1. Exosome Liberation by Human Neutrophils under L-Amino Acid Oxidase of Calloselasma rhodostoma Venom Action.
- Author
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Serrath, Suzanne N., Pontes, Adriana S., Paloschi, Mauro V., Silva, Milena D. S., Lopes, Jéssica A., Boeno, Charles N., Silva, Carolina P., Santana, Hallison M., Cardozo, Daniel G., Ugarte, Andrey V. E., Magalhães, João G. S., Cruz, Larissa F., Setubal, Sulamita S., Soares, Andreimar M., Cavecci-Mendonça, Bruna, Santos, Lucilene D., and Zuliani, Juliana P.
- Subjects
SNAKE venom ,NEUTROPHILS ,EXOSOMES ,IMMUNOREGULATION ,VENOM ,CELL communication ,BLOOD platelet aggregation - Abstract
L-Amino acid oxidase (LAAO) is an enzyme found in snake venom that has multifaceted effects, including the generation of hydrogen peroxide (H
2 O2 ) during oxidative reactions, leading to various biological and pharmacological outcomes such as apoptosis, cytotoxicity, modulation of platelet aggregation, hemorrhage, and neutrophil activation. Human neutrophils respond to LAAO by enhancing chemotaxis, and phagocytosis, and releasing reactive oxygen species (ROS) and pro-inflammatory mediators. Exosomes cellular nanovesicles play vital roles in intercellular communication, including immune responses. This study investigates the impact of Calloselasma rhodostoma snake venom-derived LAAO (Cr-LAAO) on human neutrophil exosome release, including activation patterns, exosome formation, and content. Neutrophils isolated from healthy donors were stimulated with Cr-LAAO (100 μg/mL) for 3 h, followed by exosome isolation and analysis. Results show that Cr-LAAO induces the release of exosomes with distinct protein content compared to the negative control. Proteomic analysis reveals proteins related to the regulation of immune responses and blood coagulation. This study uncovers Cr-LAAO's ability to activate human neutrophils, leading to exosome release and facilitating intercellular communication, offering insights into potential therapeutic approaches for inflammatory and immunological disorders. [ABSTRACT FROM AUTHOR]- Published
- 2023
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