» Articles » PMID: 27032392

The Effects of IFN-β 1a on the Expression of Inflammasomes and Apoptosis-Associated Speck-Like Proteins in Multiple Sclerosis Patients

Overview
Journal Mol Neurobiol
Date 2016 Apr 2
PMID 27032392
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

This study aims to evaluate the effects of treatment with IFN-β 1α on the expressions of NLRP3, NLRP1, NLRC4, and AIM2, as inflammasomes, and caspase-1, IL-1β, and IL-18, as the downstream molecules of inflammasomes, in a population of Iranian multiple sclerosis (MS) patients. In this study, 30 MS patients (22 women and 8 men) participated. Before receiving any medication and 6 months after treatment with standard doses of IFN-β 1α 30 mcg injected intramuscularly once a week, blood samples were taken and then the leukocytes isolated, total RNAs extracted, and complementary DNAs (cDNAs) synthesized. Gene expressions of NLRP3, NLRP1, NLRC4, AIM2, and ASC were evaluated at messenger RNA (mRNA) levels using real-time PCR method; for assessing caspase-1 at protein level, the Western blot method was used. The amounts of IL-1β and IL-18 were measured in plasma using enzyme-linked immunosorbent assay method. Analysis of the results before and after therapy with IFN-β 1α in all patients shows significantly decreased expressions of NLRP3, NLRC4, and AIM2. The plasma levels of IL-1β, after treatment with IFN-β 1α, were significantly decreased in the MS patients. Based on our results, it appears that NLRP3, NLRC4, and AIM2 play critical roles in the progression of MS, probably by mediating Th1 and Th17 responses. It seems that decreased expression of IL-1β is related to decreased production and also functions of inflammasomes.

Citing Articles

Inflammasomes in neurodegenerative diseases.

Wang Q, Yang S, Zhang X, Zhang S, Chen L, Wang W Transl Neurodegener. 2024; 13(1):65.

PMID: 39710713 PMC: 11665095. DOI: 10.1186/s40035-024-00459-0.


Microglial Mayhem NLRP3 Inflammasome's Role in Multiple Sclerosis Pathology.

Fan H, Fu Q, Du G, Qin L, Shi X, Wang D CNS Neurosci Ther. 2024; 30(12):e70135.

PMID: 39690733 PMC: 11652677. DOI: 10.1111/cns.70135.


Multiple sclerosis: the NLRP3 inflammasome, gasdermin D, and therapeutics.

Brint A, Greene S, Fennig-Victor A, Wang S Ann Transl Med. 2024; 12(4):62.

PMID: 39118955 PMC: 11304424. DOI: 10.21037/atm-23-1960.


Inflammasome Molecular Insights in Autoimmune Diseases.

Neamtu M, Bild V, Vasincu A, Arcan O, Bulea D, Ababei D Curr Issues Mol Biol. 2024; 46(4):3502-3532.

PMID: 38666950 PMC: 11048795. DOI: 10.3390/cimb46040220.


Inflammasomes in neurological disorders - mechanisms and therapeutic potential.

Ravichandran K, Heneka M Nat Rev Neurol. 2024; 20(2):67-83.

PMID: 38195712 DOI: 10.1038/s41582-023-00915-x.


References
1.
Szabo G, Csak T . Inflammasomes in liver diseases. J Hepatol. 2012; 57(3):642-54. DOI: 10.1016/j.jhep.2012.03.035. View

2.
Anderson G, Rodriguez M . Multiple sclerosis, seizures, and antiepileptics: role of IL-18, IDO, and melatonin. Eur J Neurol. 2010; 18(5):680-5. DOI: 10.1111/j.1468-1331.2010.03257.x. View

3.
McDonald W, Compston A, Edan G, Goodkin D, Hartung H, Lublin F . Recommended diagnostic criteria for multiple sclerosis: guidelines from the International Panel on the diagnosis of multiple sclerosis. Ann Neurol. 2001; 50(1):121-7. DOI: 10.1002/ana.1032. View

4.
Inoue M, Williams K, Oliver T, Vandenabeele P, Rajan J, Miao E . Interferon-β therapy against EAE is effective only when development of the disease depends on the NLRP3 inflammasome. Sci Signal. 2012; 5(225):ra38. PMC: 3509177. DOI: 10.1126/scisignal.2002767. View

5.
Inoue M, Williams K, Gunn M, Shinohara M . NLRP3 inflammasome induces chemotactic immune cell migration to the CNS in experimental autoimmune encephalomyelitis. Proc Natl Acad Sci U S A. 2012; 109(26):10480-5. PMC: 3387125. DOI: 10.1073/pnas.1201836109. View