IP Library Granted Patent US 8,969,081
Granted Patent B2
US 8,969,081 · App. 12/653,217 · Granted Mar 3, 2015

Caudal motor neuron derived from embryonic stem cells under conditions essentially free of any retinoid

Inventors: Hynek Wichterle (New York, NY); Thomas M. Jessell (Bronx, NY); Mirza Peljto (New York, NY)
Assignee: The Trustees of Columbia University in the City of New York
C12N5/0619C12N2501/385C12N5/0696C12N5/0606C12N2506/45C12N5/0623C12N2501/155C12N2501/41A61K35/30C12N2501/115C12N2501/13C12N2501/19C12N2506/02
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,969,081
App. No.
12/653,217
Granted
Mar 3, 2015
Kind
B2
Abstract

Disclosed are methods for generating a neuron expressing Hoxc8 transcription factor or a caudal motor neuron comprising culturing an embryonic stem cell in a composition which is essentially free of retinoids and comprises an isotonic salt solution, so as to generate the neuron which expresses Hoxc8 transcription factor or the caudal motor neuron. Disclosed are also methods for generating a caudal brachial motor neuron, a thoracic motor neuron, or a lumbar motor neuron from an embryonic stem cell in a composition essentially free of retinoids and comprising ADFNK medium, an amount of FGF-2, or Gdf11 respectively. Disclosed are also methods of transplanting a motor neuron into a subject comprising generating the motor neuron and transplanting the motor neuron into the subject. Disclosed is also a population of motor neuron cells enriched for motor neuron cells expressing Foxp1 and expressing a gene associated with Spinal Muscular Atrophy (SMA) or Amyotrophic Lateral Sclerosis (ALS).

Claims (22)

1. A method for producing a caudal brachial motor neuron from an embryonic stem cell, comprising

a) culturing the embryonic stem cell in a composition essentially free of any retinoid and comprising Advanced Dulbecco's Modified Eagle's Medium/F12 and Neurobasal medium that has been supplemented with 10% Knockout-Serum Replacement (ADFNK medium) wherein the amount of the composition is effective to generate the caudal brachial motor neuron under conditions such that the caudal brachial motor neuron is produced, and

b) recovering the caudal brachial motor neuron so produced.

2. The method of claim 1 , wherein during culturing the embryonic stem cell is contacted with at least one neurotrophic factor.

3. The method of claim 1 , wherein the embryonic stem cell is a murine embryonic stem cell.

4. The method of claim 1 , wherein the embryonic stem cell is a human embryonic stem cell.

5. The method of claim 1 , wherein the caudal brachial motor neuron is transfected so that it expresses enhanced green fluorescent protein (eGFP).

6. The method of claim 1 , wherein the culturing is effected in vivo in a subject.

7. The method of claim 1 , wherein the culturing is effected in vitro.

8. A method for producing a caudal motor neuron comprising

a) culturing an embryonic stem cell in a serum-free neural induction composition which is essentially free of any retinoid and comprises an isotonic salt solution, wherein the amount of the composition is effective to generate the caudal motor neuron under condition such that the caudal motor neuron is produced, and

b) recovering the caudal motor neuron so produced.

9. The method of claim 8 , wherein during culturing the embryonic stem cell is contacted with at least one neurotrophic factor.

10. The method of claim 8 , wherein the embryonic stem cell is a murine embryonic stem cell.

11. The method of claim 8 , wherein the embryonic stem cell is a human embryonic stem cell.

12. The method of claim 8 , wherein the caudal motor neuron is transfected so that it expresses enhanced green fluorescent protein (eGFP).

13. The method of claim 8 , wherein the culturing is effected in vivo in a subject.

14. The method of claim 8 , wherein the culturing is effected in vitro.

15. The method of claim 8 , wherein composition further comprises an amount of Fibroblast Growth Factor-2 (FGF-2).

16. The method of claim 8 , wherein composition further comprises an amount of Growth differentiation factor 11 (Gdf11).

17. The method of claim 8 , wherein composition further comprises an amount of a Wnt factor.

18. The method of claim 8 , wherein composition further comprises an amount of Fibroblast Growth Factor-2 (FGF-2), an amount of Growth differentiation factor 11 (Gdf11), and an amount of a Wnt factor.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2010
From: WICHTERLE, HYNEK; JESSELL, THOMAS M.; PELJTO, MIRZA
To: TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK, THE
Reel/Frame 024221/0475 →
CONFIRMATORY LICENSE Recorded Feb 16, 2010
From: COLUMBIA UNIV NEW YORK MORNINGSIDE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 023936/0982 →
Continuity (2)
Provisional Application 61201491 · Dec 10, 2008
Related Publication 20100196332A1 · Aug 5, 2010