FACS Detection of RASSLs in Blood Cells

Overview

List of reagents is not yet complete

Procedure

By Charles H. Redfern & Bruce R. Conklin

February 28, 1999

Note: This protocol has been used successfully to detect Ro1 in tetO-Ro1/MMTV-tTA mice. The original data were cut from of our 1999 Nature Biotechnology paper (Redfern et al.) at the request of our reviewers. In this section of the paper we demonstrated inducible Ro1 expression in lymphocytes of MMTV-tTA/tetO-Ro1 mice by flow cytometry. The mean percentage of cells with Ro1 expression in total peripheral blood lymphocyteswas 10.8 ± 3.7% (SD, n = 13) and was almost equally divided betweenT- and B-lymphocytes. This expression was completely suppressed by feeding the mice doxycycline.

FACS remains a powerful means of detecting RASSLs in rare subpopulations of cells, such as stem cells, certain immune cells and neural cells. If you have any corrections or additions to this protocol, please e-mail us so that we can assist other people trying to use RASSLs in rare subpopulations of cells.

Methods (short version)

Flow cytometry. Mouse whole blood (200 mlas mixed in PBS containing heparin (2 units/ml) at 4°C, centrifuged, and lysed in standard lysis buffer (150 mM NH4Cl, 10 mM NaHCO3,and 0.4% EDTA). The white blood cells were resuspended in Dulbecco's modified eagles medium (2% fetal calf serum), centrifuged three times, stained with phycoerythrin-conjugated M1-Ab (Custom conjugation by Chromaprobe Mountain View CA, or Molecular Probes, Oregon), and preserved in PBS with 1.0% paraformaldehydeat 4°C until analyzed by flow cytometry (Becton Dickinson).

Methods (long version)

1. Cut mouse tail with sharp razor. 2. Collect 200 ml of blood in 15 ml Falcon conical tube containing 12 ml of fresh PBS and heparin 1-2 units/ml. 3. Invert tube several times, store on ice while cutting other tails. 4. Spin Falcon tubes in centrifuge at 1000-1200 rpm for 5 minutes. 5. Pour off supernatant (careful, the pellet is not tight) and resuspend in 3 ml of 1x Lysis Buffer. 6. Let stand in Lysis Buffer for 5-10 minutes at room temperature. 7. Spin for 3 minutes at 1000 rpm. 8. Resuspend in media (DME + 2% FCS) and spin again for 3 minutes at 1000 rpm. 9. Resuspend in Fluorescent Staining solution (~1 ml) and shake on ICE for 20-30 minutes (in Light-tight Box). 10. Pellet, wash in 2 ml of media, pellet, and wash in 1% PFA/PBS. 11. Pellet, and resuspend in 500 ml of 1% PFA/PBS in FALCON TUBE (2054). 12. Cover with tin foil and refrigerate until FACS time.

Lysis Buffer (10x)

NH4Cl (ammonium chloride) NaHCO3 (sodium bicarb) EDTA (disodium)

80.2 g 8.4 g 3.7 g

• Add to 1 liter millipore water
• Store at 4°C.
• Dilute in millipore water

Antibody Staining Solution

• Mix 1 ml of media solution with approximately 1 mg of antibody for each reaction.
• Keep fluorescent antibody light protected at all times.

Notes

No further notes are available at this time.

References

Relevant papers and books

If this protocol has papers or books associated with it, list those references here. Below is an example for formatting purposes. See the OpenWetWare:Biblio page for more information.

1. Goldbeter A and Koshland DE Jr. An amplified sensitivity arising from covalent modification in biological systems. Proc Natl Acad Sci U S A. 1981 Nov;78(11):6840-4. DOI:10.1073/pnas.78.11.6840 |
2. JACOB F and MONOD J. Genetic regulatory mechanisms in the synthesis of proteins. J Mol Biol. 1961 Jun;3:318-56. DOI:10.1016/s0022-2836(61)80072-7 |
3. ISBN:0879697164

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