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Differential dependence of eosinophil chemotactic responses on phosphoinositide 3-kinase (PI3K)

Differential dependence of eosinophil chemotactic responses on phosphoinositide 3-kinase (PI3K)
Differential dependence of eosinophil chemotactic responses on phosphoinositide 3-kinase (PI3K)
Background: Control of eosinophil migration to sites of inflammatory responses is a potentially therapeutic intervention in diseases such as bronchial asthma. Chemoattractants, their receptors and the associated signalling pathways may, therefore, be important targets for novel therapeutics. While several potentially important chemoattractants have been identified, the signalling pathways mediating their actions are incompletely understood.
Aims of the study: The role of phosphoinositide 3-kinase (PI3K) in responses of human eosinophils to two important eosinophil chemoattractants – platelet-activating factor (PAF) and eotaxin (CCL11) – was studied to determine whether this enzyme activity might be crucial for eosinophil migration.
Methods: Eosinophils were isolated from atopic donor blood by immunomagnetic selection. Chemotaxis was assayed in a 96-well blind-chamber cell fluorescence assay. Respiratory burst and leukotriene C4 secretion were also assayed.
Results: Two PI3K inhibitors, wortmannin and LY294002, caused concentration-dependent inhibition of PAF-induced eosinophil chemotaxis (IC50 = 0.54 nM and 0.15 ?M, respectively) but exhibited at least 100-fold lower potency against eotaxin-induced responses (IC50 = 48 nM and >100 ?M, respectively), indicating that these responses were not dependent upon PI3K. Wortmannin and LY294002 also inhibited PAF induced respiratory burst but not PAF-induced LTC4 secretion.
Conclusions: We conclude that PI3K-dependence varies with stimulus and response, and that eotaxin-induced eosinophil migration is not controlled by PI3K. This may indicate a limit to the potential of PI3K inhibitors to suppress tissue eosinophilia in diseases such as asthma.
chemotaxis, eosinophils, leukotriene C4, respiratory burst, signal transduction
0105-4538
1204-1207
Mishra, R.K.
ce0c4d3d-d7ce-4263-8ebd-78b3b783cd95
Scaife, J.E.
7aeec81d-8500-4484-ba4d-2a9a978a886a
Harb, Z.
9cfbbe9f-7153-4669-9327-da31cbd295a6
Gray, B.C.
a244fdd1-41ec-4d1a-866f-ef6ec93e18da
Djukanovic, R.
d9a45ee7-6a80-4d84-a0ed-10962660a98d
Dent, G.
16599b3c-5c6c-4d43-a4a2-9168456e57d9
Mishra, R.K.
ce0c4d3d-d7ce-4263-8ebd-78b3b783cd95
Scaife, J.E.
7aeec81d-8500-4484-ba4d-2a9a978a886a
Harb, Z.
9cfbbe9f-7153-4669-9327-da31cbd295a6
Gray, B.C.
a244fdd1-41ec-4d1a-866f-ef6ec93e18da
Djukanovic, R.
d9a45ee7-6a80-4d84-a0ed-10962660a98d
Dent, G.
16599b3c-5c6c-4d43-a4a2-9168456e57d9

Mishra, R.K., Scaife, J.E., Harb, Z., Gray, B.C., Djukanovic, R. and Dent, G. (2005) Differential dependence of eosinophil chemotactic responses on phosphoinositide 3-kinase (PI3K). Allergy, 60 (9), 1204-1207. (doi:10.1111/j.1398-9995.2005.00845.x).

Record type: Article

Abstract

Background: Control of eosinophil migration to sites of inflammatory responses is a potentially therapeutic intervention in diseases such as bronchial asthma. Chemoattractants, their receptors and the associated signalling pathways may, therefore, be important targets for novel therapeutics. While several potentially important chemoattractants have been identified, the signalling pathways mediating their actions are incompletely understood.
Aims of the study: The role of phosphoinositide 3-kinase (PI3K) in responses of human eosinophils to two important eosinophil chemoattractants – platelet-activating factor (PAF) and eotaxin (CCL11) – was studied to determine whether this enzyme activity might be crucial for eosinophil migration.
Methods: Eosinophils were isolated from atopic donor blood by immunomagnetic selection. Chemotaxis was assayed in a 96-well blind-chamber cell fluorescence assay. Respiratory burst and leukotriene C4 secretion were also assayed.
Results: Two PI3K inhibitors, wortmannin and LY294002, caused concentration-dependent inhibition of PAF-induced eosinophil chemotaxis (IC50 = 0.54 nM and 0.15 ?M, respectively) but exhibited at least 100-fold lower potency against eotaxin-induced responses (IC50 = 48 nM and >100 ?M, respectively), indicating that these responses were not dependent upon PI3K. Wortmannin and LY294002 also inhibited PAF induced respiratory burst but not PAF-induced LTC4 secretion.
Conclusions: We conclude that PI3K-dependence varies with stimulus and response, and that eotaxin-induced eosinophil migration is not controlled by PI3K. This may indicate a limit to the potential of PI3K inhibitors to suppress tissue eosinophilia in diseases such as asthma.

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More information

Published date: 2005
Additional Information: Short Communication
Keywords: chemotaxis, eosinophils, leukotriene C4, respiratory burst, signal transduction

Identifiers

Local EPrints ID: 27272
URI: http://eprints.soton.ac.uk/id/eprint/27272
ISSN: 0105-4538
PURE UUID: 0492da90-9331-4eea-a544-1be535dfd7ba
ORCID for R. Djukanovic: ORCID iD orcid.org/0000-0001-6039-5612

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Date deposited: 25 Apr 2006
Last modified: 16 Mar 2024 02:36

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Contributors

Author: R.K. Mishra
Author: J.E. Scaife
Author: Z. Harb
Author: B.C. Gray
Author: R. Djukanovic ORCID iD
Author: G. Dent

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