2 - CELLS Flashcards

1
Q

What is an antigen?

A

A foreign body that stimulates the body’s immune response leading to the production of an antibody

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2
Q

Describe phagocytosis of pathogens (non-specific immune response)

A
  • phagocyte is attracted to/detects foreign antigen on pathogen
  • engulfs pathogen and forms a phagosome around it
  • lysosomes fuse with phagosome and release lysozymes
  • lysozymes hydrolyse and digest pathgoen
  • phagocyte absorbs its products and presents its antigen on the outside of its membrane to stimulate the specific immune response
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3
Q

Describe the response of B lymphocytes to a foreign antigen (the humoral
response)

A
  • antigen binds to specific B cell receptors
  • specific B cell cloned rapidly by mitosis
  • B cell differentiates into plasma and memory cells
  • plasma cells secrete specific antibodies into the blood
  • antibodies stimulate agglutination
  • phagocytosis occurs
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4
Q

Describe the response of T lymphocytes to a foreign antigen (the cellular
response)

A
  • After phagocytosis, phagocyte displays antigen on outside of its membrane
  • Specific T cells bind to antigen, then clones rapidly by mitosis
  • Produces specialised T cells:
    Killer T cells - hydrolyse pathogen
    Helper T cells - stimulate antibody response
    Memory T cells - remember antigen for next exposure
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5
Q

What is clonal selection?

A

When a specific T cell becomes activated after binding to its antigen

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6
Q

What is clonal expansion?

A

When a T cell divides by mitosis to produce clones

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7
Q

What’s the difference between primary and secondary immune response?

A
  • antibodies are released much quicker the second time around because the immune system recognises the antigen
  • It so quick that the pathogen is suppressed before you are able to experience symptoms because you are immune to the pathogen
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8
Q

What is a vaccine?

A
  • Injection of antigens from attenuated (dead or weakened) pathogens
  • Stimulating formation of memory cells
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9
Q

Describe the replication of HIV in helper T cells

A
  1. HIV attachment proteins bind to receptors on helper T cell
  2. Lipid envelope fuses with cell-surface membrane of T cell and releases capsid into cell
  3. Capsid uncoats, releasing RNA and reverse transcriptase
  4. Reverse transcriptase (enzyme) converts the 2 single strands of RNA to DNA
  5. Viral DNA incorporated into helper T cell DNA
  6. DNA transcribed into HIV mRNA then the HIV mRNA is translated into new HIV proteins forming Viral proteins
  7. Virus particles assembled and released from cell (via budding)
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10
Q

How do you use/set up a light microscope?

A
  • clip prepared slide onto stage
  • select lowest powered objective lens
  • use course adjustment knob to bring stage up to just under the objective lens
  • look down the eyepiece and move the coarse knob down until the image becomes more in focus
  • adjust the fine adjustment knob until you get a clear image
  • ## if you need to see the slide with a higher magnification then change to a higher objective lens
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11
Q

What are the 2 types of electron microscope?

A
  • transmission
  • scanning
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12
Q

How does a transmission electron microscope work?

A
  • they use electromagnets to transmit a beam of electrons through the specimen
  • denser parts absorb more electrons making them appear darker on the image while less dense areas are lighter, forming an image
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13
Q

How does a scanning electron microscope work?

A
  • they scan a beam of electrons across a specimen
  • this knocks off electrons off the cells surface and these electrons come together to form an image
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14
Q

What are artefacts?

A

Visible details that aren’t part of the specimen being observed
- eg dust or fingerprints when looking through a microscope

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15
Q

State the advantages and disadvantages of the 2 types of electron microscope

A

Transmission:
✅ - high resolution so can be used to see small objects
❌ - 2D images
❌ - can only be used of non living specimens as they are placed in a vacuum

Scanning:
✅ - can be used on thick specimen that are 3D
❌ - gives lower resolution images than TEMs
❌ - can only be used on non living

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16
Q

Describe how viruses replicate

A
  1. The virus uses its attachment proteins to bind to specific receptor proteins on host cells.
  2. The virus injects its viral DNA or RNA into the host cell.
  3. The virus uses the host cell’s machinery and resources, such as enzymes and ribosomes, to replicate viral particles.
  4. New viral particles are released from the host cell.
17
Q

Describe the process of mitosis

A

I:
- DNA replicates semi conservatively to form 2 identical chromatids
- Cell growth
P:
- chromosomes condense becoming shorter/thicker and appear as sister chromatids held by a centromere
- nuclear envelope breaks down
- centrioles move to opposite poles forming spindle network
M:
- spindle fibres attach to chromosomes by their centromeres and move chromosomes to equator
A:
- spindle fibres shorten and contract
- centromere divides pulling chromatids to opposite poles of cell
T:
- chromosomes uncoil becoming longer and thinner
- nuclear envelope reforms
C:
- two identical daughter cells formed

18
Q

Describe how prokaryotic cells replicate

A
  1. Replication of circular DNA
    2 replication of plasmids
  2. division of cytoplasm to produce 2 daughter cells
19
Q

Describe how cancer treatments control rate of cell division

A
  • some disrupts spindle fibre activity/formation
    -> spindle fibres pull chromatids to opposite poles, so prevents/slows mitosis
  • some prevent DNA replication in interphase
    -> so canes make 2 copies of each chromosome
20
Q

Explain the importance of mitosis in the life of an organism

A
  • growth of multicellular organisms by increasing cell number
  • replacing cells to repair damaged tissues
  • asexual reproduction
21
Q

Describe how tumours and cancers form

A

Mutations in DNA/genes controlling mitosis can lead to uncontrolled cell division
Mass of abnormal cells formed (tumour)

22
Q

What are the 2 types of tumour?

A

Malignant - cancerous (can spread)
Benign - non cancerous

23
Q

Describe the structure and function of the nucleus

A
  • Stores DNA for polynucleotide production
  • produces mRNA from DNA for protein synthesis
  • DNA stored as chromosomes in the nucleus
24
Q

How many daughter cells does binary fission produce?

A

2

25
Q

Explain how you would use cell fractionation and ultracentrifugation to separate cell components

A
  1. homogenise tissue (blends cells gently to disrupt cell membrane, breaking open cell and releasing organelles)
  2. place in a cold, isotonic, buffered solution
    - cold to slow down enzyme activity (so organelles not broken down)
    - isotonic so water doesn’t move in or out of organelles by osmosis (so they don’t burst)
    - buffered to keep pH constant (so enzymes don’t denature)
  3. Filter homogenate (to remove unwanted debris eg. whole cells)
  4. Ultracentrifugation to separate organelles in order of density/mass
    - centrifuge homogenate in a tube a high speed
    - remove pellet containing heaviest organelle
    - respin supernatant at a higher speed
    - repeat at increasing speeds until all organelles separated out
    Order of heaviest to lightest organelles:
    Nuclei -> chloroplasts/mitochondria -> lysosomes -> ER -> ribosomes
26
Q

Describe how to convert into different units (e.g meters to millimeters etc)

A

X1000⬇️ Metre ⬆️ /1000
X1000⬇️ Millimetre ⬆️ /1000
X1000⬇️ Micrometer ⬆️ /1000
X1000⬇️ Nanometre ⬆️ /1000