Structure and Function of RBCs Flashcards

1
Q

What is the stain used for a basic blood smear?

A

Wright-Giemsa stain.

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2
Q

What stops collected blood from clotting?

A

EDTA in the collection tube.

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3
Q

How does EDTA work?

A

Chelates calcium

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4
Q

Acidic Aromatic stain?

A

Eosin

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5
Q

What does Eosin stain?

A

Hydrophobic basic macro-molecules (Haemoglobin and some other proteins)

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6
Q

Which cell does Eosin stain particularly well?

A

Eosinophil

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7
Q

What percentage of blood is made up of Eosinophils?

A

Less than 5%

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8
Q

Functions of Eosinophils

A

Mediators of innate immunity

Increase in context of allergic and parasitic infections

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9
Q

Aromatic Basic stain?

A

Methylene Blue

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10
Q

What does Methelene Blue stain adhere to?

A

Hydrophobic acidic macro-molecules such as Nucleic Acids

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11
Q

What cells does methelene Blue predominantly stain?

A

Basophils

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12
Q

What percentage of Blood cells are Basophils?

A

Less than 1%

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13
Q

Functions of Basophils

A

Degranulation during allergic reactions

Related to tissue mast cells

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14
Q

Which cells stain with a little of either dyes?

A

Neutrophils

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15
Q

Lifespan of Neutrophils

A

1 day

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16
Q

Neutrophils make up what percentage of Leukocytes?

A

40-70%

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17
Q

When do Leukocytes increase their numbers? (up to 10 fold?)

A

During Bacterial and Fungal infections.

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18
Q

How do Neutrophils do their duty?

A

Phagocytosis
Degranulation
Formation of extracellular traps

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19
Q

Defining features of Monocytes?

A

Few or no cytoplasmic granules

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20
Q

What percentage of blood leukocytes are Monocytes?

A

3-8%

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21
Q

Functions of Monocytes?

A
Phagocytes that present antigen on MHC class II
Macrophages are derived from Monocytes.
Numbers increase in wide variety of diseases.
22
Q

Lymphocytes life span?

A

Days to years.

23
Q

What is different about reactive forms of lymphocytes?

A

Have more cytoplasm and more prominent nucleoli

24
Q

What is the structure of platelets?

A

Small anucleate fragments

25
Functions of Platelets
1. Primary Hemostatic plug via aggregation 2. Stimulate coagulation cascade 3. Stimulate wound healing (secretion of PDGF which recruits fibroblasts) 4. Present Antigen
26
How are Bands morphologically different from mature neutrophils?
Horseshoe shaped nuclei Bean shaped nuclei in even less mature neutrophils (metamyelocytes) Round nuclei in myelocytes
27
What is different about neutrophil appearance during bacterial infection?
Increased cytoplasmic toxic granules.
28
Describe the red cell design
Flexible shape Bi-concave disc Cable reinforce alpha beta spectrin heterodimer anchored to Ankyrin and Band 3 Haemoglobin packed in just short of crystallization concentrations Na/K ATPase pump maintains osmotic pressure (Failure of ATPase pump results in swelling and bursting)
29
Effect of Oxidants on Haemoglobin
Radicals damage Haemoglobin leading to formation of inter and intra di-sulfide bonds which further leads to precipitation and or denaturation of haemoglobin.
30
What protects red cells from oxidants?
The Glutathione system
31
What is required for efficient operation of the Glutathione
NADPH and The enzyme Gluthathione reductase.
32
What does Iron oxidized to the Fe3+ state produce?
Methemoglobin
33
How is Methemoglobin reduced?
Via cytochrome b5 reductase
34
What is required for reduction of Methemoglobin by cytochrome B5 reductase.
NADH
35
What are 2 of the essential metabolic processes of RBCs?
Glycolysis to make ATP and NADH | Pentose shunt to make NADPH
36
What is the first enzyme of the pentose phosphate shunt?
G-6-PD
37
What is the most common cause of NONSPHEROCTIC HEMOLYTIC ANEMIA?
Pyruvate Kinase deficiency.
38
When is NONSPHEROCTIC HEMOLYTIC ANEMIA first diagnosed?
In Neonates (available screening test)
39
Facts about PK deficiency?
``` Autosomal recessive Over 100 possible mutations Causes right shift in O2 dissociation curve Increased intracellular 2,3-DPG Depleted ATP formation ```
40
Clinical features of PK deficiency
Marked aniso-and poikilocytosis Red cell Fragments Xerocytes High reticulocyte count >30-40%
41
How do RBCs protect themself from complement?
DAF and CD55
42
Lack of DAF results in?
PMH Paroxysmal Nocturnal Hemoglobinuria
43
Terms decribing insufficient Haemoglobin in red cells?
Hypochromic and/or microcytic
44
What is meant by Aniscytosis?
RBC morphology characterized by highly varied RBC sizes/volume
45
What is Poikilocytosis
RBC Morphology characterized by highly varied Shape
46
What is Polychromasia?
Appearance of residual mRNA in RBCs, usually associated with accelerated production. (Basophilic staining in center of the RBC)
47
What are the causes of Heinz-Bodies? (Precipitated Haemoglobin in RBCs)
1. Due to genetic defect in haemoglobin structure (haemoglobinopathy) 2. Failure of antioxidant systems can lead to precipitation of haemoglobin.
48
Results of Heinz body formations?
1. Cell shape can be altered i.e sickling 2. Tissue based Phagocytes can do damage to repair on oxidized haemogolbin removing chunks of the RBC creating bite cells.
49
What are Schistocytes?
Red cell fragments.
50
How are schistocytes formed?
1. Mechanical lysis (artificial valves) | 2. Microangiopathic processes