11 - blood Flashcards

1
Q

What are the three components of blood that can be seen when you centrifuge a blood sample with anticoagulant?

A

Plasma (55%), red blood cells (45%) and the buffy coat which is composed of white blood cells and platelets

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2
Q

What is contained in the blood plasma?

A

Water, electrolytes and plasma proteins

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3
Q

What are the three formed elements of blood and what is there main role?

A

Red blood cells - transport of oxygen and carbon dioxide
White blood cells - immunity
Platelets - control of bleeding and blood clotting cascade

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4
Q

What is the scientific name for the development of red blood cells?

A

Haemopoiesis

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5
Q

What hormone stimulates haemopoiesis?

A

Erythropoietin

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6
Q

Which type of stem cell develops into red blood cells, megakaryocytes, monocytes and granular leukocytes?

A

Myeloid stem cell

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7
Q

Which type of stem cell develops into T and B lymphocytes?

A

Lymphoid stem cells

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8
Q

From what cell are platelets formed from?

A

Megakaryocytes

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9
Q

Where are blood cells produced?

A

red bone marrow in spongy bone

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10
Q

Describe the structure of an erythrocyte

A
  • biconcave disc
  • 7.8um diameter
  • no nucleus
  • contains haemoglobin and enzymes
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11
Q

What does a eosinophil look like when stained with Wright’s stain?

A
  • purple double lobed nucleus

- a strongly stained pink cytoplasm

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12
Q

What does a basophil look like when stained with wright’s stain?

A
  • dark purple nucleus and cytoplasm

verty concentrated purple area that takes up most of cell

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13
Q

What does a neutrophil look like when stained with wright’s stain?

A
  • light purple/pink cytoplasm

- dark purple, multi-lobed nucleus

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14
Q

What does a monocyte look like when stained with wright’s stain?

A
  • light purple cytoplasm

- irregular purple nucleus

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15
Q

What does a lymphocyte look like when stained with wright’s stain?

A
  • large purple nucleus that covers the majority of the cell

- small area of light purple cytoplasm

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16
Q

Describe the structure of haemoglobin

A

A globular protein made of two beta haemoglobin and two alpha haemoglobin chains, which each contain a haem residue

17
Q

How does sickle cell anemia occur?

A
  • mutation causes a glutamic acid in the beta haemoglobin chain to become a valine.
  • causes haemoglobin chains to stick together when deoxygenated which deforms the erythrocytes.
  • causes the erythrocytes to get stuck in capillaries which starves tissues of oxygen.
18
Q

What causes thalassemia?

A

A reduced rate of synthesis of alpha and beta globin chains results in the formation of small and weakly staining erythrocytes. These erythrocytes are destroyed which leads to anaemia.

19
Q

What are the features of type A blood?

A
  • A antigen presentation on red blood cells

- Anti-B antibody in the plasma

20
Q

What are the features of type B blood?

A
  • B antigen presentation on red blood cells

- Anti-A antibody in the plasma

21
Q

What are the features of type AB blood?

A
  • A and B antigen presentation on red blood cells

- Neither A or B antibodies are present in the plasma

22
Q

What are the features of type O blood?

A
  • neither A or B antigens are present in the red blood cells

- plasma contains both anti-A and anti-B antibodies

23
Q

What are three possible complications of blood transfusions?

A
  • wrong blood type given (ABO incompatibility)
  • iron overload that causes iron deposits on organs (in repeated transfusions)
  • infection