TRPM2.

Handb Exp Pharmacol

Center for Biomedical Research, The Queen's Medical Center, 1301 Punchbowl Street, Honolulu, HI, 96813, USA,

Published: July 2014

TRPM2 is the second member of the transient receptor potential melastatin-related (TRPM) family of cation channels. The protein is widely expressed including in the brain, immune system, endocrine cells, and endothelia. It embodies both ion channel functionality and enzymatic ADP-ribose (ADPr) hydrolase activity. TRPM2 is a Ca(2+)-permeable nonselective cation channel embedded in the plasma membrane and/or lysosomal compartments that is primarily activated in a synergistic fashion by intracellular ADP-ribose (ADPr) and Ca(2+). It is also activated by reactive oxygen and nitrogen species (ROS/NOS) and enhanced by additional factors, such as cyclic ADPr and NAADP, while inhibited by permeating protons (acidic pH) and adenosine monophosphate (AMP). Activation of TRPM2 leads to increases in intracellular Ca(2+) levels, which can serve signaling roles in inflammatory and secretory cells through release of vesicular mediators (e.g., cytokines, neurotransmitters, insulin) and in extreme cases can induce apoptotic and necrotic cell death under oxidative stress.

Download full-text PDF

Source
http://dx.doi.org/10.1007/978-3-642-54215-2_16DOI Listing

Publication Analysis

Top Keywords

adp-ribose adpr
8
trpm2 trpm2
4
trpm2 second
4
second member
4
member transient
4
transient receptor
4
receptor potential
4
potential melastatin-related
4
melastatin-related trpm
4
trpm family
4

Similar Publications

In-Source Collision-Induced Dissociation (CID) Improves Higher-Energy Collisional Dissociation (HCD)-Dependent Fragmentation of ADP-Ribosyl Peptides.

Rapid Commun Mass Spectrom

February 2025

Department of Medicine, Center for Interdisciplinary Cardiovascular Sciences, Division of Cardiovascular Medicine, Brigham Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Rationale: ADP-ribosylation is a posttranslational modification whose higher-energy collisional dissociation (HCD) products are dominated by complete or partial modification losses, complicating peptide sequencing and acceptor site localization efforts. We tested whether in-source collision-induced dissociation (CID) performed on a quadrupole-Orbitrap could convert ADPr to the smaller phosphoribose-HO derivative to facilitate HCD-dependent peptide sequencing.

Methods: ADP-ribosyl (ADPr) peptides derived from the human macrophage-like cell line THP-1 were analyzed on a quadrupole-Orbitrap.

View Article and Find Full Text PDF

From oxidative stress to metabolic dysfunction: The role of TRPM2.

Int J Biol Macromol

January 2025

Intravenous Drug Administration Center, Department of Pharmacy, Qingdao Third People's Hospital affiliated with Qingdao University, Qingdao, Shandong 266041, PR China. Electronic address:

Metabolic syndromes including atherosclerosis, diabetes, obesity, and hypertension are increasingly prevalent worldwide. The disorders are the primary attributes of oxidative stress and inflammation. The transient receptor potential M2 (TRPM2) channel is a pivotal mediator linking oxidative stress to metabolic dysfunction.

View Article and Find Full Text PDF

Insights into mechanisms of ubiquitin ADP-ribosylation reversal.

Biochem Soc Trans

December 2024

Department of Chemistry, Purdue University, West Lafayette, IN 47907, U.S.A.

Ubiquitination and ADP-ribosylation are two types of post-translational modification (PTM) involved in regulating various cellular activities. In a striking example of direct interplay between ubiquitination and ADP-ribosylation, the bacterial pathogen Legionella pneumophila uses its SidE family of secreted effectors to catalyze an NAD+-dependent phosphoribosyl ubiquitination of host substrates in a process involving the intermediary formation of ADP-ribosylated ubiquitin (ADPR-Ub). This noncanonical ubiquitination pathway is finely regulated by multiple Legionella effectors to ensure a balanced host subjugation.

View Article and Find Full Text PDF
Article Synopsis
  • ADP-ribosylation is a process where ADP-ribose units are transferred from NAD+ to proteins, and its dysregulation is linked to neurodegenerative diseases.
  • A study used genetic testing on two siblings suffering from developmental issues, seizures, and muscle weakness, identifying a new variant in the ADPRS gene that contributes to their diagnosis of childhood-onset neurodegeneration with stress-induced ataxia and seizures (CONDSIAS).
  • The identified genetic variant affects the protein ARH3, leading to its instability, improper localization, and accumulation of harmful compounds, helping to explain the disease's mechanisms and the importance of ARH3 in maintaining nervous system health.
View Article and Find Full Text PDF

Transient Receptor Potential Melastatin 2 (TRPM2) cation channels contribute to immunocyte activation, insulin secretion, and central thermoregulation. TRPM2 opens upon binding cytosolic Ca and ADP ribose (ADPR). We present here the 2.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!