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Bi 1 “Drugs and the Brain” Lecture 24 Tuesday, May 23, 2006 Cell cycle, Stem Cells, and Stem Cell Therapy (Thanks to Prof David Anderson for some of the slides) 1 Bi 1 in the next 2 weeks (for undergraduates) Tuesday, May 23. Lecture 26. Cycle Cycle / Stem Cells Problem Set 8 posted. Parkinson’s disease, stem cells, cell cycle Thursday, May 25. Lecture 27. Evolution 1: Molecular Biology. Thursday-Friday, May 25/26. Section meetings as usual. 5:30 Fri Undergrad BBQ Monday, 5/28. Memorial day, no lecture. Tuesday, 5/29. Lecture 28. Evolution 2. The eye. Problem Set 8 due, 11 AM (seniors too) Thursday 6/1. Lecture 29. Last lecture. Evolution 3. Voyages to the Galapagos; the Physiology of Diving. Final exam review Session: 4 PM here, 119 Kerckhoff Thursday 6/1: Final Exam posted Thursday-Friday 6/1-2 Section meetings as usual Friday 6/9. Final exam due 4:30 PM, Bi 1 closet. for the “official word”, see http://www.its.caltech.edu/~bi1/schedule.html 2 Overview of the cell cycle mitosis gap2 (growth2) mammals 24 h gap1 (growth1) yeast 90 min DNA synthesis based on Little Alberts 19-2 © Garland publishing 3 ”Checkpoints” in the cell cycle based on Little Alberts 18-4 4 © Garland publishing Cdk-cyclin complexes govern progression through the checkpoints (simplified view) These proteins are regulated by 1. Kinase-mediated protein phosphorylation (lecture 14); 2. Ubiquitin-mediated proteolysis (lecture 18). a cyclin-dependent kinase (Cdk): phosphorylates many proteins a cyclin: required for kinase activity P Cdk is itself activated by phosphorylation based on Little Alberts 18-7 © Garland publishing Cdk is deactivated by dephosphorylation when the cyclin is destroyed 5 Cdk-cyclin complex is a “mitosis promoting factor” (MPF) also assayed by injecting into frog eggs based on Little Alberts 18-6 © Garland publishing 6 Yeast uses the same Cdk at both checkpoints; mammals use different Cdks at each checkpoint. A yeast whose own Cdk is mutated, and therefore fails to divide, can be rescued by expressing human Cdk. the cell cycle machinery arose > 109 y ago ! Lectures 27, 28, 29 will concern evolution. Little Alberts 18-13 © Garland publishing 7 Some growth factors instruct cells to continue in the cell cycle 8 9 onco-, cancer But many molecules in this pathway can mutate to form oncogenes inactive growth factor receptor activated growth factor receptor abnormally active growth factor receptor abnormally active GPCR based on Little Alberts 1st edition 18-23 © Garland publishing 10 A final stage, cell death, is also regulated by multiple mechanisms dying nerve cells Some autistic people have abnormally large brains. There is speculation about insufficient cell death. Little Alberts 18-27 © Garland publishing 11 After Several Cell Cycle Divisions, most Cells Eventually Differentiate . . . 12 . . . But Undifferentiated Cells Called “Stem Cells” Persist in some Adult Tissues Embryo Persistent Undifferentiated Cell Adult 13 Stem Cells can Both Differentiate and Continue Cycling (Self-Renewal) 14 Stem Cells can Generate Several Types of Differentiated Cells D1 D2 ........ Dn 15 As noted in slide 13, Stem Cells Exist in both Embryos and Adults Embryonic Stem Cells Adult Stem Cells Newly formed tissues and organs Natural turnover Regeneration 16 Isolating Stem Cells Piece of Tissue Multipotency Self-renewal 17 Stem Cells are Sometimes Purified Using Specific Cell Surface Markers 18 Early example: a “Tissue-Specific” Stem Cell for the Blood and Immune System . . . 19 . . . now we can work with Neural Stem Cells Neural Tube Peripheral neurons and related cells, some muscles CNS Neurons Some types of glia 20 “Regenerative Medicine”: Stem Cells for Repair of Diseased or Injured Tissue? •Blood •Skin •Pancreas •Heart •Liver •Muscle •Brain 21 Cell Replacement Therapy for Neurodegenerative Disease? Parkinson’s Huntington’s Alzheimer’s Amyotrophic lateral sclerosis (ALS) Spinal cord injury Multiple sclerosis (MS) 22 Theoretical example: Cell Transplant Therapy for Parkinson’s Disease 23 Approaches to Stem Cell Therapies For Neurological Disease 1. Transplantation of neural stem cells Donor: fetal brain Advantages Disadvantages What Organism Should Supply the Stem Cells? People Lawyers Animals 25 True Embryonic Stem Cells Can Generate All Cell Types in the Body Tissue-specific stem cells: Germ-line 26 1998: Human ES Cells 27 Contribution of ES Cells to Internal Tissues in Chimeras (Carrying a GFP reporter gene) Chimeric embryo reveals ES-derived GFP-expressing cells 28 Approaches to Stem Cell Therapies For Neurological Disease 2. Transplantation of ES cell-derived neural stem cells 3. Advantages Donor: blastocyst Disadvantages Material comes from IVF clinics; access to aborted fetal tissue not required • Risk of graft vs. host disease; Immunosuppression needed Cloning: 1960’s 30 1997: Dolly, a Cloned Mammal Success rate: 1/277. Dolly is now dead 31 Step 1: The Egg’s Nucleus is Removed (= the Egg is Enucleated) 32 Step 2: A Somatic Nucleus is Injected into the Enucleated Egg 33 Step 3: The Injected Egg is Chemically Activated to Induce Nuclear Division 34 Step 5: The Embryoid is Cultured Until a Blastocyst Develops 35 Step 6: The Inner Cell Mass (A) is Removed from the Blastocyst and Cultured 36 Step 7: Individual Human ES Colonies are Isolated 37 Approaches to Stem Cell Therapies For Neurological Disease 3. Transplantation of ES cell-derived neural stem cells Donor: nuclear transfer “somatic cell nuclear transfer” aka “therapeutic cloning” Advantages Disadvantages -economics Pending legislation to criminalize procedure Some Unsolved Questions in Cloning and Stem Cell Research • Why is producing ES cells by nuclear transplantation so inefficient? • What events are involved in reprogramming a somatic cell nucleus to regain pluripotency? • How do we differentiate ES cells along particular lineages? • How do we move from cell differentiation, to organogenesis? 39 2004: California Takes the Lead with Prop 71 • Establishes the California Institute of Regenerative Medicine (CIRM) • Allocates $3 billion over a 10-year period for stem cell research • Provides funding for research with hES lines not fundable with federal funds – ie, all hES lines generated after 8/9/01 • Funding can be used for somatic cell nuclear transplantation 40 Neurogenesis: new neurons are born in the adult rat and mouse brain . . . but we don’t know whether it happens in primate brain. Hippocampus Gage, F.H. (2000) Science 287:1433-1438 Olfactory Bulb 41 Approaches to Stem Cell Therapies For Neurological Disease 4. Transplantation of adult brain cells Donor: adult brain Advantages Disadvantages 42 Adult Stem Cell Plasticity: Bone Marrow-Derived Stem Cells for Brain Would Provide Stem Cell Therapy without Transplantation ? 43 Approaches to Stem Cell Therapies For Neurological Disease 5. In vivo mobilization of endogenous brain stem cells with growth factors Advantages Disadvantages • Not all brain regions may respond to the factors Bi 1 “Drugs and the Brain” Lecture 24 Tuesday, May 23, 2006 Cell cycle, Stem Cells, and Stem Cell Therapy 45 Adult Stem Cell Therapies for Neurological Disease? • Adult neural stem cells • Adult bone-marrow-derived stem cells • In vivo mobilization 46 Mouse ES Cells Differentiated into Motor Neurons Wichterle et al. (2002) Cell 110:385 47 Does Any of This Have a Prayer of Working? I SEE CELLS IN YOUR BRAIN! HOW LONG DO I HAVE TO WAIT?! 48 We Need More Basic Research on Stem Cells ? 49