Journal article
Authors list: Kühne, Sina; Ockenga, Wymke; Banning, Antje; Tikkanen, Ritva
Publication year: 2015
Pages: 6447-6463
Journal: International Journal of Molecular Sciences
Volume number: 16
Issue number: 3
ISSN: 1422-0067
Open access status: Gold
DOI Link: https://doi.org/10.3390/ijms16036447
Publisher: MDPI
Abstract:
Acetylcholine and its receptors regulate numerous cellular processes in keratinocytes and other non-neuronal cells. Muscarinic acetylcholine receptors are capable of transactivating the epidermal growth factor receptor (EGFR) and, downstream thereof, the mitogen-activated protein kinase (MAPK) cascade, which in turn regulates transcription of genes involved in cell proliferation and migration. We here show that cholinergic stimulation of human HaCaT keratinocytes results in increased transcription of matrix metalloproteinase MMP-3 as well as several ligands of the epidermal growth factor family. Since both metalloproteinases and the said ligands are involved in the transactivation of the EGFR, this transcriptional upregulation may provide a positive feed-forward loop for EGFR/MAPK activation. We here also show that the cholinergic EGFR and MAPK activation and the upregulation of MMP-3 and EGF-like ligands are dependent on the expression of flotillin-1 which we have previously shown to be a regulator of MAPK signaling.
Citation Styles
Harvard Citation style: Kühne, S., Ockenga, W., Banning, A. and Tikkanen, R. (2015) Cholinergic Transactivation of the EGFR in HaCaT Keratinocytes Stimulates a Flotillin-1 Dependent MAPK-Mediated Transcriptional Response, International Journal of Molecular Sciences, 16(3), pp. 6447-6463. https://doi.org/10.3390/ijms16036447
APA Citation style: Kühne, S., Ockenga, W., Banning, A., & Tikkanen, R. (2015). Cholinergic Transactivation of the EGFR in HaCaT Keratinocytes Stimulates a Flotillin-1 Dependent MAPK-Mediated Transcriptional Response. International Journal of Molecular Sciences. 16(3), 6447-6463. https://doi.org/10.3390/ijms16036447
Keywords
COLON-CANCER CELLS; COUPLED RECEPTORS; EPIDERMAL-GROWTH-FACTOR; FACTOR RECEPTOR TRANSACTIVATION; HUMAN GINGIVAL FIBROBLASTS; INDUCED PROLIFERATION; MATRIX METALLOPROTEINASES; METALLOPROTEINASE GENE-EXPRESSION