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      Long‐distance regressive signaling in neural development and disease

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          Abstract

          Nervous system development proceeds via well-orchestrated processes involving a balance between progressive and regressive events including stabilization or elimination of axons, synapses, and even entire neurons. These progressive and regressive events are driven by functionally antagonistic signaling pathways with the dominant pathway eventually determining whether a neural element is retained or removed. Many of these developmental sculpting events are triggered by final target innervation necessitating a long-distance mode of communication. While long-distance progressive signaling has been well characterized, particularly for neurotrophic factors, there remains relatively little known about how regressive events are triggered from a distance. Here we discuss the emergent phenomenon of long-distance regressive signaling pathways. In particular, we will cover (a) progressive and regressive cues known to be employed after target innervation, (b) the mechanisms of long-distance signaling from an endosomal platform, (c) recent evidence that long-distance regressive cues emanate from platforms like death receptors or repulsive axon guidance receptors, and (d) evidence that these pathways are exploited in pathological scenarios.

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          Most cited references169

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              The cytoplasmic dynein transport machinery and its many cargoes

              Cytoplasmic dynein-1 is an important microtubule-based motor in many eukaryotic cells. Dynein has critical roles both in interphase and during cell division. Here we focus on interphase cargoes of dynein, which include membrane-bound organelles, RNAs, protein complexes and viruses. A central challenge in the field is to understand how a single motor can transport such a diverse array of cargoes and how this process is regulated. The molecular basis by which each cargo is linked to dynein and its cofactor dynactin has started to emerge. Of particular importance for this process is a set of coiled coil proteins — ‘activating adaptors’ — which both recruit dynein–dynactin to their cargoes and activate dynein motility.
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                Author and article information

                Journal
                WIREs Developmental Biology
                WIREs Dev Biol
                Wiley
                1759-7684
                1759-7692
                May 11 2020
                Affiliations
                [1 ]Department of Biochemistry and Vanderbilt Brain InstituteVanderbilt University School of Medicine Nashville Tennessee USA
                [2 ]Neuroscience Graduate ProgramUniversity of Virginia Charlottesville Virginia USA
                [3 ]Institute of Biomedical Sciences (ICB), Faculty of Medicine, Faculty of Life ScienceUniversidad Andres Bello Santiago Chile
                [4 ]Departments of Biology, Cell Biology, Biomedical Engineering, and NeuroscienceUniversity of Virginia Charlottesville Virginia USA
                Article
                10.1002/wdev.382
                7655682
                32391977
                7c22d9dd-a6e6-4a74-80ac-35e0a2062309
                © 2020

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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