Intro Flashcards

1
Q

What are the three types of cell division?

A

Asymmetrical cell division (ACD), proliferation or differentiation

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2
Q

What is the major thing controlling differentiation?

A

The niche of the stem cell

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3
Q

What is a transit amplifying cell? what is it’s purpose?

A

A comitted stem cell, that rapidly divide before becoming terminally differentiated. They increase stem cell output

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4
Q

What type of cell potency can create a zygote?

A

Totipotent

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5
Q

What are PSCs?

A

Pluripotent stem cells, they give rise to all somatic and germ cell types of the embryo

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6
Q

What type of cells can be derived from the blastocyst?

A

embryonic stem cells

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7
Q

What type of cells can be derived from the epiblast?

A

epiblast stem cells

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8
Q

What are ES cells?

A

embryonic stem cells, they can be derived from blastocysts and cultured

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9
Q

Cells are pluripotent due to…

A

Intracellular signals, transscription factors and chromatin structure (epigenetics)

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10
Q

What are the different stages of pluripotency in a stem cell culture?

A

Totipotent, naive, primed, region-selective primed, multipotent

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11
Q

What are iPS cells?

A

Induced pluripotent stem cells. Can be derived from fibroblasts, hepatocytes, gastric epithelial cells, neural stem cells etc.

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12
Q

What are the applications for pluripotent stem cells?

A

Functional genetics, cell replacement therapies, disease models, drug screening and toxicology

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13
Q

What are the limitations of iPS and ES cells in therapy?

A

Tumorigenicity, immunogenicity, heterogeneity

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14
Q

What are the most used model organisms?

A

c. elegans, drosophila, xenopus, zebrafish and mice

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15
Q

When does gastrulation start in mouse development? when does organogenesis occur?

A

Gastrulation E6.5-7.5
Organogenesis E9.5-13.5

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16
Q

What are the most important familis of signaling molecules?

A

Hedgehog
Wnt
Bone morphogenic protein (BMP)
Fibroblast growth factor (FGF)

17
Q

What are the function of ‘master regulatory’ transcription factors

A

To regulate expression of genes specific for a cell type.
They are able to redirect a cells fate to this cell type

18
Q

What are the two mechanisms of patterning by morphogens?

A

French flag and reaction diffusion

19
Q

Explain the reaction diffusion model of patterning

A

In it’s simplest form it requires only two diffusible molecules: and activator and its inhibitor
Draw: A with arrow to it self and I. I with inhibitory arrow to A.

20
Q

What cellular processes drive morphogenesis?

A

Division, apoptosis, morphology changes, polarization, migration, reorganization, changes in adhesive properties

21
Q

What cell layers are created during gastrulation?

A

Ectoderm (outer layer)
Mesoderm (middle layer)
Endoderm (inner layer)
Germ cells

22
Q

What cells types does the endoderm create?

A

Digestive tube and its associated organs:
Stomach cells
Thyroid cells
Lung cells

23
Q

What cell types does the mesoderm create?

A

Notochord
Bone tissue
Heart
Kidney
Muscles
Connective tissue
Red blood cells
Facial muscle

24
Q

What cell types does the ectoderm create?

A

Epidermal cells of skin
Neurons in the CNS
Neural crest

25
Q

What is the difference between epithelial and mesenchymal cells?

A

the cells of an embryo are either epithelial or mesenchymal. Epithelial cells adhere to one another and can form sheets and tubes, whereas mesenchymal cells often migrate individually and form extensive extracellular matrices that can keep individual cells separate.

26
Q

What is the epithelial-mesenchymal transition?

A

In this transition, a polarized stationary epithelial cell,
which normally interacts with basal lamina through its basal surface, becomes a migratory mesenchymal cell that can invade tissues and help form organs in new places.

27
Q

How are metastasis and the epithelial-mesenchymal transition related?

A

Metastasis is the process in which cancer cells detach from the tumor and migrate to other tissues. This resembles EMT: Cadherins are downregulated, the actin cytoskeleton is reorganized, and the cells secrete enzymes such as metalloproteinases to degrade the basal lamina and mesenchymal extracellularmatrix while also under going cell division

28
Q

What initiates the epithelial-mesenchymal transition?

A

EMT is usually initiated when para-
crine factors from neighboring cells activate gene expression in
the target cells, thereby instructing the target cells to downregulate their cadherins, release their attachment to laminin and other basal lamina components, rearrange their actin cytoskeleton, and secrete new extracellular matrix molecules characteristic of mesenchymal cells.