Mesenchymal cells derived from human embryonic stem cells
First Claim
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1. A set of two isolated cell populations for generating human mesodermal cell populations, consisting of:
- a first cell population comprising pluripotent stem (pPS) cells isolated from a human blastocyst, and a second cell population that proliferates in culture, comprising at least ˜
30% pPS derived mesenchymal cells, identifiable by the criteria that they express either CD29 or CD44.
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Abstract
This invention provides populations of mesenchymal cells obtained from pluripotent stem cells by differentiating them ex vivo. Multipotent mesenchymal cells can in turn be differentiated into more specialized cell types such as osteoblasts, with properties that make them suitable for reconstituting musculoskeletal cell function in an individual. The compositions, methods, and techniques described in this disclosure can be used for a variety of commercially important diagnostic, drug screening, and therapeutic applications.
27 Citations
14 Claims
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1. A set of two isolated cell populations for generating human mesodermal cell populations, consisting of:
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a first cell population comprising pluripotent stem (pPS) cells isolated from a human blastocyst, and a second cell population that proliferates in culture, comprising at least ˜
30% pPS derived mesenchymal cells, identifiable by the criteria that they express either CD29 or CD44.
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2. The set of cell populations of claim 1, wherein the mesenchymal cells express at least 3 of the following:
- CD166 (ALCAM), CD29, CD44, GATA-4, and STRO-1.
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3. The set of cell populations of claim 1, wherein the mesenchymal cells express either osteonectin or osteocalcin, and either type 1 collagen or vimentin.
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4. The set of cell populations of claim 1, wherein the mesenchymal cells have increased alkaline phosphatase activity when cultured with bone morphogenic protein.
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5. The set of cell populations of claim 1, wherein medium preconditioned by the mesenchymal cells causes proliferation of human embryonic stem cells without differentiation.
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6. The set of cell populations of claim 1, wherein the osteoblasts or osteoblast precursors form an extracellular matrix comprising calcium when cultured in vitro.
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7. The set of cell populations of claim 1, wherein the second cell population has been obtained by culturing the pPS cells so as to form embryoid bodies, plating the embryoid bodies onto a solid substrate, and then selecting cells having said criteria.
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8. The set of cell populations of claim 1, wherein the second cell population has been genetically altered to express telomerase reverse transcriptase.
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9. The set of cell populations of claim 1, wherein the pPS cells are a line of human embryonic stem cells.
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10. The human cell line designated HEF1.
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11. A method of screening a compound for mesenchymal cell toxicity or modulation, comprising combining the compound with the second cell population of claim 1, and determining any mesenchymal cell toxicity or modulation resulting from the compound.
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12. The method of claim 11, comprising determining whether the compound is toxic to the cell population.
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13. The method of claim 11, comprising determining whether the compound affects proliferation of the cell population.
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14. The method of claim 11, comprising determining whether the compound causes the second cell population to form progeny comprising at least ˜
- 10% osteoblasts, chondrocytes, hematopoietic cells, myoblasts, or adipocytes.
Specification