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CD33 and SIGLECL1 Immunoglobulin Superfamily Involved in Dementia

Authors :
Rendina, Antonella
Drongitis, Denise
Donizetti, Aldo
Fucci, Laura
Milan, Graziella
Tripodi, Francesca
Giustezza, Francesca
Postiglione, Alfredo
Pappatà, Sabina
Ferrari, Raffaele
Bossù, Paola
Angiolillo, Antonella
di Costanzo, Alfonso
Caiazzo, Massimiliano
Vitale, Emilia
Rendina, Antonella
Drongitis, Denise
Donizetti, Aldo
Fucci, Laura
Milan, Graziella
Tripodi, Francesca
Giustezza, Francesca
Postiglione, Alfredo
Pappatà, Sabina
Ferrari, Raffaele
Bossù, Paola
Angiolillo, Antonella
di Costanzo, Alfonso
Caiazzo, Massimiliano
Vitale, Emilia
Source :
Journal of Neuropathology and Experimental Neurology vol.79 (2020) date: 2020-07-31 nr.8 p.891-901 [ISSN 0022-3069]
Publication Year :
2020

Abstract

Sialic acid-binding immunoglobulin-type lectins, which are predominantly expressed in immune cells, represent a family of immunomodulatory receptors with inhibitory and activating signals, in both healthy and disease states. Genetic factors are important in all forms of dementia, especially in early onset dementia. CD33 was recently recognized as a genetic risk factor for Alzheimer disease (AD). Here, we present a 2-generation family with 4 members, the father and the 3 siblings, characterized by an early form of unusual dementia exhibiting a behavioral variant close to behavioral variant frontotemporal dementia phenotype and severe forms of memory loss suggestive of AD. We analyzed the CD33 gene in this family and identified 10 single nucleotide polymorphisms (SNPs) in a linkage disequilibrium block associated with the disease. We also identified a tag SNP, rs2455069-A>G, in CD33 exon 2 that could be involved with dementia risk. Additionally, we excluded the presence of C9orf72 expansion mutations and other mutations previously associated with sporadic FTD and AD. The tag SNP association was also analyzed in selected sporadic AD patients from the same Southern Italy region. We demonstrate that CD33 and SIGLECL1 have a significantly increased level of expression in these patients.

Details

Database :
OAIster
Journal :
Journal of Neuropathology and Experimental Neurology vol.79 (2020) date: 2020-07-31 nr.8 p.891-901 [ISSN 0022-3069]
Notes :
DOI: 10.1093/jnen/nlaa055, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1445814967
Document Type :
Electronic Resource