A Soluble Factor from Trypanosoma cruzi Inhibits Transforming Growth Factor-ß-Induced MAP Kinase Activation and Gene Expression in Dermal Fibroblasts
| dc.career | Biology | es |
| dc.category.author | principal | es |
| dc.contributor.author | Costales Cordero, Jaime Alfredo | en_US |
| dc.contributor.corresponding | Mott, Adam G. | es |
| dc.date.accessioned | 2023-11-04T21:30:35Z | |
| dc.date.available | 2023-11-04T21:30:35Z | |
| dc.date.issued | 2011 | |
| dc.dedication.author | TC | es |
| dc.description.abstract | The protozoan parasite Trypanosoma cruzi, which causes human Chagas´disease, exerts a variety of effects on host extracellular matrix (ECM) including proteolytic degradation of collagens and dampening of ECM gene expression. Exposure of primary human dermal fibroblasts to live infective T. cruzi trypomastigotes or their shed/secreted products results in a rapdi down-regulation of the fibrogenic genes collagen a1, fibronectin and connective tissue growth factor (CTGF/CCN2). Here we demonstrate the ability of a secreted/released T. cruzi factor to antagonize ctgf/ccn2 expression in dermal fibroblasts in response to TGF-B, lysophosphatidic acid or serum, where agonist-induced phosphorylation of the mitogen-activated protein (MAP) kinases Erk1/2, p38 and JNK was also inhibited. Global analysis of gene expression in dermal fibroblasts identified a discrete subset of TGF-B-inducible genes involved in cell proliferation, wound repair, and immune regulation that are inhibited by T. cruzi secreted/released factors, where the genes exhibiting the highest sensitivity to T. cruzi are known to be regulated by MAP kinase-activated transcription factors. Consistent with this observation, the Ets-family transcription factor binding site in the proximal promoter region of the ctgf/ccn2 gene (-91bp to -84 bp) was shown to be required for T. cruzi-mediated down-regulation of ctgf/ccn2 reporter expression. The cumulative data suggest a model in which T. cruzi-derived molecules secreted/released early in the infective process dampen MAP kinase signaling and the activation of transcription factors that regulate expression of fibroblast genes invoved in wound repair and tissue remodelling, including ctfg/ccn2. These findings have broader implications for local modulation of ECM synthesis/remodelling by T. cruzi during the early establishment of infection in the mammalian host and highlight the potencial for pathogen-derived molecules to be exploited as tools to modulate the fibrogenic response. | es |
| dc.faculty | Biology | es |
| dc.id.author | - | es |
| dc.identifier.doi | 10.1371/journal.pone.0023482 | es |
| dc.identifier.issn | - | en_US |
| dc.identifier.uri | https://repositorio.puce.edu.ec/handle/123456789/4585 | |
| dc.indexed.database | Other | es |
| dc.list.authors | Mott, Adam G., Costales, Jaime A., Burleigh, Barbara A. | es |
| dc.magazine.pageRange | 01-11 | es |
| dc.magazine.title | Plos One | es |
| dc.magazine.volumeChapter | 6 | es |
| dc.rights | OpenAccess | es |
| dc.state | published | es |
| dc.subject | - | es |
| dc.title | A Soluble Factor from Trypanosoma cruzi Inhibits Transforming Growth Factor-ß-Induced MAP Kinase Activation and Gene Expression in Dermal Fibroblasts | es |