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      Toll-6 and Toll-7 function as neurotrophin receptors in the Drosophila central nervous system

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          Abstract

          Neurotrophin receptors corresponding to vertebrate Trk, p75 NTR or Sortilin have not been identified in Drosophila, thus it is unknown how neurotrophism may be implemented in insects. Two Drosophila neurotrophins, DNT1 and DNT2, have nervous system functions, but their receptors are unknown. The Toll receptor superfamily has ancient evolutionary origins and a universal function in innate immunity. Here we show that Toll paralogues unrelated to the mammalian neurotrophin receptors function as neurotrophin receptors in fruit-flies. Toll-6 and Toll-7 are expressed in the central nervous system throughout development, and regulate locomotion, motoraxon targeting and neuronal survival. DNT1 and 2 interact genetically with Toll-6 and 7, bind to Toll-7 and 6 promiscuously, and are distributed in vivo in complementary or overlapping domains. We conclude that in fruit-flies, Tolls are not only involved in development and immunity but also in neurotrophism, revealing an unforeseen relationship between the neurotrophin and Toll protein families.

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          Most cited references48

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          Sea anemone genome reveals ancestral eumetazoan gene repertoire and genomic organization.

          Sea anemones are seemingly primitive animals that, along with corals, jellyfish, and hydras, constitute the oldest eumetazoan phylum, the Cnidaria. Here, we report a comparative analysis of the draft genome of an emerging cnidarian model, the starlet sea anemone Nematostella vectensis. The sea anemone genome is complex, with a gene repertoire, exon-intron structure, and large-scale gene linkage more similar to vertebrates than to flies or nematodes, implying that the genome of the eumetazoan ancestor was similarly complex. Nearly one-fifth of the inferred genes of the ancestor are eumetazoan novelties, which are enriched for animal functions like cell signaling, adhesion, and synaptic transmission. Analysis of diverse pathways suggests that these gene "inventions" along the lineage leading to animals were likely already well integrated with preexisting eukaryotic genes in the eumetazoan progenitor.
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            The dorsoventral regulatory gene cassette spätzle/Toll/cactus controls the potent antifungal response in Drosophila adults.

            The cytokine-induced activation cascade of NF-kappaB in mammals and the activation of the morphogen dorsal in Drosophila embryos show striking structural and functional similarities (Toll/IL-1, Cactus/I-kappaB, and dorsal/NF-kappaB). Here we demonstrate that these parallels extend to the immune response of Drosophila. In particular, the intracellular components of the dorsoventral signaling pathway (except for dorsal) and the extracellular Toll ligand, spätzle, control expression of the antifungal peptide gene drosomycin in adults. We also show that mutations in the Toll signaling pathway dramatically reduce survival after fungal infection. Antibacterial genes are induced either by a distinct pathway involving the immune deficiency gene (imd) or by combined activation of both imd and dorsoventral pathways.
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              Regulation of innate immune responses in the brain.

              Microglial cells are the main innate immune cells of the complex cellular structure of the brain. These cells respond quickly to pathogens and injury, accumulate in regions of degeneration and produce a wide variety of pro-inflammatory molecules. These observations have resulted in active debate regarding the exact role of microglial cells in the brain and whether they have beneficial or detrimental functions. Careful targeting of these cells could have therapeutic benefits for several types of trauma and disease specific to the central nervous system. This Review discusses the molecular details underlying the innate immune response in the brain during infection, injury and disease.
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                Author and article information

                Journal
                9809671
                21092
                Nat Neurosci
                Nat. Neurosci.
                Nature neuroscience
                1097-6256
                1546-1726
                2 November 2015
                28 July 2013
                September 2013
                05 November 2015
                : 16
                : 9
                : 1248-1256
                Affiliations
                [1 ]School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK
                [2 ]Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge, UK
                Author notes
                [* ]Corresponding author contact details: Phone: 00 44 (0)121 4145416 Fax: 00 44 (0)121 4145445 a.hidalgo@ 123456bham.ac.uk www.biosciences-labs.bham.ac.uk/hidalgo

                AUTHOR CONTRIBUTIONS

                G.McI., I.F., J.A., J.S.W., M.A.L, J.C.F. and A.H. performed experiments; A.H. and N.J.G. conceived and directed the project; A.H., N.J.G. and G.McI. wrote the paper; all authors contributed to planning experiments and analysing data, and to discussions and improvements to the manuscript.

                [‡]

                Equal contribution first authors

                Article
                EMS53784
                10.1038/nn.3474
                4634317
                23892553
                38a0d33a-2bd0-4756-bf13-b4a9988ccd55

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                History
                Categories
                Article

                Neurosciences
                drosophila,toll-6,toll-7,toll,tlr,nfκb,neurotrophin,dnt1,dnt2,cns,survival,axon,locomotor,neuron,receptor,hb9,eve,lim3
                Neurosciences
                drosophila, toll-6, toll-7, toll, tlr, nfκb, neurotrophin, dnt1, dnt2, cns, survival, axon, locomotor, neuron, receptor, hb9, eve, lim3

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