Preprimitive streak and mesendoderm cells

US9732318B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9732318-B2
Application numberUS-201113190390-A
CountryUS
Kind codeB2
Filing dateJul 25, 2011
Priority dateDec 23, 2003
Publication dateAug 15, 2017
Grant dateAug 15, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

This disclosure relates to compositions comprising human preprimitive streak cells and/or human mesendoderm cells as well as methods for their production. Additionally, disclosed herein are methods of identifying factors useful in the further differentiation of preprimitive streak and mesendoderm cell types.

First claim

Opening claim text (preview).

What is claimed is: 1. An in vitro method of producing mesendoderm cells, the method comprising the steps of: (a) obtaining a cell population comprising human pluripotent stem cells; (b) providing the human pluripotent stem cells with at least one TGFβ superfamily growth factor in an amount sufficient to promote differentiation of the human pluripotent stem cells to mesendoderm cells, said mesendoderm cells being multipotent cells that can differentiate into mesoderm or definitive endoderm cells; and (c) allowing sufficient time for the mesendoderm cells to form, wherein the sufficient time for the mesendoderm cells to form has been determined by detecting the presence of mesendoderm cells in the cell population. 2. The method of claim 1 , wherein, the TGFβ superfamily growth factor is selected from the group consisting of Nodal, activin A and activin B. 3. The method of claim 2 , wherein the TGFβ superfamily growth factor is activin A. 4. The method of claim 3 , wherein at least 10 ng/ml activin A is provided. 5. The method of claim 3 , wherein at least 100 ng/ml activin A is provided. 6. The method of claim 1 , wherein the human pluripotent stem cells comprise human embryonic stem cells. 7. The method of claim 1 , wherein the human pluripotent stem cells are derived from a tissue selected from the group consisting of the morula, the ICM of an embryo and the gonadal ridges of an embryo. 8. The method of claim 1 further comprising the step of providing serum to the human pluripotent stem cells. 9. The method of claim 1 further comprising a medium that comprises less than about 2% (v/v) serum. 10. The method of claim 1 , wherein the population of mesendoderm cells express at least one marker selected from the group consisting of brachyury, FGF4 or SNAI1 and at least one marker from the group consisting of OCT4, SOX17, CXCR4, FOXA2, SOX7 or SOX1. 11. The method of claim 10 , wherein the expression of the marker selected from the group consisting of brachyury, FGF4 and/or SNAI1 is greater than the expression of the marker selected from the group consisting of OCT4, SOX17, CXCR4, FOXA2, SOX7 and/or SOX1 in the population of mesendoderm cells. 12. The method of claim 1 , wherein at least about 15% of the pluripotent human stem cells differentiate into mesendoderm cells. 13. The method of claim 1 , wherein at least about 50% of the pluripotent human stem cells differentiate into mesendoderm cells. 14. The method of claim 1 , wherein at least about 90% of the pluripotent human stem cells differentiate into mesendoderm cells. 15. The method of claim 1 , wherein the said pluripotent human stem cells are further provided with one or more growth factors selected from the group consisting of FGF10, FGF4, FGF2 or Wnt3B. 16. An in vitro method of producing human mesendoderm cells, the method comprising: obtaining a cell population comprising human pluripotent stem cells; and providing said cell population with a TGFβ superfamily growth factor, thereby generating a cell population comprising at least 10% mesendoderm cells. 17. The method of claim 16 , further comprising allowing sufficient time for the population of mesendoderm cells to form. 18. The method of claim 1 , further comprising a medium that comprises no serum. 19. The method of claim 18 , further comprising a medium that comprises no serum replacement. 20. The method of claim 2 , further comprising a medium that comprises no serum.

Assignees

Inventors

Classifications

  • Basic fibroblast growth factor (bFGF, FGF-2) · CPC title

  • Activin; Inhibin; Mullerian inhibiting substance · CPC title

  • from embryonic cells · CPC title

  • C12N5/0603Primary

    Embryonic cells (production of embryos, nuclear transfer A01K67/027); Embryoid bodies · CPC title

  • C12N5/0606Primary

    Pluripotent embryonic cells, e.g. embryonic stem cells [ES] (embryonic germ cells C12N5/0611, induced pluripotent stem cells C12N5/0696) · CPC title

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What does patent US9732318B2 cover?
This disclosure relates to compositions comprising human preprimitive streak cells and/or human mesendoderm cells as well as methods for their production. Additionally, disclosed herein are methods of identifying factors useful in the further differentiation of preprimitive streak and mesendoderm cell types.
Who is the assignee on this patent?
D'Amour Kevin Allen, Agulnick Alan D, Eliazar Susan, and 3 more
What technology area does this patent fall under?
Primary CPC classification C12N5/0603. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).