Red Blood Corpuscles Flashcards

1
Q

Describe the structure of erythrocytes

A

No organelles (including nucleus) –> increased volume for hemoglobin
Shaped as biconcave discs
7.5 µm in diameter

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2
Q

What is Mean Corpuscular Volume (MCV)?

A

MCV measures the average size of your red blood cells
MCV ≈ 90 μm3

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3
Q

What is Mean Corpuscular Hemoglobin (MCH)?

A

Average amount of hemoglobin in each RBC
MCH ≈ 30 picograms

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4
Q

What is Mean Corpuscular Hemoglobin Concentration (MCHC)?

A

Measure of the average concentration of hemoglobin inside a single RBC.
MCHC ≈ 33%

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5
Q

Why are RBCs biconcave?

A

Increases its flexibility (allows it to fit into capillaries and gaps between endothelial cells in splenic sinusoids)
Increase SA for diffusion of gases

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6
Q

What are RBC cytoskeletal membrane proteins?

A

Proteins forming a lattice network that is anchored to the inner surface of the RBC plasma membrane.

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7
Q

What is the function of the RBC cytoskeletal proteins?

A

Allows RBCs to bend while passing through the circulation

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8
Q

What proteins form the RBC cytoskeleton?

A

Spectrin (most abundant) and actin form the cytoskeleton
Ankyrin, band 3, band 4.1 and band 4.2 bind the cytoskeletal lattice to the plasma membrane

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9
Q

What are some disorders caused by defects in cytoskeletal membrane proteins?

A

Hereditary Spherocytosis (HS)
Hereditary Elliptocytosis (HE)

HS is caused by mutations in RBC cytoskeletal proteins; it affects their spherical shape, leading to cytoskeletal instabilities and frequent hemolysis (which causes hemolytic anemia)

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10
Q

What is Sickle Cell Disease (SCD)?

A

Hemoglobin S forms a rod inside the RBCs, making them form a sickle shape.
Because they are not flexible, they accumulate in small blood vessels, blocking the flow of blood causing oxygen deprivation and pain crises.

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11
Q

What is the average RBC count per mm3?

A

Men: 4.7 – 6.1 million cells /mm3 or (µl)
Women: 4.2 – 5.4 million cells/mm3

Average number: 5 million/mm3

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12
Q

What are the functions of RBCs?

A
  1. Contain hemoglobin for transporting respiratory gases and acid-base buffering.
  2. Contain carbonic anhydrase which catalyses the revesible reaction between CO2 and H2O to form H2CO3 which facilitates the transport of CO2.
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13
Q

What are the types of chains which can form hemoglobin?

A

Alpha chains, Beta chains, Gamma chains, and Delta chains

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14
Q

What is the composition of adult hemoglobin?

A

Adult hemoglobin (hemoglobin A1) is formed from two alpha and two beta chains

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15
Q

What is the composition of fetal hemoglobin?

A

Fetal hemoglobin (hemoglobin F) is formed from two alpha and two gamma chains

Binds to oxygen better than A1 enabling oxygen extracting from the mother’s bloodstream

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16
Q

When does hemoglobin switch from F to A1?

A

At around 4 months, gamma chain production begins diminishing.
Hemoglobin F switches to Hemoglobin A1 at around 6 months.
At 8 months, the switch is virtually complete

Production of gamma chains never ceases entirely, so ~1% of hemoglobin is hemoglobin F

17
Q

What is hemoglobin A2?

A

Hemoglobin A2 is formed from two alpha and two delta chains and forms ~1-2% of total hemoglobin

18
Q

Describe how the hemoglobin chains vary throughout life.

A
19
Q

How many oxygen molecules can one hemoglobin molecule bind to?

A

Each hemoglobin molecule can bind reversibly to four oxygen molecules

20
Q

What are the normal hemoglobin values?

A

Male: 13–18 gram/100 ml
Females: 12–16 gram/100 ml

Average: 15 gram/100 ml

21
Q

What are some RBC disorders?

A

Anemia: Decrease oxygen delivery to tissues causing anemia hypoxia
Polycythemia: Increase blood viscosity causing cause heart failure