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Evaluation of inflammasome requirement in neutrophilic inflammation induced by pore-forming toxins, Natterins

Grant number: 18/17413-0
Support type:Regular Research Grants
Duration: March 01, 2019 - February 29, 2020
Field of knowledge:Biological Sciences - Immunology - Cellular Immunology
Principal researcher:Carla Lima da Silva
Grantee:Carla Lima da Silva
Home Institution: Instituto Butantan. Secretaria da Saúde (São Paulo - Estado). São Paulo , SP, Brazil

Abstract

Neutrophils, the most abundant immune cells in the circulation, are key players in acute inflammation. Excessive neutrophil recruitment is observed in traumatic and ischemic injuries, autoimmunity, and sterile liver injury and consequent neutrophil activation results host tissue injury. Therefore, understanding mechanisms of neutrophil recruitment is of major physiological and pathophysiological importance. Neutrophil trafficking is orchestrated by adhesion molecules, such as b2 integrins, chemokines, and cytokines as IL-1b. Neutrophils express a large number of cell surface receptors for recognition of pathogens and the inflammatory environment, including Toll-like receptors (TLRs) and NLR (nucleotide binding domain (NOD) leucine-rich repeat-like receptor) family of proteins. The processing of the 31-kDa inactive cytosolic pro-IL-1² precursor into the bioactive 17-kDa IL-1², mostly depends on autocatalytic cleavage of the cysteine protease caspase-1. Such cleavage is triggered by several structures termed as inflammasome, which consist of a group of related multiprotein cellular complexes, among which the best characterized include receptors of the NLR family of proteins, namely NLRP1, NLRP3 and NLRC4. While canonical inflammasome activation results in caspase-1 cleavage and activation, the activation of a non-canonical inflammasome results in activation of pro-caspase-11 that promotes cell death as well as IL-1a and IL-1b secretion and neutrophil recruitment during infection response. The family Natterins was first discovered in the venom gland of Brazilian venomous fish Thalassophryne nattereri with five orthologues 1-4 and -P. Natterin proteins contain at the N-terminal region two DM9 domains first discovered in Drosophila, followed by an aerolysin domain at the C-terminal. The aerolysin family belongs to the large class of pore-forming proteins/toxins (b-PFTs) and is considered to be the principal virulence factors contributing to severe inflammatory diseases in humans and animals. Our objective is to verify the role of the activation of canonical or non-canonical platform members of the inflammasome in the recruitment of neutrophils to the site of injury induced by pore-forming toxins Natterins as well as the direct influence of these members in the activation of neutrophils modulating their capacity to produce mediators that amplify the inflammatory response. (AU)

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VEICULO: TITULO (DATA)
VEICULO: TITULO (DATA)

Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
LIMA, CARLA; FALCAO, MARIA ALICE PIMENTEL; ANDRADE-BARROS, ALINE INGRID; SENI-SILVA, ANA CAROLINA; GRUND, LIDIANE ZITO; BALOGH, ENIKO; CONCEICAO, KATIA; QUENIAUX, VALERIE F.; RYFFEL, BERNHARD; LOPES-FERREIRA, MONICA. Natterin an aerolysin-like fish toxin drives IL-1 beta-dependent neutrophilic inflammation mediated by caspase-1 and caspase-11 activated by the inflammasome sensor NLRP6. International Immunopharmacology, v. 91, FEB 2021. Web of Science Citations: 0.

Please report errors in scientific publications list by writing to: cdi@fapesp.br.