Erythrocyte Flashcards

1
Q

Average MCV of RBC

A

90fL

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2
Q

Surface of RBC

A

140 um2

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3
Q

The narrowest capillary diameter that RBC can pass through?

A

2.5 times smaller of RBC’s diameter

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4
Q

How does viscosity change when MCHC increase?

A

MCHC increase: Viscosity increase (Deformability decrease)

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5
Q

The percentage of each composition of RBC Membrane?

A

Lipid: 40%
Protein: 50%
Carbohydrate: 10%

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6
Q

What determines ABO group?

A

Carbohydrates

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7
Q

The outer later of Phospholipid membrane

A

Phosphatidyl Choline and Sphingomyelin

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8
Q

Inner layer of Phospholipid Membrane

A

Phosphatidyl Serine 28%

Phosphatidyl Ethanolamine 14%

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9
Q

Where does Cholesterol locate in RBC?

A

Esterified Cholesterol locate between the phospholipid layer

Unesterified Cholesterol locate in the plasma (1:1 with membrane cholesterol)

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10
Q

Name key Integral Proteins

A
  1. Aquaporin 5%
  2. Band 3 (anion transporter) 25%
  3. Glycophorin
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11
Q

Function of Aquaporin

A

Allow water cross freely when osmotic changes

HCO3 and Cl - also across

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12
Q

Active transporters include?

A

Na+ pump keep the ration (1:12 in:out)
K+ pump keep the ration (25:1 in:out)
Ca+ pump keep Ca inside low

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13
Q

What controls function of Ca2+ pump?

A

Calmodulin and Cytoplasmic Ca2+ binding protein.

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14
Q

Function of band3 protein

A
  1. Anion transporter
  2. Interact with skeleton (Ankyrin, Protein 4.2 and secondarily Protein 4.1)
  3. Prevention of surface loss.
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15
Q

What makes RBC negative charge?

A

Sialic acid-rich glycophorins

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16
Q

Structure of Glycophorin

A

Single spanning alpha helix

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17
Q

Function of Glycophorin

A
  1. Glycophorin A & B: Carry blood group

2. Glycophorin C (protein 4.1 and p55): Maintain cell shape

18
Q

Peripheral Protein

Skeleton

A
  1. Spectrin alpha, beta
  2. Ankyrin
  3. Protein 4.1
  4. Pallidin (band 4.2)
19
Q

Spectrin structure

A

2 subunits: alpha and beta entwined to form a dimer

Flexible, rod-like, 100nm

20
Q

Function of Spectrin

A

Make RBC biconcave shape

Bind Ankyrin at C terminus (connect to Band 3) and 4.1 Protein (connect to Glycophorin C)

21
Q

Function of Ankyrin

A

Interacts with:

  • Band 3
  • Spectrin
  • Protein 4.2
22
Q

The cause of Target Cells

A

Incr RBC surface
Decr Hgb content
Decr Osmotic fragility (easy to break) due to the incre of S/V

23
Q

What lead to Target cell?

A

Liver disease (incre Cholesterol/phopholipid)
Thalassemia
Hemoglobin C

24
Q

The cause of Acanthocytes

A

No Apoprotein B

Cholesterol, Triglyceride decre + Sphingomyelin incre.

25
Affect of Acanthocytes
Decre of membrane fluidity
26
What is “Spur cell Anemia”?
Hemolytic anemia in Severe Chronic Liver Disease (CLD)
27
What happens in Spur Cell Anemia?
Free plasma cholesterol (increase) accumulate and equilibrate membrane cholesterol —> Splenic remodeling of RBC: spheroidal, longer projection, poorly deformable.
28
Treatment for Spur cell anemia
Resolve CLD and spenectomy (remove spleen)
29
The cause of Stomatocyte (uniconcave)
1. Hereditary - Dehydration (decre ions and cell volume) - Overhydration (incre ions and cell volume) 2. Acquired - Decre cell membrane - Qualitative change in cell membrane composition
30
Can Stomatocytes be found in healthy people?
Yes, up to 3%
31
What is Spherocytosis and Elliptocytosis?
Disease caused by Membrane Protein Mutation.
32
What proteins mutated in Spherocytosis
``` Autosomal dominant mutations affect: Band 3 Ankyrin Protein 4.2 Spectrin —> Vertical anchorages Disruption. ```
33
What protein affected in Elliptocytosis?
Mutation to Spectrin + protein 4.1 complex | —> Horizontal disruption
34
Affect of Spherocytosis
Results in loss of lipid membrane support —> loss lipid membrane —> decrease ratio surface/volume
35
What is cation concentration in Spherocytes?
Abnormal permeability of cation: Higher intra Na+ Lower intra K+ Eventually removed by Spleen.
36
Where Ellipcytosis has high prevalence?
West Africa and South East Asia
37
Where can Tear Drop cells be found?
Myelofibrosis Pernicious Anemia Myeloid Metaplasia Hemolytic Anemia
38
What cause Tear drop cells
External disruption of membrane
39
Blister Cells and Bite cells
Oxidant induced hemolytic anemia | G6PD Deficiency
40
How Blister cells formed?
Spleen remove Heinz body (caused by denatured Hgb) and creating Blister cell.