL) ion channels are upregulated in 1b MNs several folds, which indicates that CNGL could be a candidate ion channel that might specify diversity in electrical properties . To test this hypothesis, we misoverexpress CNGL in 1s MNs so that we could investigate how this ion channel contributes to the diversity between them. We developed an analysis toolset in MATLAB that can be used to analyze whole-cell patch-clamp physiology data and obtain excitability properties. Using the Izhikevich model, we were able to quantify and predict the spiking properties of 1s and 1b MNs. Using a ball and stick model, we were able to reproduce the tonic firing pattern of 1b neurons and tested tonic firing patterns in different compartments of 1b neurons. Taken together, this thesis work laid the foundation to begin characterizing biophysical mechanisms of intrinsic diversity of Drosophila neurons by combining experimental data with modeling. === by Yasmin Siahpoosh. === M. Eng. === M.Eng. Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science
author2 Troy Littleton.
author_facet Troy Littleton.
Siahpoosh, Yasmin(Yasmin H.)
author Siahpoosh, Yasmin(Yasmin H.)
author_sort Siahpoosh, Yasmin(Yasmin H.)
title Investigating mechanisms of biophysical diversity between phasic and tonic motor neurons
title_short Investigating mechanisms of biophysical diversity between phasic and tonic motor neurons
title_full Investigating mechanisms of biophysical diversity between phasic and tonic motor neurons
title_fullStr Investigating mechanisms of biophysical diversity between phasic and tonic motor neurons
title_full_unstemmed Investigating mechanisms of biophysical diversity between phasic and tonic motor neurons
title_sort investigating mechanisms of biophysical diversity between phasic and tonic motor neurons
publisher Massachusetts Institute of Technology
publishDate 2021
url https://hdl.handle.net/1721.1/130197
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