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Blood 101
  Peter Jean
What is blood?
• Functions:
  • Transport of nutrients and
    waste
  • Defense against internal
    damage
  • Repair of damaged tissues




                                 Image: http://static.ddmcdn.com/gif/blood-cells.jpg
Hematopoiesis: The
 Differentiation of Progenitor Cells




http://apbrwww5.apsu.edu/thompsonj/Anatomy%20&%20Physiology/2020/2020%20Exam%20Reviews/Exam%201/hematopoiesis00.gif
Progenitor Cells

• Differentiated stem cells from bone marrow

• In hemapoiesis, progenitor cells are the starting
  material.

• Can be differentiated further into specific blood
  cells such as platelets, T-cells, and red blood cells
  (erythrocytes).
Platelets

• Not true cells, meaning
  they lack a nucleus.

• Membrane bound
  fragments derived cells in
  the bone marrow.

• Play a major role in blood
  clotting.


                               Image: http://www.daviddarling.info/images/blood_clotting.gif
Plasma
                                                              • The natural environment of
                                                                blood cells, or the liquid
                                                                phase of blood.
                                                                    • When blood is centrifuged, 3
                                                                      layers form.
                                                                    • Top layer: plasma
                                                                    • Middle layer: the “buffy” layer
                                                                      (mostly platelets)
                                                                    • Bottom layer: Red Blood
                                                                      Cells (RBCs)

Image: http://2.bp.blogspot.com/_FoiEZNQLqOI/TIi_PXga-eI/AAAAAAAABpU/NslutpCNkZ0/s1600/plasma-blood.gif
Leukocytes

• Also known as White Blood Cells (WBCs)
  • Different subgroups, including lymphocytes and
    granulocytes.

• Protect against infection

• Mostly produced in bone marrow

• Have the ability to migrate out of the bloodstream
  into surrounding tissues.
Iron Transport and
                    Storage
•   Iron is essential for life, two
    oxidation states:
    • Fe2+ Fe3+

•   A protein called ceruloplasmin
    donates a free electron,
    changing the oxidation state of
    iron.

•   Transferrin protein protects the
    body against free iron, which
    has toxic effects, and
    TRANSFERS the protein to
    different parts of cell.

•   Iron is important in RBCs
    because that is where oxygen
    (O2) binds to the Hemoglobin
    protein in the cell, and can be
    released in various tissues.
                                       Image: http://sickle.bwh.harvard.edu/tf-endocytosis.gif
Hemoglobin

• Two structural figures:
  oxygenated and
  deoxygenated.
• Affected by the binding of
  O2.
• The chemical bonds
  between different “chains”
  are broken and others are
  formed, effectively
                               Image:
  rotating the shape of the    http://alexandria.healthlibrary.ca/documents/notes/bom/unit_2/Hemo

  protein.                     globin%20fig%201.jpg
What about Blood Type?

• Types: A, B, AB, O
• The difference? Antigens
  on the surface of RBCs
  recognize the differing
  types floating in the
  plasma. “O negative” type
  is the universal red blood
  cell donor, while “AB
  positive” is the universal
  plasma donor.
• There is also an Rh          Image: http://waynesword.palomar.edu/images/blood1.gif
  factor, which can be
  present (+) or absent (-).
The Fate of Red Blood Cells

                                                                         • Last approximately 60 to 120
                                                                           days.
                                                                         • Cells that are ready to die are
                                                                           taken up (phagocytosed) by
                                                                           macrophages. The amino acids
                                                                           that make up the protein, are
                                                                           recycled.
                                                                         • The hemoglobin is broken
                                                                           down into bilirubin. Bilirubin is
                                                                           toxic, so it must be transported
                                                                           to the liver via albumin where it
                                                                           is broken down and eventually
                                                                           excreted.
Image: http://ars.sciencedirect.com/content/image/1-s2.0-S1074552109002919-gr8.jpg
Blood Related Diseases:
           Hemophilia
• Inherited disease, caused by single gene mutation.
• All female children of men with hemophilia are carriers,
  very rare for a woman to have (1:25,000,000)
• Symptoms: bleeding into muscle, bruising easily, blood
  in urine, first sign usually bleeding gums.
• Testing: Bleeding time, Thrombin time (used to look at
  deficiencies in fibrinogen, also tests for liver disease).
• Hemophilia spread throughout royal houses in Europe
  as marriages were arranged to set up political
  alliances.
Blood Related Diseases:
    Acute Intermittent Porphyria
•   Deficiency of the enzyme
    porphobilinogendeaminase (PBGD)

•   More than 250 mutations have been
    identified.

•   Symptoms include abdominal pain,
    irregular heart beat (tachycardia), acute
    psychosis, and respiratory paralysis.

•   Treatment: family screening (DNA testing),
    aviodance of factors that are known to
    cause attacks, heme derivatives. Future
    treatment may include liver transplantation,
    gene and enzyme therapy.

•   Vincent van Gogh may have been a case
    for AIP, as he worked tirelessly, fasted, and
    excessive consumption of absinthe.

                                        “Self-Portrait”
                                                    Image: http://www.framedcanvasart.com/images/site/Van_Gogh.jpg

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Blood

  • 1. Blood 101 Peter Jean
  • 2. What is blood? • Functions: • Transport of nutrients and waste • Defense against internal damage • Repair of damaged tissues Image: http://static.ddmcdn.com/gif/blood-cells.jpg
  • 3. Hematopoiesis: The Differentiation of Progenitor Cells http://apbrwww5.apsu.edu/thompsonj/Anatomy%20&%20Physiology/2020/2020%20Exam%20Reviews/Exam%201/hematopoiesis00.gif
  • 4. Progenitor Cells • Differentiated stem cells from bone marrow • In hemapoiesis, progenitor cells are the starting material. • Can be differentiated further into specific blood cells such as platelets, T-cells, and red blood cells (erythrocytes).
  • 5. Platelets • Not true cells, meaning they lack a nucleus. • Membrane bound fragments derived cells in the bone marrow. • Play a major role in blood clotting. Image: http://www.daviddarling.info/images/blood_clotting.gif
  • 6. Plasma • The natural environment of blood cells, or the liquid phase of blood. • When blood is centrifuged, 3 layers form. • Top layer: plasma • Middle layer: the “buffy” layer (mostly platelets) • Bottom layer: Red Blood Cells (RBCs) Image: http://2.bp.blogspot.com/_FoiEZNQLqOI/TIi_PXga-eI/AAAAAAAABpU/NslutpCNkZ0/s1600/plasma-blood.gif
  • 7. Leukocytes • Also known as White Blood Cells (WBCs) • Different subgroups, including lymphocytes and granulocytes. • Protect against infection • Mostly produced in bone marrow • Have the ability to migrate out of the bloodstream into surrounding tissues.
  • 8. Iron Transport and Storage • Iron is essential for life, two oxidation states: • Fe2+ Fe3+ • A protein called ceruloplasmin donates a free electron, changing the oxidation state of iron. • Transferrin protein protects the body against free iron, which has toxic effects, and TRANSFERS the protein to different parts of cell. • Iron is important in RBCs because that is where oxygen (O2) binds to the Hemoglobin protein in the cell, and can be released in various tissues. Image: http://sickle.bwh.harvard.edu/tf-endocytosis.gif
  • 9. Hemoglobin • Two structural figures: oxygenated and deoxygenated. • Affected by the binding of O2. • The chemical bonds between different “chains” are broken and others are formed, effectively Image: rotating the shape of the http://alexandria.healthlibrary.ca/documents/notes/bom/unit_2/Hemo protein. globin%20fig%201.jpg
  • 10. What about Blood Type? • Types: A, B, AB, O • The difference? Antigens on the surface of RBCs recognize the differing types floating in the plasma. “O negative” type is the universal red blood cell donor, while “AB positive” is the universal plasma donor. • There is also an Rh Image: http://waynesword.palomar.edu/images/blood1.gif factor, which can be present (+) or absent (-).
  • 11. The Fate of Red Blood Cells • Last approximately 60 to 120 days. • Cells that are ready to die are taken up (phagocytosed) by macrophages. The amino acids that make up the protein, are recycled. • The hemoglobin is broken down into bilirubin. Bilirubin is toxic, so it must be transported to the liver via albumin where it is broken down and eventually excreted. Image: http://ars.sciencedirect.com/content/image/1-s2.0-S1074552109002919-gr8.jpg
  • 12. Blood Related Diseases: Hemophilia • Inherited disease, caused by single gene mutation. • All female children of men with hemophilia are carriers, very rare for a woman to have (1:25,000,000) • Symptoms: bleeding into muscle, bruising easily, blood in urine, first sign usually bleeding gums. • Testing: Bleeding time, Thrombin time (used to look at deficiencies in fibrinogen, also tests for liver disease). • Hemophilia spread throughout royal houses in Europe as marriages were arranged to set up political alliances.
  • 13. Blood Related Diseases: Acute Intermittent Porphyria • Deficiency of the enzyme porphobilinogendeaminase (PBGD) • More than 250 mutations have been identified. • Symptoms include abdominal pain, irregular heart beat (tachycardia), acute psychosis, and respiratory paralysis. • Treatment: family screening (DNA testing), aviodance of factors that are known to cause attacks, heme derivatives. Future treatment may include liver transplantation, gene and enzyme therapy. • Vincent van Gogh may have been a case for AIP, as he worked tirelessly, fasted, and excessive consumption of absinthe. “Self-Portrait” Image: http://www.framedcanvasart.com/images/site/Van_Gogh.jpg