Regulation of nerve growth and patterning by cell surface protein disulphide isomerase
Geoffrey MW Cook,
Catia Sousa,
Julia Schaeffer,
Katherine Wiles,
Prem Jareonsettasin,
Asanish Kalyanasundaram,
Eleanor Walder,
Catharina Casper,
Serena Patel,
Pei Wei Chua,
Gioia Riboni-Verri,
Mansoor Raza,
Nol Swaddiwudhipong,
Andrew Hui,
Ameer Abdullah,
Saj Wajed,
Roger J Keynes
Affiliations
Geoffrey MW Cook
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom
Catia Sousa
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom; Grenoble Institute des Neurosciences, La Tronche, France
Julia Schaeffer
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom
Katherine Wiles
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom; Independent researcher, London, United Kingdom
Prem Jareonsettasin
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom; Exeter College, Oxford, United Kingdom
Asanish Kalyanasundaram
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom; School of Clinical Medicine, Cambridge University Hospitals, Cambridge, United Kingdom
Eleanor Walder
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom; School of Clinical Medicine, Cambridge University Hospitals, Cambridge, United Kingdom
Catharina Casper
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom; Winter, Brandl, Fürniss, Hübner, Röss, Kaiser & Polte, Partnerschaft mbB, Patent und Rechtsanwaltskanzlei, München, Germany
Serena Patel
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom; School of Clinical Medicine, Cambridge University Hospitals, Cambridge, United Kingdom
Pei Wei Chua
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom; School of Medicine and Health Sciences, Monash University, Bandar Sunway, Malaysia
Gioia Riboni-Verri
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom; School of Medicine, Medical Science and Nutrition, University of Aberdeen, Aberdeen, United Kingdom
Mansoor Raza
Cambridge Innovation Capital, Cambridge, United Kingdom
Nol Swaddiwudhipong
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom
Andrew Hui
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom
Ameer Abdullah
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom
Saj Wajed
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom; University of Exeter Medical School, Exeter, United Kingdom
Contact repulsion of growing axons is an essential mechanism for spinal nerve patterning. In birds and mammals the embryonic somites generate a linear series of impenetrable barriers, forcing axon growth cones to traverse one half of each somite as they extend towards their body targets. This study shows that protein disulphide isomerase provides a key component of these barriers, mediating contact repulsion at the cell surface in chick half-somites. Repulsion is reduced both in vivo and in vitro by a range of methods that inhibit enzyme activity. The activity is critical in initiating a nitric oxide/S-nitrosylation-dependent signal transduction pathway that regulates the growth cone cytoskeleton. Rat forebrain grey matter extracts contain a similar activity, and the enzyme is expressed at the surface of cultured human astrocytic cells and rat cortical astrocytes. We suggest this system is co-opted in the brain to counteract and regulate aberrant nerve terminal growth.