Passage timing calculation device, passage timing calculation method, and recording medium for recording program
US-2024352397-A1 · Oct 24, 2024 · US
US11976303B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11976303-B2 |
| Application number | US-202016994336-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 14, 2020 |
| Priority date | Sep 20, 2013 |
| Publication date | May 7, 2024 |
| Grant date | May 7, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Described herein are methods for enhancing the nuclear reprogramming of somatic cells to become induced pluripotent stem cells. In particular, the methods disclosed herein involve the use of damage-associated molecular pattern molecules (DAMP). In certain embodiments the DAMPs are aluminum compositions such as aluminum hydroxide. Such DAMPs have unexpectedly and surprisingly been found to enhance the nuclear reprogramming efficiency of the reprogramming factors commonly used to induce somatic cells to become induced pluripotent stem cells. Accordingly, this disclosure describes methods of nuclear reprogramming as well as cells obtained from such methods along with therapeutic methods for using such cells for the treatment of disease amendable to treatment by stem cell therapy; as well as kits for such uses.
Opening claim text (preview).
What is claimed is: 1. An in vitro method of enhancing nuclear reprogramming of a human somatic cell, the method comprising: contacting a population of-human somatic cells with (a) an effective dose of an aluminum composition; and (b) a cocktail of reprogramming factors; for a period of time sufficient to reprogram the human somatic cells to induced pluripotent stem cells, wherein the aluminum composition is selected from the group consisting of aluminum hydroxide, aluminum phosphate and aluminum sulfate. 2. The method of claim 1 , wherein the aluminum composition and reprogramming factors are provided sequentially or simultaneously. 3. The method of claim 1 , wherein the aluminum composition is aluminum hydroxide. 4. The method of claim 3 , wherein the effective dose of aluminum hydroxide is about or at least 40-80 micrograms/ml. 5. The method of claim 1 , wherein the aluminum composition is aluminum phosphate. 6. The method of claim 1 , wherein the aluminum composition is aluminum sulfate. 7. The method of claim 1 , wherein the cocktail of reprogramming factors comprises the use of nucleic acids encoding Oct4, Sox2, Lin28, and Nanog, or corresponding cell permeant peptides of the same, and the cells are reprogrammed to pluripotency. 8. The method of claim 1 , wherein the cocktail of reprogramming factors comprises the use of nucleic acids encoding Oct4, Sox2, c-Myc, and KLF4, or corresponding cell permeant peptides of the same, and the cells are reprogrammed to pluripotency. 9. The method of claim 1 , wherein the human somatic cell type is peripheral blood mononuclear cell (PBMC), cord blood mononuclear cells, or fibroblasts. 10. The method of claim 1 , wherein the reprogramming factors are provided as cell permeant proteins. 11. The method of claim 1 , wherein the reprogramming factors are provided as nucleic acids encoding the proteins. 12. The method of claim 1 , resulting in a nuclear reprogramming efficiency wherein the nuclear reprogramming efficiency is greater than if the method was carried out without the aluminum composition. 13. The method of claim 12 wherein the nuclear reprogramming efficiency is about 1 to about 5 fold greater with respect to the expression of at least one key pluripotency marker. 14. The method of claim 12 wherein the nuclear reprogramming efficiency is about 1 to about 5 fold greater with respect to an amount of the induced pluripotent stem cells produced.
Artificially induced pluripotent stem cells, e.g. iPS · CPC title
Oxides; Hydroxides · CPC title
Light metals, i.e. alkali, alkaline earth, Be, Al, Mg · CPC title
Serum-free medium, which may still contain naturally-sourced components · CPC title
from blood or immune system cells · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.