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Article: TLR9 is expressed in idiopathic interstitial pneumonia and its activation promotes in vitro myofibroblast differentiation.

Meneghin, A / Choi, E S / Evanoff, H L / Kunkel, S L / Martinez, F J / Flaherty, K R / Toews, G B / Hogaboam, C M

Histochemistry and cell biology

2008  Volume 130, Issue 5, Page(s) 979–992

Abstract: ... its activation can have a key role in myofibroblast differentiation promoting the progression of disease during ... the expression of alpha smooth muscle actin, the main marker of myofibroblast differentiation. These data ... with IIP compared with normal lung biopsies and its expression is localized to areas of marked interstitial ...

Abstract Infectious diseases can be cofactors in idiopathic interstitial pneumonias (IIP) pathogenesis; recent data suggests that toll-like receptors 9 (TLR9) ligands contribute to experimental chronic tissue remodeling. Real-time TAQMAN and immunohistochemical analysis of IIP normal surgical lung biopsies (SLBs), primary fibroblast lines grown from both IIP and normal SLBs indicate that TLR9 is prominently and differentially expressed in a disease-specific manner. TLR9 expression was increased in biopsies from patients with IIP compared with normal lung biopsies and its expression is localized to areas of marked interstitial fibrosis. TLR9 in fibroblasts appeared to be increased by profibrotic Th2 cytokines (IL-4 and IL-13) and this was true in fibroblasts cultured from the most severe form of IIP, idiopathic pulmonary fibrosis (IPF) SLBs, in non-specific interstitial pneumonia fibroblast lines, and in normal fibroblasts. Finally, confocal microscopy studies have shown that TLR9 activation by its synthetic agonist CpG-ODN significantly increased the expression of alpha smooth muscle actin, the main marker of myofibroblast differentiation. These data indicate that TLR9 expression may drive the abnormal tissue healing response in severe forms of IIP and its activation can have a key role in myofibroblast differentiation promoting the progression of disease during the terminal phase of IPF.
MeSH term(s) Actins/metabolism ; Cell Differentiation/drug effects ; Cells, Cultured ; Fibroblasts/drug effects ; Fibroblasts/immunology ; Fibroblasts/pathology ; Humans ; Idiopathic Interstitial Pneumonias/genetics ; Idiopathic Interstitial Pneumonias/immunology ; Idiopathic Interstitial Pneumonias/pathology ; Idiopathic Pulmonary Fibrosis/genetics ; Idiopathic Pulmonary Fibrosis/immunology ; Idiopathic Pulmonary Fibrosis/pathology ; Immunohistochemistry ; Interleukin-13/metabolism ; Interleukin-4/metabolism ; Lung/drug effects ; Lung/immunology ; Lung/pathology ; Microscopy, Confocal ; Oligodeoxyribonucleotides/pharmacology ; Polymerase Chain Reaction ; RNA, Messenger/metabolism ; Recombinant Proteins/metabolism ; Toll-Like Receptor 9/agonists ; Toll-Like Receptor 9/genetics ; Toll-Like Receptor 9/metabolism
Chemical Substances Actins ; CPG-oligonucleotide ; Interleukin-13 ; Oligodeoxyribonucleotides ; RNA, Messenger ; Recombinant Proteins ; TLR9 protein, human ; Toll-Like Receptor 9 ; Interleukin-4 (207137-56-2)
Language English
Publishing date 2008-07-17
Publishing country Germany
Document type Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID 1222930-1
ISSN 1432-119X ; 0948-6143 ; 0301-5564
ISSN (online) 1432-119X
ISSN 0948-6143 ; 0301-5564
DOI 10.1007/s00418-008-0466-z
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