Role of keratinocyte-fibroblast cross-talk in development of hypertrophic scar
- PMID: 17727467
- DOI: 10.1111/j.1524-475X.2007.00225.x
Role of keratinocyte-fibroblast cross-talk in development of hypertrophic scar
Erratum in
- Wound Repair Regen. 2008 Jul-Aug;16(4):582
Abstract
The ability to generate or repair injured tissue is essential to the continuity of human life. As in all other organs, wound healing in the skin is a dynamic process involving tissue response to different types of insults. This process involves a continuous sequence of signals and responses in which platelets, fibroblasts, epithelial, endothelial, and immune cells come together outside their usual domains to orchestrate a very complex event that results in tissue repair. These signals, which are mainly growth factors and cytokines, orchestrate the initiation, continuation, and termination of wound healing. An imbalance in the synthesis and release of these cytokines and growth factors at the wound site, therefore, may result in either retarded wound healing, as is seen in diabetic patients and the elderly population, or overhealing wounds such as fibroproliferative disorders frequently seen following surgical incision, traumatic wounds, and severe electrical and thermal injury. In general, regardless of the site of injury, in any phase of the dynamic healing process, a fine balance between synthesis of extracellular matrix and degradation by a large family of enzymes, known as matrix metalloproteinases, is required for maintaining the structural integrity of healing tissue. The availability of new models such as organotypic co-culture systems have allowed us to gain new insight into the cell-cell interactions at both cellular and molecular levels. Recent evidence indicates that mesenchymal-epithelial interactions play a critical role in regulation of skin homeostasis and this cross-talk is mediated by soluble factors acting as autocrine/paracrine regulators of fibroblast and keratinocyte growth, function, and differentiation. In this review we address the question of how keratinocyte-fibroblast interaction plays a role in controlling the expression of key extracellular matrix molecules such as matrix metalloproteinases, which are critical in the healing process following any types of insults to the skin.
Similar articles
-
Fibroblast extracellular matrix gene expression in response to keratinocyte-releasable stratifin.J Cell Biochem. 2006 May 15;98(2):383-93. doi: 10.1002/jcb.20782. J Cell Biochem. 2006. PMID: 16440305
-
Development of fungal mycelia as a skin substitute: characterization of keratinocyte proliferation and matrix metalloproteinase expression during improvement in the wound-healing process.J Biomed Mater Res A. 2005 Feb 1;72(2):220-7. doi: 10.1002/jbm.a.30235. J Biomed Mater Res A. 2005. PMID: 15625685
-
Control of wound contraction. Basic and clinical features.Hand Clin. 2000 May;16(2):289-302. Hand Clin. 2000. PMID: 10791174 Review.
-
A simple in vitro model for investigating epithelial/mesenchymal interactions: keratinocyte inhibition of fibroblast proliferation and fibronectin synthesis.Wound Repair Regen. 2005 Nov-Dec;13(6):543-50. doi: 10.1111/j.1524-475X.2005.00076.x. Wound Repair Regen. 2005. PMID: 16283869
-
Macrophages in skin injury and repair.Immunobiology. 2011 Jul;216(7):753-62. doi: 10.1016/j.imbio.2011.01.001. Epub 2011 Jan 8. Immunobiology. 2011. PMID: 21281986 Review.
Cited by
-
Keratinocytes in the treatment of severe burn injury: an update.Int Wound J. 2013 Feb;10(1):6-12. doi: 10.1111/j.1742-481X.2012.01083.x. Epub 2012 Sep 7. Int Wound J. 2013. PMID: 22958654 Free PMC article.
-
STAT3-BDNF-TrkB signalling promotes alveolar epithelial regeneration after lung injury.Nat Cell Biol. 2020 Oct;22(10):1197-1210. doi: 10.1038/s41556-020-0569-x. Epub 2020 Sep 28. Nat Cell Biol. 2020. PMID: 32989251 Free PMC article.
-
Modelling the interaction of keratinocytes and fibroblasts during normal and abnormal wound healing processes.Proc Biol Sci. 2012 Aug 22;279(1741):3329-38. doi: 10.1098/rspb.2012.0319. Epub 2012 May 23. Proc Biol Sci. 2012. PMID: 22628464 Free PMC article.
-
Partial epithelial-mesenchymal transition in keloid scars: regulation of keloid keratinocyte gene expression by transforming growth factor-β1.Burns Trauma. 2016 Aug 23;4(1):30. doi: 10.1186/s41038-016-0055-7. eCollection 2016. Burns Trauma. 2016. PMID: 27574697 Free PMC article.
-
Nanoceutical Adjuvants as Wound Healing Material: Precepts and Prospects.Int J Mol Sci. 2021 Apr 29;22(9):4748. doi: 10.3390/ijms22094748. Int J Mol Sci. 2021. PMID: 33947121 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials