Evolutionary Biology 8: Comparative development 3 Flashcards

1
Q

How is body axis patterning established?

A

Early differentiating cells collectively called ‘Organiser’ region

Organiser cells generate signals that instruct the development of neighbouring cells

Triggers differentiation of correct cell types -> correct tissue types in correct spatial locations

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2
Q

What cell changes are important for gastrulation-related rearrangements? What are they all controlled by?

A

Cells can:

  • change shape
  • change adhesion between one another
  • divide or stop dividing
  • migrate
  • undergo apoptosis

All controlled by changes in gene expression

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3
Q

What is ‘epithelium’ in embryos?

A

Epithelium:
Sheets or tubes of tightly connected cells
(connected via tight junctions, gap junctions, desmosomes) that are attached to a basement membrane

  • No extracellular matrix between cells
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4
Q

What is ‘Mesenchyme’ in embryos?

A

Mesenchyme:
Cells that are physically separated from one another but are loosely connected by large amounts of extracellular matrix (which keeps cells physically separated)

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5
Q

Can cells transition between epithelial and mesenchymal states? How?

A

Yes - Through changes in cell adhesion and cell shape

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6
Q

Differential cell affinity is important why? How is the affinity mediated?

A

Differential cell affinity important for developmental process
-> changes affinity for extracellular interactions, allows changes in behaviour e.g. epithelial to mesenchyme

  • Mediated by adhesion proteins; expression of different adhesions proteins can change drastically which governs interactions
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7
Q

How does cell migration arise? Differences in mesenchymal and epithelial migration?

A

Arises from combination of cell motility and guidance (along the write path)

Epithelial: Orchestrated by cells at leading edge, cells behind pulled passively

Mesenchymal: Cells migrate as individuals

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8
Q

Four steps of cell migration?

A

1) Cell polarises
- external signal causes shape change via cytoskeletal rearrangements. Leading + trailing edge is well defined

2) Cell extend leading edge
- filopodia or lamellopodia form from actin polymerisation

3) Leading edge forms adhesions with extracellular substrate (via Integrins)
- Contraction of actin filaments generates force to pull cell forward

4) As leading edge extends, stretch activated calcium channels open on trailing edge -> activates proteases which degrade adhesion points at trailing end -> cell move forward

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9
Q

What are integrins and what are their function?

A

Cell adhesion proteins used during migration

  • act as receptors for extracellular matrix (ECM) proteins, weakly associate and connect to cytoskeleton
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10
Q

6 basic processes of gastrulation rearrangement

A
Ingression
Invagination
Involution
Delamination
Epiboly
Convergent extension
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11
Q

Summarise ingression + steps

A

Cells migrate as mesenchyme into embryo interior:

  • Epithelial to mesenchyme transition
  • Cells lose adhesion to epithelial sheet + polarise
  • Squeeze out of epithelium + migrate as individuals to interior
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12
Q

Summarise invagination

A

Epithelial sheet of cells folds inwards to form a pocket that points to interior of embryo

  • often starting point for migration of cells (such as mesoderm) into embryo
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13
Q

Summarise involution

A

Multi-layered cell sheets begins to roll into interior of embryo

-> previously external cells fold in and become internal

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14
Q

Summarise delamination + steps

A

Similar to ingression: epithelial to mesenchymal transition
- cells arrange into new sheet once migrated

  • Single continuous sheet splits into multiple sheets
  • New sheet delaminates into interior of embryo

Marks gastrulation in humans + birds

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15
Q

Summarise Epiboly

A

Movement of epithelial sheets - spread as a unit to enclose the inner layers of the embryo

  • Ectoderm often undergoes epiboly to cover whole surface of the embryo
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16
Q

Summarise convergent extension

A

Cell sheet narrows in one direction and expands in another

  • used to establish body plan