Target intelligence / Profile preview

Arginase-2, mitochondrial (Arginase II (ARG2))

Target
Arginase II (ARG2)
Molecular classification
Enzyme, Metalloenzyme (binuclear manganese), Urea cycle enzyme (mitochondrial isoform)
01

Overview

Arginase-2, mitochondrial is a manganese-dependent hydrolase located principally in mitochondria. Unlike cytosolic arginase I, which drives the hepatic urea cycle, arginase-2 has a broader tissue distribution (notably kidney, immune cells, vascular endothelium), and is crucial for extrahepatic arginine metabolism. By regulating local arginine availability, it competes with nitric oxide synthase, influencing production of NO and thereby impacting immune responses, vascular tone, and cell survival. Dysregulated arginase-2 activity fosters immunosuppressive environments (notably in tumors), exacerbates cardiac aging and inflammation, and influences systemic metabolic processes. Emerging therapeutic strategies target arginase-2 to reverse immune suppression in cancer, abate inflammation, and address metabolic and cardiovascular disorders. Inhibitors like C0021158 modulate enzyme activity via allosteric mechanisms, restoring T cell function and anti-tumor immunity.

Other names
Arginase IIKidney-type arginaseNon-hepatic arginaseType II arginaseAII type II arginaseMitochondrial arginase
02

Mechanism of action

Enzymatic inhibition (competitive or noncompetitive, including allosteric inhibitors like C0021158) Allosteric modulation leading to conformational changes that impair substrate binding and enzyme activity Restoration of T cell proliferation by reversing immunosuppression Indirect modulation of NO production and vascular/immune effects

03

Biological functions

Arginine hydrolysis (conversion to urea and ornithine)Regulation of nitric oxide synthesis (competes with nitric oxide synthase for L-arginine)Immune regulation (suppresses T-cell responses, promotes immunosuppression)Modulation of mitochondrial dynamics and oxidative phosphorylation in macrophages (especially under influence of IL-10)Influences hepatic glucose and lipid metabolismNegative regulation of inflammation, survival of activated T cells, and endothelial cell functionInvolved in vascular smooth muscle cell senescence and apoptosis
04

Disease associations

Cancer (promotes tumor immune evasion; immunosuppressive microenvironments)Inflammation (regulates inflammatory signaling, influences cytokine production)Cardiovascular disease (cardiac aging, endothelial dysfunction, vascular stiffness)Asthma (suppresses inflammation in airway epithelium)Infection (immune evasion, e.g., by H. pylori)Metabolic disease (affects glucose/lipid metabolism, insulin sensitivity)
05

Safety considerations

Potential risk of excess NO and related vascular effects when arginase-2 is inhibited, which may contribute to hypotension or endothelial dysfunctionOff-target immunomodulation (suppression or overstimulation depending on context)Unresolved long-term effects of enzymatic blockade on broader arginine metabolism (e.g., polyamine synthesis, cell proliferation)
06

Interacting drugs

C0021158 (high-affinity antibody inhibitor)

1 more in the full profile.

07

Biomarkers

ARG2 expression levels (immunohistochemistry, mRNA quantification)L-arginine and urea concentration in tissue/circulationIL-1β and other inflammatory cytokinesCD4+ and CD8+ T cell activity (functional assays)

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