Methods of reprogramming renal cells

US9770469B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9770469-B2
Application numberUS-201314027256-A
CountryUS
Kind codeB2
Filing dateSep 16, 2013
Priority dateFeb 26, 2009
Publication dateSep 26, 2017
Grant dateSep 26, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method of reprogramming a differentiated renal cell towards a progenitor phenotype is disclosed. The method comprises up-regulating in the differentiated renal cell an expression of at least one pluripotency associated gene and/or at least one renal stem cell associated gene, thereby reprogramming the differentiated renal cell towards a progenitor phenotype. Cell populations generated thereby and uses thereof are also disclosed.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of reprogramming a differentiated adult epithelial renal cell to a cell having a progenitor phenotype, the method comprising transfecting the differentiated renal cell with a nucleic acid construct comprising a nucleic acid sequence encoding Oct4, thereby reprogramming the differentiated adult epithelial renal cell to a cell having a progenitor phenotype, and wherein said progenitor phenotype comprises Six2 and/or Osr1 expression and cell clonogenicity. 2. The method of claim 1 , further comprising isolating the cell having the progenitor phenotype. 3. The method of claim 1 , further comprising contacting the differentiated adult epithelial renal cell with at least one chromatin modifying agent. 4. The method of claim 1 , wherein said differentiated adult epithelial renal cell is a human differentiated adult epithelial renal cell. 5. The method of claim 3 , wherein said chromatin modifying agent is selected from the group consisting of valporic acid, 5-aza-2′-deoxycytidine and TSA. 6. A method of reprogramming a differentiated adult epithelial renal cell to a cell having a renal progenitor phenotype, the method comprising transfecting the differentiated adult epithelial renal cell with a nucleic acid construct comprising a nucleic acid sequence encoding at least one polypeptide which comprises Six2, thereby reprogramming the differentiated renal cell to a cell having a renal progenitor phenotype. 7. The method of claim 6 , wherein said at least one polypeptide comprises Osr1 and Six2.

Assignees

Inventors

Classifications

  • Serum-free medium, which may still contain naturally-sourced components · CPC title

  • from renal cells, from cells of the urinary tract · CPC title

  • for animal cells · CPC title

  • Modulators of histone acetylation · CPC title

  • Artificially induced pluripotent stem cells, e.g. iPS · CPC title

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What does patent US9770469B2 cover?
A method of reprogramming a differentiated renal cell towards a progenitor phenotype is disclosed. The method comprises up-regulating in the differentiated renal cell an expression of at least one pluripotency associated gene and/or at least one renal stem cell associated gene, thereby reprogramming the differentiated renal cell towards a progenitor phenotype. Cell populations generated thereby…
Who is the assignee on this patent?
Tel Hashomer Medical Res Infrastructure & Services Ltd
What technology area does this patent fall under?
Primary CPC classification A61K35/22. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Sep 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).