IP Library Granted Patent US 9,181,315
Granted Patent B2
US 9,181,315 · App. 13/143,645 · Granted Nov 10, 2015

Compositions and methods for induced brown fat differentiation

Inventors: Bruce M. Spiegelman (Waban, MA); Shingo Kajimura (Boston, MA)
Assignee: Dana-Farber Cancer Institute, Inc.
C07K14/4702A61K38/00C07H21/04C12N5/16C12N15/63
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Quick Facts
Patent No.
US 9,181,315
App. No.
13/143,645
Granted
Nov 10, 2015
Kind
B2
Abstract

The invention provides methods and compositions for inducing brown fat cell differentiation through modulation of both Prdm1β and C/EBPβ activity and/or expression. Also provided are methods for preventing or treating obesity or an obesity related disorder in a subject through stimulation of both Prdm1β and C/EBPβ expression and/or activity. Further provided are methods for identifying compounds that are capable of modulating both Prdm1β and C/EBPβ expression and/or activity.

Claims (10)

1. A method for inducing differentiation of autologous fibroblast, autologous myoblast, or autologous fibroblast and myoblast cells into brown fat cells at a subcutaneous transplantation site in a mammal comprising:

a) expressing both Prdm16 and C/EBPβ in vitro using genetically engineered autologous fibroblast, autologous myoblast, or autologous fibroblast and myoblast cells, comprising recombinant DNA encoding Prdm16 and C/EBPβ; and

b) transplanting the genetically engineered autologous cells expressing both Prdm16 and C/EBPβ into a transplantation site in the mammal by subcutaneous transplantation.

2. The method of claim 1 , wherein the autologous fibroblast cells are selected from the group consisting of skin fibroblasts, dermal fibroblasts, primary embryonic fibroblasts, immortalized embryonic fibroblasts, and human foreskin fibroblasts.

3. A method for inducing differentiation of autologous fibroblast, autologous myoblast, or autologous fibroblast and myoblast cells into brown fat cells at a subcutaneous transplantation site in a mammal comprising:

a) obtaining autologous fibroblast, autologous myoblast, or autologous fibroblast and myoblast cells from the mammal;

b) genetically engineering the autologous fibroblast, autologous myoblast, or autologous fibroblast and myoblast cells with recombinant DNA encoding Prdm16 and C/EBPβ and expressing both Prdm16 and C/EBPβ in the genetically engineered autologous cells; and

c) transplanting the genetically engineered autologous cells expressing both Prdm16 and C/EBPβ into a transplantation site in the mammal by subcutaneous transplantation.

4. The method of claim 3 , wherein the autologous fibroblast cells are selected from the group consisting of skin fibroblasts, dermal fibroblasts, embryonic fibroblasts, and human foreskin fibroblasts.

5. The method of claim 1 or 3 , wherein the mammal is a human.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 26, 2016
From: DANA-FARBER CANCER INST
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039462/0207 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2015
From: SPIEGELMAN, BRUCE M.; KAJIMURA, SHINGO
To: DANA-FARBER CANCER INSTITUTE, INC.
Reel/Frame 034785/0735 →
Continuity (2)
Provisional Application 61204607 · Jan 8, 2009
Related Publication 20120022500A1 · Jan 26, 2012