IP Library Granted Patent US 11,261,461
Granted Patent B2
US 11,261,461 · App. 15/503,649 · Granted Mar 1, 2022

Methods and compositions for selective generation of dopaminergic precursors

Inventors: Jialin Zheng (Omaha, NE); Changhai Tian (Omaha, NE)
Assignees: Tongji University; Board of Regents of the University of Nebraska
C12N15/86A61K35/12C12N5/0619C12N2501/60C12N2510/00
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Quick Facts
Patent No.
US 11,261,461
App. No.
15/503,649
Granted
Mar 1, 2022
Kind
B2
Abstract

Provided are methods and compositions for transdifferentiation of a somatic cell, e.g., a fibroblast to a dopaminergic precursor, Specifically, provided are induced dopaminergic (iDP) cells, or master transcription factors (TFs) therefore, methods for making iDP cells, and methods and compositions for using them in, e.g., treating neurodegenerative diseases such as Parkinson's disease.

Claims (15)

1. An in vitro induced dopaminergic precursor cell (iDP), consisting essentially of ectopically expressed genes or proteins of:

(1) one or both of Bm2 and Bm4, or a variant thereof,

(2) Sox2 or a variant thereof, and

(3) one or both of Foxa2 and Lmx1a, or a variant thereof,

wherein the iDP is transdifferentiated from a somatic cell that is not a dopaminergic precursor, the iDP expresses relative to the somatic cell high levels of neural progenitor markers Sox1, PAX6, ZBTB16, Sox3, CD133 and Nestin, high levels of ventral mesencephalon markers Aldh1A1, Corin (Lrp4), Lmx1a, Msx1, Ngn2, Otx2, Mash1, Pitx3 and Nkx6.1 and minimum levels of telencephalon related markers FoxG1, GSX2, and Nkx2.1, and the iDP is a dopaminergic neuronal lineage-restricted progenitor possessing dopaminergic neuronal-restricted differentiation potential.

2. The iDP of claim 1 , consisting essentially of ectopically expressed Bm2 or a variant thereof, Sox2 or a variant thereof, and Foxa2 or a variant thereof.

3. The iDP of claim 1 , wherein the ectopically expressed genes are expressed from one or more vectors carrying them, or the ectopically expressed proteins are expressed from one or more mRNA encoding them.

4. The iDP of claim 1 , wherein the iDP does not differentiate into a glial cell.

5. The iDP of claim 1 , wherein differentiation of the iDP is independent of morphogens selected from SHH and FGF8.

6. The iDP of claim 1 , wherein the iDP is self-renewable and further comprises ectopically expressed L-Myc.

7. The iDP of claim 6 , wherein the ectopically expressed L-Myc is expressed under the control of doxycycline.

8. The iDP of claim 1 , wherein the somatic cell is a fibroblast.

9. The iDP of claim 8 , wherein the somatic cell is present in vitro.

10. The iDP of claim 1 , wherein the iDP is capable of being administrated to a patient for treating a neurodegenerative disease selected from Parkinson's disease, depression, dementia and schizophrenia.

11. A population of the iDPs of claim 1 , wherein more than 80% or more than 90% of the population is capable of differentiating into dopaminergic neurons.

Assignments (2)
CONFIRMATORY LICENSE Recorded Mar 8, 2017
From: UNIVERSITY OF NEBRASKA MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 041908/0833 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 14, 2017
From: ZHENG, JIALIN; TIAN, CHANGHAI
To: BOARD OF REGENTS OF THE UNIVERSITY OF NEBRASKA; TONGJI UNIVERSITY
Reel/Frame 041252/0905 →
Continuity (2)
Provisional Application 62038914 · Aug 19, 2014
Related Publication 20170268021A1 · Sep 21, 2017