Blood

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Anatomy and Physiology II - Unit 1

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24 Terms

1
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List the functions of blood

Transport

  • gases (O2 + CO2)

  • metabolic waste products

  • hormones

Regulation

  • temperature → blood flow

  • pH → bicarbonate

  • fluid volume → body and interstitial tissues

Protection

  • clotting to prevent blood loss upon acute damage

  • immune system elements to fight infection → innate and adaptive

2
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What is blood made of in simple terms?

  • suspension of cells in a liquid

    • cell = erthyrocytes, leukocytes and platelets

    • liquid = plasma

3
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Percent composition of blood

  • separate out via centrifugation

    • Anti-coagulant added

      • upper layer plasma

        • 55% by volume '

        • contains 92% water, 7% protein, and 1% solutes

        • least dense

      • thin buffy coat of leukocytes + platelets on top

        • less than 1% of whole blood

      • thick red layer of erythrocytes on bottom

        • 45% of whole blood and most dense component

4
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Why blood is a connective tissue

  • progenitor cells derived from embryonic mesoderm

    • formed in red bone marrow

    • progenitor → early descendants of stem cells that cannot divide and reproduce indefinitely like stem cells

    • these cells became HSCs which then differentiate into various blood cells

  • has cells, suspended in ECM (plasma) and can form fibers to aid in clotting

  • leukocytes can migrate into collagenous connective tissues + epithelial cells

5
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Describe the composition and function of plasma.

  • involved in osmotic balance, protection, and transport of vitamins and minerals

  • Albumin

    • made of 60% of plasma protein

    • made by liver

    • major colloidal osmotic agent in blood

    • binds/transports hydrophobic biomolecules

  • Immunoglobulins

    • 18% of plasma protein

    • product of immune system cells in lymphoid organs

    • involved in humoral/adaptive immune response

  • Fibrinogens

    • 4% of plasma proteins

    • made by liver

    • blood clotting proteins

  • Hormone, fat-soluble vitamins, lipids and redox metal binding proteins

    • hormones: IGF-binding protein, thyroxine binding protein, transcortin

    • Vitamins: retinol binding protein, Vitamin D binding protein

    • Lipids: apolipoproteins

    • Redox metals: ceruloplasmin, transferrin

    • most made in liver

  • Ions and Solutes

    • Ions

      • high in Na+, CI-, and Ca2+ relative to cytosol

      • major buffer is bicarbonate

      • other minerals in low concentration

    • Solutes

      • glucose

      • amino acids

      • waste products

      • hormones

      • lipids

6
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Describe the structure, function and production of erythrocytes.

  • 99%

  • lack nucleus and mitochrondria

  • biconcave

  • hemoglobin

    • binds gases

      • high affinity for O2, NO, and CO at home

      • weak affinity for CO2, and HCO3- at other amino acid sites

  • Function: carry oxygen (high affinity), carbon dixoide (low affinity), and assist pH balance

  • lifetime of about 120 days with removal from macrophages + hemoglobin degradation

  • produced:

    • in red bone marrow

    • stimulated by erythropoietin (in kidneys)

    • requires iron, b12, folic acid and amino acids

7
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Describe the chemical composition of hemoglobin.

  • Proteins with heme groups bind gases

    • O2, CO, and NO bind heme iron

    • CO2, HCO3- binds global amino acids

8
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Hematopoiesis

  • occurs in adult in the red bone marrow of axial skeleton, girdles, and epiphyses of humerus and femur

  • stem cells divide and develop into mature erythrocyte

    • blast → cyte cells

    • Hematocytoblast (stem) → proerythroblast (committed) → erythroblast → reticulocyte → erythrocyte

  • during development

    • genes are turned on to make hemoglobin, mRNA, and protein

    • accumulate hemoglobin proteins

    • Loose nucleus → reticulocyte

    • loose mRNAmature erthrocyte

  • stimulated by erthropoietine produced by kidney

    • stimulated by low oxygen

    • stimulates development of committed cells

  • requires adequate iron, vitamins and amino acids for synthesis of hemoglobin

9
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Anemia (LOW TYPES)

  • lacking blood

  • hemorrhagic anemia → blood loss is greater than the production

  • Iron deficiencyinsufficient iron

  • Pernicious → vitamin deficiency (B12)

  • Renallack of EPO production by kidney

  • Aplastic → destruction of stem/progenitor cells → bone marrow damage

10
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Anemia (HIGH TYPES)

  • hemolytic → lysis of blood cells for acute reasons

  • Thalassemiasgenetic hemoglobin deficit

  • Sickle cell anemiapoint mutation in aggregations of hemoglobin + easy rupture

11
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Polycythemia

  • many blood cells

  • excess of RBC that makes blood too thick

  • vera → bone marrow cancer → proliferation of RBC

  • Secondary → EPO over stimulation → high altitiude

  • Blood doping → aerobic athletes artifically increase RBC to improve performance

12
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Leukocytes definition

  • nucleated cells that can migrate between tissues and blood

  • for inflammation and immune response

13
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Granulocytes

  • secretory granules with effector molecules for the innate immune response

  • 75% of leukocytes

  • Neutrophils

    • small granules

    • phagocytes and destroy bacteria

    • 50-70%

  • Eosinophils

    • large pink granules

    • contains protein which kills worms and proteases

    • 2%-4%

  • Basophils

    • very large purple granules

    • lobed nucleus

    • bind to activated IgE and release histamines to induce inflammatory response

    • <1%

14
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Agranulocytes

  • 25% of leukocytes

  • Lymphocytes

    • round nucleus with little cytoplasm

    • involved in adaptive immune system

    • classified into T-cells and B-cells which helps kill cancer cells and produce antibodies

    • 30%

  • Monocytes

    • large cell with dented nucleus

    • becomes macrophages in tissues and phagocytic cleaning debri cells

    • 5%

15
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Leukocyte production

  • develops from stem cells → blast via mature forms

  • gain granules + modify nucleus shape for granulocytes

  • myeloid stem cells: neutrophils, eosinophils, basophils, and monocytes

  • Lymphoid: T-cells, B-cell lymphocytes

  • develops from hematopoietic stem cells in red bone marrow

16
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Leukocytes disorders

Leukemias

  • cancerous overproduction of WBCs

  • acuterapid in young

  • chronicslow in elderly

  • Myeloid or Lymphoid

Infectious Mononucleosis

  • caused by infection of lymphocytes

  • highly contagious

Consequences: weakened immunity, infection risk, anemia, bleeding

17
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Platelets

  • small cell fragments from megakaryocytes

  • contains granules with clotting chemicals

  • sticks to damaged BV sites and initates clotting cascade

  • production regulated by thrombopoietin

18
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Hemostasis

  • process preventing blood loss at sites of damage involving platelets and blood clotting

  • Steps

    • vascular spasm (smooth muscle shortening stimulate by damage from endothelial cells or platelets)

    • Platelet plug formation (injury to endothelial cells lining the vessel exposes underlying fibers to which platelets adhere + platelets stick to each other → matrix → clot)

    • Coagulation/blood clotting fibrin proteins form a mesh that traps RBC and platelets → blood clot

    • Clot retraction → shortening of threads within interconnected plateletspulls clot together to close wound

    • Clot dissolution → protease called plasmin degrades fibrin fibrils

19
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Hemostasis Limiting Factors

  • anticoagulants

    • aspirin

      • inhibits the production of prostaglandin signaling molecules

    • Warfarin

      • prevents vitamin K-dependent + liver

    • Heparin

  • smooth endothelium

  • dilution of clotting factors

20
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Give examples of hemostatic disorders and the consequences of these disorders

  • thromboembolictoo much clotting

    • thrombostationary clot → tissue becomes ischemic and dies → heart attack

    • embolism → clot released and blocks vesselsstroke

  • Thrombocytopenialow platelet count

  • impaired liver functionlack of clotting factors

  • Hemophilia A,B,C missing clotting factors (VIII, IX, XI)

21
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Explain the basis of transfusion reactions.

  • Transfusion reactions

    • aggulination → aggregation of erthrocytes by antibodiesclogging small vessels

    • lysis of erthyrocytes cells → release of hemoglobinoverload of kidney

  • blood types are antigenic structures on the blood cell that fall into two groups with there being three types for one group and two types for the other group

22
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ABO blood group

  • three different alleles code for an enzyme that attaches carbs to an erythrocyte surface protein

  • A allele attaches N-acetylgalactosamine

  • B allele attaches galactose

  • O allele enzyme is inactive

  • Individuals produce antibodies against foreign blood group antigens and these can agglutinate RBCs

  • A, anti-B antibodies can receive A or O

  • AB, no antibodies can receive A, AB, B, or O

  • B, anti-A antibodies can receive B, O

  • O, anti-A and anti-B antibodies, O

  • Rh

    • Rh+ and Rh-

    • Rh- an individual develops antibodies after exposure to Rh+

  • Reactions:

    • agglutinationclogged BV

    • hemolysiskidney failure

23
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Describe the fluids uses to replace blood volume ant the circumstances for their use.

  • transfusions of whole blood or packed RBCs

  • isotonic saline or plasma expanders for short-term volume restoration

  • used during blood loss, surgery, or trauma

24
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Explain the diagnostic importance of blood testing.

Measures

  • cell counts

  • protein/enzyme levels

  • electrolytes, hormones, and waste

compares results to normal reference ranges

performed by automated machines

crucial for disease diagnosis and monitoring

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