Clonal culture of human pluripotent stem cells
While culture medium and systems have been described that permit the culture and proliferation of human embryonic stem cells in feeder free and animal product free conditions, these conditions will not readily support cloning of an embryonic stem cell culture meaning, at least here, the initiation of a sub-culture using one or a very few originating cells. It has been found here that a class of small molecules that are inhibitors of kinase enzymes will increase the efficiency of cloning of stem cell cultures sufficiently to make such cloning practical in the defined medium and in other media as well.
1. A method of creating a clonal culture of human pluripotent stem cells comprising the steps of:
providing a culture of human pluripotent stem cells in culture in a fibroblast growth factor-containing culture medium in a culture vessel;
selecting a single pluripotent stem cell from the stem cells in culture;
initiating a new culture of pluripotent stem cells with the single pluripotent stem cell in a culture vessel containing an extracellular matrix coating a surface inside the culture vessel and a fibroblast growth factor-containing culture medium, the culture medium including an agent selected to increase the cloning efficiency of the pluripotent stem cell culture relative to a pluripotent stem cell culture that does not contain the agent, the agent being a small molecule having the formula:
wherein R 1 and R 2 can form a cyclic group, or R 1 is H or an alkyl, and R 2 is H or an alkyl, and R 1 is not the same as R 2 unless R 1 and R 2 are part of a cyclic group; and wherein R 3 and R 4 are attached to any atom in the isoquinoline and are a hydrogen or an alkyl; and
culturing the single pluripotent stem cell to create a clonal culture of human pluripotent stem cells.
2. The method as claimed in claim 1 , wherein the agent is a kinase inhibitor.
3. The method as claimed in claim 1 , wherein the agent is a protein kinase A inhibitor, a protein kinase C inhibitor, a protein kinase G inhibitor or a Rho-associated kinase (ROCK) inhibitor.
4. The method as claimed in claim 1 , wherein the agent is selected from the group consisting of
5. A method of creating a clonal culture of human pluripotent stem cells comprising the steps of;
providing a culture of human pluripotent stem cells in culture in a fibroblast growth factor-containing culture medium in a culture vessel;
selecting a single pluripotent stem cell from the stem cells in culture;
initiating a new culture of pluripotent stem cells with the single pluripotent stem cell in a culture vessel containing an extracellular matrix coating a surface inside the culture vessel and a fibroblast growth factor-containing culture medium, the culture medium including an agent selected to increase the cloning efficiency of the pluripotent stem cell culture relative to a pluripotent stem cell culture that does not contain the agent, the agent being selected from the group consisting of
culturing the single pluripotent stem cell to create a clonal culture of human pluripotent stem cells.
6. A human pluripotent stem cell culture comprising:
a culture vessel containing an extracellular matrix coating a surface inside the culture vessel;
a fibroblast growth factor-containing culture medium;
human pluripotent stem cells growing in the fibroblast growth factor-containing culture medium; and
the fibroblast growth factor-containing culture medium containing an agent selected to increase the cloning efficiency of the stem cell culture relative to a stem cell culture that does not contain the agent, the agent being a kinase inhibitor having the formula:
wherein R 1 and R 2 can form a cyclic group, or R 1 is H or an alkyl, and R 2 is H or an alkyl, and R 1 is not the same as R 2 unless R 1 and R 2 form a cyclic group; and wherein R 3 and R 4 are attached to any atom in the isoquinoline and are a hydrogen or an alkyl.
7. A human pluripotent stem cell culture of claim 6 , wherein the agent is selected from the group consisting of
8. An improvement in a fibroblast growth factor-containing medium in which to culture relative to a stem cell culture medium that does not contain the agent human pluripotent stem cells, the improvement comprising including in the medium an agent selected to increase the cloning efficiency of the stem cell culture, wherein the agent is selected from the group consisting of