The broad long term objectives of this proposal are to understand on a molecular level intracellular signals that are involved in receptor-mediated alterations of salivary cells, particularly those signals that are initiated by secretagogues involved in saliva formation (fluid secretion) by parotid acinar cells. Fluid secretion is controlled by neurotransmitters that act on muscarinic, Substance P, and alpha-adrenergic receptors, which are linked to phospholipase C (PLC) by heterotrimeric GTP- binding (G) proteins. These receptors promote the PLC-mediated generation of DAG, which activates Protein Kinase C (PKC), and IP3, which mobilizes Ca2+. Parotid acinar cells also have multiple P2X ATP-binding receptors, including P2X7 receptors, that are nonselective cation channels, and these also elevate [Ca2+]i. ATP may be a neurotransmitter or act as an autocrine signal on salivary cells. P2X receptors are not coupled to G proteins, yet activation of the P2X7 receptor appears to stimulate PKC-dependent pathways in common with the muscarinic receptor in parotid acinar cells. These pathways may require the activation of PKCdelta, the one PKC family member that is activated by phosphorylation on tyrosine residues. PKCs and MAPKs play important roles in salivary and epithelial functions, and our data indicates that diverse receptor types, including the P2X7 receptor/ion channel and the muscarinic receptor, activate both of these proteins, which may be differentially regulated by these receptors.
Aim 1 is to determine the effects of signaling molecules/events, including tyrosine phosphorylation, MAPK, and Src, on indices of fluid/electrolyte/protein secretion.
Aim 2 is to define and compare the signal transduction cascades that activate MAPKs in secretagogue-treated and Na pump-inhibited rat parotid acinar cells, and to use MAPK activation as a paradigm to study receptor crosstalk and other aspects of cellular control. Na pump inhibition appears to activate a distinct signaling cascade that links pump activity to MAPK.
Aim 3 is to study the activation of PKC by P2X7 and other receptors.
Aim 4 is to determine downstream targets of PKCdelta and other proteins by identifying binding partners of these proteins in parotid acinar cells. PKCs and MAPKs have important functions in salivary cells and epithelia, although most studies have been performed using cell lines. Tyrosine phosphorylation, Src, PKCs, and MAPK may affect ion transport proteins, tight junction permeability, exocytosis, and other salivary functions. Understanding the signaling events that control their activation, as well as the effects of these proteins on secretion, is critical to providing a basis for understanding the regulation of salivary cells in health and in disease states.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE010877-12
Application #
6847146
Study Section
Special Emphasis Panel (ZRG1-OBM-1 (01))
Program Officer
Shum, Lillian
Project Start
1993-05-01
Project End
2006-12-31
Budget Start
2005-01-01
Budget End
2005-12-31
Support Year
12
Fiscal Year
2005
Total Cost
$371,025
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02215
Soltoff, Stephen P; Lannon, William A (2013) Activation of ERK1/2 by store-operated calcium entry in rat parotid acinar cells. PLoS One 8:e72881
Hedden, Lee; Benes, Cyril H; Soltoff, Stephen P (2011) P2X(7) receptor antagonists display agonist-like effects on cell signaling proteins. Biochim Biophys Acta 1810:532-42
Soltoff, Stephen P; Asara, John M; Hedden, Lee (2010) Regulation and identification of Na,K-ATPase alpha1 subunit phosphorylation in rat parotid acinar cells. J Biol Chem 285:36330-8
Soltoff, Stephen P; Hedden, Lee (2010) Isoproterenol and cAMP block ERK phosphorylation and enhance [Ca2+]i increases and oxygen consumption by muscarinic receptor stimulation in rat parotid and submandibular acinar cells. J Biol Chem 285:13337-48
Soltoff, Stephen P; Hedden, Lee (2008) Regulation of ERK1/2 by ouabain and Na-K-ATPase-dependent energy utilization and AMPK activation in parotid acinar cells. Am J Physiol Cell Physiol 295:C590-9
Soltoff, Stephen P (2007) Rottlerin: an inappropriate and ineffective inhibitor of PKCdelta. Trends Pharmacol Sci 28:453-8
Plourde, Deana; Soltoff, Stephen P (2006) Ouabain potentiates the activation of ERK1/2 by carbachol in parotid gland epithelial cells; inhibition of ERK1/2 reduces Na(+)-K(+)-ATPase activity. Am J Physiol Cell Physiol 290:C702-10
Benes, Cyril H; Wu, Ning; Elia, Andrew E H et al. (2005) The C2 domain of PKCdelta is a phosphotyrosine binding domain. Cell 121:271-80
Soltoff, Stephen P (2004) Evidence that tyrphostins AG10 and AG18 are mitochondrial uncouplers that alter phosphorylation-dependent cell signaling. J Biol Chem 279:10910-8
Bradford, Michelle D; Soltoff, Stephen P (2002) P2X7 receptors activate protein kinase D and p42/p44 mitogen-activated protein kinase (MAPK) downstream of protein kinase C. Biochem J 366:745-55

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