General Flashcards

1
Q

Describe the process of light microscopy

A

Preserve sample using formalin to prevent rotting
Embed tissue in melted paraffin, so that when it is cooled it sets hard allowing it to be thinly sliced by a microtome
Stain tissue using haematoxylin (stains nucleus blue) and/ or eosin (to stain cytoplasm& extracellular matrix pink).

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2
Q

What are the benefits of using a frozen section under a light microscope? How is the sample frozen and cut?

A

Sample is frozen in a cryostat and then cut using a microtome. This technique is much faster but lower quality. Can be done mid surgery.

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3
Q

What is electron microscopy? What are two types?

A

Using electrons to see higher resolution images. TEM is electrons in a vacume and using the proportion of electrons that pass through the sample as an indicator of where dense structures are. SEM looks at the electrons bouncing off the structures, and creates a 3D image of the structures surface

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4
Q

How does an ultrasound scanner work?

A

Piezo electrical crystal expands when voltage applied, so voltage applied and removed very quickly causing disturbances to air around it (ultra sound). The piezo electrical crystal also detects ultrasound waves hitting it and creates a voltage. The waves will return when they hit dense structures and so it can detect structures within the body.

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5
Q

Why is there a need to find a balance between short and long wavelengths when using ultrasound scanners?

A
short= higher resolution but low penetrance
long= deep penetrance, but high energy (bad for baby) and low resolution
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6
Q

What main way are intestinal epithelial cells integrated in the lateral domain? (side by side)

A

Tight junctions:

plasma membranes fuse so molecules cannot pass between them.

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7
Q

What cell junction is found next to tight junctions? What is their role and where are they found?

A

Desmosomes:
Each cell has a hemidesmosome which bind to form a desmosome. They form strong adhesions to to strengthen tight junctions and resist physical stress. They’re found lots in the skin.

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8
Q

Describe the structure, role and example of gap junctions

A

Connexons form junctions between cells in which substances can move through and so adjacent cells can directly communicate. They’re found in the cilia cells to help them move together.

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9
Q

How are cells integrated into connective tissue (basal domain)

A

Either:

  • Hemidesmosomes: attach to integrin which attach the cells cytoskeleton to the extracellular matrix in the connective tissue.
  • Focal adhesions: They anchor actin filaments within the cell to the basement membrane via an integrin which spans the plasma membrane to the extracellular matrix. They play a prominent role in cell movement, such as migration of epithelial cells in cell movement.
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10
Q

Describe 5 methods of cell communication

A
  • Gap junctions
  • autocrine: signal released binds to receptor on its own cell
  • paracrine: local communication, signals to nearby cells (histamine)
  • endocrine: long range communications, hormones travel in blood from endocrine gland to target tissues
  • synaptic: one neurone to another using neurotransmitters
  • Neurocrine: neurone releases neurotransmitter into blood which communicates with cells- anterior pituitary, posterior pituitary and adrenal medulla
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11
Q

How is a tissue isolated?

A

Seperate from connective tissue using collagenase, then culture

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12
Q

What are the issues with cell culturing?

A

They behave differantly within a culture
Cells stop growing in culture when they touch eachother
Cells have a limited life span in culture

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13
Q

What are the two methods of cell death?

A

Apoptosis- contolled, purposeful cell death

Necrosis- death due to distruption/ injury/ toxins/ lack of nutrients

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14
Q

describe the process of apoptosis

A

BCl-2 is inactivated by inhibitor release.
Enzymes digest components and fragment DNA (catabolism).
Capases digest specific proteins in nucleus and cytoskeleton
Cell is repackaged for safe removal, chromatin condense and cell shrinks then fragments
Fragments of cell digested by phagocytosis

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15
Q

Describe the process of Necrosis

A

Cell looses functional control
Na-K pump stops
Water diffuses in, cell swells and bursts
Cytotoxic components (Ca2+) spill out the membrane inducting tissue damage and inflammation

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16
Q

State 3 example of stable, renewing and static cells

A

static: CNS, cardiac and smooth muscle
stable: fibroblasts, endothilium, smooth muscle cells
renewing: blood, skin & gut epithilium

17
Q

Sate the 4 basic types of tissue

A
  • Epithelial
  • Muscle
  • Nerve
  • `Connective tissue
18
Q

State the 6 types of specialised connective tissue

A
  • adipose
  • lymphatic
  • blood
  • Haemopoietic
  • Cartilage
  • Bone
19
Q

Will water move from Hypertonic to Hypotonic solution?

A

No, Hypertonic has lots of solution (HYPER), hypotonic has low solute conc, so water moves from hypo to hyper to create equal water potentials

20
Q

What is the difference between osmolality and oncotic pressure?

A

Osmolality is the conc of particles in a solution (290 mOsm/kg is normal)
Oncotic pressure is a measure of the concentration of proteins (eg mainly albumin) in a solution

21
Q

Why does the Na- K pump stop cells bursting?

A

Normally water would move in because the cells of have lots of solutes- proteins ect. But Na - K pump removes 3na and only puts one K in so overal loss of ions of lower osmolality.

22
Q

what is normal pH?

A

7.4

23
Q

What is normal body temp?

A

36.5-37.2 C

24
Q

Below what temp is hypothermia?

A

35C

25
Q

Describe the fluid volumes of a avg human (70kg)

A

60% water- 42L
2/3 of this is in cells (intracellular) this must stay constant for survival of cells
1/3 is extracellular (14L)
of this:
11L (80%) is interstitial (between cells) this is variable and will increase/ decrease depending on need by vascular system and cells
3L (20%) is in the blood plasma

26
Q

How much blood do you have in body? How much can you loose before death? How much is a unit of blood?

A

You have 5L of circulating blood volume, of this 2L is RBCs (40%)
A unit of blood is 300ml, but this is isolated from a 500ml sample taken- they remove platelets, WBCs and some plasma
You therefor have about 6 units of blood (2,000ml/300ml= 6.2)
Loosing 3 units will kill you

27
Q

Describe creation and removal of tissue fluid

A
  • Oncotic/ osmotic pressure in capillary remains constant as proteins do not move out capillaries.
  • at arteriole end, there is high hydrostatic pressure, and so this over comes inward osmotic pressure
  • at venous end, lower blood volume means lower hydrostatic pressure than oncotic pressure, and so net movement of fluid back in
  • excess tissue fluid removed by lymph