IP Library Granted Patent US 9,532,994
Granted Patent B2
US 9,532,994 · App. 10/569,994 · Granted Jan 3, 2017

Agents and methods for enhancing bone formation by oxysterols in combination with bone morphogenic proteins

Inventor: Farhad Parhami (Los Angeles, CA)
Assignee: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
A61K31/56A61K31/22A61K31/59A61K31/66A61K33/06A61K38/1875C12N5/0654C12N2501/155C12N2501/999
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Quick Facts
Patent No.
US 9,532,994
App. No.
10/569,994
Granted
Jan 3, 2017
Kind
B2
Abstract

The present invention discloses agents and methods for inducing osteoblastic cellular differentiation, as well as the use of such agents and methods to treat patients to maintain bone mass, enhance bone formation and/or bone repair. Exemplary agents include oxysterols, alone or in combination with particular oxysterols, or other agents, such as bone morphogenic proteins, known to assist in bone formation. The invention further includes medicaments including oxysterols for the treatment of bone disorders and implants to facilitate bone repair.

Claims (49)

1. A method of inducing osteoblastic differentiation and inhibiting adipocyte differentiation of mammalian mesenchymal stem cells comprising administering a combination of 20S-hydroxycholesterol and 22S-hydroxycholesterol and at least one bone morphogenic protein to contact the mammalian mesenchymal stem cells and induce osteoblastic differentiation and inhibit adipocyte differentiation of the mammalian mesenchymal stem cells,

wherein the at least one bone morphogenic protein is selected from the group consisting of BMP7, BMP14, and combinations.

2. The method of claim 1 , further comprising treating the mammalian mesenchymal stem cells with a cytochrome P450 inhibitor.

3. The method of claim 1 , further comprising treating the mammalian mesenchymal cells with at least one secondary agent selected from the group consisting of parathyroid hormone, sodium fluoride, insulin-like growth factor I, insulin-like growth factor II or transforming growth factor beta, bisphosphonates, estrogen receptor modulators, calcitonin, vitamin D, and calcium.

4. The method of claim 1 , wherein the mammalian mesenchymal stem cells are of a patient.

5. The method of claim 1 ,

wherein the mammalian mesenchymal stem cells are in a patient affected by bone loss, and

wherein inducing osteoblastic differentiation and inhibiting adipocyte differentiation of the mammalian mesenchymal stem cells results in increased bone mass and enhanced bone repair in the patient.

6. The method of claim 1 ,

wherein the mammalian mesenchymal stem cells are in a patient exhibiting clinical symptoms of osteoporosis, and

wherein inducing osteoblastic differentiation and inhibiting adipocyte differentiation of the mammalian mesenchymal stem cells ameliorates the symptoms of osteoporosis in the patient.

7. The method of claim 1 ,

wherein the mammalian mesenchymal stem cells are in a patient in need of bone formation, and

wherein inducing osteoblastic differentiation and inhibiting adipocyte differentiation of the mammalian mesenchymal stem cells induces bone formation in the patient.

8. The method of claim 7 , wherein the bone formation is endochondral or intramembraneous bone formation.

9. The method of claim 1 ,

wherein the mammalian mesenchymal stem cells are ex vivo, and

wherein the method further comprises administering the osteoblastic differentiated cells to a patient in need of bone formation by applying the osteoblastic differentiated cells to a selected site in the patient where bone formation is desired.

10. The method of claim 1 , wherein the at least one bone morphogenic protein is BMP7.

11. The method of claim 1 , wherein the at least one bone morphogenic protein is BMP14.

12. The method of claim 1 , wherein the at least one bone morphogenic protein is the combination of BMP7 and BMP14.

13. A method of stimulating mammalian cells to express a level of a biological marker of osteoblastic differentiation which is greater than the level of the biological marker in untreated mammalian cells, comprising administering a combination of 20S-hydroxycholesterol and 22S-hydroxycholesterol and at least one bone morphogenic protein to the mammalian cells in an amount sufficient to induce the osteoblastic differentiation of the mammalian cells,

wherein the at least one bone morphogenic protein is selected from the group consisting of BMP7, BMP14, and combinations, and

wherein the mammalian cells are selected from the group consisting of mammalian mesenchymal stem cells, mammalian preosteoblast cells, and mammalian pluripotent embryonic fibroblast cells.

14. The method of claim 13 , wherein the biological marker of osteogenic differentiation is at least one of calcium incorporation, mineralization, expression of osteocalcin mRNA, activation of the ERK pathway, and expression of Cbfa1.

15. The method of claim 13 , further comprising treating the mammalian cells with a cytochrome P450 inhibitor.

16. The method of claim 13 , further comprising treating the mammalian cells with at least one secondary agent selected from the group consisting of parathyroid hormone, sodium fluoride, insulin-like growth factor I, insulin-like growth factor II or transforming growth factor beta, bisphosphonates, estrogen receptor modulators, calcitonin, vitamin D, and calcium.

17. The method of claim 13 , wherein the mammalian cells are mammalian mesenchymal stem cells.

18. The method of claim 13 , wherein the at least one bone morphogenic protein is BMP7.

19. The method of claim 13 , wherein the at least one bone morphogenic protein is BMP14.

20. The method of claim 13 , wherein the at least one bone morphogenic protein is the combination of BMP7 and BMP14.

21. A method for treating a patient to induce bone formation comprising:

harvesting mammalian mesenchymal stem cells;

treating the mammalian mesenchymal cells by the method of claim 1 ; and

administering the differentiated cells to the patient to induce bone formation.

22. An implant for use in the human body for bone formation comprising a substrate having a surface,

wherein at least the surface comprises a combination of 20S-hydroxycholesterol and 22S-hydroxycholesterol and at least one bone morphogenic protein,

wherein after implantation the implant administers the combination of 20S-hydroxycholesterol and 22S-hydroxycholesterol and at least one bone morphogenic protein in an amount sufficient to induce osteoblastic differentiation and inhibit adipocyte differentiation of mammalian mesenchymal stem cells for bone formation in bone tissue proximate to the implant, and

wherein the at least one bone morphogenic protein is selected from the group consisting of BMP7, BMP14, and combinations.

23. The implant of claim 22 , wherein the substrate is formed into the shape of a pin, screw, plate, or prosthetic joint.

24. The implant of claim 22 , wherein the at least one bone morphogenic protein is BMP7.

25. The implant of claim 22 , wherein the at least one bone morphogenic protein is BMP14.

26. The implant of claim 22 , wherein the at least one bone morphogenic protein is the combination of BMP7 and BMP14.

27. A medicament for inducing osteoblastic differentiation and inhibiting adipocyte differentiation of mammalian mesenchymal stem cells, comprising a therapeutically effective dosage of a combination of 20S-hydroxycholesterol and 22S-hydroxycholesterol and at least one bone morphogenic protein,

wherein the at least one bone morphogenic protein is selected from the group consisting of BMP7, BMP14, and combinations and

wherein upon administration to a patient the medicament induces osteoblastic differentiation and inhibits adipocyte differentiation of mammalian mesenchymal stem cells.

28. The medicament of claim 27 , wherein the at least one bone morphogenic protein is BMP7.

29. The medicament of claim 27 , wherein the at least one bone morphogenic protein is BMP14.

30. The medicament of claim 27 , wherein the at least one bone morphogenic protein is the combination of BMP7 and BMP14.

Assignments (4)
CONFIRMATORY LICENSE Recorded Jul 16, 2010
From: UNIVERSITY OF CALIFORNIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024701/0169 →
CONFIRMATORY LICENSE Recorded Dec 18, 2008
From: UNIVERSITY OF CALIFORNIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021999/0621 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 8, 2008
From: PARHAMI, FARHAD
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 021361/0776 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2007
From: PARHAMI, FARHAD, PHD
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 019238/0645 →
Continuity (2)
Provisional Application 60499040 · Aug 29, 2003
Related Publication 20060251735A1 · Nov 9, 2006