Week 2 Flashcards

5 sets of 2

1
Q

The second week of development is characterized by what?

What are they?

A

(5) Sets of two

  1. (2) Trophoblasts
  2. (2) Embryoblasts
  3. (2) Cavities
  4. (2) Yolk Sacs
  5. (2) Layers of Extraembryonic Mesoderm
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2
Q

What causes the Trophoblast to differentiate?
What are the resulting cells called?

A
  1. During Implantation, the trophoblast comes in direct contact with the endometrium, causing proliferation and invasion into the endometrium, thereby imbedding it self and giving rise to a multi-layered (stratified) mass
  2. The Trophoblast in direct contact with (and invading) the Endometrium is now called Syncytiotrophoblasts, while the trophoblasts not in direct contact with the endometrium are now referred to as Cytotrophoblasts
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3
Q

What is the roll of the Syncytiotrophoblast and Cytotrophoblast?

A

Syncytiotrophoblast; Invades the endometrium, allowing the embryo to embed itself into the uterine lining

Cytotrophoblasts; remain as a single layer of cells, continuing to divide and produce new cells to be assimilated into the growing syncytiotrophoblast

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4
Q

Once fully embedded into the uterine lining, what temporarily marks the site of implantation?

A

The Coagulation Plug temporarily marks the site of implantation until the epithelial cells reseal

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5
Q

The Embryoblast reorganizes into what (2) Distinct layers?
What is this process called?

A

Bilaminar Germ Disc formation;

Epiblast (primary ectoderm): The layer of cells in direct contact with the cytotrophoblast

Hypoblast (Primary Endoderm): The layer of cells closer to the abembryonic pole

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6
Q

What are the (2) Cavities?

A

Amniotic Cavity & Chorionic cavity (EE Coelom)

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7
Q

How does the Amniotic cavity form?

A

Fluid accumulates in the center of the Epiblast tissue, following Bilaminar Disc Formation, splitting the Epiblast into (2) sections;

Epiblast cells in contact with the cytotrophoblasts become Amnioblasts, while cells in contact with the hypoblast retain their name and function.

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8
Q

How does the Chorionic Cavity form?

A

Fluid accumulation in the Extraembryonic Mesoderm layer, splitting it (near completely) in two sections, with the exception of the Connecting Stalk near the Amnioblasts

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9
Q

What are the (2) Yolk sacs that form?

A

Primary Yolk sac (exocoelomic cavity) & Secondary Yolk Sac (Definitive Yolk Sac)

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10
Q

How does the Primary Yolk Sac form?

A

Hypoblast Cells lining the Blastocyst cavity begin migrating along the inside of the Cytotrophoblast, forming Heusers Membrane.

Once migration is complete, Hypoblast cells completely encircles the Blastocyst Cavity, now called the Primary Yolk Sac

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11
Q

How does the Secondary (Definitive) Yolk Sac form?

A

Following the formation of the Chorionic Cavity, a 2nd migration of Hypoblast cells pushes a portion of the Primary Yolk Sac across the Chorionic cavity, pinched off, and becomes buried within the Extraembryonic Mesoderm.

The Yolk Sac remaining associated with the Bilaminar Germ Disc is considered the Definitive Yolk Sac

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12
Q

What are the roles of the Definitive Yolk Sac?

A
  • Major site of Hematopoeisis
  • Thought to be involved in Nutrient Metabolism
  • Generation of Primordial Germ cells (PGC)
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13
Q

What process gives rise to (2) layers of Extraembryonic Mesoderm?

A

Chorionic Cavity formation leads to (technically speaking) (3) layers of extraembryonic Mesoderm.

EEM between the Chorionic cavity & EE Endoderm contributes to the Primary Yolk Sac

EEM between the Chorionic Cavity and Cytotrophoblast contributes to the Placenta

EEM between the Amnioblasts & Cytotrophoblast forms the Connecting Stalk (and future umbilical cord)

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14
Q

What begins to form on Day 9 within the Syncytiotrophoblast, to facilitate Waste/Nutrient exchange with the mother?

What simultaneously occurs in the mother?

How are they physically connected?

A
  1. Trophoblastic Lacunae (Vacuoles)
  2. Maternal Uterine Capillaries expand, forming Maternal Sinusoids
  3. Sinusoids connect to the Lacunae via Anastomoses, connecting bloodflow
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15
Q

When approximately does Primary Stem Villi form?

How do they form?

A
  1. Day 11-13
  2. EE Mesoderm induces the Cytotrophoblast to proliferate and migrate into the overlying Syncytiotrophoblast, forming Primary Stem Villi
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16
Q

What must occur to the Primary Stem villi to convert them into Secondary Stem Villi?

A

Day 16: EE Mesoderm penetrates the core of the Primary Stem Villi

17
Q

What must occur to give rise to Tertiary Stem Villi?

A

Blood vessel formation within the EE Mesenchyme.

18
Q

What is a Hydatidiform Mole?

A

A mass of vesicular tissue (resembling a bunch of grapes) that results from the build up of fluid and swelling of placental villi, due to failed embryo development (which normally absorbs the fluid).

* The trophoblast will stil form a placenta (and placental villi) regardless of failed embryo development.

19
Q

What are the (2) types of Hydatidiform moles and how do they differ?

A
  1. Complete & Partial Hyditidiform Moles
  2. Complete H. Moles contain no Embryo at all, while Partial H. Moles contain an embryo which is underdeveloped.
20
Q

How do Complete Hyditidiform Moles occur?

A

These occur when the Ovulated egg lacks it’s own Pronucleus & receives (2) Paternal Genomes through either

Dispermic Fertilization

Monospermic Fertilization and subsequent mitosis of the Male Pronucleus w/o Cleavage

21
Q

How do Partial Hyditidiform Moles occur?

A

Occurs when a Normal egg is fertilized by either

Two Sperm (Dispermic)

One abnormal Diploid sperm (2N)

22
Q

While Hydatidiform Moles can be aborted spontaneously, a __&__ (surgical procedure) may be necessary to prevent what disease?

A
  1. D&C procedure: Dilation of the Cervix, followed by suction and curettage
  2. Gestational Trophoblastic Disease
23
Q

Persistent Trophoblastic Disease will occur if what occurs?

What are they two outcomes?

A
  1. Persistent Trophoblastic Disease will occur if any residual trophoblastic tissue remains following a D&C
  2. The remnants can grow into a benign tumor (Non-Life-threatening) or into Invasive Moles or Metastatic Choriocarcinoma (May be Life-threatening)
24
Q

What are the symptoms experienced by women with Gestational Trophoblastic Diseases?

A
  1. Vaginal Bleeding
  2. Severe Morning sickness (due to high levels of hCG secreted by trophoblastic tissues)
25
How are women with these symptoms diagnosed?
1. Check hCG levels in the blood and urine following a miscarriage or D&C procedure to ensure they return to baseline 2. Confirm with Ultrasound \*Patients are advised to avoid pregnancy for about 1 year.
26
What does Hydatidiform Moles suggest about the Paternal & Maternal Genome? What is this model called?
**Genomic Imprinting** **Paternal Genome**: Important for the development of the _Trophoblast_ (& Placenta) **Maternal Genome**: Important for the development of the _Embryoblast_
27
How is Genomic Imprinting accomplished (biochemically speaking)
Zygotic genes are labeled as Maternal or Paternal via Methylation (or lack there of)
28
Which (2) Syndromes exemplify Genomic Imprinting
Prader-Willi Syndrome & Angelman Syndrome Both syndromes aries from a deletion of a specific region of Chr 15
29
The Prader-Willi gene is switched off (methylated) on the (Maternal / Paternal) copy. The Angelman gene is switched off (methylated) on the (Maternal / Paternal) copy.
1. The Prader-Willi gene is methylated on the Maternal Copy 2. The Angelman gene is methylated on the Paternal Copy
30
If normal development requires intact copies of the Prader-Willi & Angelman genes; A deletion of the Prader-Willi gene on the (Maternal / Paternal) copy will result in the syndrome A deletion of the Angelman gene on the (Maternal / Paternal) copy will result in the syndrome
1. A deletion of the Paternal Prader-Willi gene will result in the Prader-Willi Syndrome 2. A deletion of the Maternal Angelman gene will result in Angelman Syndrome
31
What are the symptoms seen in Prader-Willi Syndrome?
* Poor muscle Tone * Weak crying * Difficulty feeding at first but subsequently becomes obsessed with food and develops obesity problems
32
What are the symptoms seen in patients with Angleman syndrome?
* Mental retardation * Poor speech * stiff, uncoordinated limbs
33
In uniparental Disomy; Inheriting both copies from which parent will result in Prader-Willi Syndrome?
Maternal: Inheriting both copies of Maternal Chr 15 will result in neither gene being accessible due to methylation.
34
In uniparental Disomy; Inheriting both copies from which parent will result in Angelman Syndrome?
Paternal: Inheriting both copies of Paternal Chr 15 will result in neither gene being accessible due to methylation.