IP Library Granted Patent US 12,018,286
Granted Patent B2
US 12,018,286 · App. 17/012,651 · Granted Jun 25, 2024

Generating human podocyte cells

Inventors: Oliver Wessely (Cleveland Heights, OH); Uyen Wessely (Cleveland Heights, OH); Jan Jensen (Shaker Heights, OH); Michael Bukys (Cleveland, OH)
Assignee: The Cleveland Clinic Foundation
C12N5/0684C12N2500/90C12N2501/155C12N2501/415C12N2501/42C12N2501/999C12N2506/25
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Quick Facts
Patent No.
US 12,018,286
App. No.
17/012,651
Granted
Jun 25, 2024
Kind
B2
Abstract

Provided herein are compositions, systems, kits, and methods for generating human podocyte cells by contacting human nephron progenitor cells with an FGFR pathway inhibitor, a BMP pathway inhibitor, and a WNT pathway inhibitor. In certain embodiments, the nephron progenitor cells are further contacted with at least one factor selected from: BMP4, BMP7, lysophosphatidic acid, and gamma-secretase inhibitor XX. In certain embodiments, the contacting the nephron progenitor cells is performed under serum-free conditions.

Claims (14)

1. A method of generating podocyte cells comprising:

a) contacting a population of nephron progenitor cells with an FGFR pathway inhibitor, a BMP pathway inhibitor, a γ secretase inhibitor BMP4, BMP7, and a WNT pathway inhibitor; and

b) culturing at least a portion of said population of nephron progenitor cells such that a population of podocyte cells is generated.

2. The method of claim 1 , wherein said podocytes express the following genes: WT1, MAFB, and FOXC2.

3. The method of claim 1 , wherein said nephron progenitor cells are not exposed to serum during said culturing or during said contacting.

4. The method of claim 1 , wherein said FGFR pathway inhibitor comprises BGJ398.

5. The method of claim 1 , wherein said BMP pathway inhibitor comprise LDN193189.

6. The method of claim 1 , wherein said WNT pathway inhibitor comprises IWP2.

7. The method of claim 1 , further comprising, prior to step b), contacting said nephron progenitor cells with lysophosphatidic acid (LPA).

8. The method of claim 1 , wherein said γ secretase inhibitor is gamma-secretase inhibitor XX.

9. The method of claim 1 , wherein said BMP pathway inhibitor is selected from the group consisting of: DMIH1, DMH2, Dorsopmorphin, K02288, LDN214117, ML347, and Noggin.

10. The method of claim 1 , wherein said FGFR pathway inhibitor is selected from the group consisting of: PD0325901, Arctigenin, PD184352, PD198306, PD334581, SL 327, U0126, a MEK inhibitor, a FGFR inhibitor, a MAPK inhibitor, MEK162, GSK1120212, PD325901, CI-1040, TAK-733, Selumetinib and XL518.

11. The method of claim 1 , wherein said culturing is conducted for 1-5 days or 2-4 days.

12. The method of claim 1 , wherein said nephron progenitor cells are not exposed to a transforming growth factor beta (TGFβ) pathway agonist during said culturing or during said contacting.

Assignments (2)
CONFIRMATORY LICENSE Recorded Oct 17, 2023
From: CLEVELAND CLINIC FOUNDATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 065257/0132 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 8, 2021
From: WESSELY, OLIVER; WESSELY, UYEN; JANSEN, JAN; BUKYS, MICHAEL
To: THE CLEVELAND CLINIC FOUNDATION
Reel/Frame 055183/0381 →
Continuity (2)
Provisional Application 62899582 · Sep 12, 2019
Related Publication 20210079357A1 · Mar 18, 2021