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J Biol Chem. 2016 Aug 19;291(34):17510-22. doi: 10.1074/jbc.M116.728782. Epub 2016 Jun 30.

The Molecular Chaperone Hsc70 Interacts with Tyrosine Hydroxylase to Regulate Enzyme Activity and Synaptic Vesicle Localization.

Author information

1
From the Departments of Neurobiology and.
2
Neurology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261.
3
the Centro de Investigación y Modelamiento de Fenómenos Aleatorios Valparaíso, Faculty of Engineering, Universidad de Valparaíso, 2362905 Valparaíso, Chile.
4
the Division of Pharmaceutical Sciences, Duquesne University, Pittsburgh, Pennsylvania 15282, and.
5
the Department of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville, Florida 32610.
6
the Department of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville, Florida 32610 gonzalotorres@ufl.edu.

Abstract

We previously reported that the vesicular monoamine transporter 2 (VMAT2) is physically and functionally coupled with Hsc70 as well as with the dopamine synthesis enzymes tyrosine hydroxylase (TH) and aromatic amino acid decarboxylase, providing a novel mechanism for dopamine homeostasis regulation. Here we expand those findings to demonstrate that Hsc70 physically and functionally interacts with TH to regulate the enzyme activity and synaptic vesicle targeting. Co-immunoprecipitation assays performed in brain tissue and heterologous cells demonstrated that Hsc70 interacts with TH and aromatic amino acid decarboxylase. Furthermore, in vitro binding assays showed that TH directly binds the substrate binding and carboxyl-terminal domains of Hsc70. Immunocytochemical studies indicated that Hsc70 and TH co-localize in midbrain dopaminergic neurons. The functional significance of the Hsc70-TH interaction was then investigated using TH activity assays. In both dopaminergic MN9D cells and mouse brain synaptic vesicles, purified Hsc70 facilitated an increase in TH activity. Neither the closely related protein Hsp70 nor the unrelated Hsp60 altered TH activity, confirming the specificity of the Hsc70 effect. Overexpression of Hsc70 in dopaminergic MN9D cells consistently resulted in increased TH activity whereas knockdown of Hsc70 by short hairpin RNA resulted in decreased TH activity and dopamine levels. Finally, in cells with reduced levels of Hsc70, the amount of TH associated with synaptic vesicles was decreased. This effect was rescued by addition of purified Hsc70. Together, these data demonstrate a novel interaction between Hsc70 and TH that regulates the activity and localization of the enzyme to synaptic vesicles, suggesting an important role for Hsc70 in dopamine homeostasis.

KEYWORDS:

Hsc70; complex; dopamine; enzyme; protein targeting; synapse

PMID:
27365397
PMCID:
PMC5016148
DOI:
10.1074/jbc.M116.728782
[Indexed for MEDLINE]
Free PMC Article

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