Passage timing calculation device, passage timing calculation method, and recording medium for recording program
US-2024352397-A1 · Oct 24, 2024 · US
US9562218B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9562218-B2 |
| Application number | US-201615178190-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 9, 2016 |
| Priority date | Dec 5, 2011 |
| Publication date | Feb 7, 2017 |
| Grant date | Feb 7, 2017 |
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The present invention relates in part to methods for producing tissue-specific cells from patient samples, and to tissue-specific cells produced using these methods. Methods for reprogramming cells using RNA are disclosed. Therapeutics comprising cells produced using these methods are also disclosed.
Opening claim text (preview).
What is claimed is: 1. A method for reprogramming a cell to a less differentiated state comprising: (a) providing a non-pluripotent cell; (b) culturing the cell in a medium containing albumin and ingredients that support reprogramming of the cell to a less differentiated state, wherein the albumin is treated with an ion-exchange resin or charcoal; (c) transfecting the cell with a synthetic RNA molecule, wherein the RNA molecule encoding one or more reprogramming factor(s) selected from the group consisting of Oct4 protein, Sox2 protein, Klf4 protein, c-Myc protein, I-Myc protein, Tert protein, Nanog protein, and Lin28 protein, wherein the transfecting results in the cell expressing the one or more reprogramming factor(s) which reprograms the cell to a less differentiated state. 2. The method of claim 1 , wherein the non-pluripotent cell is derived from a biopsy. 3. The method of claim 1 , wherein the non-pluripotent cell is harvested from a human subject. 4. The method of claim 2 , wherein the non-pluripotent cell is harvested from a dermal punch biopsy sample. 5. The method of claim 1 , wherein the non-pluripotent cell is a skin cell. 6. The method of claim 1 , wherein the albumin is treated with sodium octanoate. 7. The method of claim 1 , wherein the albumin is brought to a temperature of at least 40° C. 8. The method of claim 1 , wherein the albumin is recombinant. 9. The method of claim 1 , further comprising contacting the cell with at least one member of the group: poly-L-lysine, poly-L-ornithine, RGD peptide, fibronectin, vitronectin, collagen, and laminin. 10. The method of claim 1 , wherein the synthetic RNA molecule contains at least one of a pseudouridine or a 5-methylcytidine residue.
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