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Association of Cadherin-Related Family Member 1 with Traumatic Brain Injury.

Authors :
Jiang Y
Chen P
Zhao Y
Zhang Y
Source :
Cellular and molecular neurobiology [Cell Mol Neurobiol] 2024 Apr 24; Vol. 44 (1), pp. 41. Date of Electronic Publication: 2024 Apr 24.
Publication Year :
2024

Abstract

The cadherin family plays a pivotal role in orchestrating synapse formation in the central nervous system. Cadherin-related family member 1 (CDHR1) is a photoreceptor-specific calmodulin belonging to the expansive cadherin superfamily. However, its role in traumatic brain injury (TBI) remains largely unknown. CDHR1 expression across various brain tissue sites was analyzed using the GSE104687 dataset. Employing a summary-data-based Mendelian Randomization (SMR) approach, integrated analyses were performed by amalgamating genome-wide association study abstracts from TBI with public data on expressed quantitative trait loci and DNA methylation QTL from both blood and diverse brain tissues. CDHR1 expression and localization in different brain tissues were meticulously delineated using western blotting, immunohistochemistry, and enzyme-linked immunosorbent assay. CDHR1 expression was consistently elevated in the TBI group compared to that in the sham group across multiple tissues. The inflammatory response emerged as a crucial biological mechanism, and pro-inflammatory and anti-inflammatory factors were not expressed in either group. Integrated SMR analyses encompassing both blood and brain tissues substantiated the heightened CDHR1 expression profiles, with methylation modifications emerging as potential contributing factors for increased TBI risk. This was corroborated by western blotting and immunohistochemistry, confirming augmented CDHR1 expression following TBI. This multi-omics-based genetic association study highlights the elevated TBI risk associated with CDHR1 expression coupled with putative methylation modifications. These findings provide compelling evidence for future targeted investigations and offer promising avenues for developing interventional therapies for TBI.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1573-6830
Volume :
44
Issue :
1
Database :
MEDLINE
Journal :
Cellular and molecular neurobiology
Publication Type :
Academic Journal
Accession number :
38656449
Full Text :
https://doi.org/10.1007/s10571-024-01476-3