نتایج جستجو برای: tlr4 gene

تعداد نتایج: 1150600  

Journal: :International journal of clinical and experimental medicine 2015
Lihua Zhang Huiqing He Jing Wang Deqiao Sheng

OBJECTIVE To investigate Cartilage glycoprotein 39 (Cgp-39) expression in peripheral blood monocytes of septic rats, and analyze the relationship between Toll-like receptor 4 (TLR4)-NF-κB signalling pathway and Cgp-39 expression. METHODS The ligation puncture was performed to establish rat sepsis model, and ELISA was used to measure serum Cgp-39 concentration. Peripheral blood mononuclear cel...

Journal: :Physiological genomics 2005
Hye-Youn Cho Anne E Jedlicka Robert Clarke Steven R Kleeberger

The mechanisms of susceptibility to particle-induced lung injury are not clearly understood. To evaluate the contribution of genetic background to pulmonary pathogenesis, we compared the lung injury responses to residual oil fly ash (ROFA) in inbred mouse strains and calculated heritability estimates. Significant interstrain (genetic) variation was observed in ROFA-induced lung inflammation and...

Journal: :Journal of immunology 2007
Françoise Debierre-Grockiego Marco A Campos Nahid Azzouz Jörg Schmidt Ulrike Bieker Marianne Garcia Resende Daniel Santos Mansur Ralf Weingart Richard R Schmidt Douglas T Golenbock Ricardo T Gazzinelli Ralph T Schwarz

GPIs isolated from Toxoplasma gondii, as well as a chemically synthesized GPI lacking the lipid moiety, activated a reporter gene in Chinese hamster ovary cells expressing TLR4, while the core glycan and lipid moieties cleaved from the GPIs activated both TLR4- and TLR2-expressing cells. MyD88, but not TLR2, TLR4, or CD14, is absolutely needed to trigger TNF-alpha production by macrophages expo...

Journal: :American journal of physiology. Lung cellular and molecular physiology 2006
Lauranell H Burch Ivana V Yang Gregory S Whitehead Frank G Chao Katherine G Berman David A Schwartz

Neutrophil recruitment to the lung after lipopolysaccharide (LPS; endotoxin) inhalation is primarily dependent on Toll-like receptor 4 (Tlr4) signaling, because it is virtually absent in mice deficient in Tlr4. However, among strains wild type for Tlr4, the magnitude of neutrophil recruitment to the lung after LPS inhalation is variable, suggesting the involvement of genes other than Tlr4. To i...

Journal: :Journal of immunology 2006
Prasad Rallabhandi Jessica Bell Marina S Boukhvalova Andrei Medvedev Eva Lorenz Moshe Arditi Val G Hemming Jorge C G Blanco David M Segal Stefanie N Vogel

TLR4 is the signal-transducing receptor for structurally diverse microbial molecules such as bacterial LPS, respiratory syncytial virus fusion (F) protein, and chlamydial heat shock protein 60. Previous studies associated two polymorphic mutations in the extracellular domain of TLR4 (Asp(299)Gly and Thr(399)Ile) with decreased LPS responsiveness. To analyze the molecular basis for diminished re...

Journal: :American journal of physiology. Heart and circulatory physiology 2012
Baojun Dong Dake Qi Long Yang Yan Huang Xiaoyan Xiao Ningwen Tai Li Wen F Susan Wong

Toll-like receptor (TLR)4 regulates inflammation and metabolism and has been linked to the pathogenesis of heart disease. TLR4 is upregulated in diabetic cardiomyocytes, and we examined the role of TLR4 in modulating cardiac fatty acid (FA) metabolism and the pathogenesis of diabetic heart disease in nonobese diabetic (NOD) mice. Both wild-type (WT) NOD and TLR4-deficient NOD animals had increa...

Journal: :Japanese journal of infectious diseases 2015
Kyoko Aki Yoichiro Okubo Hiroshi Nanjo Takao Ishiwatari Yasuhiro Nihonyanagi Naobumi Tochigi Megumi Wakayama Tetsuo Nemoto Katsunori Fukutake Minoru Shinozaki Yasuhiro Hori Hirotake Masuda Kazutoshi Shibuya

Single nucleotide polymorphisms (SNPs) 1063A/G (Asp299Gly) and 1363C/T (Thr399Ile) in the gene encoding Toll-like receptor 4 (TLR4) increase susceptibility to invasive aspergillosis. However, limited information is available on the prevalence of these SNPs in Japan. Therefore, we surveyed these TLR4 SNPs by using formalin-fixed and paraffin-embedded tissue blocks obtained from autopsies of pati...

Journal: :International immunology 2000
O Takeuchi K Takeda K Hoshino O Adachi T Ogawa S Akira

MyD88 is an adaptor molecule essential for signaling via the Toll-like receptor (TLR)/IL-1 receptor family. TLR4 is a member of the TLR family and a point mutation in the Tlr4 gene causes hyporesponsiveness to lipopolysaccharide (LPS) in C3H/HeJ mice. We have previously shown that both TLR4- and MyD88-deficient mice are hyporesponsive to LPS. In this study we examined the responsiveness of thes...

Journal: :The Journal of infectious diseases 2001
R C Read J Pullin S Gregory R Borrow E B Kaczmarski F S di Giovine S K Dower C Cannings A G Wilson

Human Toll-like receptor 4 (TLR4) transduces proinflammatory cytokine release by human cells in response to lipopolysaccharide (LPS). This study tested the hypothesis that, if TLR4 is rate limiting for a successful response to bacterial LPS in humans, a human gene polymorphism that results in the amino acid substitution Asp299Gly and causes reduced expression and function of TLR4 should influen...

Journal: :Frontiers in bioscience 2009
Yasuchika Takeishi Isao Kubota

Stimulation of TLRs by exogenous and endogenous ligands triggers expression of several genes that are involved in innate immune responses. Recently, a role of TLR4 in the myocardial response to injury separate from microbial pathogens has been examined in experimental studies. TLR4 deficient mice sustain significantly smaller infarctions compared with wild-type control mice given similar areas ...

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