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Literature summary for 2.3.2.13 extracted from

  • Maiuri, L.; Luciani, A.; Giardino, I.; Raia, V.; Villella, V.R.; DApolito, M.; Pettoello-Mantovani, M.; Guido, S.; Ciacci, C.; Cimmino, M.; Cexus, O.N.; Londei, M.; Quaratino, S.
    Tissue transglutaminase activation modulates inflammation in cystic fibrosis via PPARgamma down-regulation (2008), J. Immunol., 180, 7697-7705.
    View publication on PubMed

Application

Application Comment Organism
medicine central role of TG2 in the mechanistic pathway of CF inflammation, opening a possible new wave of therapies for sufferers of chronic inflammatory diseases Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
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Source Tissue

Source Tissue Comment Organism Textmining
bronchial epithelial cell ex vivo cultures of nasal polyp mucosal explants of Cystic fibrosis patients and controls, cystic fibrosis transmembrane conductance regulator-defective IB3-1 bronchial epithelial cells, C38 isogenic CFTR corrected, and 16HBE normal bronchial epithelial cell lines. A defective cystic fibrosis transmembrane conductance regulator induces a remarkable up-regulation of tissue transglutaminase in both tissues and cell lines. The increased TG2 activity leads to functional sequestration of the anti-inflammatory peroxisome proliferator-activated receptor gamma and increase of the classic parameters of inflammation Homo sapiens
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