期刊
BIO-PROTOCOL
卷 11, 期 6, 页码 -出版社
BIO-PROTOCOL
DOI: 10.21769/BioProtoc.3928
关键词
Bone marrow isolation; Monocyte culture; BMDMs; Macrophage differentiation; Monocyte differentiation
类别
资金
- Genentech, Inc.
- References 8 and 9
This article describes a simple and rapid method to isolate monocytes from murine bone marrow, culture them for up to 5 days and differentiate them into bone marrow derived macrophages. This approach helps to further understand and study the role of myeloid cell types in mammalian physiology.
Myeloid progenitors in the bone marrow generate monocytes, macrophages, granulocytes and most dendritic cells. Even though these innate immune cells are part of the same lineage, each cell type plays a specific and critical role in tissue development, host defense and the generation of adaptive immunity. Protocols have been developed in the past to differentiate myeloid cell types from bone marrow cells, enabling functional investigation and furthering our understanding about their contribution to mammalian physiology. In this protocol, we describe a simple and rapid method to isolate monocytes from murine bone marrow, culture them for up to 5 days and lastly, differentiate them into bone marrow derived macrophages (Figure 1). [GRAPHICS]
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