Potentiation of ATP- and bradykinin-induced [Ca2+]c responses by PTHrP peptides in the HaCaT cell line

Burrell, Helen E, Simpson, Alec W M, Mehat, Sharonpreet, McCreavy, David T, Durham, Brian, Fraser, William D, Sharpe, Graham R and Gallagher, James A (2008) Potentiation of ATP- and bradykinin-induced [Ca2+]c responses by PTHrP peptides in the HaCaT cell line. Journal of Investigative Dermatology, 128 (5). pp. 1107-1115. ISSN 0022-202X

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In the epidermis, local and systemic factors including extracellular nucleotides and parathyroid hormone-related protein (PTHrP) regulate keratinocyte proliferation and differentiation. Extracellular nucleotides increase proliferation via activation of P2 receptors and induction of calcium transients, while endoproteases cleave PTHrP, resulting in fragments with different cellular functions. We investigated the effects of adenosine 5'-triphosphate (ATP) alone and in combination with synthetic PTHrP peptides on calcium transients in HaCaT cells. ATP induced calcium transients, while PTHrP peptides did not. C-terminal and mid-molecule PTHrP peptides (1-100 pM) potentiated ATP-induced calcium transients independently of calcium influx. 3-Isobutyl-1-methylxanthine potentiated ATP-induced calcium transients, suggesting that a cyclic monophosphate is responsible. Cyclic AMP is not involved, but cyclic GMP is a likely candidate since the protein kinase G inhibitor, KT5823, inhibited potentiation. Co-stimulation with ATP and either PTHrP (43-52) or PTHrP (70-77) increased proliferation, suggesting that this is important in the regulation of cell turnover and wound healing and may be a mechanism for hyperproliferation in skin disorders such as psoriasis. Finally, PTHrP fragments potentiated bradykinin-induced calcium transients, suggesting a role in inflammation in the skin. Since PTHrP is found in many normal and malignant cells, potentiation is likely to have a wider role in modulating signal transduction events.

Item Type: Article
Uncontrolled Keywords: 1-methyl-3-isobutylxanthine,adenosine triphosphate,bradykinin,calcium,carbazoles,cell division,cell line,cyclic amp,cyclic gmp,drug synergism,forskolin,humans,indoles,keratinocytes,parathyroid hormone-related protein,peptide fragments,phosphodiesterase inhibitors,protein kinase inhibitors,signal transduction
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
UEA Research Groups: Faculty of Medicine and Health Sciences > Research Groups > Musculoskeletal Medicine
Faculty of Medicine and Health Sciences > Research Centres > Metabolic Health
Depositing User: Rhiannon Harvey
Date Deposited: 10 May 2011 15:44
Last Modified: 19 Oct 2023 00:42
URI: https://ueaeprints.uea.ac.uk/id/eprint/30161
DOI: 10.1038/sj.jid.5701159

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