54
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Mechanosensing is critical for axon growth in the developing brain

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          During nervous system development, neurons extend axons along well-defined pathways. The current understanding of axon pathfinding is based mainly on chemical signalling. However, growing neurons interact not only chemically but also mechanically with their environment. Here we identify mechanical signals as important regulators of axon pathfinding. In vitro, substrate stiffness determined growth patterns of Xenopus retinal ganglion cell (RGC) axons. In vivo atomic force microscopy revealed striking stiffness gradient patterns in the embryonic brain. RGC axons grew towards the tissue’s softer side, which was reproduced in vitro in the absence of chemical gradients. To test the importance of mechanical signals for axon growth in vivo, we altered brain stiffness, blocked mechanotransduction pharmacologically, and knocked down the mechanosensitive ion channel Piezo1. All treatments resulted in aberrant axonal growth and pathfinding errors, suggesting that local tissue stiffness–read out by mechanosensitive ion channels–is critically involved in instructing neuronal growth in vivo.

          Related collections

          Most cited references48

          • Record: found
          • Abstract: not found
          • Article: not found

          Dendritic organization in the neurons of the visual and motor cortices of the cat.

          D SHOLL (1953)
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Piezos are pore-forming subunits of mechanically activated channels

            Mechanotransduction plays a crucial role in physiology. Biological processes including sensing touch and sound waves require yet unidentified cation channels that detect pressure. Mouse piezo1 (mpiezo1) and mpiezo2 induce mechanically activated cationic currents in cells; however, it is unknown if piezos are pore-forming ion channels or modulate ion channels. We show that Drosophila piezo (dpiezo) also induces mechanically activated currents in cells, but through channels with remarkably distinct pore properties including sensitivity to the pore blocker ruthenium red and single channel conductances. mpiezo1 assembles as a ~1.2 million-Dalton tetramer, with no evidence of other proteins in this complex. Finally, purified mpiezo1 reconstituted into asymmetric lipid bilayers and liposomes forms ruthenium red-sensitive ion channels. These data demonstrate that piezos are an evolutionarily conserved ion channel family involved in mechanotransduction.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Stretch-activated ion channel Piezo1 directs lineage choice in human neural stem cells.

              Neural stem cells are multipotent cells with the ability to differentiate into neurons, astrocytes, and oligodendrocytes. Lineage specification is strongly sensitive to the mechanical properties of the cellular environment. However, molecular pathways transducing matrix mechanical cues to intracellular signaling pathways linked to lineage specification remain unclear. We found that the mechanically gated ion channel Piezo1 is expressed by brain-derived human neural stem/progenitor cells and is responsible for a mechanically induced ionic current. Piezo1 activity triggered by traction forces elicited influx of Ca(2+), a known modulator of differentiation, in a substrate-stiffness-dependent manner. Inhibition of channel activity by the pharmacological inhibitor GsMTx-4 or by siRNA-mediated Piezo1 knockdown suppressed neurogenesis and enhanced astrogenesis. Piezo1 knockdown also reduced the nuclear localization of the mechanoreactive transcriptional coactivator Yes-associated protein. We propose that the mechanically gated ion channel Piezo1 is an important determinant of mechanosensitive lineage choice in neural stem cells and may play similar roles in other multipotent stem cells.
                Bookmark

                Author and article information

                Journal
                9809671
                21092
                Nat Neurosci
                Nat. Neurosci.
                Nature neuroscience
                1097-6256
                1546-1726
                26 September 2016
                19 September 2016
                December 2016
                27 July 2017
                : 19
                : 12
                : 1592-1598
                Affiliations
                [1 ]Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK
                [2 ]Institute of Physics at São Carlos, University of São Paulo, São Carlos, SP, Brazil
                [3 ]Department of Physics, Cavendish Laboratory, University of Cambridge, Cambridge, UK
                Author notes
                Correspondence should be addressed to K.F. ( kf284@ 123456cam.ac.uk )
                [4]

                Present address: Department of Clinical Neurobiology, Medical Faculty of Heidelberg University and German Cancer Research Center (DKFZ), Heidelberg, Germany

                [5]

                Present address: School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton, UK

                [6]

                Present address: Biotechnology Center, Technische Universität Dresden, Dresden, Germany

                Article
                EMS69760
                10.1038/nn.4394
                5531257
                27643431
                17bb4797-fa26-405c-b1f8-ee68320b44a0

                Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms

                History
                Categories
                Article

                Neurosciences
                mechanosensitivity,durotaxis,afm,axon guidance,biomechanics,stretch-activated ion channels,brain stiffness,stiffness gradient

                Comments

                Comment on this article