Brief Report: Astrogliosis Promotes Functional Recovery of Completely Transected Spinal Cord Following Transplantation of hESC‐Derived Oligodendrocyte and Motoneuron Progenitors

Spinal cord injury results in neural loss and consequently motor and sensory impairment below the injury. Reactive astrocytes contribute to formation of glial scar, thus impeding axonal regeneration, through secretion of extracellular matrix molecules, chondroitin sulfate proteoglycans (CSPGs). In this study, we analyze lesion site tissue to reveal the possible mechanism underlying the functional recovery after cell transplantation of human embryonic stem cell (hESC)‐derived oligodendrocyte progenitor cell (OPC) and motoneuron progenitors (MP) and propose that transplanted cells increase astrogliosis through the regenerative signaling pathways activated in the host tissue that may crucial for restoring locomotor ability. We show that the transplantation of hESC‐derived OPC and MP promotes astrogliosis, through activation of Jagged1‐dependent Notch and Jak/STAT signaling that support axonal survival. The transplanted cells in synergism with reactive astrocytes create permissive environment in which the expression of detrimental genes (Cspg, Tenascins, and genes involved in SLIT/ROBO signaling) was significantly decreased while expression of beneficial ones (Laminins and Fibronectin) was increased. According to our data, this mechanism is activated in all transplantation groups independently of the level of locomotor recovery. These results indicate that modifying the beneficial function of reactive astrocytes could be a feasible therapeutic strategy for spinal cord injury in future. Stem Cells 2014;32:594–599

[1]  N. Sueyoshi,et al.  Ependymal Cell Reactions in Spinal Cord Segments after Compression Injury in Adult Rat , 2003, Journal of neuropathology and experimental neurology.

[2]  X. Navarro,et al.  Acute and delayed transplantation of olfactory ensheathing cells promote partial recovery after complete transection of the spinal cord , 2006, Neurobiology of Disease.

[3]  Clive N Svendsen,et al.  Leukocyte Infiltration, Neuronal Degeneration, and Neurite Outgrowth after Ablation of Scar-Forming, Reactive Astrocytes in Adult Transgenic Mice , 1999, Neuron.

[4]  Ó. González-Pérez Neural stem cells in the adult human brain. , 2012, Biological and biomedical reports.

[5]  S. Dunlop,et al.  Metallothionein induces a regenerative reactive astrocyte phenotype via JAK/STAT and RhoA signalling pathways , 2010, Experimental Neurology.

[6]  F. Gage,et al.  Nerve Growth Factor Delivery by Gene Transfer Induces Differential Outgrowth of Sensory, Motor, and Noradrenergic Neurites after Adult Spinal Cord Injury , 1996, Experimental Neurology.

[7]  J. Guest,et al.  The Ability of Human Schwann Cell Grafts to Promote Regeneration in the Transected Nude Rat Spinal Cord , 1997, Experimental Neurology.

[8]  Sara G. Becker-Catania,et al.  A positive autoregulatory loop of Jak-STAT signaling controls the onset of astrogliogenesis , 2005, Nature Neuroscience.

[9]  A. Wanaka,et al.  Slit and glypican‐1 mRNAs are coexpressed in the reactive astrocytes of the injured adult brain , 2003, Glia.

[10]  J. Silver,et al.  CNS injury, glial scars, and inflammation: Inhibitory extracellular matrices and regeneration failure , 2008, Experimental Neurology.

[11]  M. Hediger,et al.  Knockout of Glutamate Transporters Reveals a Major Role for Astroglial Transport in Excitotoxicity and Clearance of Glutamate , 1996, Neuron.

[12]  S. Paul,et al.  Apolipoprotein E promotes astrocyte colocalization and degradation of deposited amyloid-β peptides , 2004, Nature Medicine.

[13]  H. Okano,et al.  Beneficial compaction of spinal cord lesion by migrating astrocytes through glycogen synthase kinase-3 inhibition , 2011, Neuroscience Research.

[14]  Hideyuki Okano,et al.  Conditional ablation of Stat3 or Socs3 discloses a dual role for reactive astrocytes after spinal cord injury , 2006, Nature Medicine.

[15]  Jerry Silver,et al.  Regeneration beyond the glial scar , 2004, Nature Reviews Neuroscience.

[16]  Oswald Steward,et al.  Human Embryonic Stem Cell-Derived Oligodendrocyte Progenitor Cell Transplants Remyelinate and Restore Locomotion after Spinal Cord Injury , 2005, The Journal of Neuroscience.

[17]  S. Akira,et al.  STAT3 is a Critical Regulator of Astrogliosis and Scar Formation after Spinal Cord Injury , 2008, The Journal of Neuroscience.

[18]  Jesús Avila,et al.  Functional Recovery of Paraplegic Rats and Motor Axon Regeneration in Their Spinal Cords by Olfactory Ensheathing Glia , 2000, Neuron.

[19]  Hossein Baharvand,et al.  Human embryonic stem cell-derived neural precursor transplants in collagen scaffolds promote recovery in injured rat spinal cord. , 2009, Cytotherapy.

[20]  A. Manira,et al.  Marrow stromal cells form guiding strands in the injured spinal cord and promote recovery , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Hideyuki Okano,et al.  Spinal cord injury: emerging beneficial role of reactive astrocytes' migration. , 2008, The international journal of biochemistry & cell biology.

[22]  R. Swanson,et al.  Astrocytes protect neurons from nitric oxide toxicity by a glutathione‐dependent mechanism , 2001, Journal of neurochemistry.

[23]  F. Gage,et al.  Proliferation and Differentiation of Progenitor Cells Throughout the Intact Adult Rat Spinal Cord , 2000, The Journal of Neuroscience.

[24]  L. Weaver,et al.  Sprouting of primary afferent fibers after spinal cord transection in the rat , 1998, Neuroscience.

[25]  Austin G Smith,et al.  Treatment of a Mouse Model of Spinal Cord Injury by Transplantation of Human Induced Pluripotent Stem Cell‐Derived Long‐Term Self‐Renewing Neuroepithelial‐Like Stem Cells , 2012, Stem cells.

[26]  M. Sofroniew,et al.  Reactive Astrocytes in Neural Repair and Protection , 2005, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[27]  N. Kleitman,et al.  Axonal regeneration into Schwann cell‐seeded guidance channels grafted into transected adult rat spinal cord , 1995, The Journal of comparative neurology.

[28]  N. Lago,et al.  Astrocyte-targeted expression of IL-6 protects the CNSagainst a focal brain injury , 2003, Experimental Neurology.

[29]  Xiao-Ming Xu,et al.  GDNF modifies reactive astrogliosis allowing robust axonal regeneration through Schwann cell-seeded guidance channels after spinal cord injury , 2011, Experimental Neurology.

[30]  R. U. Margolis,et al.  Functional characterization of chondroitin sulfate proteoglycans of brain: interactions with neurons and neural cell adhesion molecules , 1993, The Journal of cell biology.

[31]  Marion Murray,et al.  Direct Agonists for Serotonin Receptors Enhance Locomotor Function in Rats that Received Neural Transplants after Neonatal Spinal Transection , 1999, The Journal of Neuroscience.

[32]  M. Sofroniew Molecular dissection of reactive astrogliosis and glial scar formation , 2009, Trends in Neurosciences.

[33]  S. Wiegand,et al.  BDNF and NT-4/5 Prevent Atrophy of Rat Rubrospinal Neurons after Cervical Axotomy, Stimulate GAP-43 and Tα1-Tubulin mRNA Expression, and Promote Axonal Regeneration , 1997, The Journal of Neuroscience.

[34]  J. Silver,et al.  Changing role of forebrain astrocytes during development, regenerative failure, and induced regeneration upon transplantation , 1986, The Journal of comparative neurology.

[35]  B. Song,et al.  Reactive Astrocytes Form Scar-Like Perivascular Barriers to Leukocytes during Adaptive Immune Inflammation of the CNS , 2009, The Journal of Neuroscience.

[36]  Hideyuki Okano,et al.  Therapeutic potential of appropriately evaluated safe-induced pluripotent stem cells for spinal cord injury , 2010, Proceedings of the National Academy of Sciences.

[37]  S. Davies,et al.  Astrocytes Derived from Glial-restricted Precursors Promote Spinal Cord Repair , 2005 .

[38]  M. Tuszynski,et al.  Neurotrophic factors, cellular bridges and gene therapy for spinal cord injury , 2001, The Journal of physiology.

[39]  J. Silver,et al.  Injury-Induced Proteoglycans Inhibit the Potential for Laminin-Mediated Axon Growth on Astrocytic Scars , 1995, Experimental Neurology.

[40]  H. Tozaki-Saitoh,et al.  JAK-STAT3 pathway regulates spinal astrocyte proliferation and neuropathic pain maintenance in rats. , 2011, Brain : a journal of neurology.

[41]  F. Gomez-Pinilla,et al.  Epidermal growth factor receptor immunoreactivity in rat brain astrocytes. Response to injury , 1988, Neuroscience Letters.

[42]  J. Mcdonald,et al.  Robust CNS regeneration after complete spinal cord transection using aligned poly-L-lactic acid microfibers. , 2011, Biomaterials.

[43]  Gord Fishell,et al.  The role of notch in promoting glial and neural stem cell fates. , 2002, Annual review of neuroscience.

[44]  H. Okano,et al.  Cell Therapy for Spinal Cord Injury by Neural Stem/Progenitor Cells Derived from iPS/ES Cells , 2011, Neurotherapeutics.

[45]  S. David,et al.  Molecular approaches to spinal cord repair. , 2003, Annual review of neuroscience.

[46]  L. Jakeman,et al.  Don't fence me in: harnessing the beneficial roles of astrocytes for spinal cord repair. , 2008, Restorative neurology and neuroscience.

[47]  M. Norenberg,et al.  Astrocytes Protect Neurons from Ammonia Toxicity , 2005, Neurochemical Research.

[48]  R. Swanson,et al.  Astrocyte influences on ischemic neuronal death. , 2004, Current molecular medicine.

[49]  S. Lalwani,et al.  Spinal cord injury. , 2011, Journal of neurosurgery. Spine.

[50]  Ngan B. Doan,et al.  Reactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury , 2004, The Journal of Neuroscience.

[51]  H. Okano,et al.  Roles of ES Cell-Derived Gliogenic Neural Stem/Progenitor Cells in Functional Recovery after Spinal Cord Injury , 2009, PloS one.

[52]  Victoria Moreno-Manzano,et al.  Transplanted Oligodendrocytes and Motoneuron Progenitors Generated from Human Embryonic Stem Cells Promote Locomotor Recovery After Spinal Cord Transection , 2010, Stem cells.

[53]  B. Stokes,et al.  Brain-Derived Neurotrophic Factor Stimulates Hindlimb Stepping and Sprouting of Cholinergic Fibers after Spinal Cord Injury , 1998, Experimental Neurology.

[54]  H. Okano,et al.  Grafted human-induced pluripotent stem-cell–derived neurospheres promote motor functional recovery after spinal cord injury in mice , 2011, Proceedings of the National Academy of Sciences.

[55]  V. Edgerton,et al.  Local and Remote Growth Factor Effects after Primate Spinal Cord Injury , 2010, The Journal of Neuroscience.