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The NLR family of innate immune and cell death sensors.
Sundaram, Balamurugan; Tweedell, Rebecca E; Prasanth Kumar, Sivakumar; Kanneganti, Thirumala-Devi.
  • Sundaram B; Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Tweedell RE; Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Prasanth Kumar S; Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Kanneganti TD; Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. Electronic address: thirumala-devi.kanneganti@stjude.org.
Immunity ; 57(4): 674-699, 2024 Apr 09.
Article en En | MEDLINE | ID: mdl-38599165
ABSTRACT
Nucleotide-binding oligomerization domain (NOD)-like receptors, also known as nucleotide-binding leucine-rich repeat receptors (NLRs), are a family of cytosolic pattern recognition receptors that detect a wide variety of pathogenic and sterile triggers. Activation of specific NLRs initiates pro- or anti-inflammatory signaling cascades and the formation of inflammasomes-multi-protein complexes that induce caspase-1 activation to drive inflammatory cytokine maturation and lytic cell death, pyroptosis. Certain NLRs and inflammasomes act as integral components of larger cell death complexes-PANoptosomes-driving another form of lytic cell death, PANoptosis. Here, we review the current understanding of the evolution, structure, and function of NLRs in health and disease. We discuss the concept of NLR networks and their roles in driving cell death and immunity. An improved mechanistic understanding of NLRs may provide therapeutic strategies applicable across infectious and inflammatory diseases and in cancer.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Receptores de Reconocimiento de Patrones / Inflamasomas Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Receptores de Reconocimiento de Patrones / Inflamasomas Idioma: En Año: 2024 Tipo del documento: Article