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      Postnatal Development and Distribution of Sympathetic Innervation in Mouse Skeletal Muscle

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          Abstract

          Vertebrate neuromuscular junctions (NMJs) have been conceived as tripartite synapses composed of motor neuron, Schwann cell, and muscle fiber. Recent work has shown the presence of sympathetic neurons in the immediate vicinity of NMJs and experimental and clinical findings suggest that this plays an eminent role in adult NMJ biology. The present study examined the postnatal development and distribution of sympathetic innervation in different muscles using immunofluorescence, confocal microscopy, and Western blot. This demonstrates the proximity of sympathetic neurons in diaphragm, extensor digitorum longus, tibialis anterior, soleus, and levator auris longus muscles. In extensor digitorum longus muscle, sympathetic innervation of NMJs was quantified from perinatal to adult stage and found to increase up to two months of age. In diaphragm muscle, an extensive network of sympathetic neurons was prominent along the characteristic central synapse band. In summary, these data demonstrate that an elaborate sympathetic innervation is present in several mouse skeletal muscles and that this is often next to NMJs. Although the presence of sympathetic neurons at the perisynaptic region of NMJs increased during postnatal development, many synapses were already close to sympathetic neurons at birth. Potential implications of these findings for treatment of neuromuscular diseases are discussed.

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          Development of the vertebrate neuromuscular junction.

          We describe the formation, maturation, elimination, maintenance, and regeneration of vertebrate neuromuscular junctions (NMJs), the best studied of all synapses. The NMJ forms in a series of steps that involve the exchange of signals among its three cellular components--nerve terminal, muscle fiber, and Schwann cell. Although essentially any motor axon can form NMJs with any muscle fiber, an additional set of cues biases synapse formation in favor of appropriate partners. The NMJ is functional at birth but undergoes numerous alterations postnatally. One step in maturation is the elimination of excess inputs, a competitive process in which the muscle is an intermediary. Once elimination is complete, the NMJ is maintained stably in a dynamic equilibrium that can be perturbed to initiate remodeling. NMJs regenerate following damage to nerve or muscle, but this process differs in fundamental ways from embryonic synaptogenesis. Finally, we consider the extent to which the NMJ is a suitable model for development of neuron-neuron synapses.
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            Mechanisms Regulating Neuromuscular Junction Development and Function and Causes of Muscle Wasting.

            The neuromuscular junction is the chemical synapse between motor neurons and skeletal muscle fibers. It is designed to reliably convert the action potential from the presynaptic motor neuron into the contraction of the postsynaptic muscle fiber. Diseases that affect the neuromuscular junction may cause failure of this conversion and result in loss of ambulation and respiration. The loss of motor input also causes muscle wasting as muscle mass is constantly adapted to contractile needs by the balancing of protein synthesis and protein degradation. Finally, neuromuscular activity and muscle mass have a major impact on metabolic properties of the organisms. This review discusses the mechanisms involved in the development and maintenance of the neuromuscular junction, the consequences of and the mechanisms involved in its dysfunction, and its role in maintaining muscle mass during aging. As life expectancy is increasing, loss of muscle mass during aging, called sarcopenia, has emerged as a field of high medical need. Interestingly, aging is also accompanied by structural changes at the neuromuscular junction, suggesting that the mechanisms involved in neuromuscular junction maintenance might be disturbed during aging. In addition, there is now evidence that behavioral paradigms and signaling pathways that are involved in longevity also affect neuromuscular junction stability and sarcopenia.
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              Neuromuscular Junction Formation, Aging, and Disorders.

              Synapses, the fundamental unit in neuronal circuits, are critical for learning and memory, perception, thinking, and reaction. The neuromuscular junction (NMJ) is a synapse formed between motoneurons and skeletal muscle fibers that is covered by Schwann cells (SCs). It is essential for controlling muscle contraction. NMJ formation requires intimate interactions among motoneurons, muscles, and SCs. Deficits in NMJ formation and maintenance cause neuromuscular disorders, including congenital myasthenic syndrome and myasthenia gravis. NMJ decline occurs in aged animals and may appear before clinical presentation of motoneuron disorders such as amyotrophic lateral sclerosis. We review recent findings in NMJ formation, maintenance, neuromuscular disorders, and aging of the NMJ, focusing on communications among motoneurons, muscles and SCs, and underlying mechanisms.
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                01 July 2018
                July 2018
                : 19
                : 7
                : 1935
                Affiliations
                [1 ]Institute of Molecular and Cell Biology, Mannheim University of Applied Sciences, 68163 Mannheim, Germany; t.straka@ 123456hs-mannheim.de (T.S.); rina90pro@ 123456web.de (K.P.); hoerner@ 123456kooperationen.hs-mannheim.de (S.J.H.); muzamil.m.khan@ 123456embl.de (M.M.K.); marion@ 123456g.clemson.edu (M.P.I.W.); m.hafner@ 123456hs-mannheim.de (M.H.)
                [2 ]Interdisciplinary Center for Neurosciences, Heidelberg University, 69120 Heidelberg, Germany
                [3 ]Institute of Toxicology and Genetics, Karlsruhe Institute of Technology, 76344 Eggenstein-Leopoldshafen, Germany
                [4 ]Venetian Institute of Molecular Medicine, 35129 Padua, Italy; verovita92@ 123456gmail.com (V.V.); marcopiraz@ 123456gmail.com (M.P.); tania.zaglia@ 123456unipd.it (T.Z.)
                [5 ]Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy
                [6 ]Department of Cardiac Thoracic and Vascular Sciences, University of Padua, 35128 Padua, Italy
                Author notes
                [* ]Correspondence: r.rudolf@ 123456hs-mannheim.de ; Tel.: +49-621-292-6804
                Author information
                https://orcid.org/0000-0002-4485-8346
                https://orcid.org/0000-0003-4127-254X
                https://orcid.org/0000-0002-0833-1053
                Article
                ijms-19-01935
                10.3390/ijms19071935
                6073285
                29966393
                9c15488d-013d-4707-8817-2ad509bd0c6e
                © 2018 by the authors.

                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 ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 03 June 2018
                : 29 June 2018
                Categories
                Article

                Molecular biology
                endplate,neuromuscular junction,sympathetic neuron,tyrosine hydroxylase,neuropeptide y

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