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Stem Cells SG
Stem Cells
| Question | Answer |
|---|---|
| Are stem cells terminally differentiated? | No. It has the potential to differentiate |
| What is the name of the cell that stem cells are in? | Niche cell |
| What can stem cells give rise to? | Another stem cell or a progenitor cell |
| What is invariant asymmetry? | If a signal is present it will divide asymmetrically and give rise to one lineage of differentiated cells |
| What is population asymmetry? | Some randomness is involved. It can renew itself and give rise to one lineage or differentiate into cells from one lineage or another lineage. Randomness more choices involved |
| What is meant by embryo cells are totipotent? | Can give rise to all cells and make the extraembryonic membranes and placenta |
| What does pluripotent mean? | It can give rise to all somatic cells |
| What does multipotent mean? | It can give rise to several different lineages |
| What does unipotent mean? | It can give rise to one lineage |
| The more developed primitive cells are what is more likely? | More likely it can give rise to tumors |
| What is the benefits and cons to using a progenitor cell that is regionally specified? | Benefit: Fewer steps and lose fewer cells. Cons: Doesn't divide as well |
| What is meant by the later in lineage a cell is the less myologenic it is? | Too few cells but more reliabel to get what you want. |
| What is the marker form cardiac myocytes? | Cardiac myosin |
| What is the marker for smoothe muscle cells? | Smooth muscle actin |
| What is the marker for endothelial cells? | Von Willebrand Factor |
| Name problems with using stem cells on sick people? | Sometimes not reproducible in different laboratories. It is hard to take a sick person and isolate cells from them and wait for them to mature |
| Why can you get stem cells from embryos? | Because the inner cell mass gives rise to all tissues in the body (Pluripotent but not stem cells yet) |
| Name things the ectoderm gives rise to | Skin, nerves and eye tissues |
| Name things the mesoderm gives rise to | Bone, blood and muscles |
| Name things that endoderm give rise to | Lungs, liver, lining of the gut |
| What was the feeder layer when stem cells were being made in the lab? | Feeder layer was mice cells that were putting nutrients into the culture |
| What is the major problem with using embryo stem cells? | They have a high capacity for producing tumors when injected in adult recipient |
| Describe therapeutic cloning | Pull out the nucleus of eff from embryo and replace it with a somatic cell from the adult. Then do electrofusion. Now the embryo has the same kind of genotype except for mitochondrail DNA that comes from the egg. |
| Why might therapeutic cloning be useful? | To overcome the problem that the genotype from the embryo might not be compatible with the adult it is bing injected into |
| Name some alternatives to using embryo stem cells | Somatic stem cell, Human ES cell and Trans differentiation |
| Name some transcription factors that are necessary for pluripotency | Oct-4, Sox-2 and NANOG |
| What defines pluripotency? | The little circuit created by factors that can inhibit or cause the synthesis of another factor in the group |
| What is a characteristic transcription factor across all animals? | NKX 2.5 |
| Are iPS (induced Pluripotent stem cells)cells totipotent? | No because they can't make extraembryonic membranes |
| How can you make iPS cells? | By taking somatic cells and placing reprogramming genes in the culture |
| What does tetraploid complementation mean? | You have embryos that are mutated |
| In the experiment involving the pancreas they tried to induced what cells to secrete insulin? | beta cells |
| What are the problems associated with iPS cells? | They can induce an immune response and may still bear oncogenioic property even after differentiated |
| What was different about the experiment involving direct reprogramming of fibroblast? | They didn't send them through a stem cell stage. |