B4 W1 Flashcards

1
Q

B12 and folate sources

A

Meat, salmon, eggs, soy

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2
Q

Phagocytic cells of the CNS

A

Microglia

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3
Q

MCH

A

Mean corpuscular Hb

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4
Q

Which progenitor gives rise to neutrophils?

A

Myeloid

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4
Q

Which progenitor gives rise to neutrophils?

A

Myeloid

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5
Q

Anaemia due to bone marrow change

A

Infection, cancer, autoimmune disease, pregnancy, drugs and renal failure

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6
Q

What transports B12 in enterocytes?

A

Transcobalamin II protein and takes it to the plasma

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7
Q

Least common blood type

A

AB-

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8
Q

WBC with lifespan of 14 days

A

NK cells

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9
Q

What reduces iron absorption?

A

Tea and coffee, Proton pump inhibitors and antacids

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10
Q

How is bilirubin metabolised?

A

Into urobilinogen to be excreted by intestinal bacteria

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11
Q

Lectin pathway

A

Mannose binds to pathogen via lectin enzyme and induces complement activation

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12
Q

Schistocytes

A

Fragmented RBC with different shapes, found in areas with a central pallor. Indicator of haemolytic anaemia

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13
Q

Schistocytes

A

Fragmented part of RBC with different shapes.

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14
Q

Number of allelic variants for ABO

A

3

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15
Q

Which WBC are mononuclear?

A

Lymphocytes and monocytes

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16
Q

How is iron from animal diet source absorbed?

A

In the duodenum and jejunum as haem iron. It is taken in via endocytosis and released into enterocyte by haem oxidase

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17
Q

Cells which contribute to tissue and blood cell development.

A

Stromal cells in the bone marrow

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18
Q

Stromal cells

A

Specifically in the bone marrow, give rise to bone, cartilage, adipocytes and contribute to sustained proliferation and self-renewal of haematopoietic stem cells

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19
Q

Difference between stromal cell and stem cell?

A

Stem cell is originated from mesenchyme. Stromal cell is a non-haematopoetic mesenchymal stem cell of the bone marrow.

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20
Q

Why does haematopoeisis not occur in adult long bones?

A

Fat deposition

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21
Q

What is glossitis an indication for?

A

B12 and folate deficiency and iron

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22
Q

What is a lymphatic trunk?

A

Lymph vessel formed from the convergence of efferent lymph vessels. It includes lumbar, intestinal, bronchomediastinal

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23
Q

What are the formed elements of blood?

A

RBC, WBC and platelets

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24
How much of formed elements of blood do RBC make up?
99%
25
Substance on surface of RBC which induces antibody formation
Isoagglutinogen
26
What are the carriers of A and B antigens on RBC?
N-glycosylated glycoproteins, anion exchanger and Glut-2 transporter
27
What substance allows B12 to be absorbed?
Intrinsic factor produced by parietal cells, absorption occurs in the terminal ileum.
28
Complement pathway initiated by antibody-antigen complex
Classical pathway
29
How does an antibody interact with secondary lymphoid tissue?
Antigen interacts with cells in the follicle. This causes cells in the Germinal centre to divide
30
Polychromasia
Disorder with high number of immature RBC
31
Main storage site for folic acid
Liver
32
When does the liver release folate?
To maintain plasma folate levels. Released with bile
33
What is the recessive allele in the ABO blood group?
i
34
Condition where only RBC are affected
Pure red cell aplasia
35
Indication of haemolytic anaemia
Dark urine, splenomegaly, jaundice, heart murmur, schistocyte count is high
36
Types of pure red cell aplasia
Primary which is congenital and secondary caused by drug or infection
37
How do erythrocytes form?
Differentiates -> haemoglobin accumulation -> ribosome synthesis -> nuclear ejection Pro-erythroblast -> erythroblast -> normoblast -> reticulocyte -> erythrocyte
38
Diamond Black Fan anaemia
Congenital Pure red cell aplasia with reduced erythroblast production
39
Cortex
Area of thymus containing large numbers of T cells and dendritic cells
40
Normocytic anaemia
Haemolytic anaemia, bone marrow disorder, hypersplenism, chronic disease anaemia
41
Cytokine produced by cytoxic T cells which prevents macrophages leaving the site of infection
Macrophage migration inhibiting factor
42
Stem cell gives rise to megakaryocytes, erythrocytes, granulocytes and macrophages
Common myeloid progenitor
43
What causes B12 or folate deficiency?
Malnutrition, malabsorption, pernicious anaemia, pancreatitis, antacids
44
What is the site of T cell death?
Thymic corpsucles composed of epithelial cells in concentric layers of flat cells
45
How is the porphyrin ring degraded?
By haem oxygenase Into green biliverdin. This is catalysed by biliverdin reductase -> bilirubin.
46
How does an erythroblast become a normoblast?
Haemoglobin accumulation
47
What part of the spleen contains lymphocytes?
White pulp
48
What are the components of the innate immune system?
NK cells, dendritic cells, phagocytic leukocytes, epithelial cell barriers
49
Which granulocyte stains bright red by eosin?
Eosinophils
50
Iron rich granules formed when there is failure of iron incorporation, when iron is not deficient
Sideroblasts
51
Interferon
Produced by virally infected cells to inhibits viral replication and cell division. Activates NK cells
52
Pancytopenia
Issue with haematopoietic stem cell. Condition affecting RBC, WBC and platelet production
53
Cytokine produced by macrophage which causes neutrophil and macrophage accumulation
TNF- Tumour necrosis factor. Blockade can cause reactivation of TB and increased secondary infection
54
Kinins
Polypeptides formed from inactive precursors. Induce vasodilation and increase permeability.
55
Site where T cells mature
Thymus
56
What is the composition of the red pulp?
Granulocytes, platelets, plasma and RBC. It is a large resorvoir for monocytes
57
What does white pulp contain?
Mainly lymphocytes
58
Leukotrienes
Substance produced by basophils and mast cells to increase permeability and attract phagocytes
59
Microcytic anaemia
TAILS T: thalasemia A: autoimmune disease I: Iron deficiency, L: lead poisoning S: sideroblastic anaemia
60
A antigen
N-acetylgalactosamine
61
Which cells transfer antigens to lymphocytes on Peyer's patches?
Microfold cells
62
Myeloblast
Gives rise to the granulocytes
63
What stimulates phagocyte migration and intensifies histamine and kinin effect?
Prostaglandins
64
Chemotactic pathogenic agent produced by basophils and mast cells
Leukotrienes
65
Mononuclear phagocytic system
System of phagocytic cells in the reticular connective tissue
66
Macrocytic anaemia causes unrelated to B12 and folate
Liver disease, reticulocytosis and hypothyroidism
67
Complement system activated by antibody binding to antigen
Classical pathway
68
A antigen
N-acetylgalactosaminyltransferse which transfers N-acetylgalactoseamine from UDP-Nacetylgalactosemaine to H antigen fucosylated galactosyl residue
69
Cell where erythropoeisis begins
Haematopoietic pluripotent stem cell
70
EPO stages
Riboome synthesis -> Hb accumulation -> nuclear ejection
71
EPO synthesis
Juxtatubular intestitial cells detect o2 levels via oxygen dependent prolyl hydroxylase which regulates stability of HIF
72
Receptors in macrophage membrane
TLR- Toll like receptor
73
Phagocytes of kidney
Intraglomerular mesanglial cells
74
Formation of blood cells
Haematopoesis
75
Phagocytic cell of CNS
Microglia
76
Protein which protects B12 from stomach acid
Transcobalamin I in the saliva.
77
Porphyrin ring metabolised and excreted in faeces
Porphyrin is metabolised to biliverdin-> bilirubin-> urobilinogen -> stercobilin
78
EPO transcription factor
HIF- hypoxia inducible factor
79
Closed tubes which drain fluid from tissues and respond to fluid pressure. Consist of endothelial cells
Lymph capillaries
80
Adult haematopoeisis
Flat bones such as pelvis, cranium, vertebrae and sternum
81
Universal recipient
AB+
82
Stem cells which form the granulocytes
Myeloblast
83
RBC with nuclear fragments
Howell-Jolly bodies
84
Macrophages of lymph nodes
Sinus histocytes
85
Least common blood type
AB-
86
Not enough Hb is produced
Thalassemia
87
Agranulocyte
Lymphocyte, monocyte
88
Follicle
Aggregation of B cells in secondary lymphoid tissue
89
Reticulocytosis
High reticulocyte count- indication of high RBC count, related to macrocytic anaemia