Assessment of expression of RELN signaling pathway in multiple sclerosis patients.


Journal

Immunobiology
ISSN: 1878-3279
Titre abrégé: Immunobiology
Pays: Netherlands
ID NLM: 8002742

Informations de publication

Date de publication:
05 2019
Historique:
received: 12 01 2019
revised: 02 02 2019
accepted: 08 02 2019
pubmed: 20 2 2019
medline: 28 2 2020
entrez: 20 2 2019
Statut: ppublish

Résumé

Multiple sclerosis (MS) is a chronic demyelinating disease of the central nervous system. Nearly 85% of MS patients are recognized with relapsing-remitting MS (RRMS), a typical clinical course of disease which is distinguished by several episodes of relapses, separated by remissions of neurological impairment. Failure of repair mechanisms is a main factor in progression of neurological dysfunction in MS. Several lines of evidence suggest that Reelin (RELN) signaling pathway can contribute in the regulation of repair mechanisms in MS patients. In the present study, we assessed expression levels of RELN and Disabled-1 (DAB1), two key genes in RELN signaling pathway, in peripheral blood of 50 RRMS patients and 50 matched healthy subjects. RELN was significantly down-regulated in total MS patients, and total female patients compared with the matched controls. However, no statistically significant difference was found in DAB1 mRNA expression between MS patients and controls. Furthermore, considerable correlations were detected between expression levels of RELN and DAB1 in the patients group. There were no significant correlations between expression levels of genes and EDSS, disease duration or age at onset. Our study provides evidences for the role of RELN signaling pathway in the pathogenesis of MS. Further studies are required to clarify the exact clinical significance of this pathway in MS patients.

Identifiants

pubmed: 30777599
pii: S0171-2985(19)30010-5
doi: 10.1016/j.imbio.2019.02.007
pii:
doi:

Substances chimiques

Adaptor Proteins, Signal Transducing 0
Cell Adhesion Molecules, Neuronal 0
DAB1 protein, human 0
Extracellular Matrix Proteins 0
Nerve Tissue Proteins 0
RNA, Messenger 0
Reelin Protein 0
RELN protein, human EC 3.4.21.-
Serine Endopeptidases EC 3.4.21.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

402-407

Informations de copyright

Copyright © 2019 Elsevier GmbH. All rights reserved.

Auteurs

Shahrzad Talebian (S)

Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

Jalal Gharesouran (J)

Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Soudeh Ghafouri-Fard (S)

Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Behnaz Salek Esfahani (BS)

Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

Shahram Arsang-Jang (S)

Clinical Research Development Center (CRDU), Qom University of Medical Sciences, Qom, Iran.

Mir Davood Omrani (MD)

Urogenital Stem Cell Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Mohammad Taheri (M)

Student Research Committee, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: Mohammad.taheri@sbmu.ac.ir.

Maryam Rezazadeh (M)

Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran; Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. Electronic address: rezazadehma@tbzmed.ac.ir.

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Classifications MeSH