IP Library Granted Patent US 8,354,521
Granted Patent B2
US 8,354,521 · App. 12/870,991 · Granted Jan 15, 2013

Compositions and methods for inhibiting adipogenesis by inhibition of constitutive coactivator of ppargamma

Inventor: Dechun Li (Fenton, MO)
Assignee: Saint Louis University
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Quick Facts
Patent No.
US 8,354,521
App. No.
12/870,991
Granted
Jan 15, 2013
Kind
B2
Abstract

This invention relates generally to compositions and methods which utilization nuclear receptors for regulating adipogenesis in cells. Specifically, the invention is directed to compositions which regulate transcription factor PPARγ, and enhance or inhibit the transcription of genes responsible for directing cell differentiation towards a pathway of adipogenesis. More specifically, disclosed herein is a novel polypeptide coactivator of PPARγ, and fragments thereof, which possess coactivator or corepressor activity. Also related are nucleotide sequences which express these polypeptides. Also disclosed is an interfering RNA that may be used to inhibit adipogenesis.

Claims (20)

1. An isolated RNAi with sufficient complementarity to an RNA encoding a Constitutive Coactivator of PPARgamma polypeptide to inhibit expression of a nucleotide sequence encoding a Constitutive Coactivator of PPARgamma polypeptide.

2. The RNAi of claim 1 , consisting of at least 10 contiguous nucleic acid residues of SEQ ID NO: 11, whereby the oligonucleotide reduces levels of Constitutive Coactivator of PPARgamma polypeptide.

3. The RNAi of claim 1 , consisting of at least 20 contiguous nucleic acid residues of SEQ ID NO: 11, whereby the oligonucleotide reduces levels of Constitutive Coactivator of PPARgamma polypeptide.

4. The RNAi of claim 1 , consisting of at least 30 contiguous nucleic acid residues of SEQ ID NO: 11, whereby the oligonucleotide reduces levels of Constitutive Coactivator of PPARgamma polypeptide.

5. The RNAi of claim 1 , consisting of at least 40 contiguous nucleic acid residues of SEQ ID NO: 11, whereby the oligonucleotide reduces levels of Constitutive Coactivator of PPARgamma polypeptide.

6. The RNAi of claim 1 , consisting of SEQ ID NO: 11, and conservatively modified variants thereof, whereby the oligonucleotide reduces levels of Constitutive Coactivator of PPARgamma polypeptide.

7. The RNAi of claim 1 , consisting of SEQ ID NO: 11.

8. The RNAi of claim 1 , consisting of at least 10 contiguous nucleic acid residues of SEQ ID NO: 12, whereby the oligonucleotide reduces levels of Constitutive Coactivator of PPARgamma polypeptide.

9. The RNAi of claim 1 , consisting of at least 20 contiguous nucleic acid residues of SEQ ID NO: 12, whereby the oligonucleotide reduces levels of Constitutive Coactivator of PPARgamma polypeptide.

10. The RNAi of claim 1 , consisting of at least 30 contiguous nucleic acid residues of SEQ ID NO: 12, whereby the oligonucleotide reduces levels of Constitutive Coactivator of PPARgamma polypeptide.

11. The RNAi of claim 1 , consisting of at least 40 contiguous nucleic acid residues of SEQ ID NO: 12, whereby the oligonucleotide reduces levels of Constitutive Coactivator of PPARgamma polypeptide.

12. The RNAi of claim 1 , consisting of SEQ ID NO: 12, and conservatively modified variants thereof, whereby the oligonucleotide reduces levels of Constitutive Coactivator of PPARgamma polypeptide.

13. The RNAi of claim 1 , consisting of a nucleic acid sequence set forth in SEQ ID NO: 12.

14. The isolated RNAi of claim 1 , further comprising a pharmaceutical formulation.

15. The isolated RNAi of claim 1 , further comprising a gene delivery system selected from the group consisting of cells, liposomes, liposome-derived systems, and artificial viral envelopes.

16. The isolated RNAi of claim 1 , further comprising an expression vector, the RNAi operably linked to control elements of the expression vector, and the expression vector selected from the group consisting of a plasmid, retrovirus, lentiviruses, adenovirus, parvoviruses, and an adeno-associated virus herpes simplex virus.

17. The isolated RNAi of claim 1 , further comprising an adenovirus, the RNAi operably linked to control elements of the adenovirus.

18. A method of reducing adipogenesis in a mammal cell, comprising administering the composition of claim 17 to the mammal cell.

19. A method of reducing adipogenesis in a mammal cell in vivo, comprising, injecting intravenously, intramuscularly, or subcutaneously, an isolated RNAi with sufficient complementarity to an RNA encoding a Constitutive Coactivator of PPARgamma polypeptide to inhibit ex ession of a nucleotide sequence encoding a Constitutive Coactivator of PPARgamma polypeptide and an adenovirus, the RNAi operably linked to control elements of the adenovirus.

20. A method of reducing adipogenesis in a mammal cell, in vivo comprising, administering through topical application or direct application to tissue exposed through surgery, an isolated RNAi with sufficient complementarity to an RNA encoding a Constitutive Coactivator of PPARgamma polypeptide to inhibit expression of a nucleotide sequence encoding a Constitutive Coactivator of PPARgamma of polypeptide and an adenovirus, the RNAi operably linked to control elements of the adenovirus.

Assignments (1)
CONFIRMATORY LICENSE Recorded Oct 26, 2012
From: ST. LOUIS UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029198/0913 →
Continuity (3)
Division 11870736 · Oct 11, 2007
Provisional Application 60851156 · Oct 12, 2006
Related Publication 20110014275A1 · Jan 20, 2011