1. Chapter 11: Blood 11.1 The Composition and Functions of Blood
11.2 The Blood Cells
11.3 Platelets and Hemostasis
11.4 Capillary Exchange
11.5 Blood Typing and Transfusions
11.6 Effects of Aging

2. 11.1 The Composition and Functions of Blood
Objectives:
Describe, in general, the composition of _________________________.
Divide the ___________________ of blood into three categories, and discuss each category.
Describe the composition of _____________ and the specific functions of the plasma proteins.

3. Composition of Blood Plasma (55%) Buffy coat Formed elements (45%)
WBCs and blood ____________________…top
Buffy coat
Thin, shiny layer in middle
Formed elements (45%)
RBCs, heavier because of _______________
Percentage of blood attributed to formed __________________ is called the hematocrit.

4. Function 1: Transport Moves from _________________ to all organs.
Picks up __________________ from lungs and nutrients from digestive tract and transports these to tissues.
Picks up cellular __________________, such as carbon dioxide
Transports hormones and messenger chemicals for various organs and _______________.

5. Function 2: Defense
Defends against pathogens (_________________ and viruses).
Removes ______________ and dying cells
Some WBCs can ‘eat’ ____________________.
Blood clotting to prevent blood loss. (platelets and plasma __________________)

6. Function 3: Regulation
Regulate body temperature by picking up heat from ___________________ muscles.
Uses concentration gradient (________________ __________) to transfer heat to other parts of the body.
Salts and plasma proteins keep osmotic __________________ in normal range.
Buffers in the blood keep the pH relatively constant at ___________

7. Plasma Composition 92% is __________________.
8% remaining is salts (ions) and ______________ molecules.
Small: Glucose, amino acids, ______________
Large: _________________ and plasma proteins.

8. Plasma Proteins Functions
Made in __________________
Help ________________ the blood and maintain pH (homeostasis)
Albumins contribute to the osmotic __________________.
Antibodies made by WBCs help fight infection (gamma globulins)
Transport different molecules.
Fibrinogen and prothrombin are necessary for ______________________.

9. 11.2 The Blood Cells Objectives:
Explain the hematopoietic role of _________ _____________in the red bone marrow.
Describe the structure, function, and life cycle of ______________ blood cells and _______________ blood cells.

10. Production of RBCs
Hematopoiesis: Process by which formed ___________________ are made (RBCs)
Multipotent stem cells: red ________________ marrow cells that mature into all the various types of blood cells.
May be able to ________________________ the body’s tissues in the laboratory.

11. Red Blood Cells Structure
Small, bioconcave disks that lack a _________________ when mature
Function
Transport _________________________
Life Cycle
Live only about _______________ days
Aka erythrocytes, formed from red bone marrow stem cells
Erythropoietin: hormone that helps induce RBC production; abused by athletes
Macrophages in _______________ and spleen engulf and ‘eat’ RBCs

12. White Blood Cells Structure
Larger, have a nucleus, lack hemoglobin, and are ___________________
Function
Fight infection, destroy dead or dying body cells, and recognize and kill ____________________ cells…all this helps maintain homeostasis
Life Cycle
Produced by red bone marrow, can be found in tissue fluid and ___________________
Many live only a few days when they fight infection
Others live months or __________________

13. 11.3 Platelets and Hemostasis
Objectives:
Describe the structure, function, and life cycle of _____________________.
Describe the ______________ events of hemostasis and the reactions necessary to coagulation.
Discuss __________________ of hemostasis.

14. Platelets Structure Function Life Cycle
____________________________; fragmented from megakaryocytes that develop in the red bone marrow
Function
Necessary for hemostasis
_______________________________________
Life Cycle
Because they have no nucleus, they last at most _____________ days

15. Hemostasis Vascular Spasm
Constriction of _________________ muscle layer in a broken blood vessel is the immediate response to injury
Platelets ______________________ seratonin that prolongs smooth muscle contraction
Platelet __________________________ Formation
Platelets adhere to _____________________________ fibers that are exposed when blood vessels break
As platelets build up, a platelet plug forms
Coagulation
Blood _____________________
Fibrinogen and prothrombin participate in blood clotting

16. Coagulation
Requires protein clotting __________________; most produced by liver
Intrinsic mechanism: blood will coagulate in a ____________________________________
Extrinsic mechanism: activated when ______________ tissues release tissue thromboplastin
Four steps: 1) Prothrombin activator is formed. 2) Prothrombin activator converts prothrombin to thrombin. 3) Thrombin severs two short amino acid chains from each fibrinogen molecules; they join end-to-end, forming fibrin. 4) Fibrin threads wind around the platelet plug in the damaged area of the blood vessel and provide framework for clot.

17. Hemostasis Disorders Thrombocytopenia Hemophilia
__________________ platelet count
autoimmune; your antibodies ________________ platelets
Megakaryocytes in red bone marrow are destroyed
Hemophilia
_______________________ (inherited)
Deficiencies of clotting factors
Hemophilia A: lack clotting factor _____________ and is most severe

18. 11.4 Capillary Exchange Objectives:
Describe capillary _______________ within the tissues.
Oxygen and nutrients leave a capillary. Cellular _______________ (carbon dioxide) enter the capillary.
In the lungs, it’s reversed. ______________ enters the blood and carbon dioxide leaves.

19. 11.5 Blood Typing and Transfusions
Objectives:
Explain the ______________ and Rh systems of blood typing.
Explain agglutination and its relationship to __________________________.

20. ABO Blood Groups + Rh Factor
Type A and B blood are _____________________.
Type O blood is recessive.
Rh positive is dominant and Rh negative is ___________________.

21. Transfusions Agglutination: __________________ of RBCs
Happens when transfusions are not _______________________.

22. 11.6 Effects of Aging Objectives:
Name the blood ___________________ that are commonly seen as we age.
Anemias, leukemias, and clotting disorders.
_______________ deficiency anemia and pernicious anemia (B12 deficient).
Leukemia is ________________ that is genetic and environmental.
Thromboembolism occurs because arteries contain ________________________.