Embryo Formation Flashcards

1
Q

Maternal to zygotic transition (MZT)

A

Period during which zygotic genes are activated and maternal transcripts are cleared

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2
Q

What are the molecules involved in morula compaction?

A
  • E-cadherin

* Occludin

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3
Q

Describe cell-cell adhesion via E-cadherin

A

Extracellular domain is attached to extracellular domain of neighbouring cell
Intracellular domain –> anchored to a and b catenins –> actin cytoskeleton

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4
Q

Describe expression of E-cadherin during embryo development.

A

Expressed from early cleavage

Expression relocated to regions of cell-cell contact at the time of compaction

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5
Q

Describe cell-cell adhesion via occludin

A

occludin –> ZO-1 and ZO-2 –> cingulin –> actin cytoskeleton

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6
Q

Describe JAM=1 expression during embryo development

A

No JAM-1 expression detected until pre-compact 8 cell stage

At the onset of compaction, there is intense JAM-1 expression at the apical poles of blastomeres and contact sites

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7
Q

Describe tight junction biogenesis

A
  • From the pre-compact 8 cell stage to the 16-cell morula stage, the embryo is permeable:
  • Pre-compact 8 cell stage expresses non-adhesive E-cadherin
  • Compact 8 cell stage onwards expresses adhesive E-cadherin. Number of junctional proteins expressed increases as the embryo progresses further.
  • JAM is expressed at the compact 8 cell stage
  • At the early blastocyst stage, junctional proteins are localised at the apical surface of the cells, forming a tight junction. At this point, the embryo is sealed, which is helpful for blastulation
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8
Q

Describe energy metabolism in the pre-implantation embryo

A
  • There is a switch from pyruvate metabolism to glucose metabolism which happens at the time of pre and post-compaction morula stage
  • At the time of compaction (morula stage), the embryo switches from dependence on TCA cycle to glycolysis
  • In the early stages of embryo development, there are high levels of pyruvate and lactate. High ATP:ADP ratio allosterically inhibits PFK enzyme (converts ATP to ADP), limiting flux of glucose through the glycolytic pathway before compaction
  • After compaction, pyruvate energy source is used up and embryo expresses more GLUTs. Reduced ATP:ADP ratio, increase in ADP has a positive allosteric effect on PFK, facilitating higher flux of glucose through glycolytic pathway
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9
Q

Describe expression of glucose transporters during pre-implantation embryo development

A
  • GLUT4 starts to be expressed at the blastocyst stage

* GLUT5 starts to be expressed from the 8 cell stage onwards

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10
Q

What could be used as biomarkers to predict the fate of embryos?

A
  • Glycolysis profile - viable embryos had higher levels of glucose uptake and low levels of glycolysis. too much glycolysis is toxic for the embryos, indicates stress –> non-viable.
  • Oxygen consumption/respiratory activity - higher O2 consumption resulted in pregnancy.
  • Amino acid profile
  • Amino acid depletion - steady increase in amino acid depletion from day 2-3 to morula to blastocyst stage rather than high consumption in cleavage stages = increased viability, reach blastocyst stage
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11
Q

Describe oxygen consumption during embryo development

A

During oviductal development (early embryo stages), the embryo has more O2 supplied to them
During uterine development (post-compaction stage), O2 transport in the embryo decreases

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12
Q

What is the impact of oxygen concentration on mammalian embryo development?

A

5% oxygen (low) improves embryo development - associated with fewer perturbations in global pattern of gene expression
(increased blastocyst formation and cell number)

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13
Q

What is the impact of oxygen concentration on amino acid turnover?

A

Cleavage stage embryos cultured in 20% oxygen (high) - amino acid turnover is higher than those cultured in 5% oxygen
Blastocyst stage embryos cultured in 20% oxygen (low) - amino acid turnover is lower than those cultured in 5% oxygen - high oxygen damages embryos at the blastocyst stage

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14
Q

What is the impact of oxygen concentration on glucose uptake?

A

glucose uptake is reduced in embryos cultured in 20% oxygen –> reduced viability

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15
Q

Give examples of amino acids used as energy sources by the early embryo

A

Glutamine

Aspartate

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16
Q

What are some methods of assessing embryo quality?

A
  • Metabolomic analysis
  • Staining - ratio of ICM:TE low = embryo quality poor. high number of apoptotic cells = embryo quality poor.
  • Time lapse microscopy
17
Q

What are 3 important amino acids made by the embryo during development?

A
  • Glutamine
  • Glycine
  • Alanine
18
Q

Time lapse microscopy

A

Captures images over time, providing a combination of morphological, dynamic and quantitative information about developmental events

19
Q

What information can be gained from time lapse microscopy?

A
  • Time taken for 1st cleavage to occur
  • Regularity in duration of cell cycles
  • Embryo morphology, fragmentation
20
Q

What are some other biomarkers of embryo metabolism that are controversial?

A
  • sHLA-G

* Follicular IL-15 and GM-CSF

21
Q

What can stress in the embryo cause?

A
  • Apoptosis and fragmentation
  • Modified gene expression
  • Modified metabolism