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Am J Physiol Lung Cell Mol Physiol (June 17, 2005). doi:10.1152/ajplung.00286.2004
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Submitted on July 26, 2004
Accepted on June 7, 2005

The human endogenous antibiotic LL-37 stimulates airway epithelial cell proliferation and wound closure

Renat Shaykhiev1, Christoph Beisswenger1, Kerstin Kaendler1, Judith Senske1, Annette Puechner1, Thomas Damm1, Juergen Behr2, and Robert Bals1*

1 Department of Internal Medicine, Hospital of the University of Marburg, Marburg, Hessen, Germany
2 Department of Internal Medicine I, Hospital of the University of Munich, Munich, Bavaria, Germany

* To whom correspondence should be addressed. E-mail: bals{at}mailer.uni-marburg.de.

Antimicrobial peptides are endogenous antibiotics that directly inactivate microorganisms and in addition have a variety of receptor mediated functions. LL-37/hCAP-18 is the only cathelicidin found in humans and is involved in angiogenesis and regulation of the innate immune system. The aim of the present study was to characterize the role of the peptide LL-37 in the regulation of wound closure of the airway epithelium using the cell line NCI-H292 and primary airway epithelial cells. LL-37 stimulated healing of mechanically induced wounds in monolayers of the cell line and in differentiated primary airway epithelium. This effect was detectable at concentrations of 5 µg / ml in NCI-H292 and 1 µg / ml in primary cells. The effect of LL-37 on wound healing was dependent on the presence of serum. LL-37 induced cell proliferation and migration of NCI-H292 cells. Inhibitor studies in the wound closure and proliferation assays indicated that the effects caused by LL-37 are mediated through epidermal growth factor receptor (EGFR), a G protein-coupled receptor (GPCR), and MAP/extracellular regulated kinase (MEK). In conclusion, LL-37 induces wound healing, proliferation and migration of airway epithelial cells. The peptide is likely involved in the regulation of tissue homeostasis in the airways.




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