Lecture 17: Intro To Haemotology Flashcards

1
Q

3 functions of blood

A
  1. Transport
  2. Regulation
  3. Protection
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2
Q

What does the blood transport

A

-nutrients and cellular components
-metabolic waste to elimination sites
-hormones to target organs

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3
Q

What does the blood prevent

A

-infection from foreign bodies

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4
Q

What does the blood regulate

A

-pH of body tissues
-BP
-fluid balance and circulation
-body temp

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5
Q

How many litres of blood in an adult

A

4.5-5.5L

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6
Q

What’s the pH of the blood

A

Slightly alkaline
7.35-7.45

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7
Q

Fluid components of blood

A

90% water 10% solutes
- plasma proteins (albumin, fibrinogen, globulins

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8
Q

Cellular components of blood

A

3 main:
1. Platelets
2. Leukocytes (WBC)
3. Erythrocytes (RBC)

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9
Q

How much of the blood do erythrocytes compose

A

45%

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10
Q

Avg life span of erythrocytes

A

120 days

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11
Q

Are erythrocytes able to change shape

A

Yes- to facilitate movement

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12
Q

Are erythrocytes true cells

A

No- anucleuated and no organelles

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13
Q

Erythrocytes adaptations

A
  • large sa:v
    -lots of haemoglobin
    -ATP generated by anaerobic mechanisms
    -able to deform yet spring back into shape
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14
Q

How many HB molecules per erythrocyte

A

<250 million

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15
Q

How are erythrocytes formed

A

Haematopoiesis

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16
Q

Where does haemotopoiesis occur

A

Largely in red bone marrow (axial skeleton, girdles, proximal epiphysis of humerus and femur)

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17
Q

How many erythrocytes produced each day

A

100 billion

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18
Q

What does erythrocyte production depend on

A

Body needs and regulatory factors

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19
Q

What are the steps in haematopoiesis

A
  1. Stem cell (haemocytoblast)
  2. Committed cell (proerythroblast)
  3. Developmental pathway
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20
Q

What are the 3 steps in the developmental pathway

A

Phase 1- ribosome synthesis
Phase 2- haemoglobin accumulation
Phase 3- ejection of nucleus

21
Q

Phase 1- ribosome synthesis

A

Basophilic erythroblast

22
Q

Phase 2- haemoglobin accumulation

A

Polychromatic erythroblast
Orthochromatic erythroblast

23
Q

Phase 3- ejection of the nucleus

A

Reticulocyte

24
Q

How do leukocytes leave the circulation

A

Via diapedesis

25
How much of blood volume do leukocytes account for
<1% (4,800- 10,800 per microliter
26
What 2 categories are leukocytes divided into
Granulocytes and agranulocytes
27
What is categorised as granulocytes
- neutrophils (50-70%) - eosinophils (2-4%) - basophils (0.5-1%)
28
What is categorised as agranulocytes
- lymphocytes (25-45%) - monocytes (3-8%)
29
WBC functions
- protect against bacteria, viruses, toxins, tumour cells - leave circulation at inflammation sites - gather in large numbers due to chemotaxis and destroy foreign substances
30
Neutrophil function
- destroy foreign antigens by phagocytosis - cytoplasmic granules released on lysis with a phagosome
31
Eosinophil function
- parasite protection e.g. worms by releasing granules which digest them
32
Basophil function
- histamine granules (potent vasodilator) to attract other leukocytes to site of infection
33
Lymphocyte function
-immune response T- directly respond to tumour and virus infected cells B- produce specific AB against antigens
34
Monocyte function
- activating lymphocytes in mounting the secondary immune response - those leaving the bloodstream become macrophages - destroy antigen and infected cells by phagocytosis
35
How and where are leukocytes formed
Leukopoiesis in bone marrow of large bones
36
Where do lymphocytes undergo additional maturation
In thymus to T and B lymphocytes
37
Granulocytes life span
<9 days
38
Lymphocytes life span
Hours-decades (memory cells)
39
Monocytes life span
Several months
40
How are platelet cell fragments formed
Budding off a megakaryocyte
41
What do platelets contain
Ca2+ important in coagulation
42
Platelet lifespan
10 days
43
What is haemostasis
Multi step, localised process in stopping bleeding at site of vessel injury
44
Haemostasis overview
Begins with formation of platelet plug, ends with formation of fibrin blood clot to prevent blood loss
45
Coagulation cascade
Formation of a blood clot via the activation of ‘factors’, leading to fibrin formation and resulting clot
46
How is coagulation cascade activated
1. Vessel damage and exposure to underlying tissues- contact or intrinsic pathway 2. Exposure to tissue factor via extrinsic pathway
47
What do both the intrinsic and extrinsic pathway do
Converge to form the common coagulation cascade leading to fibrin clot formation
48
Activation of what initiates the first step of the common pathway
Factor X
49
Final common pathway
Factor X activated Xa which converts prothrombin (II) to thrombin (IIa) via Va Fibrinogen (I) converted to fibrin (Ia) then produces cross-linked fibrin clot via XIIIa