Unknown/enigmatic functions of extracellular ASC

Autor(es)

de Souza, Jean Gabriel ^{[1, 2, 3]} ; Starobinas, Nancy ^{[1, 2]} ; Ibanez, Olga Celia Martinez ^{[1, 2]}

Afiliação do(s) autor(es)

^[1] Butantan Inst, Lab Immunogenet, Sao Paulo - Brazil

^[2] Butantan Inst, Ctr Excellence New Target Discovery, CENTD, Sao Paulo - Brazil

^[3] GlaxoSmithKline, Immunol Catalyst, Stevenag - England

• Tipo de documento: Artigo de Revisão
• Fonte: IMMUNOLOGY; v. 163, n. 4, p. 377-388, AUG 2021.
• Citações Web of Science: 1

Resumo

Apoptosis-associated speck-like protein containing a caspase recruit domain (ASC), encoded by PYCARD gene, is a 22 kDa small molecule, which aggregates into ASC specks during inflammasome activation. ASC protein is an adaptor protein present in several inflammasome complexes that performs several intra- and extracellular functions, in monomeric form or as ASC specks, during physiological and pathological processes related to inflammation and adaptive immunity. Extracellular ASC specks (eASC specks) released during cell death by pyroptosis can contribute as a danger signal to the propagation of inflammation via phagocytosis and activation of surrounding cells. ASC specks are found in the circulation of patients with chronic inflammatory diseases and have been considered as relevant blood biomarkers of inflammation. eASC amplifies the inflammatory signal, may induce the production of autoantibodies, transports molecules that bind to this complex, contributing to the generation of antibodies, and can induce the maturation of cytokines promoting the modelling of the adaptive immunity. Although several advances have been registered in the last 21 years, there are numerous unknown or enigmatic gaps in the understanding of the role of eASC specks in the organism. Here, we provide an overview about the ASC protein focusing on the probable roles of eASC specks in several diseases, up to the most recent studies concerning COVID-19. (AU)

• Processo FAPESP: 19/20713-8 - Papel do ASC extracelular na inflamação da artrite reumatoide
• Beneficiário: Jean Gabriel de Souza
• Modalidade de apoio: Bolsas no Exterior - Estágio de Pesquisa - Pós-Doutorado
• Processo FAPESP: 15/50040-4 - Rational approach for searching molecular targets involved in inflammatory events and cell survival
• Beneficiário: Ana Marisa Chudzinski-Tavassi
• Modalidade de apoio: Auxílio à Pesquisa - Programa Centros de Pesquisa em Engenharia
• Processo FAPESP: 17/06736-0 - Identificação/elucidação e validação de novos alvos/vias envolvidos na osteoartrite
• Beneficiário: Jean Gabriel de Souza
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado