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Receptor protein tyrosine phosphatase ? binds to neurons in the adult mouse brain.


ABSTRACT: The role of type IIA receptor protein tyrosine phosphatases (RPTPs), which includes LAR, RPTP? and RPTP?, in the nervous system is becoming increasingly recognized. Evidence supports a significant role for these RPTPs during the development of the nervous system as well as after injury, and mutations in RPTPs are associated with human disease. However, a major open question is the nature of the ligands that interact with type IIA RPTPs in the adult brain. Candidates include several different proteins as well as the glycosaminoglycan chains of proteoglycans. In order to investigate this problem, we used a receptor affinity probe assay with RPTP?-AP fusion proteins on sections of adult mouse brain and to cultured neurons. Our results demonstrate that the major binding sites for RPTP? in adult mouse brain are on neurons and are not proteoglycan GAG chains, as RPTP? binding overlaps with the neuronal marker NeuN and was not significantly altered by treatments which eliminate chondroitin sulfate, heparan sulfate, or both. We also demonstrate no overlap of binding of RPTP? with perineuronal nets, and a unique modulation of RPTP? binding to brain by divalent cations. Our data therefore point to neuronal proteins, rather than CSPGs, as being the ligands for RPTP? in the adult, uninjured brain.

SUBMITTER: Yi JH 

PROVIDER: S-EPMC3999219 | biostudies-literature | 2014 May

REPOSITORIES: biostudies-literature

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Receptor protein tyrosine phosphatase σ binds to neurons in the adult mouse brain.

Yi Jae-Hyuk JH   Katagiri Yasuhiro Y   Yu Panpan P   Lourie Jacob J   Bangayan Nathanael J NJ   Symes Aviva J AJ   Geller Herbert M HM  

Experimental neurology 20140214


The role of type IIA receptor protein tyrosine phosphatases (RPTPs), which includes LAR, RPTPσ and RPTPδ, in the nervous system is becoming increasingly recognized. Evidence supports a significant role for these RPTPs during the development of the nervous system as well as after injury, and mutations in RPTPs are associated with human disease. However, a major open question is the nature of the ligands that interact with type IIA RPTPs in the adult brain. Candidates include several different pro  ...[more]

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