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A TCF7L2-responsive suppression of both homeostatic and compensatory remyelination in Huntington disease mice

Authors :
Benraiss, Abdellatif
Mariani, John N.
Tate, Ashley
Madsen, Pernille M.
Clark, Kathleen M.
Welle, Kevin A.
Solly, Renee
Capellano, Laetitia
Bentley, Karen
Chandler-Militello, Devin
Goldman, Steven A.
Benraiss, Abdellatif
Mariani, John N.
Tate, Ashley
Madsen, Pernille M.
Clark, Kathleen M.
Welle, Kevin A.
Solly, Renee
Capellano, Laetitia
Bentley, Karen
Chandler-Militello, Devin
Goldman, Steven A.
Source :
Benraiss , A , Mariani , J N , Tate , A , Madsen , P M , Clark , K M , Welle , K A , Solly , R , Capellano , L , Bentley , K , Chandler-Militello , D & Goldman , S A 2022 , ' A TCF7L2-responsive suppression of both homeostatic and compensatory remyelination in Huntington disease mice ' , Cell Reports , vol. 40 , no. 9 , 111291 .
Publication Year :
2022

Abstract

Huntington’s disease (HD) is characterized by defective oligodendroglial differentiation and white matter disease. Here, we investigate the role of oligodendrocyte progenitor cell (OPC) dysfunction in adult myelin maintenance in HD. We first note a progressive, age-related loss of myelin in both R6/2 and zQ175 HD mice compared with wild-type controls. Adult R6/2 mice then manifest a significant delay in remyelination following cuprizone demyelination. RNA-sequencing and proteomic analysis of callosal white matter and OPCs isolated from both R6/2 and zQ175 mice reveals a systematic downregulation of genes associated with oligodendrocyte differentiation and myelinogenesis. Gene co-expression and network analysis predicts repressed Tcf7l2 signaling as a major driver of this expression pattern. In vivo Tcf7l2 overexpression restores both myelin gene expression and remyelination in demyelinated R6/2 mice. These data causally link impaired TCF7L2-dependent transcription to the poor development and homeostatic retention of myelin in HD and provide a mechanism for its therapeutic restoration.<br />Huntington's disease (HD) is characterized by defective oligodendroglial differentiation and white matter disease. Here, we investigate the role of oligodendrocyte progenitor cell (OPC) dysfunction in adult myelin maintenance in HD. We first note a progressive, age-related loss of myelin in both R6/2 and zQ175 HD mice compared with wild-type controls. Adult R6/2 mice then manifest a significant delay in remyelination following cuprizone demyelination. RNA-sequencing and proteomic analysis of callosal white matter and OPCs isolated from both R6/2 and zQ175 mice reveals a systematic downregulation of genes associated with oligodendrocyte differentiation and myelinogenesis. Gene co-expression and network analysis predicts repressed Tcf7l2 signaling as a major driver of this expression pattern. In vivo Tcf7l2 overexpression restores both myelin gene expression and remyelination in demyelinated R6/2 mice. These data causally link impaired TCF7L2-dependent transcription to the poor development and homeostatic retention of myelin in HD and provide a mechanism for its therapeutic restoration.

Details

Database :
OAIster
Journal :
Benraiss , A , Mariani , J N , Tate , A , Madsen , P M , Clark , K M , Welle , K A , Solly , R , Capellano , L , Bentley , K , Chandler-Militello , D & Goldman , S A 2022 , ' A TCF7L2-responsive suppression of both homeostatic and compensatory remyelination in Huntington disease mice ' , Cell Reports , vol. 40 , no. 9 , 111291 .
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1382500199
Document Type :
Electronic Resource