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Regulation of M2-type pyruvate kinase mediated by the high-affinity IgE receptors is required for mast cell degranulation.

Publication ,  Journal Article
Ryu, H; Walker, JKL; Kim, S; Koo, N; Barak, LS; Noguchi, T; Kang, BY; Kim, K-M
Published in: Br J Pharmacol
July 2008

BACKGROUND AND PURPOSE: M2-type pyruvate kinase (M2PK) was found to interact directly with the 'ITAM' region of the gamma chain of the high-affinity IgE receptor (FcvarepsilonRI). Our hypothesis was that mast cell degranulation might require the FcvarepsilonRI-mediated inhibition of M2PK activity. EXPERIMENTAL APPROACH: In rat basophilic leukaemia (RBL-2H3) cells, the effects of directly inhibiting M2PK or preventing the FcvarepsilonRI-mediated inhibition of M2PK (disinhibition) on degranulation was measured by hexosaminidase release. Effects of blocking the FcvarepsilonRI-mediated inhibition of M2PK was also assessed in vivo in a mouse model of allergen-induced airway hyper-responsiveness. KEY RESULTS: Activation of FcvarepsilonRI in RBL-2H3 cells caused the rapid phosphorylation of tyrosine residues in M2PK, associated with a decrease in M2PK enzymatic activity. There was an inverse correlation between M2PK activity and mast cell degranulation. FcvarepsilonRI-mediated inhibition of M2PK involved Src kinase, phosphatidylinositol 3-kinase, PKC and calcium. Direct inhibition of M2PK potentiated FcvarepsilonRI-mediated degranulation and prevention of the FcvarepsilonRI-mediated inhibition of M2PK attenuated mast cell degranulation. Transfection of RBL-2H3 cells with M1PK which prevents FcvarepsilonRI-induced inhibition of M2PK, markedly reduced their degranulation and exogenous M1PK (i.p.) inhibited ovalbumin-induced airway hyper-responsiveness in vivo. CONCLUSIONS AND IMPLICATIONS: We have identified a new control point and a novel biochemical pathway in the process of mast cell degranulation. Our study suggests that the FcvarepsilonRI-mediated inhibition of M2PK is a crucial step in responses to allergens. Moreover, the manipulation of glycolytic processes and intermediates could provide novel strategies for the treatment of allergic diseases.

Duke Scholars

Published In

Br J Pharmacol

DOI

ISSN

0007-1188

Publication Date

July 2008

Volume

154

Issue

5

Start / End Page

1035 / 1046

Location

England

Related Subject Headings

  • src-Family Kinases
  • Transfection
  • Signal Transduction
  • Receptors, IgE
  • Rats
  • Pyruvate Kinase
  • Protein Kinase C
  • Phosphorylation
  • Phosphatidylinositol 3-Kinases
  • Pharmacology & Pharmacy
 

Citation

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Ryu, H., Walker, J. K. L., Kim, S., Koo, N., Barak, L. S., Noguchi, T., … Kim, K.-M. (2008). Regulation of M2-type pyruvate kinase mediated by the high-affinity IgE receptors is required for mast cell degranulation. Br J Pharmacol, 154(5), 1035–1046. https://doi.org/10.1038/bjp.2008.148
Ryu, H., J. K. L. Walker, S. Kim, N. Koo, L. S. Barak, T. Noguchi, B. Y. Kang, and K. -. M. Kim. “Regulation of M2-type pyruvate kinase mediated by the high-affinity IgE receptors is required for mast cell degranulation.Br J Pharmacol 154, no. 5 (July 2008): 1035–46. https://doi.org/10.1038/bjp.2008.148.
Ryu H, Walker JKL, Kim S, Koo N, Barak LS, Noguchi T, et al. Regulation of M2-type pyruvate kinase mediated by the high-affinity IgE receptors is required for mast cell degranulation. Br J Pharmacol. 2008 Jul;154(5):1035–46.
Ryu, H., et al. “Regulation of M2-type pyruvate kinase mediated by the high-affinity IgE receptors is required for mast cell degranulation.Br J Pharmacol, vol. 154, no. 5, July 2008, pp. 1035–46. Pubmed, doi:10.1038/bjp.2008.148.
Ryu H, Walker JKL, Kim S, Koo N, Barak LS, Noguchi T, Kang BY, Kim K-M. Regulation of M2-type pyruvate kinase mediated by the high-affinity IgE receptors is required for mast cell degranulation. Br J Pharmacol. 2008 Jul;154(5):1035–1046.
Journal cover image

Published In

Br J Pharmacol

DOI

ISSN

0007-1188

Publication Date

July 2008

Volume

154

Issue

5

Start / End Page

1035 / 1046

Location

England

Related Subject Headings

  • src-Family Kinases
  • Transfection
  • Signal Transduction
  • Receptors, IgE
  • Rats
  • Pyruvate Kinase
  • Protein Kinase C
  • Phosphorylation
  • Phosphatidylinositol 3-Kinases
  • Pharmacology & Pharmacy