Separation of cells by velocity sedimentation

Journal of Cellular Physiology - Tập 73 Số 3 - Trang 191-201 - 1969
Richard G. Miller1, Robert A. Phillips1
1Department of Medical Biophysics, University of Toronto, and the Ontario Cancer Institute, Toronto, Ontario, Canada

Tóm tắt

Abstract

A system for fractionating populations of living cells by velocity sedimentation in the earth's gravitational field is described. The cells start in a thin band near the top of a shallow gradient of 3% to 30% fetal calf serum in phosphate buffered saline at 4°C. Cell separation takes place primarily on the basis of size and is approximately independent of cell shape. A sharply‐defined upper limit, called the streaming limit, exists for the cell concentration in the starting band beyond which useful cell separations cannot be achieved. This limit, which varies with the type of cell being sedimented, can be significantly increased by proper choice of gradient shape. For sheep erythrocytes (sedimentation velocity of 1.6 mm/hour) it is 1.5 × 107 cells/ml. Measured and calculated sedimentation velocities for sheep erythrocytes are shown to be in agreement. The technique is applied to a suspension of mouse spleen cells and it is shown, using an electronic cell counter and pulse height analyzer, that cells are fractionated according to size across the gradient such that the sedimentation velocity (in mm/hour) approximately equals r2/4 where r is the cell radius in microns. Since cells of differing function also often differ in size, the system appears to have useful biological applications.

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Tài liệu tham khảo

Altman P. L., 1964, Biology Data Book, 269

Beresford J., 1967, Size analysis of organic pigments using the ICI‐Joyce Loebel disc centrifuge, J. Oil Col. Chem. Assoc., 50, 594

Bergsagel D. E. andR. G.Miller1969(in preparation).

10.1083/jcb.36.2.369

10.1111/j.1749-6632.1962.tb45310.x

10.1126/science.131.3392.32

10.1084/jem.99.2.167

10.1126/science.150.3698.910

10.1016/S0006-3495(65)86724-8

10.1038/2161229a0

Hodgman C. D., 1963, Handbook of Chemistry and Physics

10.1126/science.140.3565.405

10.1073/pnas.51.3.520

MacDonald H. R. andR. G.Miller1969(in preparation)

McCool D. R. J. Miller W. R.Bruce R. H.PainterandC. M.Warby1969(in preparation).

Magath T. B., 1960, Electronic blood‐cell counting, Am. J. Clin. Path., 34, 203, 10.1093/ajcp/34.3.203

10.3181/00379727-127-32719

10.1038/200423a0

10.1016/0022-5193(64)90026-8

II Laminar flow and density gradient stability, J. Theor. Biol., 6, 181

III Migration principles – sedimentation and electrophoresis, J. Theor. Biol., 6, 307

Mel H. C. andJ. C.Schooley1965La greffe des cellules hématopoiétiques allogeniques. G. Mathe J. L. Amiel and L. Schwarzenberg (eds.)

10.1073/pnas.58.6.2261

10.1038/214824a0

Phillips R. A. andR. G.Miller1969(in preparation).

10.1038/2161227a0

Tanford C., 1961, Physical Chemistry of Macromolecules, 327

10.1002/jcp.1040690110

10.3181/00379727-125-32093

Worton R. G., 1967, Partial purification of hemopoietic colony‐forming cells, Biophys. J. (Abstr.), 7, 100

Worton R. G. J. E. TillandE. A.McCulloch1969(in preparation).