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Interleukin-lb

Epps, P.E. et al. (1992) Spectral characterization of environment-sensitive adducts of interleukin lb. J. Biol. Chem. 267, 3129. [Pg.1061]

Welsh, N., and Sandler, S. (1992). Interleukin-lb induces nitric oxide prodution and inhibits the activity of aconitase without decreasing glucose oxidation rates in isolated mouse pancreatic islets. Biochem. Biophys. Res. Commun. 182, 333-340. [Pg.216]

Selegiline stimulates the biosynthesis of interleukin-lb and interleukin-6, is an immu-noenhancing substance, possesses antiapoptotic action, and is a neuroprotectant. [Pg.165]

Yuan J, Shaham S, Ledoux S, Ellis HM, Horvitz HR. The C. elegans cell death gene ced-3 encodes a protein similar to mammalian interleukin-lb-converting enzyme. Cell 1993 75 641-652. [Pg.74]

Zoja C, Wang JM, Bettoni S, Sironi M, Renzi D, Chiaffarino F, Abboud HE, Van Damme J, Mantovani A, Remuzzi G, Rambaldi A. Interleukin-lb and tumor necrosis factor-a induce gene expression and production of leukocyte chemotactic factors, colony-stimulating factors, and interleukin-6 in human mesangial cells. Am J Pathol 1991 138 991-1003. [Pg.653]

Rivera, S., Gold, S.J. and Gall, C.M. (1994) Interleukin-lb increases basic fibroblast growth factor mRNA expression in adult rat brain and organotypic hippocampal cultures. Mol. Brain Res. 27 12-26. [Pg.372]

Metal ions released from metal implants by osteoclastic bio-corrosion are distributed through- out the body and are eventually taken up by dendritic cells, the most potent anti-gen-presenting cells [14, 15, 18]. Besides changing phenotypic and functional properties of dendritic cells [18], metal ions complex with cellular proteins and peptides. In case of titanium, the ions form complexes with phosphorus-containing proteins and peptides (usually signaling molecules), nucleotides (DNA in the nuclease and RNA in the cytoplasm) and lipids (phospholipids of the cellular membranes) [15]. The new antigenic metal-peptides are presented by dendritic cells to specific T-lymphocytes that react and are activated [15]. The dendritic cells and activated T-lymphocytes accumulate in tissues with high metal concentrations, usually close to the metal implant, and form inflammatory reactions [7] that include secretion of inflammatory cytokines, such as TNF-a, TGF-b, interleukin-6 and interleukin-lb [19]. Most important is secretion of RANK-L by the activated T-lymphocytes, an essential factor for maturation, survival and function of osteoclasts [19]. [Pg.176]

Martinez-Cacenes EM (1998) Amelioration of flu-like symptoms at the onset of interferon beta-lb therapy in multiple sclerosis by low dose oral steroids is related to a decrease in interleukin-6 mduc-tion. Arm Neurol 44(4) 682-685. [Pg.601]

Gillio AP, Faulkner LB, Alter BP, Reilly L, Klafter R, Heller G, Young DC, Lipton JM, Moore MA, O Reilly RJ. Treatment of Diamond-Blackfan anemia with recombinant human interleukin-3. Blood 1993 82(3) 744-51. [Pg.1845]

The interferon beta-la form (Avonex ) is similarly a immunomodulator used by injection in the treatment of multiple sclerosis. Interferons derived through recombinant DNA technology are labelled (rbe). interferon beta — interferon p. interferon beta-la interferon p. interferon beta-lb interferon p. interferon P2 interleukin 6. interferon yOFN-y MAF immune interferon interferon gamma [ban, inn] formerly called immune interferon Polyferon ) can be isolated from immunologically stimulated T-lymphocytes (hence its former name), and is an IMMUNOMODULAIOR that can be used to treat arthritis and shows activity as an ANTICANCER AGENT. [Pg.155]

Tamura M, Arakaki N, Tsubouchi H, Takada H, Daikuhara Y (1993) Enhancement of human hepatocyte growth factor production by interleukin-1 alpha and -1 beta and tumor necrosis factor-alpha by fibroblasts in culture. J Biol Chem 268 8140-8145 Tee LB, Boobis AR, Huggett AC, Davies DS (1986) Reversal of acetaminophen toxicity in isolated hamster hepatocytes by dithiothreitol. Toxicol Appl Pharmacol 83 294—314... [Pg.404]

Nanney LB, Mueller SG, Bueno R, Peiper SC, Richmond A. Distributions of melanoma growth stimulatory activity or growth-related gene and the interleukin-8 receptor type B in human wound repair. Ann J Pathol 1995 147 1248-1260. [Pg.320]

Kasahara, K., Stricter, R. M., Standiford, T. J., and Kunkel, S. L. (1993) Adherence in combination with lipopolysaccharide, tumor necrosis factor or inierleukin-lb potentiates the induction of monocyte-derived interleukin-8. Pathobiol. 61,57-66. [Pg.122]


See other pages where Interleukin-lb is mentioned: [Pg.744]    [Pg.240]    [Pg.430]    [Pg.246]    [Pg.724]    [Pg.382]    [Pg.126]    [Pg.151]    [Pg.32]    [Pg.744]    [Pg.240]    [Pg.430]    [Pg.246]    [Pg.724]    [Pg.382]    [Pg.126]    [Pg.151]    [Pg.32]    [Pg.886]    [Pg.236]    [Pg.241]    [Pg.18]    [Pg.549]    [Pg.24]    [Pg.886]    [Pg.155]    [Pg.308]    [Pg.396]    [Pg.81]    [Pg.295]    [Pg.85]   


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