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Intergrin α9β1 potentially plays a role in reducing airway smooth muscle contraction
  1. Mark Spears
  1. Correspondence to Dr Mark Spears, University of Glasgow and Respiratory Department, Glasgow Royal Infirmary, G4 OSF, UK; mark.spears{at}glasgow.ac.uk

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Contraction of airway smooth muscle in response to innocuous stimuli is pathognomonic of asthma. However the mechanisms responsible for the loss of normal control are only partially understood. Therefore the authors sought to explore the modulatory role of integrin α9β1 on airway smooth muscle contraction given previous results demonstrating high expression levels in mouse airway smooth muscle and the respiratory phenotype of α9 knockout (KO) mice.

Through a number of elegant experiments the protective effect of intergrin α9β1 was found to be related to control of calcium release from the sarcoplasmic reticulum following G protein coupled receptor ligation. The authors established that ligation of α9β1 reduces local levels of phosphatidylinositol 4,5-bisphosphate (PIP2) through co-localisation of the enzymes phosphatidylinositol-4-phosphate 5-kinase 1α (PIP5K1γ (responsible for production of PIP2)) and spermidine/spermine N1-acetyltransferase (SSAT). As PIP5K1γ activity requires the presence of higher order polyamines for full function the co-localisation with SSAT and hence its activity resulted in a localised reduction of higher order polyamines leading to reduced PIP2 and hence Inositol trisphosphate (IP3). The reduction in IP3 resulted in a reduction in intracellular calcium oscillations from the sacroplasmic reticulum and hence airway smooth muscle contraction. The authors also confirmed some of their findings in ex vivo human airways.

Further exploration and confirmation of the role for intergrin α9β1 in the airway hyper-responsiveness characteristic of human asthma should be considered. Pharmacological manipulation of either PIP5K1γ or SSAT or promotion of their co-localisation may be of clinical relevance.

References

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Footnotes

  • Competing interests None.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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