Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The . gov means it’s official. Federal government websites often end in . gov or . mil. Before sharing sensitive information, make sure you’re on a federal government site VSports app下载. .

Https

The site is secure V体育官网. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. .

Review
. 2013 Dec 9:4:440.
doi: 10.3389/fimmu.2013.00440.

VSports手机版 - An Update on PYRIN Domain-Containing Pattern Recognition Receptors: From Immunity to Pathology

Affiliations
Review

An Update on PYRIN Domain-Containing Pattern Recognition Receptors: From Immunity to Pathology

Rojo A Ratsimandresy et al. Front Immunol. .

Abstract

Cytosolic pattern recognition receptors (PRRs) sense a wide range of endogenous danger-associated molecular patterns as well as exogenous pathogen-associated molecular patterns. In particular, Nod-like receptors containing a pyrin domain (PYD), called NLRPs, and AIM2-like receptors (ALRs) have been shown to play a critical role in host defense by facilitating clearance of pathogens and maintaining a healthy gut microflora. NLRPs and ALRs both encode a PYD, which is crucial for relaying signals that result in an efficient innate immune response through activation of several key innate immune signaling pathways. However, mutations in these PRRs have been linked to the development of auto-inflammatory and autoimmune diseases VSports手机版. In addition, they have been implicated in metabolic diseases. In this review, we summarize the function of PYD-containing NLRPs and ALRs and address their contribution to innate immunity, host defense, and immune-linked diseases. .

Keywords: AIM2-like receptor; ALR; NLR; Nod-like receptor; PYRIN domain; inflammasome; innate immunity; pattern recognition receptor V体育安卓版. .

PubMed Disclaimer

Figures

Figure 1
Figure 1
Domain architecture of PYD-containing proteins involved in innate immunity. Depicted are human and mouse (A) Nod-like receptors, (B) AIM2-like receptors, and (C) regulatory proteins.
Figure 2
Figure 2
Mechanism of NLRP1 activation in human and mice. MDP, muramyl dipeptide; LF, lethal factor; PA, protective antigen.
Figure 3
Figure 3
Mechanism of NLRP3 activation in response to pathogen infection.
Figure 4
Figure 4
Mechanism of NLRP3 activation in response to endogenous and exogenous danger signals.
Figure 5
Figure 5
Function of NLRP6, NLRP10, and NLRP12 in intestinal homeostasis and dendritic cell (DC) homing.
Figure 6
Figure 6
Pro- and anti-inflammatory mechanisms of NLRP7.
Figure 7
Figure 7
Signaling of AIM2 and IFI16 leading to inflammasome activation and induction of IFNβ in response to bacterial and viral infection.

References

    1. Martinon F, Burns K, Tschopp J. The inflammasome: a molecular platform triggering activation of inflammatory caspases and processing of proIL-1b. Mol Cell (2002) 10:417–2610.1016/S1097-2765(02)00599-3 - V体育ios版 - DOI - PubMed
    1. Khare S, Luc N, Dorfleutner A, Stehlik C. Inflammasomes and their activation. Crit Rev Immunol (2010) 30:463–8710.1615/CritRevImmunol.v30.i5.50 - DOI - PMC - PubMed
    1. Srinivasula SM, Poyet J-L, Razmara M, Datta P, Zhang Z, Alnemri ES. The PYRIN-CARD protein ASC is an activating adaptor for caspase-1. J Biol Chem (2002) 277:21119–2210.1074/jbc.C200179200 - DOI - PubMed
    1. Groß O, Yazdi A, Thomas C, Masin M, Heinz L, Guarda G, et al. Inflammasome activators induce interleukin-1α secretion via distinct pathways with differential requirement for the protease function of caspase-1. Immunity (2012) 36:388–40010.1016/j.immuni.2012.01.018 - VSports - DOI - PubMed
    1. Fettelschoss A, Kistowska M, LeibundGut-Landmann S, Beer H-D, Johansen P, Senti G, et al. Inflammasome activation and IL-1β target IL-1α for secretion as opposed to surface expression. Proc Natl Acad Sci U S A (2011) 108:18055–6010.1073/pnas.1109176108 - DOI - PMC - PubMed

"VSports" Publication types

"V体育官网" LinkOut - more resources