New Insights into Endogenous Retrovirus-K Transcripts in Amyotrophic Lateral Sclerosis

Author:

Moreno-Martinez Laura1234ORCID,Macías-Redondo Sofía5,Strunk Mark5,Guillén-Antonini María Isabel3,Lunetta Christian678,Tarlarini Claudia8,Penco Silvana8,Calvo Ana Cristina1234ORCID,Osta Rosario1234ORCID,Schoorlemmer Jon359

Affiliation:

1. Laboratory of Genetics and Biochemistry (LAGENBIO), Faculty of Veterinary, University of Zaragoza, Miguel Servet 177, 50013 Zaragoza, Spain

2. Centro de Investigación Biomédica en Red en Enfermedades Neurodegenerativas, Instituto de Salud Carlos III (CIBER-CIBERNED-ISCIII), 28029 Madrid, Spain

3. Instituto de Investigación Sanitaria Aragón (IIS Aragón), 50009 Zaragoza, Spain

4. Instituto Agroalimentario de Aragón (IA2), University of Zaragoza-CITA, C/Miguel, Servet 177, 50013 Zaragoza, Spain

5. Instituto Aragonés de Ciencias de la Salud (IACS), Centro de Investigación Biomédica de Aragón (CIBA), 50009 Zaragoza, Spain

6. NEMO (NEuroMuscular Omnicentre) Clinical Center, Fondazione Serena Onlus, 20162 Milan, Italy

7. Neurorehabilitation Department of Milano Institute, Istituti Clinici Scientifici Maugeri IRCCS, 20138 Milan, Italy

8. Medical Genetics Unit, Department of Laboratory Medicine, ASST Grande Ospedale Metropolitano Niguarda, 20162 Milan, Italy

9. ARAID Foundation, 50009 Zaragoza, Spain

Abstract

Retroviral reverse transcriptase activity and the increased expression of human endogenous retroviruses (HERVs) are associated with amyotrophic lateral sclerosis (ALS). We were interested in confirming HERVK overexpression in the ALS brain, its use as an accessory diagnostic marker for ALS, and its potential interplay with neuroinflammation. Using qPCR to analyze HERVK expression in peripheral blood mononuclear cells (PBMCs) and in postmortem brain samples from ALS patients, no significant differences were observed between patients and control subjects. By contrast, we report alterations in the expression patterns of specific HERVK copies, especially in the brainstem. Out of 27 HERVK copies sampled, the relative expression of 17 loci was >1.2-fold changed in samples from ALS patients. In particular, the relative expression of two HERVK copies (Chr3-3 and Chr3-5) was significantly different in brainstem samples from ALS patients compared with controls. Further qPCR analysis of inflammation markers in brain samples revealed a significant increase in NLRP3 levels, while TNFA, IL6, and GZMB showed slight decreases. We cannot confirm global HERVK overexpression in ALS, but we can report the ALS-specific overexpression of selected HERVK copies in the ALS brain. Our data are compatible with the requirement for better patient stratification and support the potential importance of particular HERVK copies in ALS.

Funder

Ayudas de Investigación sobre Medicamentos Huérfanos y Enfermedades Raras 2016

Instituto de Salud Carlos III

Fondo Europeo de Desarrollo Regional

Government of Aragon

DGA

Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca, IMIB

Publisher

MDPI AG

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