Mapa mental
Normal and Abnormal Brain Development
Conteúdo do mapa
Normal and Abnormal Brain Development
Cell Proliferation
- Non-Embryonic Cell Cycle
- G1: mitogens signal the start, G1 checkpoint, restriction point
- S phase: unwinds into 2, ATCG = DNA per daughter cell
- G2: new cell organelles, checkpoint, high p53 = apoptosis
- Mitosis: organelles, split, QA checkpoint = daughter cells
- Either G0 or G1
- In mature organism neurones are permanently/semi G0
- Either G0 or G1
- Mitosis: organelles, split, QA checkpoint = daughter cells
- G2: new cell organelles, checkpoint, high p53 = apoptosis
- S phase: unwinds into 2, ATCG = DNA per daughter cell
- Mitogens (>50: broad or specific)
- G1: mitogens signal the start, G1 checkpoint, restriction point
- Non-Embryonic Cell Cycle
Cell Differentiation
- Gene Expression
- Transcription: RNA polymerase makes a RNA copy of DNA - cytoplasm as mRNA
- Transcription factors block or induce RNA polymerase
- Translation: GM of mRNA into a protein by ribosomes in RER
- Transcription factors block or induce RNA polymerase
- Transcription: RNA polymerase makes a RNA copy of DNA - cytoplasm as mRNA
- Gene Expression
When proteins go wrong...
- Alzheimer's: Faulty APP & Tau
- Autism: Cereblon (thalidomide exposure and foetal development) - 20-24 days
- Rett Syndrome - MECP2 gene (Guy et al., 2007: mice, 4 weeks- loss of neurological symptoms
- Autism: Cereblon (thalidomide exposure and foetal development) - 20-24 days
- Alzheimer's: Faulty APP & Tau
Axon Growth
- Growth cones extend extensions called filipodia (Stirling & Dunlop, 1995)
- Molecular signals attract or repel - guide the axons direction/length
- Growth cones extend extensions called filipodia (Stirling & Dunlop, 1995)
How do growth cones know where to go?
- Chemoaffinity Hypothesis: releases a specific chemical, axon attracted to the target
- Blueprint Hypothesis: chemical trails that axons follow
- By cell adhesion molecules (CAMS)- Van Vactor 1998
- Fasiculation: subsequent axons follow pioneer growth cones
- Not explain in vitro
- Transplanted reach their target (Lance-Jones & Landmesser, 1980)
- Topographic gradient hypothesis: one sheet to another by relative positions on original sheet, 2 intersecting gradients
- Anterior-posterior, medial-lateral
- Molecular gradients (retina/tectum) Holt & Harris, 1998
- Preserved across sheets in neurodevelopment (Reh & Constantine-Paton, 1984)
- Following lesions = spread out to targets
- Sperry (1943): optic nerve in frogs
- In vitro: rat VC & LGN (Yamamoto et al., 1989)
- Stoeckli & Landmesser (1989) chemical have been identified
- Transplanted- incorrect cells (Whitelaw & Hollyday, 1983)
- Axon growth indirect (Batiani et al., 1985)
- Insufficient number of genes to code individually
- Blueprint Hypothesis: chemical trails that axons follow
- Chemoaffinity Hypothesis: releases a specific chemical, axon attracted to the target
Postnatal Development
- Most neurones developed by 7th mo
- Brain volume 4x birth to adulthood (Johnson, 1997)
- Due to synaptogenesis, myelination, dendritic arborisation
Synaptogenesis (new synapses)
- Dependent on glial cells
- Increase after both, uneven in cortical (Huttenlocher, 1994)
- PFC max at 24mo
- PV & AC large increase at 4, max at 7mo
- Synapse loss in V1 density at 5yo
- Mirrors functional development (auditory, wenicke, broca)
- How do synapses in the brain know where to grow?
- Mediated by glutamate and NMDA receptor
- Activation of NDMA receptor initiates synaptogenesis by downstream products (Ghiani et al., 2007)
- Heightened NMDA receptor activity = influx of calcium = LTP of synapse
- Cell differentiation via gene expression
- Heightened NMDA receptor activity = influx of calcium = LTP of synapse
- Activation of NDMA receptor initiates synaptogenesis by downstream products (Ghiani et al., 2007)
- Mediated by glutamate and NMDA receptor
Fragile X Syndrome
- Non expression of the FMRP protein controlled by FRM1 gene (Verheij et al., 1993)
- Thin long post synaptic spines like in neo-cortical development (Comery et al., 1997)
- Bred knock out mice - FMR1 gene disrupted = dendrites longer, dendritic spine density is increased
Informações
- Descrição
- Ageing Brain (PS3061) Mapa Mental sobre Normal and Abnormal Brain Development, criado por Eleni Blakemore em 28-04-2017.
- Criado por
- Eleni Blakemore
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