FORM & FUNCTION (Subcellular Organelles) Flashcards

1
Q

nucleus

A

-usually one
-some cells have multiple (muscle) or none due to development (RBC)
-basophilic
-euchromatin (EC) and heterochromatin (HC)
-nucleolus
-active cells will have more EC and nucleoli

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2
Q

euchromatin

A

-appears lighter
-less coiled
-DNA more exposed

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3
Q

heterochromatin

A

-appears darker
-more coiled
-DNA less exposed

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4
Q

nucleolus

A

-region where rRNA is made for ribosome synthesis
-darker spots within the nucleus

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5
Q

Mitochondria

A

-primary organelle that produces energy (ATP)
-also metabolizes fatty acids
-visible appearance gives you a clue of it’s function (cristae or tubular projections)

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6
Q

mitochondria cristae

A

-energy producing
-inner folding structure

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7
Q

mitochondria tubular projections

A

-lipid producing (ex. steroids)
-tubular looking

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8
Q

endoplasmic reticulum

A

-extensive network of membranes arranged in flattened sacs
-rough ER: with ribosomes attached
-smooth ER: no ribosomes attached

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9
Q

ribosomes

A

-make proteins (Requires ATP)
-made from rRNA and proteins (basophilic)
-many free ribosomes=polyribosomes

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10
Q

2 pathways for protein synthesis depending on their function

A
  1. Proteins that function in the cytosol and have no modification (synthesized by free ribosomes)
  2. Proteins that function at specific locations (membrane, organell or outside the cell)
    >synthesized by ribosomes on rER, packaged in vesicles and often modified by Golgi apparatus
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11
Q

differential staining of free ribosomes as a diagnostic tool

A

-mature RBC have no subcellular organelles, filled with Hb=no polyribosomes
-reticulocyte (immature RBC) still contains polyribosomes (normally present in 1% in circulation)
>more basophilic

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12
Q

Golgi apparatus structure

A
  1. Stacked membrane
  2. Cis face
  3. Trans face
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13
Q

stacked membrane

A

-composed of a series of flattened, stacked pouches

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14
Q

cis face

A

-receiving side
-closest to the ER
-receives materials from ER for modification

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15
Q

trans face

A

-shipping side
-oriented toward the PM
-sends modified products to their final destinations

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16
Q

Golgi apparatus functions

A
  1. Chemical modification
  2. Packing and storage
17
Q

chemical modification (golgi)

A

-contains enzymes to chemically modify nasent proteins
Ex. glycosylation, sulfation, phosphorylation

18
Q

packing and storage (golgi)

A

-initiates packing, concentration and storage of secretory products
-prepares them for transportation to specific locations

19
Q

golgi staining

A

-primarily composed of lipids, making it challenging to visualize
-in a basophilic cytoplasm=Golgi may appear faint or unstained

20
Q

cells that make proteins to be secreted

A

-many vesicles/granules
1. Pancreatic acinar cells secrete digestive enzymes
2. Fibroblasts secret collagen
3. Plasma cells secret immunoglobulins

21
Q

secretory granules

A

-can be basophilic or acidophilic
-depends on chemical composition of their contents

22
Q

sER

A

-continuous rER
-synthesizes cholesterol, steroids, CHO, lipid, phospholipids
-detoxifies drugs or toxin (in liver)
-stores Ca2+ (in skeletal muscle)

23
Q

sER are abundant in cells that

A

-are important for synthesis of lipids and metabolism of drugs or toxins (hepatocytes)
-produce steroid hormones (adrenocortical cells, testicular and ovarian cells)

24
Q

steroid-secreting cells

A

-round nuclei
-boxy
-polyhedral shape
-conspicuous and vacuolated cytoplasm
*full of her (white=no dye)

25
Q

lysosome structure

A

-spherical, range in diameter
-appear uniformly granular and electron-dense
-less electron dense ones=heterolysosomes in which digestion of the content is underway
-typically acidic

26
Q

lysosomes function

A
  1. remove obsolete or non-functional proteins, organelles or membranes (ex. autophagosome-> lipofusion)
  2. store hydrolytic enzymes before they are secreted outsided (ex. osteoclasts:remodelling bone)
  3. store hydrolytic enzymes to digest invading pathogens (ex. macrophages and neutrophils function to detect, engulf and destroy pathogens)
27
Q

peroxisome structure

A

-similar to lysosomes
-abundant in liver and proximal convoluted tubules of kidneys
-can appear crytstalline
-contains various enzymes but work at neutral pH

28
Q

peroxisome function

A

-detoxicication
-beta-oxidation of long chain fatty acids
-removes oxygen species (ex. catalase, oxidases, peroxidases) to prevent oxidative damage

29
Q

lipid droplet structure

A

-non membrane bound (hydrophobic) droplets are found in adipocytes, steroid producing cells
-stained orange with a special dye

30
Q

lipid droplet function

A

-lipid storage

31
Q
A