Research Paper Volume 8, Issue 10 pp 2463—2487
Plasticity Related Gene 3 (PRG3) overcomes myelin-associated growth inhibition and promotes functional recovery after spinal cord injury
- 1 Department of Neurosurgery, Charité - Universitätsmedizin Berlin, D-10115 Berlin, Germany
- 2 Brain Research Institute, University of Zurich and ETHZ, CH-8057 Zurich, Switzerland
- 3 Art+Science Consulting, Zurich, Switzerland
- 4 Translational Cell Biology and Neurooncology Lab, Department of Neurosurgery, University Medical School Erlangen, Friedrich Alexander University of Erlangen – Nürnberg (FAU), D-91054 Erlangen, Germany
- 5 Center for Microscopy and Image Analysis, University of Zurich, CH-8057 Zurich, Switzerland
- 6 Department of Anesthesiology, University Medical Center, Focus Program Translational Neuroscience (FTN) of the Johannes Gutenberg-University Mainz, Germany
- 7 BiMECON Ent., Berlin, Germany
- 8 Dr. Erler Kliniken Nürnberg, Nürnberg, Germany
- 9 Present address: Department of Physics, University of California at San Diego, La Jolla, California 92093 USA
Received: June 15, 2016 Accepted: September 25, 2016 Published: October 15, 2016
https://doi.org/10.18632/aging.101066How to Cite
Abstract
The Plasticity Related Gene family covers five, brain-specific, transmembrane proteins (PRG1-5, also termed LPPR1-5) that operate in neuronal plasticity during development, aging and brain trauma. Here we investigated the role of the PRG family on axonal and filopodia outgrowth. Comparative analysis revealed the strongest outgrowth induced by PRG3 (LPPR1). During development, PRG3 is ubiquitously located at the tip of neuronal processes and at the plasma membrane and declines with age. In utero electroporation of PRG3 induced dendritic protrusions and accelerated spine formations in cortical pyramidal neurons. The neurite growth promoting activity of PRG3 requires RasGRF1 (RasGEF1/Cdc25) mediated downstream signaling. Moreover, in axon collapse assays, PRG3-induced neurites resisted growth inhibitors such as myelin, Nogo-A (Reticulon/RTN-4), thrombin and LPA and impeded the RhoA-Rock-PIP5K induced neurite repulsion. Transgenic adult mice with constitutive PRG3 expression displayed strong axonal sprouting distal to a spinal cord lesion. Moreover, fostered PRG3 expression promoted complex motor-behavioral recovery compared to wild type controls as revealed in the Schnell swim test (SST). Thus, PRG3 emerges as a developmental RasGRF1-dependent conductor of filopodia formation and axonal growth enhancer. PRG3-induced neurites resist brain injury-associated outgrowth inhibitors and contribute to functional recovery after spinal cord lesions. Here, we provide evidence that PRG3 operates as an essential neuronal growth promoter in the nervous system. Maintaining PRG3 expression in aging brain may turn back the developmental clock for neuronal regeneration and plasticity.