Wednesday, July 30, 2025 7/30/2025

Cell Type Specific Genetic Manipulation to Dissect Cholinergic Interneuron Function and Plasticity in a Symptomatic Model of DYT1 Dystonia

Award Number: R01NS110853
ORGANIZATION: NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
OPDIV: NIH
AWARD CLASS: DISCRETIONARY
AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)
PERIOD OF PERFORMANCE START DATE: 02/01/2021
PERIOD OF PERFORMANCE END DATE: 01/31/2026

Group Awards By:

View Award Description

Cell Type Specific Genetic Manipulation to Dissect Cholinergic Interneuron Function and Plasticity in a Symptomatic Model of DYT1 Dystonia - Project Summary/Abstract Cholinergic neurons (ChIs) are a central but poorly understood element of striatal circuitry. A considerable literature strongly implicates ChI dysfunction in the pathogenesis of abnormal movements, especially in dystonia and levodopa-induced dyskinesias in Parkinson disease. A common theme of these studies is that maladaptive plastic changes cause aberrant ChI output and connectivity, promoting motor dysfunction. The central goal of this proposal is to advance understanding of the cellular and synaptic mechanisms through which ChIs cause motor dysfunction by employing novel selective genetic and chemical strategies in a recently validated model of DYT1 dystonia. Conditional Knock Out of torsinA from all striatal neurons (using Dlx5/6-Cre; “Dlx-CKO”) causes selective neurodegeneration of dorsolateral striatal ChI. ChI degeneration occurs roughly coincident with the juvenile onset of abnormal twisting movements in these mice, and selective ChI abnormalities are also present in postmortem tissue from DYT1 subjects. These movements are suppressed by the same anti-muscarinic compounds used to treat patients with DYT1 dystonia, establishing model therapeutic validity and suggesting shared pathophysiology with human dystonia. Surviving striatal ChIs are enlarged and hyperexcitable, and receive aberrant synaptic inputs. Selective ablation of these surviving ChI suppresses abnormal twisting, implicating these cells as key contributors to abnormal movements. Based on these data, we hypothesize that maladaptations in surviving ChIs drive motor dysfunction. Successful completion of the proposed studies will fundamentally advance understanding of maladaptive mechanisms whereby ChI function and connectivity drive abnormal movements, information highly significant for multiple striatal diseases. We will first address our hypothesis by testing the necessity of striatal ChI dysfunction in abnormal movement generation by selectively restoring torsinA to these cells (Aim 1), decisively moving beyond the current association between these factors. We will determine if cholinergic dysfunction arises primarily from intrinsic ChI abnormalities or defects in how they respond to afferents (Aim 2), and, informed by Aims 1 and 2, will pursue translational studies (Aim 3) testing whether directly modulating the activity of surviving ChIs can suppress dystonic-like movements. This proposal is therefore highly signifiant because it will define a circuit-based model of motor dysfunction that will inform the design of targeted therapeutics.


Issue Date FY	Funding FY	Legal Entity Name	Legal Entity Address	Legal Entity City	Legal Entity State	Legal Entity Zip Code	Legal Entity COUNTY	Legal Entity COUNTRY	Assistance Listing	Award Code	Budget Year	Action Date	Action Type	Action Amount

Issue Date FY: 2025 ( Subtotal = $454,382 )
2025	2025	THE UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER	5323 HARRY HINES BLVD	DALLAS	TX	75390	DALLAS	USA	Extramural Research Programs in the Neurosciences and Neurological Disorders	000	5	2/14/2025	NON-COMPETING CONTINUATION	$454,382
														Subtotal = $454,382

Issue Date FY: 2024 ( Subtotal = $489,721 )
2024	2024	THE UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER	5323 HARRY HINES BLVD	DALLAS	TX	75390	DALLAS	USA	Extramural Research Programs in the Neurosciences and Neurological Disorders	001	4	6/6/2024	NON-COMPETING CONTINUATION	$35,339
2024	2024	UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER, THE	5323 HARRY HINES BLVD	DALLAS	TX	75390	DALLAS	USA	Extramural Research Programs in the Neurosciences and Neurological Disorders	000	4	1/26/2024	NON-COMPETING CONTINUATION	$454,382
														Subtotal = $489,721

Issue Date FY: 2023 ( Subtotal = $504,867 )
2023	2023	UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER, THE	5323 HARRY HINES BLVD	DALLAS	TX	75390	DALLAS	USA	Extramural Research Programs in the Neurosciences and Neurological Disorders	000	3	2/8/2023	NON-COMPETING CONTINUATION	$504,867
														Subtotal = $504,867

Issue Date FY: 2022 ( Subtotal = $502,161 )
2022	2022	UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER, THE	5323 HARRY HINES BLVD	DALLAS	TX	75390	DALLAS	USA	Extramural Research Programs in the Neurosciences and Neurological Disorders	000	2	1/7/2022	NON-COMPETING CONTINUATION	$451,946
2022	2022	UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER, THE	5323 HARRY HINES BLVD	DALLAS	TX	75390	DALLAS	USA	Extramural Research Programs in the Neurosciences and Neurological Disorders	001	2	3/28/2022	NON-COMPETING CONTINUATION	$50,215
														Subtotal = $502,161

Issue Date FY: 2021 ( Subtotal = $516,285 )
2021	2021	UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER, THE	5323 HARRY HINES BLVD	DALLAS	TX	75390	DALLAS	USA	Extramural Research Programs in the Neurosciences and Neurological Disorders	000	1	1/29/2021	NEW	$516,285
														Subtotal = $516,285

Grand Total All Awards = $2,467,416

Top

All Categories

About

Search

Reports

Data Submission

Award Information

Cell Type Specific Genetic Manipulation to Dissect Cholinergic Interneuron Function and Plasticity in a Symptomatic Model of DYT1 Dystonia

Award Number: R01NS110853

ORGANIZATION: NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE

OPDIV: NIH

AWARD CLASS: DISCRETIONARY

AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

PERIOD OF PERFORMANCE START DATE: 02/01/2021

PERIOD OF PERFORMANCE END DATE: 01/31/2026

Federal Websites

Department of Health & Human Services

HHS Operating Divisions

HHS Staff Divisions

Download A Document Viewer