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LAR Receptor Tyrosine Phosphatase Family in Healthy and Diseased Brain.
Cornejo, Francisca; Cortés, Bastián I; Findlay, Greg M; Cancino, Gonzalo I.
Afiliação
  • Cornejo F; Center for Integrative Biology, Facultad de Ciencias, Universidad Mayor, Santiago, Chile.
  • Cortés BI; Center for Integrative Biology, Facultad de Ciencias, Universidad Mayor, Santiago, Chile.
  • Findlay GM; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
  • Cancino GI; Center for Integrative Biology, Facultad de Ciencias, Universidad Mayor, Santiago, Chile.
Front Cell Dev Biol ; 9: 659951, 2021.
Article em En | MEDLINE | ID: mdl-34966732
ABSTRACT
Protein phosphatases are major regulators of signal transduction and they are involved in key cellular mechanisms such as proliferation, differentiation, and cell survival. Here we focus on one class of protein phosphatases, the type IIA Receptor-type Protein Tyrosine Phosphatases (RPTPs), or LAR-RPTP subfamily. In the last decade, LAR-RPTPs have been demonstrated to have great importance in neurobiology, from neurodevelopment to brain disorders. In vertebrates, the LAR-RPTP subfamily is composed of three members PTPRF (LAR), PTPRD (PTPδ) and PTPRS (PTPσ), and all participate in several brain functions. In this review we describe the structure and proteolytic processing of the LAR-RPTP subfamily, their alternative splicing and enzymatic regulation. Also, we review the role of the LAR-RPTP subfamily in neural function such as dendrite and axon growth and guidance, synapse formation and differentiation, their participation in synaptic activity, and in brain development, discussing controversial findings and commenting on the most recent studies in the field. Finally, we discuss the clinical outcomes of LAR-RPTP mutations, which are associated with several brain disorders.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Front Cell Dev Biol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Chile

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Front Cell Dev Biol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Chile