Isolation of mouse mesenchymal stem cells on the basis of expression of Sca-1 and PDGFR-α

被引:239
作者
Houlihan, Diarmaid D. [2 ]
Mabuchi, Yo [1 ,3 ]
Morikawa, Satoru [1 ,4 ]
Niibe, Kunimichi [1 ,4 ]
Araki, Daisuke [1 ,4 ]
Suzuki, Sadafumi [1 ]
Okano, Hideyuki [1 ]
Matsuzaki, Yumi [1 ]
机构
[1] Keio Univ, Sch Med, Dept Physiol, Tokyo 160, Japan
[2] Univ Birmingham, Biomed Res Unit, Natl Inst Hlth Res, Liver Res Ctr, Birmingham, W Midlands, England
[3] Tokyo Med & Dent Univ, Grad Sch Hlth Care Sci, Dept Biochem & Biophys, Tokyo, Japan
[4] Keio Univ, Sch Med, Dept Dent & Oral Surg, Tokyo 160, Japan
基金
英国医学研究理事会;
关键词
MURINE BONE-MARROW; HEMATOPOIETIC MICROENVIRONMENT; STROMAL CELLS; INBRED MICE; CULTURE; DIFFERENTIATION; SELECTION; PROTOCOL; STRAINS;
D O I
10.1038/nprot.2012.125
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Platelet-derived growth factor receptor alpha (PDGFR-alpha) and stem cell antigen 1 (Sca-1) have recently been identified as selective markers of mouse mesenchymal stem cells (MSCs). PDGFR-alpha(+)Sca-1(+) (P alpha S) MSCs have augmented growth potential and robust tri-lineage differentiation compared with standard culture-selected MSCs. In addition, the selective isolation of P alpha S MSCs avoids cellular contamination that can complicate other methods. Here we describe in detail our protocol to isolate P alpha S MSCs using flow cytometry. In brief, the tibia and femora are isolated and crushed using a pestle and mortar. The crushed bones are then chopped and incubated for 1 h at 37 degrees C in 20 ml of DMEM containing 0.2% (wt/vol) collagenase. The cell suspension is filtered before red blood cell lysis and incubated with the following antibodies: allophycocyanin (APC)-conjugated PDGFR-alpha, FITC-conjugated Sca-1, phycoerythrin (PE)-conjugated CD45 and Ter-119. Appropriate gates are constructed on a cell sorter to exclude dead cells and lineage (CD45(+)Ter-119(+))-positive cells. Approximately 10,000 P alpha S MSCs may then be isolated per mouse. The total protocol takes similar to 7 h to complete.
引用
收藏
页码:2103 / 2111
页数:9
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