Affiliations: [a]
School of Chemical Engineering and Technology, Tianjin University, Tianjin, China
| [b]
Department of Blood Transfusion, Chinese PLA General Hospital, Beijing, China
| [c]
Department of Experimental Hematology, Beijing Institute of Radiation Medicine, Beijing, China
| [d] State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, China
| [e]
Beijing Institute of Pharmacology and Toxicology, Beijing, China
| [f]
State Key Laboratory of Toxicology and Medical Countermeasures, Beijing, China
Correspondence:
[*]
Correspondence to: Xiaorui Cheng, Beijing Institute of Pharmacology and Toxicology, Tai Ping Road 27, 100850 Beijing, E-mail: cxr916@163.com.
Note: [1] These authors contributed equally to this work.
Abstract: Background:The toxicity of excessive glutamate release has been implicated in various acute and chronic neurodegenerative conditions. Vesicular glutamate transporters (VGLUTs) are the major mediators for the uptake of glutamate into synaptic vesicles. However, the dynamics and mechanism of this process in glutamatergic neurons are still largely unknown. Objective:This study aimed to investigate the candidate protein partners of VGLUT1 and their regulatory roles in the vesicles in rat brain. Methods:Pull down assay, co-immunoprecipitation assay, or split-ubiquitin membrane yeast two hybrid screening coupled with nanoRPLC-MS/MS were used to identify the candidate protein partners of VGLUT1 in the vesicles in rat brain. The in vitro and in vivo models were used to test effects of AβPP, Atp6ap2, Gja1, and Synataxin on VGLUT1 expression. Results:A total of 255 and 225 proteins and 172 known genes were identified in the pull down assay, co-immunoprecipitation assay, or split-ubiquitin yeast two-hybrid screening respectively. The physiological interactions of SV2A, Syntaxin 12, Gja1, AβPP, and Atp6ap2 to VGLUT1 were further confirmed. Knockdown of Atp6ap2, Gja1, and Synataxin increased VGLUT1 mRNA expression and only knockdown of AβPP increased both mRNA and protein levels of VGLUT1 in PC12 cells. The regulatory function of AβPP on VGLUT1 expression was further confirmed in the in vitro and in vivo models. Conclusion:These results elucidate that the AβPP and VGLUT1 interacts at vesicular level and AβPP plays a role in the regulation of VGLUT1 expression which is essential for maintaining vesicular activities.
