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The transmembrane domain of the p75 neurotrophin receptor stimulates phosphorylation of the TrkB tyrosine kinase receptor.


ABSTRACT: The function of protein products generated from intramembraneous cleavage by the ?-secretase complex is not well defined. The ?-secretase complex is responsible for the cleavage of several transmembrane proteins, most notably the amyloid precursor protein that results in A?, a transmembrane (TM) peptide. Another protein that undergoes very similar ?-secretase cleavage is the p75 neurotrophin receptor. However, the fate of the cleaved p75 TM domain is unknown. p75 neurotrophin receptor is highly expressed during early neuronal development and regulates survival and process formation of neurons. Here, we report that the p75 TM can stimulate the phosphorylation of TrkB (tyrosine kinase receptor B). In vitro phosphorylation experiments indicated that a peptide representing p75 TM increases TrkB phosphorylation in a dose- and time-dependent manner. Moreover, mutagenesis analyses revealed that a valine residue at position 264 in the rat p75 neurotrophin receptor is necessary for the ability of p75 TM to induce TrkB phosphorylation. Because this residue is just before the ?-secretase cleavage site, we then investigated whether the p75(??) peptide, which is a product of both ?- and ?-cleavage events, could also induce TrkB phosphorylation. Experiments using TM domains from other receptors, EGFR and FGFR1, failed to stimulate TrkB phosphorylation. Co-immunoprecipitation and biochemical fractionation data suggested that p75 TM stimulates TrkB phosphorylation at the cell membrane. Altogether, our results suggest that TrkB activation by p75(??) peptide may be enhanced in situations where the levels of the p75 receptor are increased, such as during brain injury, Alzheimer's disease, and epilepsy.

SUBMITTER: Saadipour K 

PROVIDER: S-EPMC5633122 | biostudies-literature | 2017 Oct

REPOSITORIES: biostudies-literature

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The transmembrane domain of the p75 neurotrophin receptor stimulates phosphorylation of the TrkB tyrosine kinase receptor.

Saadipour Khalil K   MacLean Michael M   Pirkle Sean S   Ali Solav S   Lopez-Redondo Maria-Luisa ML   Stokes David L DL   Chao Moses V MV  

The Journal of biological chemistry 20170817 40


The function of protein products generated from intramembraneous cleavage by the γ-secretase complex is not well defined. The γ-secretase complex is responsible for the cleavage of several transmembrane proteins, most notably the amyloid precursor protein that results in Aβ, a transmembrane (TM) peptide. Another protein that undergoes very similar γ-secretase cleavage is the p75 neurotrophin receptor. However, the fate of the cleaved p75 TM domain is unknown. p75 neurotrophin receptor is highly  ...[more]

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