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      Cerebral dopamine neurotrophic factor transfection in dopamine neurons using neurotensin-polyplex nanoparticles reverses 6-hydroxydopamine-induced nigrostriatal neurodegeneration

      research-article
      1 , 1 , 2 , 3 , 4 , 1 , 1 , 5 , 6 , 7 , 1 , 8 , 9 , 10 , 10 , 1 , 1 , , MD, PhD 1 , 11 , *
      Neural Regeneration Research
      Wolters Kluwer - Medknow
      axonal growth, brain-derived neurotrophic factor, gene delivery, nanoparticles, neuritogenesis, neuronal cytoskeleton, neuroregeneration, neurorestoration, neurotrophic therapy, Parkinson's disease, reinnervation, substantia nigra

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          Abstract

          Abstract

          Overexpression of neurotrophic factors in nigral dopamine neurons is a promising approach to reverse neurodegeneration of the nigrostriatal dopamine system, a hallmark in Parkinson’s disease. The human cerebral dopamine neurotrophic factor (hCDNF) has recently emerged as a strong candidate for Parkinson’s disease therapy. This study shows that hCDNF expression in dopamine neurons using the neurotensin-polyplex nanoparticle system reverses 6-hydroxydopamine-induced morphological, biochemical, and behavioral alterations. Three independent electron microscopy techniques showed that the neurotensin-polyplex nanoparticles containing the hCDNF gene, ranging in size from 20 to 150 nm, enabled the expression of a secretable hCDNF in vitro. Their injection in the substantia nigra compacta on day 21 after the 6-hydroxydopamine lesion resulted in detectable hCDNF in dopamine neurons, whose levels remained constant throughout the study in the substantia nigra compacta and striatum. Compared with the lesioned group, tyrosine hydroxylase-positive (TH +) nigral cell population and TH + fiber density rose in the substantia nigra compacta and striatum after hCDNF transfection. An increase in βIII-tubulin and growth-associated protein 43 phospho-S41 (GAP43p) followed TH + cell recovery, as well as dopamine and its catabolite levels. Partial reversal (80%) of drug-activated circling behavior and full recovery of spontaneous motor and non-motor behavior were achieved. Brain-derived neurotrophic factor recovery in dopamine neurons that also occurred suggests its participation in the neurotrophic effects. These findings support the potential of nanoparticle-mediated hCDNF gene delivery to develop a disease-modifying treatment against Parkinson’s disease. The Institutional Animal Care and Use Committee of Centro de Investigación y de Estudios Avanzados approved our experimental procedures for animal use (authorization No. 162-15) on June 9, 2019.

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          Most cited references72

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          Parkinson Disease

          The diagnosis of Parkinson disease (PD) is based on the presence of bradykinesia and either resting tremor or rigidity and there should be no features from the history or examination to suggest an alternative cause of parkinsonism. In addition to the motor manifestations of PD, there is a long list of nonmotor symptoms, several of which occur before motor signs and are considered "prodromal" PD. These are classified as neuropsychiatric, autonomic, sleep, and sensory. There are many medical options for the treatment of PD but levodopa remains the mainstay. Deep brain stimulation and other advanced therapies are also available.
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            NURR1 in Parkinson disease--from pathogenesis to therapeutic potential.

            In Parkinson disease (PD), affected midbrain dopamine (DA) neurons lose specific dopaminergic properties before the neurons die. How the phenotype of DA neurons is normally established and the ways in which pathology affects the maintenance of cell identity are, therefore, important considerations. Orphan nuclear receptor NURR1 (NURR1, also known as NR4A2) is involved in the differentiation of midbrain DA neurons, but also has an important role in the adult brain. Emerging evidence indicates that impaired NURR1 function might contribute to the pathogenesis of PD: NURR1 and its transcriptional targets are downregulated in midbrain DA neurons that express high levels of the disease-causing protein α-synuclein. Clinical and experimental data indicate that disrupted NURR1 function contributes to induction of DA neuron dysfunction, which is seen in early stages of PD. The likely involvement of NURR1 in the development and progression of PD makes this protein a potentially interesting target for therapeutic intervention.
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              Novel CDNF/MANF family of neurotrophic factors.

              Current therapeutic interventions for neurodegenerative diseases alleviate only disease symptoms, while treatments that could stop or reverse actual degenerative processes are not available. Parkinson's disease (PD) is a movement disorder with characteristic degeneration of dopaminergic neurons in the midbrain. Few neurotrophic factors (NTFs) that promote survival, maintenance, and differentiation of affected brain neurons are considered as potential therapeutic agents for the treatment of neurodegenerative diseases. Thus, it is important to search and study new NTFs that could also be used in therapy. In this review, we discuss novel evolutionary conserved family of NTFs consisting of two members in the vertebrates, cerebral dopamine neurotrophic factor (CDNF) and mesencephalic astrocyte-derived neurotrophic factor (MANF). Invertebrates, including Drosophila and Caenorhabditis have a single protein homologous to vertebrate CDNF/MANF. Characteristic feature of these proteins is eight structurally conserved cysteine residues, which determine the protein fold. The crystal structure analysis revealed that CDNF and MANF consist of two domains; an amino-terminal saposin-like domain that may interact with lipids or membranes, and a presumably unfolded carboxy-terminal domain that may protect cells against endoplasmic reticulum stress. CDNF and MANF protect midbrain dopaminergic neurons and restore motor function in 6-hydroxydopamine rat model of PD in vivo. In line, Drosophila MANF is needed for the maintenance of dopaminergic neurites and dopamine levels in the fly, suggesting that the function of CDNF/MANF proteins is evolutionary conserved. Future studies will reveal the receptors and mode of action of these novel factors, which are potential therapeutic proteins for the treatment of PD.
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                Author and article information

                Journal
                Neural Regen Res
                Neural Regen Res
                NRR
                Neural Regeneration Research
                Wolters Kluwer - Medknow (India )
                1673-5374
                1876-7958
                April 2022
                30 August 2021
                : 17
                : 4
                : 854-866
                Affiliations
                [1 ]Departamento de Fisiología, Biofísica y Neurociencias, Centro de Investigación y de Estudios Avanzados, Ciudad de México, México
                [2 ]Programa Institucional de Biomedicina Molecular, Escuela Nacional de Medicina y Homeopatía, Instituto Politécnico Nacional, Ciudad de México, México
                [3 ]Department of Biosciences, IIIT-Srikakulam, Rajiv Gandhi University of Knowledge Technologies (RGUKT), Andhra Pradesh, India
                [4 ]Department of Pharmacology, Wayne State University School of Medicine, Detroit, MI, USA
                [5 ]Departamento de Física, Centro de Investigación y de Estudios Avanzados, Ciudad de México, México
                [6 ]Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México, Tlalnepantla de Baz, Edo. de México, México
                [7 ]Departamento de Fisiología, Escuela Nacional de Ciencias Biológicas, Ciudad de México, México
                [8 ]Laboratorio de Medicina Genómica, Hospital Regional “1° de Octubre”, ISSSTE, Ciudad de México, México
                [9 ]Laboratorio de Neuropsiquiatría, Instituto de Fisiología, Benemérita Universidad Autónoma de Puebla, Puebla, Puebla, México
                [10 ]Departamento de Biociencias e Ingeniería, Centro Interdisciplinario de Investigaciones y Estudios sobre Medio Ambiente y Desarrollo, Instituto Politécnico Nacional, Ciudad de México, México
                [11 ]Programa de Nanociencias y nanotecnología, Centro de Investigación y de Estudios Avanzados, Ciudad de México, México
                Author notes
                [* ] Correspondence to: Daniel Martinez-Fong, martinez.fong@ 123456gmail.com

                Author contributions: MAFP performed immunostaining experiments, stereotaxic surgeries, HPLC assays, analyzed the data, made substantial contributions to the experimental design and manuscript writing. DRC, LOSR, and CLH participated in most immunofluorescence experiments and processed, analyzed, and interpreted the results. YMFM performed and analyzed ELISA and WB experiments. RN and MMB quantified dopamine and catabolites levels by HPLC, RN also performed assays in vitro and participated in electron microscopy characterization directed by JSS. MJB provided NBRE3× sequence, and LE designed and cloned pNBRE3×-hCDNF plasmid (4482 bp). JAD undertook the behavioral tests. JAGB supervised expression assays and statistical analysis, and PN performed and analyzed GAP43p WB experiments. GF, MEGC, AJEA, IAMD, and DMF participated in the intellectual content, conception, and design of the study, and edited the manuscript and figures. DMF also provided funding, supervised experiments and data analysis, and wrote the paper. All authors have contributed to writing and editing the manuscript and approved its final version.

                Author information
                https://orcid.org/0000-0002-2934-8380
                Article
                NRR-17-854
                10.4103/1673-5374.321001
                8530149
                34472486
                c2436433-8f9b-4e38-bbb5-717a99e30c05
                Copyright: © Neural Regeneration Research

                This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

                History
                : 21 September 2020
                : 19 November 2020
                : 04 January 2021
                Categories
                Research Article

                axonal growth,brain-derived neurotrophic factor,gene delivery,nanoparticles,neuritogenesis,neuronal cytoskeleton,neuroregeneration,neurorestoration,neurotrophic therapy,parkinson's disease,reinnervation,substantia nigra

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