Haemopoiesis, The Spleen And Bone Marrow ILOs Flashcards

1
Q

What is haemopoiesis?

A

Formation of blood cells from bone marrow

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2
Q

Bone marrow distribution in infants

A

All throughout the skeleton

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3
Q

Bone marrow distribution in Adults

A

Limited
Pelvis, skull, ribs, sternum and vertebrae

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4
Q

Haemopoiesis in the embryo

A

IN vasculature of the yolk sac to start
Then in the foetal liver between weeks 5-8

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5
Q

Haemopoiesis starts off with Haematopoietic stem cells:
They differentiate into 2 cell types:

A

Common Myeloid Progenitor Cells
Common Lymphoid Progenitor Cells

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6
Q

Common Myeloid Progenitor cells differentiate into 3 Types of cell:

A

Megakaryocytes
Erthryocytes
Myeloblasts

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7
Q

Myeoblasts differentiate into:

A

Granulocytes: Neutrophils, Eosinophils and Basophils
AND
Monocytes

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8
Q

Common Lymphoid Progenitor cell differentiations into 2 different lymphocytes

A

T-Lymphocytes
B-Lymphocytes

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9
Q

T-Lymphocyte development

A

In foetal liver and Thymus

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10
Q

B-Lymphocyte development

A

Foetal liver and Bone Marrow

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11
Q

Erythropoiesis

A

Formation of red cells

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12
Q

Protein Secreted by the KIDNEY to stimulate erythropoiesis

A

Erythropoietin

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13
Q

Thrombopoiesis

A

The formation of Thrombocytes (Platelets)

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14
Q

Thrombopoietin function

A

Protein that simulates formation of Megakaryocytes therefore stimulates THROMBOPOIESIS

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15
Q

What is a THROMBOCYTE?

A

Important in blood clotting
Membrane bound cytoplasm that has budded off from a Megakaryocyte

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16
Q

Granulopoiesis

A

Formation of Granulocytes (Neutrophils, Eosinophils and Basophils) from Myeloblast cells which originate from Common Myeloid Progenitor Cells

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17
Q

Monocytopoiesis

A

Production of monocytes from Myeoblasts which originate from Common Myeloid Progenitor Cells
Monocytes differentiate into either MACROPHAGES OR DENTRITIC CELLS

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18
Q

Macrophage function

A

Phagocytose foreign substances in the body

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19
Q

DENTRITIC Cells

A

Antigen presenting cells
Present the antigens of pathogens they have engulfed to Lymphocytes

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20
Q

Erythrocyte function

A

Transport Oxygen from lungs to tissues by carrying haemoglobin
Transport CO2 form the tissues back to the lungs

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21
Q

Erythrocyte Structure

A

No nucleus
Bioconcave
No mitochondria
Lipid bilayer contains proteins that maintain the structure of the cell so that it remains bioconcave and flexible

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22
Q

Hereditary Spherocytosis

A

A gene mutation of at least one of the proteins that is responsible in maintaining phospholipid bilayer of the erythrocyte and therefore its bioconcave shape

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23
Q

Spleen function

A

A filter of the blood

24
Q

Spleen general structures

A

Splenic Artery (Brings BLood To Spleen)
Red Pulp = Sinusoids containing Macrophages RED Cells Pass through it
White Pulp = Plasma and white cells pass through it
Splenic vein
Splenic artery linked to splenic vein by a portal system

25
BLood Pooling in the SPleen
RED Cells and platelets accumulate in the spleen so they can be quickly mobilised during bleeeding
26
WHite pulp importance
Lots of antibodies synthesised here Removes antibody covered bacteria and RBCs
27
Red Pulp Importance
Macrophages engulf and destroy old RBCs here
28
Extramedullary Haemopoiesis
When haemopoiesis occurs not in the bone marrow E.g: Spleen and Liver Can cause Splenomegaly
29
What is Splenomegaly?
Enlarged Spleen
30
Splenomegaly is caused by
-Extra-medullary Haemopoiesis -Hypertension of hepatic portal vein from liver disease (blood can’t leave spleen) -Overwork of spleen (causes increase in pulp size) -Expanding as infiltrated by cells (Blood cancers/Leukeamia) -Expanding as infiltrated by materials (Sarcoidosis)
31
Dangers of Splenomegaly
Spleen no longer fully protected by rib cage, risk of rupture Need to avoid contact sports
32
Hyposplenism is
Lack of functioning splenic tissue
33
Hyposplenism caused by
Splenectomy Sickle cell disease ( Red cells not bioconcave, get stuck in spleen) Gastrointestinal diseases (ulcerative colitis, Crohns Disease and coeliac disease) Autoimmune disorders (Rhuematioid Arthiritis and Hashimotos Disease)
34
Hyposplenism = BIG RISK OF
SEPSIS Encapsulated bacteria very hard for immune system to combat without maximum splenic function
35
Indication of Hyposplenism
Presence of Howell Jolly Bodies in Blood Film Normally are removed
36
Normal Range
Includes 95% of population Values outside range not always abnormal Results may be in normal range but it may be a significant change within the normal (this is abnormal) Normal range changes with age, sex and comorbidities
37
Significance of reticulocyte count
Indication of production of erythrocytes and therefore activity of the bone marrow
38
Haematocrit (HcT)
Proportion of blood that is made up of red blood cells
39
Haemoglobin Concentration
A Parameter for accessing Full Blood Counts
40
Red Cell Count (RCC)
Number of Red Cells in a given vol of blood
41
Mean Cell Volume (MCV)
Helps determine cause of anaemia
42
Red Cell Distribution Width (RDW)
Variation in size or red blood cells Helps determine the stage of anaemia So if anaemia has just started there will be a wide range of sizes If its been happening a long time, all cells would be small so RDW is low since they are all similar
43
Mean Cell Haemoglobin (MCH)
Average amount of haemglobin in a RBC Used to asses
44
Microcytic
Small MCV (Mean Cell Volume)
45
Macrocytic
High MCV (Mean Cell Volume)
46
Anisocytosis
Increased variation non red cell size (RDW Red Cell Distribution Width)
47
Hypochromic
Low Mean CEll Haemoglobin
48
Hyperchromic
High Mean Cell Haemoglobin (MCH)
49
Dimorphism
2 distinct populations of red cells
50
Polychromatic
Reticulocytes
51
Megakaryocyte function
Produce Thrombocytes
52
Eosinophils FUnction
MEdiator of allergic responses Immune response to parasites
53
In appropriate activation of eosinophils
Causes inflammation (asthma) and tissue damage
54
Basophils
Active in allergies and inflammatory conditions
55
Lymphocytes
B Cells make antibodies T Cells (Produce T cell receptors to recognise antigens) Natural Killer Cells