271 related articles for article (PubMed ID: 24925032)
21. Non-canonical NLRP3 inflammasome activation and IL-1β signaling are necessary to L. amazonensis control mediated by P2X7 receptor and leukotriene B4.
Chaves MM; Sinflorio DA; Thorstenberg ML; Martins MDA; Moreira-Souza ACA; Rangel TP; Silva CLM; Bellio M; Canetti C; Coutinho-Silva R
PLoS Pathog; 2019 Jun; 15(6):e1007887. PubMed ID: 31233552
[TBL] [Abstract][Full Text] [Related]
22. CD39 limits P2X7 receptor inflammatory signaling and attenuates sepsis-induced liver injury.
Savio LEB; de Andrade Mello P; Figliuolo VR; de Avelar Almeida TF; Santana PT; Oliveira SDS; Silva CLM; Feldbrügge L; Csizmadia E; Minshall RD; Longhi MS; Wu Y; Robson SC; Coutinho-Silva R
J Hepatol; 2017 Oct; 67(4):716-726. PubMed ID: 28554875
[TBL] [Abstract][Full Text] [Related]
23. Caveolin-1 forms a complex with P2X7 receptor and tunes P2X7-mediated ATP signaling in mouse bone marrow-derived macrophages.
Sawai Y; Suzuki Y; Asagiri M; Hida S; Kondo R; Zamponi GW; Giles WR; Imaizumi Y; Yamamura H
Am J Physiol Cell Physiol; 2024 Jan; 326(1):C125-C142. PubMed ID: 37955123
[TBL] [Abstract][Full Text] [Related]
24. Aging and contribution of MyD88 and TRIF to expression of TLR pathway-associated genes following stimulation with Porphyromonas gingivalis.
Shaik-Dasthagirisaheb YB; Huang N; Weinberg EO; Shen SS; Genco CA; Gibson FC
J Periodontal Res; 2015 Feb; 50(1):89-102. PubMed ID: 24862405
[TBL] [Abstract][Full Text] [Related]
25. Porphyromonas gingivalis fimbria-dependent activation of inflammatory genes in human aortic endothelial cells.
Chou HH; Yumoto H; Davey M; Takahashi Y; Miyamoto T; Gibson FC; Genco CA
Infect Immun; 2005 Sep; 73(9):5367-78. PubMed ID: 16113252
[TBL] [Abstract][Full Text] [Related]
26. Extracellular adenosine 5'-triphosphate and lipopolysaccharide induce interleukin-1β release in canine blood.
Spildrejorde M; Curtis SJ; Curtis BL; Sluyter R
Vet Immunol Immunopathol; 2014 Jan; 157(1-2):105-10. PubMed ID: 24290165
[TBL] [Abstract][Full Text] [Related]
27. TLR2-dependent inflammatory response to Porphyromonas gingivalis is MyD88 independent, whereas MyD88 is required to clear infection.
Burns E; Eliyahu T; Uematsu S; Akira S; Nussbaum G
J Immunol; 2010 Feb; 184(3):1455-62. PubMed ID: 20042569
[TBL] [Abstract][Full Text] [Related]
28. Intracellular signaling and cytokine induction upon interactions of Porphyromonas gingivalis fimbriae with pattern-recognition receptors.
Hajishengallis G; Sojar H; Genco RJ; DeNardin E
Immunol Invest; 2004 May; 33(2):157-72. PubMed ID: 15195695
[TBL] [Abstract][Full Text] [Related]
29. Enhanced monocyte migration and pro-inflammatory cytokine production by Porphyromonas gingivalis infection.
Pollreisz A; Huang Y; Roth GA; Cheng B; Kebschull M; Papapanou PN; Schmidt AM; Lalla E
J Periodontal Res; 2010 Apr; 45(2):239-45. PubMed ID: 19778327
[TBL] [Abstract][Full Text] [Related]
30. Is Porphyromonas gingivalis cell invasion required for atherogenesis? Pharmacotherapeutic implications.
Amar S; Wu SC; Madan M
J Immunol; 2009 Feb; 182(3):1584-92. PubMed ID: 19155507
[TBL] [Abstract][Full Text] [Related]
31. Differential role of pannexin-1/ATP/P2X
Parzych K; Zetterqvist AV; Wright WR; Kirkby NS; Mitchell JA; Paul-Clark MJ
FASEB J; 2017 Jun; 31(6):2439-2445. PubMed ID: 28246166
[TBL] [Abstract][Full Text] [Related]
32. Pepsin digest of wheat gliadin fraction increases production of IL-1β via TLR4/MyD88/TRIF/MAPK/NF-κB signaling pathway and an NLRP3 inflammasome activation.
Palová-Jelínková L; Dáňová K; Drašarová H; Dvořák M; Funda DP; Fundová P; Kotrbová-Kozak A; Černá M; Kamanová J; Martin SF; Freudenberg M; Tučková L
PLoS One; 2013; 8(4):e62426. PubMed ID: 23658628
[TBL] [Abstract][Full Text] [Related]
33. Distinct lipid a moieties contribute to pathogen-induced site-specific vascular inflammation.
Slocum C; Coats SR; Hua N; Kramer C; Papadopoulos G; Weinberg EO; Gudino CV; Hamilton JA; Darveau RP; Genco CA
PLoS Pathog; 2014 Jul; 10(7):e1004215. PubMed ID: 25010102
[TBL] [Abstract][Full Text] [Related]
34. Macrophage-elicited osteoclastogenesis in response to bacterial stimulation requires Toll-like receptor 2-dependent tumor necrosis factor-alpha production.
Ukai T; Yumoto H; Gibson FC; Genco CA
Infect Immun; 2008 Feb; 76(2):812-9. PubMed ID: 17998311
[TBL] [Abstract][Full Text] [Related]
35. TLR2 transmodulates monocyte adhesion and transmigration via Rac1- and PI3K-mediated inside-out signaling in response to Porphyromonas gingivalis fimbriae.
Harokopakis E; Albzreh MH; Martin MH; Hajishengallis G
J Immunol; 2006 Jun; 176(12):7645-56. PubMed ID: 16751412
[TBL] [Abstract][Full Text] [Related]
36. LOX-1 is involved in IL-1β production and extracellular matrix breakdown in dental peri-implantitis.
Che C; Liu J; Ma L; Xu H; Bai N; Zhang Q
Int Immunopharmacol; 2017 Nov; 52():127-135. PubMed ID: 28898769
[TBL] [Abstract][Full Text] [Related]
37. Macrophage depletion abates Porphyromonas gingivalis-induced alveolar bone resorption in mice.
Lam RS; O'Brien-Simpson NM; Lenzo JC; Holden JA; Brammar GC; Walsh KA; McNaughtan JE; Rowler DK; Van Rooijen N; Reynolds EC
J Immunol; 2014 Sep; 193(5):2349-62. PubMed ID: 25070844
[TBL] [Abstract][Full Text] [Related]
38. IL-27 enhances LPS-induced IL-1β in human monocytes and murine macrophages.
Petes C; Wynick C; Guzzo C; Mehta D; Logan S; Banfield BW; Basta S; Cooper A; Gee K
J Leukoc Biol; 2017 Jul; 102(1):83-94. PubMed ID: 28377398
[TBL] [Abstract][Full Text] [Related]
39. Hyperlipidemia impaired innate immune response to periodontal pathogen porphyromonas gingivalis in apolipoprotein E knockout mice.
Lei L; Li H; Yan F; Xiao Y
PLoS One; 2013; 8(8):e71849. PubMed ID: 23977160
[TBL] [Abstract][Full Text] [Related]
40. Activation of the damage-associated molecular pattern receptor P2X7 induces interleukin-1β release from canine monocytes.
Jalilian I; Peranec M; Curtis BL; Seavers A; Spildrejorde M; Sluyter V; Sluyter R
Vet Immunol Immunopathol; 2012 Sep; 149(1-2):86-91. PubMed ID: 22652409
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]