Isolation of human bone marrow stromal cells from bone marrow biopsies for single-cell RNA sequencing

被引:6
|
作者
Gleitz, Helene F. E. [1 ,2 ,3 ]
Snoeren, Inge A. M. [1 ,2 ,3 ]
Fuchs, Stijn N. R. [1 ,2 ,3 ]
Leimkuhler, Nils B. [1 ,4 ]
Schneider, Rebekka K. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Erasmus MC, Dept Hematol, NL-3015 GD Rotterdam, Netherlands
[2] Erasmus MC, Dept Dev Biol, NL-3015 GD Rotterdam, Netherlands
[3] Erasmus MC, Oncode Inst, NL-3015 GD Rotterdam, Netherlands
[4] Rhein Westfal TH Aachen, Fac Med, Dept Hematol Oncol Hemostaseol & Stem Cell Transp, Aachen, Germany
[5] Rheinisch Westfalische Tech Hsch Aachen Univ, Inst Biomed Engn, Dept Cell Biol, Aachen, Germany
来源
STAR PROTOCOLS | 2021年 / 2卷 / 02期
关键词
Cancer; Cell Biology; Cell isolation; Flow Cytometry/Mass Cytometry;
D O I
10.1016/j.xpro.2021.100538
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bone marrow (BM) mesenchymal stromal cells play an important role in regulating stem cell quiescence and homeostasis; they are also key contributors to various hematological malignancies. However, human bone marrow stromal cells are difficult to isolate and prone to damage during isolation. This protocol describes a combination of mechanical and enzymatic isolation of BM stromal cells from human BM biopsies, followed by FACS sorting to separate stromal sub-populations including mesenchymal stromal cells, fibroblasts, and Schwann cells for single-cell RNA sequencing. For complete details on the use and execution of this protocol, please refer to Leimkuhler et al. (2020).
引用
收藏
页数:12
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