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3 protocols using ter 119 biotin

1

Bone Marrow Cell Immunophenotyping

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Bone marrow single cell suspensions were obtained and washed in IMDM + 15% FBS. Cells were pre-incubated with 10% rat serum and stained with anti-CD44-APC (#559250 BD) and anti-TER119-PE (#553673 BD) antibodies. For DRAQ5 (#DR50200 Biostatus) analysis cells were stained for CD44-PE (#553134 BD) antibody and TER119-Biotin (#553672 BD) followed by Streptavidin-PE-Cy7 (#557598 BD). After washing, cells were incubated with DRAQ5 DNA binding dye (1/1000 dilution in PBS + 2% FBS) at 37°C and washed. Samples were analyzed in a FacsCanto flow cytometer (BD). Data was analyzed by FlowJo software (Treestar).
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2

Isolation and Transplantation of NG2+ Bone Stromal Cells

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To isolate enough number of NG2+ bone mesenchymal stromal cells for transplantation, the whole bone cells were prepared and pooled from the bones (femur, tibia, calvarium, sternum bones) of nine NG2-CreERTM+/−;tdRED+/+ female mice. To facilitate cell sorting, the majority of immune cells were pre-depleted by MACS sorting. Briefly, whole bone cells were incubated with CD45-biotin, CD11b-biotin, CD3e-biotin, Ly-6C/G-biotin and TER-119-biotin (BD Bioscience, Cat# 559971) in PBS with 2% serum, 1% antibiotics for 15 minutes at 4°C. After washing, cells were re-suspended and incubated with Streptavidin-bound magnetic beads (BD Bioscience, Cat# 557812) for 15 minutes at 4°C. Then cells were rinse twice and the biotin negative cells were collected by EasySep Magnet (StemCell, Cat# 18000). The CD45CD31TER119DAPING2-tdRED+ cells were immediately sorted from the enriched population by a BD Aria II cell sorter with 100 μm nozzle. About 120000 cells in total were collected and then re-suspended in 60μl PBS. Purified cells were directly transplanted into the femur bones of five 8-week-old female C57BL/6 mice (10μl per animal) through intra-femoral injection with a 28G BD insulin syringe. As sham controls, 5 age-matched female C57BL/6 mice were injected with 10μl PBS.
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3

Cardiac Cell Characterization in Ischemic Mice

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Ten- to 12-week-old CXCR4-EGFP BAC transgenic reporter mice with or without LAD ligation were either treated with saline or DMOG (80 mg/kg/day) for up to 7 days. BM mononuclear and myocyte-depleted cardiac cells were separated as previously described [4 (link)]. Cells were incubated for 40 min in the dark at 4 °C with the following fluoresceinisothiocyanate (FITC)-, phycoerythrin (PE)-, and peridininchlorophyll-protein (PerCP)-conjugated monoclonal antibodies: CD45-PerCP, CD11b-PErCP, CD11b-PE, CD4-PE, CD20-PE, CD31-PE, CD34-PE, Flk-PE, CD86-PE, CD206-PE, F4/80-PE, CD133-PE, c-kit-PE, Sca-1-PE, CD3-biotin, CD45R/B220-biotin, CD11b-biotin, TER-119-biotin, and Ly-6G-biotin (all from BD Pharmingen). Matching isotype antibodies (BD Pharmingen) served as controls. Cells were analyzed by three-color flow cytometer using a Coulter Epics XL-MCLTM flow cytometer (Beckman Coulter). Each analysis included 50,000 events.
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