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Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease

Proenkephalin (PENK) and prodynorphin (PDYN) are endogenous opioid peptides mainly produced in the striatum and, to a lesser extent, in the cerebral cortex. Dysregulated metabolism and altered cerebrospinal fluid (CSF) levels of PENK and PDYN have been described in several neurodegenerative diseases...

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Autores principales: Abu-Rumeileh, Samir, Barschke, Peggy, Oeckl, Patrick, Baiardi, Simone, Mammana, Angela, Mastrangelo, Andrea, Al Shweiki, Mhd Rami, Steinacker, Petra, Ladogana, Anna, Capellari, Sabina, Otto, Markus, Parchi, Piero
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8877714/
https://www.ncbi.nlm.nih.gov/pubmed/35216166
http://dx.doi.org/10.3390/ijms23042051
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author Abu-Rumeileh, Samir
Barschke, Peggy
Oeckl, Patrick
Baiardi, Simone
Mammana, Angela
Mastrangelo, Andrea
Al Shweiki, Mhd Rami
Steinacker, Petra
Ladogana, Anna
Capellari, Sabina
Otto, Markus
Parchi, Piero
author_facet Abu-Rumeileh, Samir
Barschke, Peggy
Oeckl, Patrick
Baiardi, Simone
Mammana, Angela
Mastrangelo, Andrea
Al Shweiki, Mhd Rami
Steinacker, Petra
Ladogana, Anna
Capellari, Sabina
Otto, Markus
Parchi, Piero
author_sort Abu-Rumeileh, Samir
collection PubMed
description Proenkephalin (PENK) and prodynorphin (PDYN) are endogenous opioid peptides mainly produced in the striatum and, to a lesser extent, in the cerebral cortex. Dysregulated metabolism and altered cerebrospinal fluid (CSF) levels of PENK and PDYN have been described in several neurodegenerative diseases. However, no study to date investigated these peptides in the CSF of sporadic Creutzfeldt–Jakob disease (sCJD). Using liquid chromatography-multiple reaction monitoring mass spectrometry, we evaluated the CSF PDYN- and PENK-derived peptide levels in 25 controls and 63 patients with sCJD belonging to the most prevalent molecular subtypes (MM(V)1, VV2 and MV2K). One of the PENK-derived peptides was significantly decreased in each sCJD subtype compared to the controls without a difference among subtypes. Conversely, PDYN-derived peptides were selectively decreased in the CSF of sCJD MV2K, a subtype with a more widespread overall pathology compared to the sCJD MM(V)1 and the VV2 subtypes, which we confirmed by semiquantitative analysis of cortical and striatal neuronal loss and astrocytosis. In sCJD CSF PENK and PDYN were associated with CSF biomarkers of neurodegeneration but not with clinical variables and showed a poor diagnostic performance. CSF PDYN and PENK-derived peptides had no significant diagnostic and prognostic values in sCJD; however, the distinct marker levels between molecular subtypes might help to better understand the basis of phenotypic heterogeneity determined by divergent neuronal targeting.
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spelling pubmed-88777142022-02-26 Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease Abu-Rumeileh, Samir Barschke, Peggy Oeckl, Patrick Baiardi, Simone Mammana, Angela Mastrangelo, Andrea Al Shweiki, Mhd Rami Steinacker, Petra Ladogana, Anna Capellari, Sabina Otto, Markus Parchi, Piero Int J Mol Sci Communication Proenkephalin (PENK) and prodynorphin (PDYN) are endogenous opioid peptides mainly produced in the striatum and, to a lesser extent, in the cerebral cortex. Dysregulated metabolism and altered cerebrospinal fluid (CSF) levels of PENK and PDYN have been described in several neurodegenerative diseases. However, no study to date investigated these peptides in the CSF of sporadic Creutzfeldt–Jakob disease (sCJD). Using liquid chromatography-multiple reaction monitoring mass spectrometry, we evaluated the CSF PDYN- and PENK-derived peptide levels in 25 controls and 63 patients with sCJD belonging to the most prevalent molecular subtypes (MM(V)1, VV2 and MV2K). One of the PENK-derived peptides was significantly decreased in each sCJD subtype compared to the controls without a difference among subtypes. Conversely, PDYN-derived peptides were selectively decreased in the CSF of sCJD MV2K, a subtype with a more widespread overall pathology compared to the sCJD MM(V)1 and the VV2 subtypes, which we confirmed by semiquantitative analysis of cortical and striatal neuronal loss and astrocytosis. In sCJD CSF PENK and PDYN were associated with CSF biomarkers of neurodegeneration but not with clinical variables and showed a poor diagnostic performance. CSF PDYN and PENK-derived peptides had no significant diagnostic and prognostic values in sCJD; however, the distinct marker levels between molecular subtypes might help to better understand the basis of phenotypic heterogeneity determined by divergent neuronal targeting. MDPI 2022-02-12 /pmc/articles/PMC8877714/ /pubmed/35216166 http://dx.doi.org/10.3390/ijms23042051 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Abu-Rumeileh, Samir
Barschke, Peggy
Oeckl, Patrick
Baiardi, Simone
Mammana, Angela
Mastrangelo, Andrea
Al Shweiki, Mhd Rami
Steinacker, Petra
Ladogana, Anna
Capellari, Sabina
Otto, Markus
Parchi, Piero
Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease
title Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease
title_full Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease
title_fullStr Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease
title_full_unstemmed Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease
title_short Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease
title_sort prodynorphin and proenkephalin in cerebrospinal fluid of sporadic creutzfeldt–jakob disease
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8877714/
https://www.ncbi.nlm.nih.gov/pubmed/35216166
http://dx.doi.org/10.3390/ijms23042051
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