Intravascular staining for discrimination of vascular and tissue leukocytes

KG Anderson, K Mayer-Barber, H Sung, L Beura… - Nature protocols, 2014 - nature.com
KG Anderson, K Mayer-Barber, H Sung, L Beura, BR James, JJ Taylor, L Qunaj, TS Griffith
Nature protocols, 2014nature.com
Abstract Characterization of the cellular participants in tissue immune responses is crucial to
understanding infection, cancer, autoimmunity, allergy, graft rejection and other
immunological processes. Previous reports indicate that leukocytes in lung vasculature fail
to be completely removed by perfusion. Several studies suggest that intravascular staining
may discriminate between tissue-localized and blood-borne cells in the mouse lung. Here
we outline a protocol for the validation and use of intravascular staining to define innate and …
Abstract
Characterization of the cellular participants in tissue immune responses is crucial to understanding infection, cancer, autoimmunity, allergy, graft rejection and other immunological processes. Previous reports indicate that leukocytes in lung vasculature fail to be completely removed by perfusion. Several studies suggest that intravascular staining may discriminate between tissue-localized and blood-borne cells in the mouse lung. Here we outline a protocol for the validation and use of intravascular staining to define innate and adaptive immune cells in mice. We demonstrate application of this protocol to leukocyte analyses in many tissues and we describe its use in the contexts of lymphocytic choriomeningitis virus and Mycobacterium tuberculosis infections or solid tumors. Intravascular staining and organ isolation usually takes 5–30 min per mouse, with additional time required for any subsequent leukocyte isolation, staining and analysis. In summary, this simple protocol should help enable interpretable analyses of tissue immune responses.
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