Stimulation of mast cells via the high affinity receptor for IgE (FcepsilonRI) leads to the release of inflammatory mediators that are responsible for allergic inflammatory diseases, such as asthma and allergic dermatitis. The release of inflammatory mediators is dependent on the increase in cytosolic free Ca2+ ([Ca2+]i), which is initiated by the mobilization of Ca2+ from the endoplasmic reticulum and followed by influx of Ca2+ from outside of the cell. It is generally believed that inositol 1,4,5-trisphosphate (IP3) is responsible for mobilizing Ca2+ from the intracellular stores. However, we have shown that FcepsilonRI-mediated production of IP3 is not sufficient to account for the increase in [Ca2+]i. This suggests an alternative mechanism for Ca2+ mobilization via sphingosine 1- phosphate, a product of sphingosine kinase. Furthermore, the increase in sphingosine 1-phosphate production and Ca2+ mobilization has been observed in an antigen-stimulated mast cell line, RBL-2H3 cells that has been overexpressed with the beta isoform of Class II phosphoinositide 3-kinase (PI3KC2beta). Our long-range goal is to understand the mechanisms underlying [Ca2+]i increase in mast cells. The objective of this particular application is to understand the role of Class II PI3K in sphingosine kinase activation and Ca2+ mobilization. The central hypothesis for the proposed research is that activation of a Class II PI3K via FcepsilonRI increases production of sphingosine 1-phosphate, which causes Ca2+ mobilization in conjunction with IP3 in RBL-2H3 Cells. We formulated this hypothesis based on strong preliminary findings, which demonstrate that overexpression of PI3KC2beta increases FcepsilonRI-mediated production of sphingosine 1-phosphate and Ca2+ mobilization. In addition, increased production of sphingosine 1-phosphate leads to increased mobilization of Ca2+ only in the presence of IP3. The rationale for the proposed research is that, once the alternative pathway of Ca2+ mobilization is elucidated, it can be targeted as a new approach to treat allergic inflammatory diseases. The central hypothesis will be tested by pursuing three specific aims: 1) Identify initiating biochemical events for FcepsilonRI-mediated Ca2+ mobilization. 2) Identify intermediate signaling molecule(s) in the alternative pathway for FcepsilonRI-mediated Ca2+ mobilization. 3) Determine how FcepsilonRI-mediated Ca2+ mobilization is regulated by sphingosine kinase and phospholipase C pathways in RBL-2H3 cells. It is our expectation that the resultant approach will delineate an alternative Ca2+ signaling pathway that involves the activation of PI3KC2beta, sphingosine kinase and phospholipase C. The research proposed in this application is significant, because the outcomes are expected to provide new targets for therapeutic interventions for the prevention and treatment of allergic inflammatory diseases. In addition, they are expected to offer a better fundamental understanding of how Ca2+ is mobilized in mast cells.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL068879-04
Application #
6699663
Study Section
Lung Biology and Pathology Study Section (LBPA)
Program Officer
Noel, Patricia
Project Start
2002-02-05
Project End
2006-01-31
Budget Start
2004-02-01
Budget End
2005-01-31
Support Year
4
Fiscal Year
2004
Total Cost
$286,125
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Ryu, Seung-Duk; Lee, Hyun Sil; Suk, Ho Young et al. (2009) Cross-linking of FcepsilonRI causes Ca2+ mobilization via a sphingosine kinase pathway in a clathrin-dependent manner. Cell Calcium 45:99-108
Jung, In Duk; Lee, Hyun-Sil; Lee, Hoi Young et al. (2009) FcepsilonRI-mediated mast cell migration: signaling pathways and dependence on cytosolic free Ca2+ concentration. Cell Signal 21:1698-705
Park, Chang Gyo; Lee, Hyun Sil; Lee, Hoi Young et al. (2007) Cloning and characterization of rat sphingosine kinase 1 with an N-terminal extension. Biochem Biophys Res Commun 364:702-7
Lee, Hyun-Sil; Park, Chang-Shin; Lee, Young Mi et al. (2005) Antigen-induced Ca2+ mobilization in RBL-2H3 cells: role of I(1,4,5)P3 and S1P and necessity of I(1,4,5)P3 production. Cell Calcium 38:581-92