2008
DOI: 10.1002/jcb.21675
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MMP‐14 mediated MMP‐9 expression is involved in TGF‐beta1‐induced keratinocyte migration

Abstract: The importance of expression of matrix metalloproteinase (MMP) in keratinocyte migration is well established, but its role remains unclear. Here we investigated the function of MMP-14 in TGF-beta1-induced keratinocyte migration. TGF-beta1 stimulated cell migration and the expression of MMP-2, -9 in HaCaT human keratinocyte cells. When we lowered MMP-14 mRNA with siRNA, cell migration, and MMP-9 expression decreased. Furthermore, the MMP-14 siRNA also reduced activation of JNK in response to TGF-beta1, and a JN… Show more

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Cited by 53 publications
(45 citation statements)
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References 31 publications
(57 reference statements)
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“…In line with these results, PDGF was found to be a powerful chemotactic factor for MSCs, including osteoblasts from human and rat tissues (Fiedler et al, 2002). In addition, TGF-β is known to be an important component of the overall process of wound healing, triggering a multitude of reactions needed for cell migration (Seomun et al, 2008).…”
Section: Discussionmentioning
confidence: 60%
“…In line with these results, PDGF was found to be a powerful chemotactic factor for MSCs, including osteoblasts from human and rat tissues (Fiedler et al, 2002). In addition, TGF-β is known to be an important component of the overall process of wound healing, triggering a multitude of reactions needed for cell migration (Seomun et al, 2008).…”
Section: Discussionmentioning
confidence: 60%
“…JNK activity has been known upregulated in migrating epidermis during wound re-epithelialization (Deng et al, 2006); the factors controlling JNK activity, however, are largely unclear. In this regard, cytokines, such as TNF-a and transforming growth factor-b, and integrins and their ligands, such as integrin a6b4 and lamin-5, are implicated to be the candidates, as they activate JNK in keratinocytes in vitro (Nguyen et al, 2000;Kadrmas et al, 2004;Seomun et al, 2008;Bahar-Shany et al, 2010). In contrast to previous findings, our in vivo study showed that JNK activity was www.jidonline.org 233 significantly altered by CD9 deficiency, suggesting a previously unreported, CD9-mediated mechanism for the regulation of JNK in migrating epidermis during wound healing.…”
Section: Discussionmentioning
confidence: 99%
“…VEGF supports wound healing by stimulation of vascular permeability and leukocyte recruitment, survival, proliferation, migration, and invasion of endothelial cells, as well as modulation of bone remodeling [5557]. TGF β , another growth factor, stimulates wound healing by its activating effects on migration, chemotaxis, and proliferation of monocytes/macrophages, fibroblasts, and endothelial cells, keratinocyte migration and reepithelialization, extracellular matrix production, and stem cell differentiation [5860]. POSTN supports formation of high stiffness collagen through effective collagen cross-linking.…”
Section: Discussionmentioning
confidence: 99%