Blood Flashcards

Week 6

1
Q

Plasma

A
  • 90% water
  • 10% solutes: proteins, gases, electrolytes, nutrient, and waste
    Proteins:
  • albumin: major constituent of plasma – colloid osmotic pressure
    • carrier proteins too (hormones)
  • Immunoglobulins: Abs (antibodies) secreted by plasma
  • Non-immune globulins: hemoblohin
  • Fibrinogen: hemostasis
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2
Q

Albumin

A

Major transporter for cholesterol and maintains osmotic balance

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3
Q

Blood smear

A

1) drop blood spread evenly over surface of slide
2) dried + stained
3) erythrocytes most abundant
4) thrombocytes (platelets)
5) leukocytes
- granulocytes: neutrophils, eosinophils, basophils
- agranulocytes (natural killer cells): lymphocytes and monocytes

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4
Q

Erythrocyte structure + function

A
  • Enucleate: lacks nucleus
  • Cytoplasm filled with hemoglobin - specialized for O2 delivery and CO2 removal
  • stains evenly with eosin
  • flexible plasma membrane:
    • integral membrane proteins - span the membrane (glycophorin)
    • peripheral membrane proteins - inner surface; lattice or mesh (spectrin)
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4
Q

Hereditary Spherocytosis + Elliptocytosis

A

Spherocytosis: mutation in spectrin
- fatigue
- yellow skin and eyes (jaundice)
- enlarged spleen
- blood smear may show elliptical rbcs
- complete blood count (cbc) may show anemia or signs rbc destruction
- ultrasound of gallbladder may show gallstones

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4
Q

hypochromia

A

RBCs appear pale in smear - anemia

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5
Q

Anemia and malaria

A
  • Protozoan parasite: Plasmodium faciparum
  • Infectious merozoites - polarized for entering erythrocytes (hide from immune system)
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6
Q

Spreading malaria

A

Parasitophosophorous vacuole: merozoite inside of a vacuole formed by RBC plasma membrane pinching off
- safe from the immune system and other killing enzymes

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7
Q

Malaria infected RBCs

A
  • Nodules form from protein-protein interactions
  • RBCs become stiff+sticky and can clog vessels
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8
Q

Sickle cell disease

A
  • Abnormal hemoglobin that can lead to blocking
    CRISPR CAS9: used to repair stem cells (specifically beta-globin gene)
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9
Q

Iron deficiency

A
  • appears paler pink around the edges with a white center
  • more flimsy because RBCs get beaten up and break down
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10
Q

Polycythemia

A
  • too many circulating RBCs and elevated hematocrit
  • primary polycythemia - polycythemia vera
    • caused by tumor-like condition of bone marrow: erythropoiesis proceeds at uncontrolled rate
  • secondary polycythemia
    • erythropoietin-induced adaptive mechanism to improve blood’s oxygen carrying capacity in response to prolonged reduced oxygen delivery to the tissue: occurs normally in people living at high altitudes
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11
Q

Polycythemia Vera

A

Symptoms: discolored skin, blurry vision, headaches, fatigue
V: Looks crazy

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12
Q

Thrombocytes

A

Platelets
- derived from megakaryocytes (blood marrow)
- platelet demarcation channels: invaginations of plasma membrane leads to pinching off of thrombocytes
- LM: foamy cytoplasm indicated platelet formation

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13
Q

Thrombocytes

A

1) Peripheral zone: plasma membrane and glycocalyx functions as receptor during hemostasis
2) Structure zone: microtubules and actin - maintain disc shape
3) Organelle zone: mitochondria and others
- granules contain
- serotonin: vasoconstrictor
- ADP and thromboxane A2: aid aggregation

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14
Q

Leukocytes

A

Granulocytes and agranulocytes

15
Q

Neutrophils

A
  • A type of granulocyte
  • polymorphonuclear: multi-lobed nuclei connected by thinner strands
  • 3 types of granules:
    • specific granules: enzymes, complement activators, and antimicrobial proteins
    • azurophilic granules: lysosomes (larger), contain myeloperoxidase (MPO)
    • tertiary granules: metalloproteinases - aid in neutrophil migration
16
Q

Neutrophil phagocytosis

A

3 types of receptors:
- Fc: recognizes IgG of opsonized bacterium
- Toll-like receptor: pattern recognition receptors - endotoxins, lipopolysaccharides
- complement receptors: facilitates binding and phagocytosis

17
Q

Chronic neutrophilic leukemia

A

rare, unknown cause
- elevation of neutropils

18
Q

Neutrophil killing

A

murderers

19
Q

Eosinophils

A
  • same size as neutrophils
  • multi-lobed nucleus with refractory granules (crystal-like)
    Two types of granules:
    1) specific granules: contain crystalloid body:
    • major basic protein (MPB- cytotoxic to invading protozoans and helminthes)
    • eosinophil-derived neurotoxin (EDN - disrupts invading organisms nervous system)
      2) azurophilic: lysosomes
20
Q

Basophils

A
  • Same size as neutrophils
  • numerous large granules in cytoplasm
  • low abundance in blood smear
  • multi-lobed nuclear obscured by granules
  • Fc receptors with high affinity for IgE concentrated on cell surface
    Two types of granules:
    1) specific granules:
  • heparin: anticoagulant
  • histamine: dilates vessels
  • IL-4: stimulates IgE production
    2) azurophillic: lysozymes
21
Q

Lymphocyte

A
  • Most common type of agranulocyte
  • same size as erythrocyte (RBC), enlargens to double when active
  • Cannot diff T, B, or natural killer cells using typical microscopy
  • Large lymphocytes: activated lymphocytes or NK cells
  • Medium: more common than large
  • Small: majority of circulating cells
  • Kidney bean shaped nucleus
  • A few mitochondria
  • golgi evident
22
Q

Monocyte

A
  • Largest leukocyte
  • bone marrow -> tissues become resident macrophages
    • osteoclasts - bone
    • alveolar macrophages - lung
    • Kupfer cells: liver
    • etc
  • even more indented nucleus than lymphocytes and larger
23
Q

Bone marrow

A
  • differentiated RBCs mostly
  • stem cells anchored to bones
  • sinusoid: specialized capillary
24
Q
A