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Death-associated protein kinase 1 phosphorylates NDRG2 and induces neuronal cell death

Authors
 Mi-Hyeon You  ;  Byeong Mo Kim  ;  Chun-Hau Chen  ;  Michael J Begley  ;  Lewis C Cantley  ;  Tae Ho Lee 
Citation
 CELL DEATH AND DIFFERENTIATION, Vol.24(2) : 238-250, 2017 
Journal Title
 CELL DEATH AND DIFFERENTIATION 
ISSN
 1350-9047 
Issue Date
2017
MeSH
Alzheimer Disease/metabolism ; Alzheimer Disease/pathology ; Amino Acid Chloromethyl Ketones/pharmacology ; Animals ; Apoptosis/drug effects ; Brain/metabolism ; Caspase 3/chemistry ; Caspase 3/metabolism ; Cells, Cultured ; Ceramides/pharmacology ; Death-Associated Protein Kinases/antagonists & inhibitors ; Death-Associated Protein Kinases/genetics ; Death-Associated Protein Kinases/metabolism* ; HEK293 Cells ; HeLa Cells ; Humans ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Neurons/cytology ; Neurons/metabolism ; Phosphorylation/drug effects ; Poly(ADP-ribose) Polymerases/metabolism ; Proteins/antagonists & inhibitors ; Proteins/genetics ; Proteins/metabolism* ; RNA Interference
Abstract
Death-associated protein kinase 1 (DAPK1) has been shown to have important roles in neuronal cell death in several model systems and has been implicated in multiple diseases, including Alzheimer's disease (AD). However, little is known about the molecular mechanisms by which DAPK1 signals neuronal cell death. In this study, N-myc downstream-regulated gene 2 (NDRG2) was identified as a novel substrate of DAPK1 using phospho-peptide library screening. DAPK1 interacted with NDRG2 and directly phosphorylated the Ser350 residue in vitro and in vivo. Moreover, DAPK1 overexpression increased neuronal cell death through NDRG2 phosphorylation after ceramide treatment. In contrast, inhibition of DAPK1 by overexpression of a DAPK1 kinase-deficient mutant and small hairpin RNA, or by treatment with a DAPK1 inhibitor significantly decreased neuronal cell death, and abolished NDRG2 phosphorylation in cell culture and in primary neurons. Furthermore, NDRG2-mediated cell death by DAPK1 was required for a caspase-dependent poly-ADP-ribose polymerase cleavage. In addition, DAPK1 ablation suppressed ceramide-induced cell death in mouse brain and neuronal cell death in Tg2576 APPswe-overexpressing mice. Finally, levels of phosphorylated NDRG2 Ser350 and DAPK1 were significantly increased in human AD brain samples. Thus, phosphorylation of NDRG2 on Ser350 by DAPK1 is a novel mechanism activating NDRG2 function and involved in neuronal cell death regulation in vivo.
Files in This Item:
T201700473.pdf.pdf Download
DOI
10.1038/cdd.2016.114
Appears in Collections:
5. Research Institutes (연구소) > Yonsei Integrative Research Institute for Cerebral & Cardiovascular Disease (뇌심혈관질환융합연구사업단) > 1. Journal Papers
Yonsei Authors
Kim, Byeong Mo(김병모) ORCID logo https://orcid.org/0000-0002-0582-3132
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/166581
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