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An optimized protocol for the isolation of rare stromal cell populations from the mouse spleen.

STAR protocols (2023-01-04)
Yannick O Alexandre, Scott N Mueller
ZUSAMMENFASSUNG

Lymphoid tissue stromal cells are important regulators of spleen homeostasis and immune responses. Here, we present an optimized protocol that describes the digestion and enrichment steps for the isolation and analysis of rare populations of stromal cells, including fibroblastic reticular cells, perivascular cells, and glial cells found in the spleen. This protocol is suitable for subsequent analysis of spleen stromal cells by flow cytometry or single-cell RNA sequencing and to analyze different disease models. For complete details on the use and execution of this protocol, please refer to Alexandre et al. (2022).1.

MATERIALIEN
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Marke
Produktbeschreibung

Roche
Collagenase D, from Clostridium histolyticum
Sigma-Aldrich
Deoxyribonuclease I aus Rinderpankreas, lyophilized powder, Protein ≥85 %, ≥400 Kunitz units/mg protein
Sigma-Aldrich
Albumin aus Rinderserum, heat shock fraction, pH 7, ≥98%
Sigma-Aldrich
Ethylendiamintetraessigsäure Dinatriumsalz Dihydrat, suitable for electrophoresis, Molecular Biology, 99.0-101.0% (titration)
Sigma-Aldrich
DAPI, for nucleic acid staining
Roche
Dispase® II (neutrale Protease, Klasse II), lyophilized, from bacterial, Roche, pkg of 5 × 1 g