GN 2.5.2 Flashcards

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1
Q

What are CB-SCs?

A

Cord blood stem cells - can be taken at time of birth, may be useful in therapeutic treatments later in life

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2
Q

In regards to cell lineage, technology has given us the ability to induce stem cell production. Describe this reverse process.

A

Differentiated cells -> progenitors/precursor cells -> Stem cells

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3
Q

How many embryos were donated to research from a pool of how many from embryos at embryo banks?

A

11,000 excess embryos of 400,000 frozen embryos

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4
Q

What are some promising purposes of stem cell research?

A

ID drug targets and test potential therapeutics, toxic testing, tissue for transplantation, study cell differentiation

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5
Q

Without the presence of extra-embryonic cells, what do ES cells lack?

A

They lack the ability to form a body plan

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6
Q

What are some functions of adult stem cells?

A

Respond to demands of growth or repair, proper tissue organization that is influenced by molecular restraints

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7
Q

Describe the process of somatic cell nuclear transfer.

A

The nucleus of a stem cell is removed. Then, a somatic cell with its nucleus is fused into the stem cell. Then, the cell stimulated into the division process. Then, the inner cell mass of the blastocyst is removed to create a culture of pluripotent embryonic stem cells.

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8
Q

What type of stem cell is known to migrate to different tissues then become different types of stem cells?

A

HSCs

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9
Q

What are some of the signaling pathways that influence the way a HSCs respond to its environment?

A

Notch, Wnt, Opn Ang-1

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10
Q

From where are embryonic stem cells derived?

A

5 day-old human embryos created during IVF before specialized tissues of the body begin to form. These can then be grown laterally in the primitive embryonic state indefinitely in culture.

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11
Q

At this point in time, what are some of the possible treatment usages of ES cells in mouse models?

A

Severe immune deficiency, diabetes, parkinson’s dz, spinal injury, demyelenation, MI

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12
Q

What type of signals must be present to cause ES cells to uniformly differentiate into mature stem cells?

A

Commitment signals and specific signals for growth and differentiation

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13
Q

What newer technology might allow us to sidestep or avoid some of the ethical implications of SCNT?

A

iPSC

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14
Q

When ES cells are injected subdermally into mice, what happens?

A

Teratoma

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15
Q

What are some of the challenges of regenerative medicine and transplantation therapy?

A

Prod of req’d cell type in sufficient #s and pure form, what cell to transplant, delivery and proper integration, probs of tissue/immune rejection, immunogenic effects of grafts

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16
Q

What is Somatic Cell Nuclear Transfer?

A

Combines cloning methods w/ embryonic stem cell tech to produce cells which are custom made for patient.

17
Q

Describe some of the advantage/disadvantages of using mature or early stem cells.

A

Insert chart.

18
Q

Define the three types of developmental capacity (toti-, pluri-, and multipotency) and provide examples of each?

A

Totipotency: ability of cell to give rise to all cells of an organism, embryonic and extraembryonic tissue. Ex: zygote Pluripotency: ability of cell to give rise to all cells of embryo and subsequently adult tissue Ex: embryonic stem cells Mulitipotency: ability of cell to give rise to different cell types of a given lineage. Ex: adult stem cells

19
Q

What is the hierarchy of stem cells?

A

Totipotent -> pluripotent -> multipotent -> unipotent

20
Q

Think of a medical condition that would benefit from SCNT treatments.

A

Type I DM

21
Q

From which blastocyst cell mass are the ES Cells derived?

A

Inner cell mass, then grown as cultured pluripotent stem cells (Image)