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Sci. STKE, 23 May 2006 EDITORS' CHOICECELL GROWTH A Growing Role for Keratins
Injuries to the skin elicit homeostatic repair responses. Nearby cells increase in size and migrate to close the wound, responses that necessitate increased protein synthesis and changes in gene expression. The expression of genes encoding keratins--which form epithelial cell intermediate filaments and thus contribute to formation of a cytoskeletal scaffolding network--is up-regulated (see Omary and Ku). Noting that mouse embryos lacking keratin 17 (K17) show delays in repairing wounds to surface ectoderm, Kim et al. took a closer look and found that neighboring epithelial cells in K17/ embryos failed to enlarge in response to injury. Cultured K17/ keratinocytes were smaller than wild-type cells and showed slower rates of peptide chain elongation and of amino acid incorporation into protein. K17/ keratinocytes also showed decreased activity of Akt and mammalian target of rapamycin (mTOR), components of a pathway that regulates protein synthesis and thereby cell growth, but not of phosphatidylinositol 3-kinase (PI3K, which acts upstream of mTOR in growth factor signaling). The mTOR inhibitor rapamycin had less effect on translation in K17/ than in wild-type keratinocytes, and both stimulation of protein synthesis in response to serum (which contains growth factors) and mTOR activation were blunted. K17 bound to 14-3-3 S. Kim, P. Wong, P. A. Coulombe, A keratin cytoskeletal protein regulates protein synthesis and epithelial cell growth. Nature 441, 362-365 (2006). [PubMed] M. B. Omary, N.-O. Ku, Skin care by keratins. Nature 441, 296-297 (2006). [PubMed]
Citation: A Growing Role for Keratins. Sci. STKE 2006, tw172 (2006). The editors suggest the following Related Resources on Science sites:In Science Signaling
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Science Signaling. ISSN 1937-9145 (pre-2008: Science's STKE. ISSN 1525-8882)