US2022265728A1PendingUtilityA1
Parthenogenic activation of human oocytes for the production of human embryonic stem cells
Est. expiryOct 21, 2025(expired)· nominal 20-yr term from priority
A61P 21/00A61P 25/00C12N 9/12A61P 17/02A61P 1/16A61P 1/00C12N 2500/14C12Y 207/11001C12N 5/0606C12N 2500/02A61K 35/35A61P 25/28A61P 3/10A61K 35/26C12N 5/0609C12N 15/8776A61P 25/16A61P 31/18C12N 2502/1323A61K 35/34A61P 9/00A61P 13/02C12N 2517/10A61P 13/12A61P 35/00C12N 2501/70A61P 21/04A61P 27/02A61K 35/32A61K 35/30A61K 35/39C12N 2501/999A61P 19/08C12N 5/00C12N 5/0602A61K 35/36A61P 19/04A61P 43/00A61P 25/14A61K 35/15
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Abstract
Methods of producing human stem cells are disclosed for parthenogenetically activating human oocytes by manipulation of O2 tension, including manipulation of Ca2+ under high O2 tension and contacting oocytes with serine threonine kinase inhibitors under low O2 tension, isolating inner cell masses (ICMs) from the activated oocytes, and culturing the cells of the isolated ICMs under high O2 tension. Moreover, methods are described for the production of stems cells from activated oocytes in the absence of non-human animal products, including the use of human feeder cells/products for culturing ICM/stem cells. Stem cells produced by the disclosed methods are also described.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A differentiated cell derived from a stem cell obtained from a parthenogenetically activated oocyte from a human donor.
2 . The differentiated cell of claim 1 , wherein the differentiated cell is histocompatible with the oocyte donor.
3 . The differentiated cell of claim 1 , wherein the differentiated cell is selected from the group consisting of a neuronal cell, cardiac cell, smooth muscle cell, striated muscle cell, endothelial cell, osteoblast, oligodendrocyte, hematopoietic cell, adipose cell, stromal cell, chondrocyte, astrocyte, dendritic cell, keratinocyte, pancreatic islet, lymphoid precursor cell, mast cell, mesodermal cell, and endodermal cell.
4 . The differentiated cell of claim 3 , wherein the cell expresses neurofiliment 68, NCAM, beta III-tubulin, GFAP, or a combination thereof.
5 . The differentiated cell of claim 3 , wherein the cell expresses alpha-actinin, desmin, or a combination thereof.
6 . The differentiated cell of claim 3 , wherein the cell expresses PECAM-1, VE-Cadherin, or a combination thereof.
7 . The differentiated cell of claim 3 , wherein the cell expresses alpha-fetoprotein.
8 . The differentiated cell of claim 3 , wherein the cell comprises homoplasmic mitochondrial DNA (mtDNA).Cited by (0)
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