Protein Expression of TXNIP in the Dopaminergic Neurons of Subjects with Parkinson’s Disease: Evidence from a Pilot Study
Parkinson’s disease (PD) is a progressive, multisystemic α-synucleinopathy, recognized as the second most prevalent neurodegenerative disorder globally. Its neuropathology is characterized by the degeneration of dopaminergic neurons, particularly in the substantia nigra pars compacta (SNpc), and the...
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Published in | Life (Basel, Switzerland) Vol. 15; no. 8; p. 1252 |
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Main Authors | , , , , |
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Language | English |
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DOI | 10.3390/life15081252 |
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Abstract | Parkinson’s disease (PD) is a progressive, multisystemic α-synucleinopathy, recognized as the second most prevalent neurodegenerative disorder globally. Its neuropathology is characterized by the degeneration of dopaminergic neurons, particularly in the substantia nigra pars compacta (SNpc), and the intraneuronal accumulation of α-synuclein-forming Lewy bodies. Oxidative stress is a key contributor to PD pathogenesis. Thioredoxin-interacting protein (TXNIP) is a crucial regulator of cellular redox balance, inhibiting the antioxidant function of thioredoxin. This pilot study aimed to investigate the protein expression and localization of TXNIP in the SNpc of PD patients compared to healthy controls. We performed immunohistochemical analyses on 12 post-mortem human brain sections (formalin-fixed, paraffin-embedded) from six subjects with PD and six healthy controls. The study was performed on PD subjects with Braak stage 6. Our findings revealed that in control samples, TXNIP protein was distinctly and closely associated with neuromelanin (NM) pigment within the cytoplasm of SNpc dopaminergic neurons. Conversely, in PD samples, there was a markedly weak cytoplasmic expression of TXNIP, and critically, this association with NM pigment was absent. Furthermore, PD samples exhibited a significant reduction in both dopaminergic neurons and NM content, consistent with advanced disease. These findings, which mirror previous transcriptomic data showing TXNIP gene under-expression in the same subjects, suggest that altered TXNIP expression and localization in SNpc dopaminergic neurons are features of late-stage PD, potentially reflecting neuronal dysfunction and loss. |
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AbstractList | Parkinson's disease (PD) is a progressive, multisystemic α-synucleinopathy, recognized as the second most prevalent neurodegenerative disorder globally. Its neuropathology is characterized by the degeneration of dopaminergic neurons, particularly in the substantia nigra pars compacta (SNpc), and the intraneuronal accumulation of α-synuclein-forming Lewy bodies. Oxidative stress is a key contributor to PD pathogenesis. Thioredoxin-interacting protein (TXNIP) is a crucial regulator of cellular redox balance, inhibiting the antioxidant function of thioredoxin. This pilot study aimed to investigate the protein expression and localization of TXNIP in the SNpc of PD patients compared to healthy controls. We performed immunohistochemical analyses on 12 post-mortem human brain sections (formalin-fixed, paraffin-embedded) from six subjects with PD and six healthy controls. The study was performed on PD subjects with Braak stage 6. Our findings revealed that in control samples, TXNIP protein was distinctly and closely associated with neuromelanin (NM) pigment within the cytoplasm of SNpc dopaminergic neurons. Conversely, in PD samples, there was a markedly weak cytoplasmic expression of TXNIP, and critically, this association with NM pigment was absent. Furthermore, PD samples exhibited a significant reduction in both dopaminergic neurons and NM content, consistent with advanced disease. These findings, which mirror previous transcriptomic data showing TXNIP gene under-expression in the same subjects, suggest that altered TXNIP expression and localization in SNpc dopaminergic neurons are features of late-stage PD, potentially reflecting neuronal dysfunction and loss.Parkinson's disease (PD) is a progressive, multisystemic α-synucleinopathy, recognized as the second most prevalent neurodegenerative disorder globally. Its neuropathology is characterized by the degeneration of dopaminergic neurons, particularly in the substantia nigra pars compacta (SNpc), and the intraneuronal accumulation of α-synuclein-forming Lewy bodies. Oxidative stress is a key contributor to PD pathogenesis. Thioredoxin-interacting protein (TXNIP) is a crucial regulator of cellular redox balance, inhibiting the antioxidant function of thioredoxin. This pilot study aimed to investigate the protein expression and localization of TXNIP in the SNpc of PD patients compared to healthy controls. We performed immunohistochemical analyses on 12 post-mortem human brain sections (formalin-fixed, paraffin-embedded) from six subjects with PD and six healthy controls. The study was performed on PD subjects with Braak stage 6. Our findings revealed that in control samples, TXNIP protein was distinctly and closely associated with neuromelanin (NM) pigment within the cytoplasm of SNpc dopaminergic neurons. Conversely, in PD samples, there was a markedly weak cytoplasmic expression of TXNIP, and critically, this association with NM pigment was absent. Furthermore, PD samples exhibited a significant reduction in both dopaminergic neurons and NM content, consistent with advanced disease. These findings, which mirror previous transcriptomic data showing TXNIP gene under-expression in the same subjects, suggest that altered TXNIP expression and localization in SNpc dopaminergic neurons are features of late-stage PD, potentially reflecting neuronal dysfunction and loss. Parkinson’s disease (PD) is a progressive, multisystemic α-synucleinopathy, recognized as the second most prevalent neurodegenerative disorder globally. Its neuropathology is characterized by the degeneration of dopaminergic neurons, particularly in the substantia nigra pars compacta (SNpc), and the intraneuronal accumulation of α-synuclein-forming Lewy bodies. Oxidative stress is a key contributor to PD pathogenesis. Thioredoxin-interacting protein (TXNIP) is a crucial regulator of cellular redox balance, inhibiting the antioxidant function of thioredoxin. This pilot study aimed to investigate the protein expression and localization of TXNIP in the SNpc of PD patients compared to healthy controls. We performed immunohistochemical analyses on 12 post-mortem human brain sections (formalin-fixed, paraffin-embedded) from six subjects with PD and six healthy controls. The study was performed on PD subjects with Braak stage 6. Our findings revealed that in control samples, TXNIP protein was distinctly and closely associated with neuromelanin (NM) pigment within the cytoplasm of SNpc dopaminergic neurons. Conversely, in PD samples, there was a markedly weak cytoplasmic expression of TXNIP, and critically, this association with NM pigment was absent. Furthermore, PD samples exhibited a significant reduction in both dopaminergic neurons and NM content, consistent with advanced disease. These findings, which mirror previous transcriptomic data showing TXNIP gene under-expression in the same subjects, suggest that altered TXNIP expression and localization in SNpc dopaminergic neurons are features of late-stage PD, potentially reflecting neuronal dysfunction and loss. |
Audience | Academic |
Author | Lanza, Giuseppe Salluzzo, Maria Grazia Salemi, Michele Ferri, Raffaele Schillaci, Francesca A. |
AuthorAffiliation | 1 Oasi Research Institute-IRCCS, 94018 Troina, Italy; glanza@oasi.en.it (G.L.); msalluzzo@oasi.en.it (M.G.S.); rferri@oasi.en.it (R.F.); msalemi@oasi.en.it (M.S.) 2 Department of Surgery and Medical-Surgical Specialties, University of Catania, 95125 Catania, Italy |
AuthorAffiliation_xml | – name: 2 Department of Surgery and Medical-Surgical Specialties, University of Catania, 95125 Catania, Italy – name: 1 Oasi Research Institute-IRCCS, 94018 Troina, Italy; glanza@oasi.en.it (G.L.); msalluzzo@oasi.en.it (M.G.S.); rferri@oasi.en.it (R.F.); msalemi@oasi.en.it (M.S.) |
Author_xml | – sequence: 1 givenname: Francesca A. orcidid: 0009-0004-7185-1176 surname: Schillaci fullname: Schillaci, Francesca A. – sequence: 2 givenname: Giuseppe orcidid: 0000-0002-5659-662X surname: Lanza fullname: Lanza, Giuseppe – sequence: 3 givenname: Maria Grazia orcidid: 0000-0001-6240-1975 surname: Salluzzo fullname: Salluzzo, Maria Grazia – sequence: 4 givenname: Raffaele orcidid: 0000-0001-6937-3065 surname: Ferri fullname: Ferri, Raffaele – sequence: 5 givenname: Michele surname: Salemi fullname: Salemi, Michele |
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Cites_doi | 10.1038/s41598-019-52829-8 10.3390/ijms18030551 10.1016/j.ejphar.2025.177806 10.1016/j.nbd.2019.104700 10.3390/ijms22052754 10.3390/biomedicines11123118 10.1101/cshperspect.a033118 10.1111/neup.12259 10.1038/s41419-018-0798-0 10.1101/cshperspect.a028035 10.1007/s11682-023-00815-0 10.1186/s12974-025-03462-y 10.3390/ijms23031535 10.3390/ijms24010712 10.1007/s12264-019-00459-5 10.1002/mds.27776 10.1016/j.clinph.2019.09.004 10.1016/j.parkreldis.2023.105448 10.1016/S0140-6736(23)01419-8 10.1111/cns.12721 10.3390/nano14020170 10.3390/jpm10040274 10.3390/brainsci11121588 10.1016/j.nbd.2007.02.009 10.1146/annurev.neuro.28.061604.135718 10.1016/j.intimp.2025.114691 10.1093/brain/awh584 10.1007/s11011-021-00689-5 10.1038/s12276-023-01019-8 10.1016/S0197-4580(02)00065-9 10.1007/978-1-4939-8935-5_25 10.1002/9780470479216 10.1038/s41531-018-0050-8 10.4103/0975-7406.100281 10.1016/j.cca.2021.08.009 10.1038/nrdp.2017.13 10.1016/S0197-0186(02)00161-4 10.3390/ijms25020707 10.2147/NSS.S266071 10.1016/bs.irn.2022.06.010 10.3390/diagnostics12020385 10.1038/s41598-025-01636-5 10.1016/0047-6374(83)90074-X 10.3390/ijms252313107 10.3389/fnagi.2022.804385 10.3390/ijms21249357 10.1007/978-3-319-30634-6_4 10.1016/j.ncl.2022.12.001 10.3389/fneur.2020.00180 |
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Keywords | substantia nigra immunohistochemistry Parkinson’s disease dopaminergic neurons TXNIP protein |
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References | Padhy (ref_36) 2025; 156 Darweesh (ref_2) 2024; 403 Zucca (ref_42) 2018; 4 Bouzou (ref_50) 2007; 26 ref_13 ref_11 ref_10 Duraiyan (ref_29) 2012; 4 Checkoway (ref_5) 2011; 163 ref_19 Poewe (ref_25) 2017; 3 ref_17 ref_16 Braak (ref_28) 2003; 24 Choi (ref_48) 2023; 55 Figorilli (ref_15) 2023; 15 Patil (ref_37) 2025; 1002 Fasano (ref_22) 2003; 42 Zaman (ref_24) 2021; 36 Su (ref_9) 2017; 23 Patel (ref_52) 2023; 41 ref_26 Araki (ref_12) 2016; 36 Mogensen (ref_44) 2025; 22 Donzuso (ref_18) 2024; 18 Magaki (ref_27) 2019; 1897 ref_35 ref_34 ref_33 Marsden (ref_38) 1983; 19 ref_32 ref_31 (ref_39) 2018; 9 ref_30 Moore (ref_23) 2005; 28 Arabia (ref_51) 2022; 164 Halliday (ref_41) 2005; 128 Salemi (ref_49) 2023; 19 ref_47 ref_46 Su (ref_45) 2020; 36 ref_1 ref_3 Vila (ref_20) 2019; 34 Mitra (ref_43) 2023; 112 Mann (ref_40) 1983; 21 Latif (ref_21) 2021; 522 ref_8 ref_4 ref_7 Terao (ref_14) 2019; 130 ref_6 |
References_xml | – ident: ref_16 doi: 10.1038/s41598-019-52829-8 – volume: 163 start-page: 407 year: 2011 ident: ref_5 article-title: Neurodegenerative Diseases publication-title: IARC Sci. Publ. – ident: ref_6 doi: 10.3390/ijms18030551 – volume: 1002 start-page: 177806 year: 2025 ident: ref_37 article-title: Thioredoxin-Interacting Protein: An Emerging Target for Alzheimer’s Disease publication-title: Eur. J. Pharmacol. doi: 10.1016/j.ejphar.2025.177806 – ident: ref_8 doi: 10.1016/j.nbd.2019.104700 – volume: 19 start-page: 678 year: 2023 ident: ref_49 article-title: mRNA Expression Profiling of Mitochondrial Subunits in Subjects with Parkinson’s Disease publication-title: Arch. Med. Sci. – ident: ref_47 doi: 10.3390/ijms22052754 – ident: ref_19 doi: 10.3390/biomedicines11123118 – ident: ref_1 doi: 10.1101/cshperspect.a033118 – volume: 36 start-page: 187 year: 2016 ident: ref_12 article-title: Progressive Supranuclear Palsy and Parkinson’s Disease Overlap: A Clinicopathological Case Report publication-title: Neuropathology doi: 10.1111/neup.12259 – volume: 9 start-page: 748 year: 2018 ident: ref_39 article-title: Can We Conclude a Potential Therapeutic Action for Parkinson’s Disease by Using Postmortem Tissue and a Preclinical Model Based on an Exogenous Neurotoxin? publication-title: Cell Death Dis. doi: 10.1038/s41419-018-0798-0 – ident: ref_3 doi: 10.1101/cshperspect.a028035 – volume: 18 start-page: 83 year: 2024 ident: ref_18 article-title: Neuroanatomical Findings in Isolated REM Sleep Behavior Disorder and Early Parkinson’s Disease: A Voxel-Based Morphometry Study publication-title: Brain Imaging Behav. doi: 10.1007/s11682-023-00815-0 – volume: 22 start-page: 136 year: 2025 ident: ref_44 article-title: Microglial Dynamics and Neuroinflammation in Prodromal and Early Parkinson’s Disease publication-title: J. Neuroinflamm. doi: 10.1186/s12974-025-03462-y – ident: ref_34 doi: 10.3390/ijms23031535 – ident: ref_33 doi: 10.3390/ijms24010712 – volume: 36 start-page: 346 year: 2020 ident: ref_45 article-title: Thioredoxin-Interacting Protein (TXNIP) Regulates Parkin/PINK1-Mediated Mitophagy in Dopaminergic Neurons Under High-Glucose Conditions: Implications for Molecular Links Between Parkinson’s Disease and Diabetes publication-title: Neurosci. Bull. doi: 10.1007/s12264-019-00459-5 – volume: 34 start-page: 1440 year: 2019 ident: ref_20 article-title: Neuromelanin, Aging, and Neuronal Vulnerability in Parkinson’s Disease publication-title: Mov. Disord. doi: 10.1002/mds.27776 – volume: 130 start-page: 2203 year: 2019 ident: ref_14 article-title: Differentiating Early Parkinson’s Disease and Multiple System Atrophy with Parkinsonism by Saccade Velocity Profiles publication-title: Clin. Neurophysiol. doi: 10.1016/j.clinph.2019.09.004 – volume: 112 start-page: 105448 year: 2023 ident: ref_43 article-title: Neuromelanin: Its Role in the Pathogenesis of Idiopathic Parkinson’s Disease and Potential as a Therapeutic Target publication-title: Park. Relat. Disord. doi: 10.1016/j.parkreldis.2023.105448 – volume: 403 start-page: 283 year: 2024 ident: ref_2 article-title: The Epidemiology of Parkinson’s Disease publication-title: Lancet doi: 10.1016/S0140-6736(23)01419-8 – volume: 23 start-page: 717 year: 2017 ident: ref_9 article-title: Thioredoxin-Interacting Protein Induced α-Synuclein Accumulation via Inhibition of Autophagic Flux: Implications for Parkinson’s Disease publication-title: CNS Neurosci. Ther. doi: 10.1111/cns.12721 – ident: ref_10 doi: 10.3390/nano14020170 – ident: ref_4 doi: 10.3390/jpm10040274 – ident: ref_7 doi: 10.3390/brainsci11121588 – volume: 26 start-page: 606 year: 2007 ident: ref_50 article-title: Effects of Gender on Nigral Gene Expression and Parkinson Disease publication-title: Neurobiol. Dis. doi: 10.1016/j.nbd.2007.02.009 – volume: 28 start-page: 57 year: 2005 ident: ref_23 article-title: Molecular Pathophysiology of Parkinson’s Disease publication-title: Annu. Rev. Neurosci. doi: 10.1146/annurev.neuro.28.061604.135718 – volume: 19 start-page: 121 year: 1983 ident: ref_38 article-title: Neuromelanin and Parkinson’s Disease publication-title: J. Neural Transm. Suppl. – volume: 156 start-page: 114691 year: 2025 ident: ref_36 article-title: Neuroprotective Potential of Tranilast in Streptozotocin-Induced Sporadic Alzheimer’s Disease Model Targeting TXNIP-NLRP3 Inflammasome Pathway publication-title: Int. Immunopharmacol. doi: 10.1016/j.intimp.2025.114691 – volume: 128 start-page: 2654 year: 2005 ident: ref_41 article-title: Alpha-Synuclein Redistributes to Neuromelanin Lipid in the Substantia Nigra Early in Parkinson’s Disease publication-title: Brain doi: 10.1093/brain/awh584 – volume: 36 start-page: 815 year: 2021 ident: ref_24 article-title: Cellular and Molecular Pathophysiology in the Progression of Parkinson’s Disease publication-title: Metab. Brain Dis. doi: 10.1007/s11011-021-00689-5 – volume: 55 start-page: 1348 year: 2023 ident: ref_48 article-title: TXNIP: A Key Protein in the Cellular Stress Response Pathway and a Potential Therapeutic Target publication-title: Exp. Mol. Med. doi: 10.1038/s12276-023-01019-8 – volume: 24 start-page: 197 year: 2003 ident: ref_28 article-title: Staging of Brain Pathology Related to Sporadic Parkinson’s Disease publication-title: Neurobiol. Aging doi: 10.1016/S0197-4580(02)00065-9 – volume: 1897 start-page: 289 year: 2019 ident: ref_27 article-title: An Introduction to the Performance of Immunohistochemistry publication-title: Methods Mol. Biol. doi: 10.1007/978-1-4939-8935-5_25 – ident: ref_31 doi: 10.1002/9780470479216 – volume: 4 start-page: 17 year: 2018 ident: ref_42 article-title: Neuromelanin Organelles Are Specialized Autolysosomes That Accumulate Undegraded Proteins and Lipids in Aging Human Brain and Are Likely Involved in Parkinson’s Disease publication-title: NPJ Park. Dis. doi: 10.1038/s41531-018-0050-8 – volume: 4 start-page: S307 year: 2012 ident: ref_29 article-title: Applications of Immunohistochemistry publication-title: J. Pharm. Bioallied Sci. doi: 10.4103/0975-7406.100281 – volume: 522 start-page: 114 year: 2021 ident: ref_21 article-title: Dopamine in Parkinson’s Disease publication-title: Clin. Chim. Acta doi: 10.1016/j.cca.2021.08.009 – volume: 3 start-page: 17013 year: 2017 ident: ref_25 article-title: Parkinson Disease publication-title: Nat. Rev. Dis. Primers doi: 10.1038/nrdp.2017.13 – volume: 42 start-page: 603 year: 2003 ident: ref_22 article-title: Residual Substantia Nigra Neuromelanin in Parkinson’s Disease Is Cross-Linked to Alpha-Synuclein publication-title: Neurochem. Int. doi: 10.1016/S0197-0186(02)00161-4 – ident: ref_26 doi: 10.3390/ijms25020707 – volume: 15 start-page: 333 year: 2023 ident: ref_15 article-title: Considering REM Sleep Behavior Disorder in the Management of Parkinson’s Disease publication-title: Nat. Sci. Sleep doi: 10.2147/NSS.S266071 – volume: 164 start-page: 101 year: 2022 ident: ref_51 article-title: Sex and Gender Differences in Movement Disorders: Parkinson’s Disease, Essential Tremor, Dystonia and Chorea publication-title: Int. Rev. Neurobiol. doi: 10.1016/bs.irn.2022.06.010 – ident: ref_17 doi: 10.3390/diagnostics12020385 – ident: ref_35 doi: 10.1038/s41598-025-01636-5 – volume: 21 start-page: 193 year: 1983 ident: ref_40 article-title: Possible Role of Neuromelanin in the Pathogenesis of Parkinson’s Disease publication-title: Mech. Ageing Dev. doi: 10.1016/0047-6374(83)90074-X – ident: ref_32 doi: 10.3390/ijms252313107 – ident: ref_13 doi: 10.3389/fnagi.2022.804385 – ident: ref_46 doi: 10.3390/ijms21249357 – ident: ref_30 doi: 10.1007/978-3-319-30634-6_4 – volume: 41 start-page: 371 year: 2023 ident: ref_52 article-title: Sex and Gender Differences in Parkinson’s Disease publication-title: Neurol. Clin. doi: 10.1016/j.ncl.2022.12.001 – ident: ref_11 doi: 10.3389/fneur.2020.00180 |
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Snippet | Parkinson’s disease (PD) is a progressive, multisystemic α-synucleinopathy, recognized as the second most prevalent neurodegenerative disorder globally. Its... Parkinson's disease (PD) is a progressive, multisystemic α-synucleinopathy, recognized as the second most prevalent neurodegenerative disorder globally. Its... |
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SubjectTerms | Antibodies Antigens Antioxidants Biomarkers Brain Brain research Cytoplasm Degeneration Development and progression Disease Diseases Dopamine receptors dopaminergic neurons Genes Immunohistochemistry Italy Lewy bodies Localization Medical research Medicine, Experimental Movement disorders Multiple sclerosis Neurodegeneration Neurodegenerative diseases Neurons Neuropathology New Mexico Oxidative stress Parkinson's disease Pathogenesis Pigments Pilot projects Protein expression Proteins Software Substantia nigra Synuclein Thioredoxin Transcriptomics TXNIP protein United Kingdom |
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Title | Protein Expression of TXNIP in the Dopaminergic Neurons of Subjects with Parkinson’s Disease: Evidence from a Pilot Study |
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