Analysis of interaction of cloned human and/or sheep fetal hemoglobin gamma-chain and LPS in augmenting induction of inflammatory cytokine production in vivo and in vitro.
Data(s) |
2005
|
---|---|
Resumo |
We have reported earlier that purified preparations of sheep fetal hemoglobin, but not adult hemoglobin, in concert with non-stimulatory doses of lipopolysaccharide (LPS) (lipid A), act cooperatively to regulate in vitro production of a number of cytokines, including TNFalpha, TGFbeta and IL-6 from murine and human leukocytes. Following in vivo treatment of mice with the same combination of hemoglobin and LPS, harvested spleen or peritoneal cells showed a similar augmented capacity to release these cytokines into culture supernatants. We report below that genetically cloned gamma-chain of human or sheep fetal hemoglobin, but not cloned alpha- or beta-chains, can produce this cooperative effect, as indeed can HPLC purified, heme-free, gamma-chains derived from cord blood fetal hemoglobin, and that purified haptoglobin completely abolishes the cooperative interaction. |
Identificador |
http://serval.unil.ch/?id=serval:BIB_37776 isbn:0165-2478 (Print) pmid:16154492 doi:10.1016/j.imlet.2005.03.004 isiid:000232420500004 |
Idioma(s) |
en |
Fonte |
Immunology Letters, vol. 100, no. 2, pp. 120-129 |
Palavras-Chave | #Age Factors; Amino Acid Sequence; Animals; Cloning, Molecular; Cricetinae; Dose-Response Relationship, Drug; Fetal Hemoglobin/biosynthesis; Fetal Hemoglobin/genetics; Globins/biosynthesis; Globins/chemistry; Haptoglobins/pharmacology; Humans; Interleukin-6/biosynthesis; Lipid A/administration & dosage; Lipid A/antagonists & inhibitors; Lipopolysaccharides/administration & dosage; Lipopolysaccharides/immunology; Lymphocytes/drug effects; Mice; Molecular Sequence Data; Sheep; Spleen/cytology; Spleen/drug effects; Transforming Growth Factor beta/biosynthesis; Tumor Necrosis Factor-alpha/biosynthesis |
Tipo |
info:eu-repo/semantics/article article |