Methods for staining cells for identification and sorting

1. A method which distinguishes bovine sperm cells based on DNA content, wherein live sperm cells are stained with a DNA-selective fluorescent dye in an osmotic gradients process, comprising:

incubating the live sperm cells in a buffer-containing first solution in a hypertonic condition to partially dehydrate the sperm cells, at a temperature between about 0° C. and about 12° C., which is substantially sufficient to maintain a comparatively high sperm viability rate, and for a time period less than about 5 minutes;

transferring the solution containing the sperm cells to a buffer-containing second solution in a hypotonic condition at said same temperature between about 0° C. and about 12° C.;

wherein the hypertonic condition is about more than 250 mOsm and the hypotonic condition is about less than 250 mOsm, for bovine sperm cells;

wherein the dye is present in at least one of the hypertonic or hypotonic condition to expedite permeation of the dye into the sperm cells when osmotic equilibrium is reached, thereby staining DNA in the sperm cells;

exposing the sperm cells to a light source to cause the stained DNA to fluoresce;

detecting a pre-determined fluorescence of the stained DNA, the predetermined fluorescence corresponding to DNA content;

distinguishing the sperm cells based on the pre-determined fluorescence; and

collecting selected sperm cells.

2. The method of claim 1 , wherein an incubation temperature of said sperm cells is less than or equal to about 4° C.

3. The method of claim 1 , wherein the high sperm viability rate is greater than 70%.

4. The method of claim 1 , wherein said dye is present in the second solution in the hypotonic condition, and said dye is drawn into the sperm cells across the cell membrane.

5. The method of claim 4 , wherein said temperature is about 4 degrees Centigrade.

6. The method of claim 4 , further comprising:

reducing one of a time or a temperature during which the sperm cells are mixed with the dye, to conserve cellular resources.

7. The method of claim 1 , wherein said fluorescence is photoactivated.

8. The method of claim 1 , further comprising:

collecting the sperm cells from a donor and subjecting the sperm cells to extension, prior to incubation; and

cooling the sperm cells to 6 degrees Centigrade.

9. The method of claim 8 , further comprising:

cooling the collected sperm cells after the collecting step, to about 4 degrees Centigrade;

subjecting the collected sperm cells to a second extension; and

freezing the collected sperm cells.

10. The method of claim 9 , further comprising:

adding a sperm-supporting substance, including eggs or egg yolks, to said collected bovine sperm cells, to extend sperm viability.

11. The method of claim 1 , wherein the selected sperm cells are sorted into X and Y chromosomes for gender sorting.

12. The method of claim 1 , further comprising:

adding a counter-stain to the sperm cells which one of diminishes fluorescence or stains in another color, to identify dead sperm cells from live sperm cells; and

removing said dead sperm from said live sperm.

13. The method of claim 1 , wherein the dye comprises at least one selected from the group consisting of SYTOX blue, SYTOX green, SYTOX orange, a cyanine dimer, POPO-1, BOBO-1, YOYO-1, TOTO-1, JOJO-1, POPO-3, LOLO-1, BOBO-3, YOYO-3, TOTO-3, a cyanine monomer, PO-PRO-1, BO-PRO-1, YO-PRO-1, TO-PRO-1, JO-PRO-1, POPRO-3, LO-PRO-1, BO-PRO-3, YO-PRO-3, TO-PRO-3, TO-PRO-5, acridine homodimer, 7-amino actinomycin D, ethidium bromide, ethidium homodimer-1, ethidium homodimer-2, ethidium nonazide, nuclear yellow, and propidium iodide.

14. The method of claim 1 , wherein the dye comprises at least one selected from the group consisting of SYTO 40 blue-fluorescent nucleic acid stain, SYTO 41 blue, SYTO 42 blue, SYTO 43 blue, SYTO 44 blue, SYTO 45 blue, a green-fluorescent SYTO dye, SYTO 9 green, SYTO 10 green, SYTO BC green, SYTO 1 green, SYTO 16 green, SYTO 24 green, SYTO 21 green, SYTO 27 green, SYTO 26 green, SYTO 23 green, SYTO 12 green, SYTO 11 green, SYTO 20 green, SYTO 22 green, SYTO 15 green, SYTO 14 green, SYTO 25 green, an orange-fluorescent SYTO dye, SYTO 86 orange, SYTO 81 orange, SYTO 80 orange, SYTO 82 orange, SYTO 83 orange, SYTO 84 orange, SYTO 85 orange, a red-fluorescent SYTO dye, SYTO 64 red, SYTO 61 red, SYTO 17 red, SYTO 59 red, SYTO 62 red, SYTO 60 red, SYTO 63 red, a Hoechst dye, Hoechst 33342, Hoechst 34580, Hoechst 33258, DAPI, LDS 751 and dihydroethidium.

15. The method of claim 1 , further comprising:

introducing nanoparticles into the sperm cells to be one of detected, or to amplify the fluorescence of the DNA.

16. The method of claim 15 , wherein said nanoparticles are quantum dots or nano-metallic particles.

17. The method of claim 1 , wherein osmolality is varied by adding salts or solutes compatible with the sperm cells, or by dilution of the second solution in the hypotonic condition, with water or buffer.

18. The method of claim 1 , wherein in the transferring step, the hypotonic condition is created by addition of buffer.

19. A method which distinguishes bovine sperm cells based on DNA content, wherein live sperm cells are stained with a DNA-selective fluorescent dye in an osmotic gradients process, comprising:

incubating the live sperm cells in a buffer-containing first solution in a hypertonic condition to partially dehydrate the sperm cells, at a temperature between about 0° C. and about 12° C., which is substantially sufficient to maintain a comparatively high sperm viability rate, and for a time period less than about 5 minutes;

transferring the solution containing the sperm cells to a buffer-containing second solution in a hypotonic condition at said same temperature between about 0° C. and about 12° C.;

wherein the hypertonic condition is about more than 500 mOsm and the hypotonic condition is about less than 250 mOsm, for bovine sperm cells;

wherein the dye is present in at least one of the hypertonic or hypotonic condition to expedite permeation of the dye into the sperm cells when osmotic equilibrium is reached, thereby staining DNA in the sperm cells;

exposing the sperm cells to a light source to cause the stained DNA to fluoresce;

detecting a pre-determined fluorescence of the stained DNA, the predetermined fluorescence corresponding to DNA content;

distinguishing the sperm cells based on the pre-determined fluorescence; and

collecting selected sperm cells.

20. A method which distinguishes bovine sperm cells based on DNA content, wherein live sperm cells are stained with a DNA-selective fluorescent dye in an osmotic gradients process, comprising:

incubating the live sperm cells in a buffer-containing first solution in a hypertonic condition to partially dehydrate the sperm cells, at a temperature between about 0° C. and about 12° C., which is substantially sufficient to maintain a comparatively high sperm viability rate, and for a time period less than about 5 minutes;

transferring the solution containing the sperm cells to a buffer-containing second solution in a hypotonic condition at said same temperature between about 0° C. and about 12° C.;

wherein the hypertonic condition is about more than 250 mOsm and the hypotonic condition is greater than 150 mOsm, but less than 250 mOsm, for bovine sperm cells;

wherein the dye is present in at least one of the hypertonic or hypotonic condition to expedite permeation of the dye into the sperm cells when osmotic equilibrium is reached, thereby staining DNA in the sperm cells;

exposing the sperm cells to a light source to cause the stained DNA to fluoresce;

detecting a pre-determined fluorescence of the stained DNA, the predetermined fluorescence corresponding to DNA content;

distinguishing the sperm cells based on the pre-determined fluorescence; and

collecting selected sperm cells.