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Isolation and differentiation of murine macrophages

Research output: Chapter in Book/Report/Conference proceeding › Chapter (peer-reviewed) › peer-review

Abstract

Macrophages play a major role in inflammation, wound healing, and tissue repair. Infiltrated monocytes differentiate into different macrophage subtypes with protective or pathogenic activities in vascular lesions. In the heart and vascular tissues, pathological activation promotes cardiovascular inflammation and remodeling and there is increasing evidence that macrophages play important mechanisms in this environment. Primary murine macrophages can be obtained from: bone marrow by different treatments (granulocyte-macrophage colony-stimulating factor—GM-CSF, macrophage colony-stimulating factor—M-CSF or supernatant of murine fibroblast L929), peritoneal cavity (resident or thioglycolate elicit macrophages), from the lung (alveolar macrophages) or from adipose tissue. In this chapter we describe some protocols to obtain primary murine macrophages and how to identify a pure macrophage population or activation phenotypes using different markers.
Original languageEnglish
Title of host publicationHypertension
Subtitle of host publicationMethods and Protocols
EditorsRhian M. Touyz, Ernesto L. Schiffrin
PublisherHumana
Pages297–309
Number of pages13
ISBN (Electronic)9781493966257
ISBN (Print)9781493966233
DOIs
Publication statusPublished - 24 Jan 2017

Publication series

NameMethods in Molecular Biology
PublisherHumana Press Inc.
Volume1527
ISSN (Print)1064-3745

Keywords

  • Macrophage
  • murine
  • peritoneum
  • bone marrow
  • resident
  • thioglycollate
  • L929 supernatant

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