Advances in the Signaling Pathways Downstream of Glial-Scar Axon Growth Inhibitors
Axon growth inhibitors generated by reactive glial scars play an important role in failure of axon regeneration after CNS injury in mature mammals. Among the inhibitory factors, chondroitin sulfate proteoglycans (CSPGs) are potent suppressors of axon regeneration and are important molecular targets...
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doaj-1994916447cf4d11b80f8de760e649772020-11-25T03:36:23ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022020-07-011410.3389/fncel.2020.00174546519Advances in the Signaling Pathways Downstream of Glial-Scar Axon Growth InhibitorsArmin Sami0Armin Sami1Michael E. Selzer2Michael E. Selzer3Shuxin Li4Shuxin Li5Shriners Hospitals Pediatric Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, United StatesDepartment of Anatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, United StatesShriners Hospitals Pediatric Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, United StatesDepartment of Neurology, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, United StatesShriners Hospitals Pediatric Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, United StatesDepartment of Anatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, United StatesAxon growth inhibitors generated by reactive glial scars play an important role in failure of axon regeneration after CNS injury in mature mammals. Among the inhibitory factors, chondroitin sulfate proteoglycans (CSPGs) are potent suppressors of axon regeneration and are important molecular targets for designing effective therapies for traumatic brain injury or spinal cord injury (SCI). CSPGs bind with high affinity to several transmembrane receptors, including two members of the leukocyte common antigen related (LAR) subfamily of receptor protein tyrosine phosphatases (RPTPs). Recent studies demonstrate that multiple intracellular signaling pathways downstream of these two RPTPs mediate the growth-inhibitory actions of CSPGs. A better understanding of these signaling pathways may facilitate development of new and effective therapies for CNS disorders characterized by axonal disconnections. This review will focus on recent advances in the downstream signaling pathways of scar-mediated inhibition and their potential as the molecular targets for CNS repair.https://www.frontiersin.org/article/10.3389/fncel.2020.00174/fullscar inhibitionCSPG receptorLARPTPσaxon regenerationintracellular signaling |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Armin Sami Armin Sami Michael E. Selzer Michael E. Selzer Shuxin Li Shuxin Li |
spellingShingle |
Armin Sami Armin Sami Michael E. Selzer Michael E. Selzer Shuxin Li Shuxin Li Advances in the Signaling Pathways Downstream of Glial-Scar Axon Growth Inhibitors Frontiers in Cellular Neuroscience scar inhibition CSPG receptor LAR PTPσ axon regeneration intracellular signaling |
author_facet |
Armin Sami Armin Sami Michael E. Selzer Michael E. Selzer Shuxin Li Shuxin Li |
author_sort |
Armin Sami |
title |
Advances in the Signaling Pathways Downstream of Glial-Scar Axon Growth Inhibitors |
title_short |
Advances in the Signaling Pathways Downstream of Glial-Scar Axon Growth Inhibitors |
title_full |
Advances in the Signaling Pathways Downstream of Glial-Scar Axon Growth Inhibitors |
title_fullStr |
Advances in the Signaling Pathways Downstream of Glial-Scar Axon Growth Inhibitors |
title_full_unstemmed |
Advances in the Signaling Pathways Downstream of Glial-Scar Axon Growth Inhibitors |
title_sort |
advances in the signaling pathways downstream of glial-scar axon growth inhibitors |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cellular Neuroscience |
issn |
1662-5102 |
publishDate |
2020-07-01 |
description |
Axon growth inhibitors generated by reactive glial scars play an important role in failure of axon regeneration after CNS injury in mature mammals. Among the inhibitory factors, chondroitin sulfate proteoglycans (CSPGs) are potent suppressors of axon regeneration and are important molecular targets for designing effective therapies for traumatic brain injury or spinal cord injury (SCI). CSPGs bind with high affinity to several transmembrane receptors, including two members of the leukocyte common antigen related (LAR) subfamily of receptor protein tyrosine phosphatases (RPTPs). Recent studies demonstrate that multiple intracellular signaling pathways downstream of these two RPTPs mediate the growth-inhibitory actions of CSPGs. A better understanding of these signaling pathways may facilitate development of new and effective therapies for CNS disorders characterized by axonal disconnections. This review will focus on recent advances in the downstream signaling pathways of scar-mediated inhibition and their potential as the molecular targets for CNS repair. |
topic |
scar inhibition CSPG receptor LAR PTPσ axon regeneration intracellular signaling |
url |
https://www.frontiersin.org/article/10.3389/fncel.2020.00174/full |
work_keys_str_mv |
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