Modelling of Neuropsychiatric Diseases Flashcards

1
Q

Disadvantages of mice

A

Lack of translational significance
No higher brain function, no polygenic variants
Disease-relevant cell types differ to humans, genetic differences
Human neocortex much more complex
Cell cycle times of neuronal progenitors are much larger

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2
Q

Other used models

A

Post mortem tissue
Imaging for structural & functional studies
GWAS (Associate traits to genes)
Primate models
iPSC

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3
Q

phNPCs

A

Primary human neuroal precursor cells
From fetal postmortem cortex
Aggregated in neurospheres, differentiated into neurons & glia = In vivo fetal cortical development up to mid gestation

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4
Q

iPSC

A

From primary human cell –> iPSC –> NPC –> Differentiated neuronal cells
Low genetic stability (CNV or SNV), epigenetic markers rest during reprogramming
Study causal links between disease variants & cellular phenotypes

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5
Q

iNeurons

A

Induced neurons
Directly from primary human cell by combination of induction factors
Retain many epigenetic markers but do no allow featl brain development study

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6
Q

Patterned 2D culture

A

Small-molecule patterning & TF induction on cellular level
Increased enriched uniform populations of targeted cell types, scalable & reproducible
Do not fully capture in vivo development

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7
Q

Patterned 3D culture

A

Small-molecule patterning on brain structure level
Capture architecture & cellular environment, interaction of different cell types
But: Much longer differentiation time & less scalable

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8
Q

Unguided organoid differentiation

A

Potential to develop into multiple neural structures
Used to observe patterning, cell-cell interactions through region, synapse formation
Composition inconsistent across experiments
Vary in size & cell type composition different regional identities

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9
Q

Guided differentiation

A

Small molecules to promote neural induction
Manipulation of relevant signaling pathways –> Different structures

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10
Q

Cortical organoids

A

Day 0: SMAD inhibition
Day6: FGF2, EGF
Day 25: BDNF, NT3

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11
Q

Strengths of organoids

A

Indistinguishable compendium of cell types, following similar developmental trajectories with a degree of organoid-to-organoid variability comparable to human brains
Consistent reproducibility if derived from different stem cell lines

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12
Q

Genome-wide transition mapping (TMAP)

A

Assess extent of overlap between in vivo cortical development & in vitro differentiation

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13
Q

Assembloids

A

Organoids generated by spatially organizing multiple cell types = Tissue function
Region-specific organoid differentiation –> 3D assembly of spheroids –> Multiregion
Long distance projections possible & interneuron migration
Use to assemble a multi-synaptic circuit in vitro

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