Dokument: Biochemistry, pharmacology, and in vivo function of arginases

Titel:Biochemistry, pharmacology, and in vivo function of arginases
URL für Lesezeichen:https://docserv.uni-duesseldorf.de/servlets/DocumentServlet?id=72667
URN (NBN):urn:nbn:de:hbz:061-20260323-115323-7
Kollektion:Publikationen
Sprache:Englisch
Dokumententyp:Wissenschaftliche Texte » Artikel, Aufsatz
Medientyp:Text
Autoren: Heuser, Sophia K. [Autor]
Li, Junjie [Autor]
Pudewell, Silke [Autor]
LoBue, Anthea [Autor]
Li, Zhixin [Autor]
Cortese-Krott, Miriam M. [Autor]
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Dateien vom 23.03.2026 / geändert 23.03.2026
Beschreibung:The enzyme arginase catalyzes the hydrolysis of l-arginine into l-ornithine and urea. The 2 existing isoforms Arg1 and Arg2 exhibit different cellular localizations and metabolic functions. Arginase activity is crucial for nitrogen detoxification in the urea cycle, synthesis of polyamines, and control of l-arginine bioavailability and nitric oxide (NO) production. Despite significant progress in the understanding of the biochemistry and function of arginases, several open questions remain. Recent studies have revealed that the regulation and function of Arg1 and Arg2 are cell type–specific, species-specific, and profoundly different in mice and humans. The main differences are in the distribution and function of Arg1 and Arg2 in immune and erythroid cells. Contrary to what was previously thought, Arg1 activity appears to be only partially related to vascular NO signaling under homeostatic conditions in the vascular wall, but its expression is increased under disease conditions and may be targeted by treatment with arginase inhibitors. Arg2 appears to be mainly a catabolic enzyme involved in the synthesis of l-ornithine, polyamine, and l-proline but may play a putative role in blood pressure control, at least in mice. The immunosuppressive role of arginase-mediated arginine depletion is a promising target for cancer treatment. This review critically revises and discusses the biochemistry, pharmacology, and in vivo function of arginases, focusing on the insights gained from the analysis of cell-specific Arg1 and Arg2 knockout mice and human studies using arginase inhibitors or pegylated recombinant arginase.
Rechtliche Vermerke:Originalveröffentlichung:
Heuser, S. K., Li, J., Pudewell, S., Lo Bue, A., Li, Z., & Cortese-Krott, M. M. (2024). Biochemistry, pharmacology, and in vivo function of arginases. Pharmacological Reviews, 77(1), Article 100015. https://doi.org/10.1124/pharmrev.124.001271
Lizenz:Creative Commons Lizenzvertrag
Dieses Werk ist lizenziert unter einer Creative Commons Namensnennung 4.0 International Lizenz
Fachbereich / Einrichtung:Medizinische Fakultät
Dokument erstellt am:23.03.2026
Dateien geändert am:23.03.2026
english
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