Summary: Introduction To Stemcells
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1 Day 1: Embryonic stem cells, pluripotency and reprogramming
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1.1 From embryo to embryonic stem cells (Roelen)
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Oocyte (egg cell)
Large immotile cell. -
Which tissues can a pluripotent stem cells differentiate towards?
Endoderm, mesoderm, germ cells (NO yolk sack and placenta). -
1.3 Reprogramming, induced pluripotent stem cells and application (Jaenisch)
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Sporadic, late onset diseases
- Common and therefore medically the most relevant
- Lack a clear genetic basis
- Generally display a more subtle phenotype
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Therapeutic applications of iPSCs?
- Can be used to generate desired cell types for individual patients
- Can be used to model disease, facilitating drug discovery.
- Patient-derived iPSCs could potentially be corrected ex vivo to be transplanted back into the patient to replenish lost/damaged cells.
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Major issue with iPSC-derived cells
They often remain poorly matured -
How can we manipulate the human (epi)genome to rectify disease-causing variants?
- Gene targeting
- CRISPR/Cas9-bases gene editing
- Gene targeting
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CRISPR/Cas9-based gene editing
- Efficient method to generate/correct mutations, based on HR on nonhomologous end joining (NHEJ)
- Involves a guide RNA (for homology search) and Cas9 (cleaves DNA).
- Can introduce multiple genetic modifications at a time.
- Efficient and rapid technique.
- Does not require extensive
selection process.
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Two main types of gene therapies?
- Somatic therapy
- Germline therapy
- Somatic therapy
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2 Day 2: Epigenetics and flavors of pluripotency
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2.1 Principles of epigenetics in stem cells (Lopes)
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Association of ATP-dependent complexes
- E.g. polycomb and trithorax proteins
- Change the distance between nucleosomes, which results in altered accessibility
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Association with non-coding RNAs
- Binding of non-coding RNAs to the DNA blocks transcription
- E.g. X-inactive specific transcript (XIST) and TSIX
- XIST and TSIX can neutralize each other
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