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Last Updated: April 25, 2024

Claims for Patent: 8,998,793


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Summary for Patent: 8,998,793
Title:Feeder-free method for culture of bovine and porcine spermatogonial stem cells
Abstract: The present invention relates to the production and culture of undifferentiated spermatogonial stem cells that can be maintained long term and are feeder free. The resultant feeder-free populations can be used in any of a number of protocols including the generation of progeny bulls. The present invention includes novel methods required for the successful enrichment of bovine spermatogonial stem cells, novel cell lines and other components used for the same, as well as the resultant stem cell compositions.
Inventor(s): Oatley; Jon Michael (Pullman, WA), Oatley; Melissa Joan (Pullman, WA)
Assignee: Washington State University (Pullman, WA)
Application Number:13/763,908
Patent Claims:1. A method of enriching spermatogonial stem cells (SSCs) from a population of testis-derived cells containing at least one SSC, said method comprising: a) providing a media that has been preconditioned with a feeder cell line, wherein said preconditioned media is created by contacting said media with cells, or parts thereof, from the feeder cell line, wherein the feeder cell line is a strain of embryonic fibroblast cells and/or somatic cells isolated from testes; b) contacting said population of testis-derived cells with said preconditioned media under conditions suitable for SSC cell maintenance and enrichment.

2. The method of claim 1 wherein said feeder cell line is bovine.

3. The method of claim 2 wherein said feeder cell line strain is selected from the group consisting of cell line BEF1 and cell line BSC1.

4. The method of claim 2 wherein preconditioning includes the steps of: a) contacting media with feeder cells selected from the group consisting of bovine embryonic fibroblast cells and/or bovine testicular somatic cells; b) allowing said cells to reproduce on said media; and thereafter c) removing said feeder cells.

5. The method of claim 4 wherein said cell feeder cells are derived from cell line BEF1 and/or BSC1.

6. The method of claim 1 wherein said SSC are bovine cells.

7. A method of isolating spermatogonial stem cells from bovine testicular tissue comprising: a. Obtaining testicular tissue from a subject b. Incubating said tissue with collagenase to separate spermatogonia and Sertoli cells c. Separating tubules from other cell types d. Digesting tubules with trypsin to yield a suspension spermatogonial cells and Sertoli cells and e. Separating the spermatogonial cells and Sertoli cells from said suspension.

8. The method of claim 7 wherein said separating of tubules from other cell types is by gravity sedimentation.

9. The method of claim 7 wherein said separating of spermatogonial cells and Sertoli cell from said suspension is by centrifugation and incubation on culture dishes to which sertoli cells preferentially bind.

10. The method of claim 1 wherein said pre-conditioned media is DMEM/F12 media.

11. The method of claim 1 wherein said media is supplemented with serum replacement supplement.

12. The method of claim 10 wherein said serum replacement supplement is StemPro.

13. A media for maintenance and enrichment of bovine spermatogonial stem cells created by the method of claim 1.

14. The media of claim 13 wherein said media is comprised within plastic culture wells pre-coated with Matrigel.

15. A population of enriched spermatogonial stem cells created by the method of claim 1.

16. The population of cells of claim 15, wherein said cells are bovine cells.

17. A method of generating at least one mammal progeny, said method comprising: a) administering a population enriched SSCs produced by the method of claim 1 to a testis of a male recipient mammal wherein feeder cells do not need to be removed from said population; b) allowing said enriched SSCs to generate a colony of spermatogenesis in said recipient mammal; and c) mating said recipient mammal with a female mammal of the same species as said recipient mammal.

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