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      Brain-Derived Neurotrophic Factor and Nerve Growth Factor Therapeutics for Brain Injury: The Current Translational Challenges in Preclinical and Clinical Research

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          Abstract

          Ischemic stroke and traumatic brain injury (TBI) are among the leading causes of death and disability worldwide with impairments ranging from mild to severe. Many therapies are aimed at improving functional and cognitive recovery by targeting neural repair but have encountered issues involving efficacy and drug delivery. As a result, therapeutic options for patients are sparse. Neurotrophic factors are one of the key mediators of neural plasticity and functional recovery. Neurotrophic factors such as brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) serve as potential therapeutic options to increase neural repair and recovery as they promote neuroprotection and regeneration. BDNF and NGF have demonstrated the ability to improve functional recovery in preclinical and to a lesser extent clinical studies. Direct and indirect methods to increase levels of neurotrophic factors in animal models have been successful in improving postinjury outcome measures. However, the translation of these studies into clinical trials has been limited. Preclinical experiments have largely failed to result in significant impacts in clinical research. This review will focus on the administration of these neurotrophic factors in preclinical and clinical stroke and TBI and the challenges in translating these therapies from the bench to the clinic.

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          Most cited references44

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          The BDNF val66met Polymorphism Affects Activity-Dependent Secretion of BDNF and Human Memory and Hippocampal Function

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            Neurotrophins: roles in neuronal development and function.

            Neurotrophins regulate development, maintenance, and function of vertebrate nervous systems. Neurotrophins activate two different classes of receptors, the Trk family of receptor tyrosine kinases and p75NTR, a member of the TNF receptor superfamily. Through these, neurotrophins activate many signaling pathways, including those mediated by ras and members of the cdc-42/ras/rho G protein families, and the MAP kinase, PI-3 kinase, and Jun kinase cascades. During development, limiting amounts of neurotrophins function as survival factors to ensure a match between the number of surviving neurons and the requirement for appropriate target innervation. They also regulate cell fate decisions, axon growth, dendrite pruning, the patterning of innervation and the expression of proteins crucial for normal neuronal function, such as neurotransmitters and ion channels. These proteins also regulate many aspects of neural function. In the mature nervous system, they control synaptic function and synaptic plasticity, while continuing to modulate neuronal survival.
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              Directed differentiation of embryonic stem cells into motor neurons.

              Inductive signals and transcription factors involved in motor neuron generation have been identified, raising the question of whether these developmental insights can be used to direct stem cells to a motor neuron fate. We show that developmentally relevant signaling factors can induce mouse embryonic stem (ES) cells to differentiate into spinal progenitor cells, and subsequently into motor neurons, through a pathway recapitulating that used in vivo. ES cell-derived motor neurons can populate the embryonic spinal cord, extend axons, and form synapses with target muscles. Thus, inductive signals involved in normal pathways of neurogenesis can direct ES cells to form specific classes of CNS neurons.
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                Author and article information

                Contributors
                Journal
                Neural Plast
                Neural Plast
                np
                Neural Plasticity
                Hindawi
                2090-5904
                1687-5443
                2022
                2 March 2022
                : 2022
                : 3889300
                Affiliations
                1Medical University of South Carolina, 173 Ashley Ave, Charleston, SC 29424, USA
                2College of Charleston, 66 George Street, Charleston, SC 29424, USA
                Author notes

                Academic Editor: Gabriela Delevati Colpo

                Author information
                https://orcid.org/0000-0001-8886-1638
                https://orcid.org/0000-0002-8518-3680
                https://orcid.org/0000-0003-4776-5839
                Article
                10.1155/2022/3889300
                8906958
                35283994
                8d1d08c3-6a08-44b1-87af-f42aae018cce
                Copyright © 2022 Serena-Kaye Sims et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 15 September 2021
                : 4 February 2022
                Funding
                Funded by: T32 Grant
                Funded by: Blueprint DSPAN Diversity training grant
                Funded by: National Institutes of Health
                Award ID: P20GM109040
                Award ID: R25GM072643
                Award ID: R01NS099595
                Award ID: HL007260
                Award ID: K00NS105220
                Categories
                Review Article

                Neurosciences
                Neurosciences

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