Related Experiment Video
Updated: Oct 20, 2025

Systemic Delivery of MicroRNA Using Recombinant Adeno-associated Virus Serotype 9 to Treat Neuromuscular Diseases in Rodents
Published on: August 10, 2018
microRNA-146a-5p, Neurotropic Viral Infection and Prion Disease (PrD)
Aileen I Pogue1, Walter J Lukiw2,3,4
1Alchem Biotech, Toronto, ON M5S 1A8, Canada.
Abstract:
The human brain and central nervous system (CNS) harbor a select sub-group of potentially pathogenic microRNAs (miRNAs), including a well-characterized NF-kB-sensitive Homo sapiens microRNA hsa-miRNA-146a-5p (miRNA-146a). miRNA-146a is significantly over-expressed in progressive and often lethal viral- and prion-mediated and related neurological syndromes associated with progressive inflammatory neurodegeneration. These include ~18 different viral-induced encephalopathies for which data are available, at least ~10 known prion diseases (PrD) of animals and humans, Alzheimer's disease (AD) and other sporadic and progressive age-related neurological disorders. Despite the apparent lack of nucleic acids in prions, both DNA- and RNA-containing viruses along with prions significantly induce miRNA-146a in the infected host, but whether this represents part of the host's adaptive immunity, innate-immune response or a mechanism to enable the invading prion or virus a successful infection is not well understood. Current findings suggest an early and highly interactive role for miRNA-146a: (i) as a major small noncoding RNA (sncRNA) regulator of innate-immune responses and inflammatory signaling in cells of the human brain and CNS; (ii) as a critical component of the complement system and immune-related neurological dysfunction; (iii) as an inducible sncRNA of the brain and CNS that lies at a critical intersection of several important neurobiological adaptive immune response processes with highly interactive associations involving complement factor H (CFH), Toll-like receptor pathways, the innate-immunity, cytokine production, apoptosis and neural cell decline; and (iv) as a potential biomarker for viral infection, TSE and AD and other neurological diseases in both animals and humans. In this report, we review the recent data supporting the idea that miRNA-146a may represent a novel and unique sncRNA-based biomarker for inflammatory neurodegeneration in multiple species. This paper further reviews the current state of knowledge regarding the nature and mechanism of miRNA-146a in viral and prion infection of the human brain and CNS with reference to AD wherever possible.
Insights
Homo sapiens microRNA hsa-miRNA-146a-5p (miRNA-146a) is over-expressed in progressive neurological disorders. This small noncoding RNA may serve as a biomarker for inflammatory neurodegeneration in various species.
Area of Science:
- Neuroscience
- Immunology
- Molecular Biology
Background:
- The human brain and central nervous system (CNS) contain pathogenic microRNAs (miRNAs), including Homo sapiens microRNA hsa-miRNA-146a-5p (miRNA-146a).
- miRNA-146a is significantly over-expressed in progressive, often lethal, viral- and prion-mediated neurological syndromes associated with inflammatory neurodegeneration, including viral encephalopathies, prion diseases, Alzheimer's disease (AD), and other age-related neurological disorders.
Purpose of the Study:
- To review current data on miRNA-146a's role in viral and prion infections of the human brain and CNS.
- To explore miRNA-146a as a potential biomarker for inflammatory neurodegeneration in multiple species, including its association with AD.
Main Methods:
- Literature review of recent data on miRNA-146a.
- Analysis of miRNA-146a's role in innate-immune responses, inflammatory signaling, complement system, and neurobiological processes.
- Examination of miRNA-146a's potential as a biomarker for neurological diseases.
Main Results:
- miRNA-146a is a key regulator of innate-immune responses and inflammatory signaling in the brain and CNS.
- It plays a critical role in the complement system and immune-related neurological dysfunction.
- miRNA-146a is an inducible small noncoding RNA (sncRNA) at the intersection of immune responses, complement factor H (CFH), Toll-like receptor pathways, cytokine production, apoptosis, and neural cell decline.
- It shows potential as a biomarker for viral infections, transmissible spongiform encephalopathies (TSEs), and AD.
Conclusions:
- miRNA-146a is a crucial sncRNA regulator in the brain's immune response and inflammatory processes.
- It is intricately linked to neuroinflammation, immune pathways, and neurodegeneration.
- miRNA-146a represents a promising novel sncRNA-based biomarker for inflammatory neurodegeneration across species.
Related Concept Videos
MicroRNAs
Subviral Agents
siRNA - Small Interfering RNAs
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...

