Flow-cytometric method for simultaneous analysis of mouse lung epithelial, endothelial, and hematopoietic lineage cells

Benjamin D. Singer, Jason R. Mock, Franco D'Alessio, Neil R. Aggarwal, Pooja Mandke, Laura Johnston, Mahendra Damarla

Research output: Contribution to journalArticle

Abstract

Flow cytometry is a powerful tool capable of simultaneously analyzing multiple parameters on a cell-by-cell basis. Lung tissue preparation for flow cytometry requires creation of a single-cell suspension, which often employs enzymatic and mechanical dissociation techniques. These practices may damage cells and cause cell death that is unrelated to the experimental conditions under study. We tested methods of lung tissue dissociation and sought to minimize cell death in the epithelial, endothelial, and hematopoietic lineage cellular compartments. A protocol that involved flushing the pulmonary circulation and inflating the lung with Dispase, a bacillus-derived neutral metalloprotease, at the time of tissue harvest followed by mincing, digestion in a DNase and collagenase solution, and filtration before staining with fluorescent reagents concurrently maximized viable yields of epithelial, endothelial, and hematopoietic lineage cells compared with a standard method that did not use enzymes at the time of tissue harvest. Flow cytometry identified each population—epithelial (CD326+CD31-CD45-), endothelial (CD326-CD31+CD45-), and hematopoietic lineage (CD326-CD31-CD45+)—and measured cellular viability by 7-aminoactinomycin D (7-AAD) staining. The Dispase method permitted discrimination of epithelial vs. endothelial cell death in a systemic lipopolysaccharide model of increased pulmonary vascular permeability. We conclude that application of a dissociative enzyme solution directly to the cellular compartments of interest at the time of tissue harvest maximized viable cellular yields of those compartments. Investigators could employ this dissociation method to simultaneously harvest epithelial, endothelial, and hematopoietic lineage and other lineage-negative cells for flow-cytometric analysis.

Original languageEnglish (US)
Pages (from-to)L796-L801
JournalAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
Volume310
Issue number9
DOIs
StatePublished - Mar 1 2016

Fingerprint

Lung
Flow Cytometry
Cell Death
Staining and Labeling
Pulmonary Circulation
Deoxyribonucleases
Capillary Permeability
Metalloproteases
Collagenases
Enzymes
Bacillus
Lipopolysaccharides
Cause of Death
Digestion
Suspensions
Endothelial Cells
Research Personnel
dispase

Keywords

  • Cell death
  • Flow cytometry
  • Lung
  • Tissue digestion
  • Tissue processing

ASJC Scopus subject areas

  • Physiology
  • Medicine(all)
  • Pulmonary and Respiratory Medicine
  • Cell Biology
  • Physiology (medical)

Cite this

Flow-cytometric method for simultaneous analysis of mouse lung epithelial, endothelial, and hematopoietic lineage cells. / Singer, Benjamin D.; Mock, Jason R.; D'Alessio, Franco; Aggarwal, Neil R.; Mandke, Pooja; Johnston, Laura; Damarla, Mahendra.

In: American Journal of Physiology - Lung Cellular and Molecular Physiology, Vol. 310, No. 9, 01.03.2016, p. L796-L801.

Research output: Contribution to journalArticle

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