Back to Search Start Over

Brain CHID1 Expression Correlates with NRGN and CALB1 in Healthy Subjects and AD Patients.

Authors :
Castrogiovanni P
Sanfilippo C
Imbesi R
Maugeri G
Lo Furno D
Tibullo D
Castorina A
Musumeci G
Di Rosa M
Source :
Cells [Cells] 2021 Apr 13; Vol. 10 (4). Date of Electronic Publication: 2021 Apr 13.
Publication Year :
2021

Abstract

Alzheimer's disease is a progressive, devastating, and irreversible brain disorder that, day by day, destroys memory skills and social behavior. Despite this, the number of known genes suitable for discriminating between AD patients is insufficient. Among the genes potentially involved in the development of AD, there are the chitinase-like proteins (CLPs) CHI3L1, CHI3L2, and CHID1. The genes of the first two have been extensively investigated while, on the contrary, little information is available on CHID1. In this manuscript, we conducted transcriptome meta-analysis on an extensive sample of brains of healthy control subjects (n = 1849) (NDHC) and brains of AD patients (n = 1170) in order to demonstrate CHID1 involvement. Our analysis revealed an inverse correlation between the brain CHID1 expression levels and the age of NDHC subjects. Significant differences were highlighted comparing CHID1 expression of NDHC subjects and AD patients. Exclusive in AD patients, the CHID1 expression levels were correlated positively to calcium-binding adapter molecule 1 ( IBA1 ) levels. Furthermore, both in NDHC and in AD patient's brains, the CHID1 expression levels were directly correlated with calbindin 1 ( CALB1 ) and neurogranin ( NRGN ). According to brain regions, correlation differences were shown between the expression levels of CHID1 in prefrontal, frontal, occipital, cerebellum, temporal, and limbic system. Sex-related differences were only highlighted in NDHC. CHID1 represents a new chitinase potentially involved in the principal processes underlying Alzheimer's disease.

Details

Language :
English
ISSN :
2073-4409
Volume :
10
Issue :
4
Database :
MEDLINE
Journal :
Cells
Publication Type :
Academic Journal
Accession number :
33924468
Full Text :
https://doi.org/10.3390/cells10040882