Blood cells Flashcards

1
Q

Average diameter of RBC

A

7.2 um

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2
Q

Shape of RBC, and how it is achieved
S_o_a_ocyte
E_h_n_cyte

R_u_e_u_

A

Three types, dependant on water content:

  • Discocyte (biconcave disk)
  • Stomatocyte (more swollen
  • Echinocyte

Deformability maintained by specialised cytoskeleton:
-e.g. spectrin, ankyrin and band 3 anchoring proteins

Stack end-to-end forming Rouleaux

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3
Q

Contents of RBC

A

No nucleus, no mitochondria
Lots of Hb each with 4 haem groups which can each carry one O2
Enzymes for glucose metabolism
Ions

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4
Q

Why is it important that RBCs are deformable, and what physical property does this give to blood?

A

So they can fit into capillaries

Visco-elasticity so hard to find artificial substitutes:
-viscosity increases with decreased velocity due to their stacking into Rouleaux

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5
Q

Normal turnover time of RBC

A

120 days

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6
Q

Where and how are old/defective RBCs cleared?

A

In the spleen via phagocytosis by macrophages

Destruction gives off iron and waste products:

  • iron is transferred by transferrin to the bone marrow
  • waste products dealt with by the liver
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7
Q

What different types of anaemia are there and what can cause each of them?

A

Two types:

  • microcytic (where there is a low average RBC size) caused by iron deficiency l - accompanied by low haematocrit
  • macrocytic (where there is a high average RBC size) caused by vitamin B12 and/or folic acid deficiency
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8
Q

Define haematocrit

A

% of RBC in blood

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9
Q

What is EPO?

A

Erythropoietin - stimulated by hypoxia or increased O2 demand by tissues

Stimulates synthesis of more RBCs

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10
Q

Where is endogenous EPO made and what can exogenous EPO be used to treat?

A

Endogenous EPO synthesised and released by kidneys

Exogenous EPO used to treat anaemia, kidney diseases and chemotherapy side effects, for example

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11
Q

Describe the appearance and size of a neutrophil

A

Multi-lobed nucleus
Granulocyte - lysosomes and toxic granules containing strong oxidisers
10um

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12
Q

When and from where does neutrophil number increase?

A

Acute bacterial infection

Mobilised from reserves and increased production from myeloid progenitors

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13
Q

Describe their pathway to sites of acute inflammation

A

Adhere to vascular endothelium

Transmigrate via diapedesis through capillary walls

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14
Q

What do neutrophils leave behind after carrying out phagocytic activity?

A

Pus - a fluid containing dead neutrophils, liquefied tissue and cellular debris

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15
Q

Which white blood cells belong to the granulocyte family?

A

Neutrophils
Eosinophils
Basophils

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16
Q

Describe appearance of eosinophils

A

Stain pink due to presence of cationic proteins within large ovoid granules
Bigger than neutrophils

17
Q

What is characteristic of eosinophil plasma membranes?

A

IgE receptors for recognising allergens or certain antigens

18
Q

When does eosinophil number increase?

A

Chronic allergic conditions and tropical parasitic infection

19
Q

What do basophils secrete on activation?

A

Histamine

Interleukins/cytokines

20
Q

Is a macrophage a blood cell?

A

No - but a monocyte is…

21
Q

Define monocyte

A

A blood cell that can give rise to a macrophage after migrating into a tissue

22
Q

What are the roles of macrophages?

A

Tissue dependant, but generally they:

  • phagocytose, and kill organisms
  • remove tissue debris (by secreting enzymes) for repair
  • involved in tissue homeostasis and remodelling (e.g. phagocytose apoptotic bodies)
23
Q

Key points of Till & McCullogh 1963 experiment showing the presence of haematopoietic stem cells

A

Heavily irradiated mice
Injected bone marrow cells, and observed small nodules later dubbed ‘spleen colonies’ in spleen, number of which was proportional to the amount of bone marrow cells injected
Around 10,000 bone marrow cells had to be injected before a nodule formed
Each nodule spawned red cells, white cells and platelets
Hypothesised that each nodule was formed from one stem cell

24
Q

What two main divisions arise from haematopoietic stem cells, and give examples for each?

A

Common myeloid progenitors - granulocytes, red blood cells, mast cells, monocytes

Common lymphoid progenitors - lymphocytes

25
Q

What are primary lymphoid organs, and which lymphocytes develop where?

A

PLOs are where lymphocytes mature

T-cells mature in Thymus
B-cells mature in Bone marrow

26
Q

What are secondary lymphoid organs, and give some examples?

A

Locations where mature lymphocytes encounter antigens, which activate them to proliferate

E.g. lymph nodes, spleen, Peyer’s patches

27
Q

General role of B cell vs T cell

A

B cells mature into antibody producing plasma cells

T cells undertake a more cell-mediated response:

  • regulate the immune response (e.g. T-helper cells secreting cytokines to summon macrophages or T-regulators which stop the immune response)
  • kill infected cells directly (e.g. cytotoxic t-cells which kill virus infected cells)

Both can form memory cells

28
Q

Natural killer cell appearance and role

A

Large, granular lymphocytes

Survey the blood in search of cells without recognisable antigens

Anti-viral and anti-tumour

29
Q

Differences between small and large lymphocytes

A

Small:

  • dormant
  • G0
  • Long-lived
  • numbers expand on stimulation
  • recirculating from vasculature to lymphatics in high endothelial venules
  • e.g. memory cells

Large:

  • activated
  • proliferating
  • called Lymphoblasts
  • large because lots of DNA synthesis
  • intermediates of B, T and natural killer cells (effector cells)
30
Q

Examples of things that can harm haematopoietic stem cells

A
Ionising radiation
Cytotoxic drugs (e.g. chemotherapy)