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Published on: August 30, 2017
The emerging interrelation between ROCO and related kinases, intracellular Ca2+ signaling, and autophagy
1KU Leuven, Laboratory for Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine & Leuven Kanker Instituut, Campus Gasthuisberg O/N-1 B-802, Herestraat 49, BE-3000 Leuven, Belgium; Cancer Research UK Beatson Institute, Garscube Estate, Switchback Road, Glasgow G61 1BD, UK.
Abstract:
ROCO kinases form a family of proteins characterized by kinase activity in addition to the presence of the so-called ROC (Ras of complex proteins)/COR (C-terminal of ROC) domains having a role in their GTPase activity. These are the death-associated protein kinase (DAPK) 1 and the leucine-rich repeat kinases (LRRK) 1 and 2. These kinases all play roles in cellular life and death decisions and in autophagy in particular. Related to the ROCO kinases is DAPK 2 that however cannot be classified as a ROCO protein due to the absence of the ROC/COR domains. This review aims to bring together what is known about the relation between these proteins and intracellular Ca2+ signals in the induction and regulation of autophagy. Interestingly, DAPK 1 and 2 and LRRK2 are all linked to Ca2+ signaling in their effects on autophagy, though in various ways. Present evidence supports an upstream role for LRRK2 that via lysosomal and endoplasmic reticulum Ca2+ release can trigger autophagy induction. In contrast herewith, DAPK1 and 2 react on existing Ca2+ signals to stimulate the autophagic pathway. Further research will be needed for obtaining a full understanding of the role of these various kinases in autophagy and to assess their exact relation with intracellular Ca2+ signaling as this would be helpful in the development of novel therapeutic strategies against neurodegenerative disorders, cancer and auto-immune diseases. This article is part of a Special Issue entitled: ECS Meeting edited by Claus Heizmann, Joachim Krebs and Jacques Haiech.
Insights
ROCO kinases, including DAPK1, DAPK2, and LRRK2, regulate autophagy through calcium (Ca2+) signaling. LRRK2 initiates autophagy via Ca2+ release, while DAPK1 and DAPK2 modulate it in response to Ca2+ signals.
Area of Science:
- Biochemistry
- Cell Biology
- Molecular Biology
Background:
- ROCO kinases, characterized by ROC/COR domains, regulate GTPase activity and cellular processes like autophagy.
- Death-associated protein kinase (DAPK) 1 and leucine-rich repeat kinase (LRRK) 1 and 2 are key ROCO kinases involved in cell life/death and autophagy.
- DAPK 2, lacking ROC/COR domains, is related to ROCO kinases but distinct.
Purpose of the Study:
- To review the relationship between ROCO kinases, DAPK 2, and intracellular calcium (Ca2+) signaling in autophagy.
- To elucidate the distinct roles of LRRK2, DAPK1, and DAPK2 in Ca2+-mediated autophagy regulation.
Main Methods:
- Literature review synthesizing current research on ROCO kinases, DAPK 2, and Ca2+ signaling in autophagy.
- Analysis of existing evidence on the mechanisms linking these proteins to autophagic pathways.
Main Results:
- LRRK2 acts upstream, inducing autophagy through lysosomal and endoplasmic reticulum Ca2+ release.
- DAPK1 and DAPK2 respond to existing Ca2+ signals to stimulate autophagy.
- All studied kinases (LRRK2, DAPK1, DAPK2) are linked to Ca2+ signaling in their regulation of autophagy.
Conclusions:
- Distinct roles of LRRK2, DAPK1, and DAPK2 in Ca2+-dependent autophagy are highlighted.
- Further research is needed to fully understand these kinases' roles in autophagy and Ca2+ signaling.
- Understanding these pathways could aid therapeutic strategies for neurodegenerative diseases, cancer, and autoimmune disorders.
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