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Macrophage chitinase 1 stratifies chronic obstructive lung disease.

American journal of respiratory cell and molecular biology (2009-06-06)
Eugene Agapov, John T Battaile, Rose Tidwell, Ramsey Hachem, G Alexander Patterson, Richard A Pierce, Jeffrey J Atkinson, Michael J Holtzman
RÉSUMÉ

Diagnosis and therapy of chronic inflammatory lung disease is limited by the need for individualized biomarkers that provide insight into pathogenesis. Herein we show that mouse models of chronic obstructive lung disease exhibit an increase in lung chitinase production but cannot predict which chitinase family member may be equivalently increased in humans with corresponding lung disease. Moreover, we demonstrate that lung macrophage production of chitinase 1 is selectively increased in a subset of subjects with severe chronic obstructive pulmonary disease, and this increase is reflected in plasma levels. The findings provide a means to noninvasively track alternatively activated macrophages in chronic lung disease and thereby better differentiate molecular phenotypes in heterogeneous patient populations.

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Sigma-Aldrich
Solution de substrat 3,3′,5,5′-tétraméthylbenzidine (TMB), peroxidase substrate
Sigma-Aldrich
Stop Reagent for TMB Substrate, powder, ELISA, 450 nm
Sigma-Aldrich
Stop Reagent for TMB Substrate, solid, ELISA, 650 nm