| Literature DB >> 31876231 |
Alexander S Brown1, Pratap Meera2, Gabe Quinones1, Jessica Magri1, Thomas S Otis3, Stefan M Pulst4, Anthony E Oro1.
Abstract
Spinocerebellar ataxias (SCA) are a genetically heterogeneous family of cerebellar neurodegenerative diseases characterized by abnormal firing of Purkinje neurons and degeneration. We recently demonstrated the slowed firing rates seen in several SCAs share a common etiology of hyper-activation of the Src family of non-receptor tyrosine kinases (SFKs). However, the lack of clinically available neuroactive SFK inhibitors lead us to investigate alternative mechanisms to modulate SFK activity. Previous studies demonstrate that SFK activity can be enhanced by the removal of inhibitory phospho-marks by receptor-protein-tyrosine phosphatases (RPTPs). In this Extra View we show that MTSS1 inhibits SFK activity through the binding and inhibition of a subset of the RPTP family members, and lowering RPTP activity in cerebellar slices with peptide inhibitors increases the suppressed Purkinje neuron basal firing rates seen in two different SCA models. Together these results identify RPTPs as novel effectors of Purkinje neuron basal firing, extending the MTSS1/SFK regulatory circuit we previously described and expanding the therapeutic targets for SCA patients.Entities:
Keywords: Mtss1; Receptor protein tyrosine phosphatase; Src family kinase; neurodegeneration; spinocerebellar ataxia
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Year: 2019 PMID: 31876231 PMCID: PMC6961678 DOI: 10.1080/15384101.2019.1695995
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534