Blood Flashcards

1
Q

Explain the composition of Blood

A

Blood

It is composed of liquid plasma and formed elements

Formed elements include:

  1. Erythrocytes, or red blood cells (RBCs)
  2. Leukocytes, or white blood cells (WBCs)
  3. Trombocytes, or platelets
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Where does Hematopoesis takes place?

A

Hematopoesis

Blood cell formation, Hematopoesis, takes place in the red bone marrow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How much percentage of body weight does Blood account for?

A

Blood accounts for approximately 8% of body weight

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the average volume of blood?

A

Average volume: 5–6 L for males, and 4–5 L for females

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Give example of solutes in Blood Plasma.

A

Blood Plasma contains over 100 solutes, including;

  1. Proteins – albumin, globulins, clotting proteins, and others
  2. Lactic acid, urea, creatinine
  3. Organic nutrients – glucose, carbohydrates, amino acids
  4. Electrolytes – sodium, potassium, calcium, chloride, bicarbonate
  5. Respiratory gases – oxygen and carbon dioxide
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Explain Erythrocytes.

A

Erythrocytes (RBCs)

  • Biconcave discs, anucleate, essentially free of organelles
  • Filled with hemoglobin (Hb), a protein that functions in gas transport
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Describe Hemoglobin and the differenet phases during gas transportation

A

Structure of Hemoglobin

  • Each Hb molecule can transport four molecules of oxygen bound to the heme groups
  • Oxyhemoglobin – Hb bound to oxygen
    • Oxygen loading takes place in the lungs
  • Deoxyhemoglobin – Hb after oxygen diffuses into tissues (reduced Hb)
  • Carbaminohemoglobin – Hb bound to carbon dioxide
    • Carbon dioxide loading takes place in the tissues
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the turnover of red blood cells (RBC)

A

Turnover of red blood cells (RBC)

  • The life span of an erythrocyte is 100–120 days
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What happens if you have too many or too few RBC:s?

A

Erythrocytes

The number of circulating erythrocytes remains constant and reflects a balance between RBC production and destruction:

  • too few RBCs leads to tissue hypoxia (pale and/or cyanotic skin!)
  • too many RBCs, polycythemia, causes undesirable blood viscosity (blushing skin!)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Explain Erythropoiesis

A

Production of Erythrocytes: Erythropoiesis

Developmental stages of erythroblasts.

Erythropoiesis requires:

  1. Iron
  2. Vitamin B12
  3. Folic acid
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Explain Hormonal Control of Erythropoiesis

A

Hormonal Control of Erythropoiesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Explain Erythrocyte Destruction and Heme Metabolism

A

Erythrocyte Destruction and Heme Metabolism

  • Dying RBCs are engulfed by macrophages mainly in the spleen
  • Heme and globin are separated and the iron is saved for reuse
  • Heme is degraded to a yellow pigment, bilirubin, that is concentrated in the liver (icterus or jaundice in liver disease!)
  • The liver secretes conjugated bilirubin into the intestines along with the bile
  • The intestines metabolize bilirubin to a brownish pigment in feces
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Explain symptoms and causes of Anemia

A

Anemia

  • Signs and symptoms include fatigue, paleness, shortness of breath, and chills
  • Various causes:
    • Iron-deficiency (secondary to hemorrhage; inadequate intake; impaired absorption)
    • Deficiency of vitamin B12 (inadequate intake; impaired absorption)
    • Premature RBC destruction (genetic; autoimmune)
    • Defective erythropoesis (leukemia and other myeloproliferative disorders)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Explain Sickle-Cell Anemia

A

Anemia: Abnormal Hemoglobin

  • Sickle-cell anemia – results from a defective gene coding for an abnormal Hb called hemoglobin S (HbS)
    • HbS has a single amino acid substitution in the beta chain; this defect causes RBCs to become sickle-shaped in low oxygen situations
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Explain Leukocytes

A

White blood cells (WBCs), also called leukocytes or leucocytes, are the cells of the immune system that are involved in protecting the body against both infectious disease and foreign invaders. All white blood cells are produced and derived from multipotent cells in the bone marrow known as hematopoietic stem cells. Leukocytes are found throughout the body, including the blood and lymphatic system.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How does the classification of Leukocytes look like?

A

White blood cells - Leukocytes
A. Granular leukocytes (contain conspicuous granules
that are visible under a light microscope after staining)
1. Neutrophils
2. Eosinophils
3. Basophils
B. Agranular leukocytes (no granules are visible under a
light microscope after staining)
1. T and B lymphocytes and natural killer cells
2. Monocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

How does the distribution of Leukocytes look like?

A

Leukocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Describe Neutrophils

A

Neutrophils

  • Neutrophils have two types of granules that:
    • Take up both acidic and basic dyes
    • Give the cytoplasm a lilac color
    • Contain peroxidases, hydrolytic enzymes, and defensins (antibiotic-like proteins)
  • Neutrophils are our body’s bacteria slayers
19
Q

Describe Eosinophils

A

Eosinophils

  • Eosinophils account for 1–4% of WBCs
    • Have red-staining, bilobed nuclei connected via a broad band of nuclear material
    • Have red to crimson (acidophilic) large, coarse, lysosome-like granules
    • Lead the body’s counterattack against parasitic worms
    • Lessen the severity of allergies by phagocytizing immune complexes
20
Q

Describe Basophils

A

Basophils

  • Account for 0.5% of WBCs and:
    • Have U- or S-shaped nuclei with two or three conspicuous constrictions
    • Are functionally similar to mast cells
    • Have large, purplish-black (basophilic) granules that contain histamine
      • Histamine – inflammatory chemical that acts as a vasodilator and attracts other WBCs (antihistamines counter this effect)
21
Q

Describe Lymphocytes

A

Lymphocytes

  • Account for 25% or more of WBCs and:
    • Have large, dark-purple, circular nuclei with a thin rim of blue cytoplasm
    • Are found mostly enmeshed in lymphoid tissue (some circulate in the blood)
  • There are two types of lymphocytes: T cells and B cells
    • T cells function in the immune response
    • B cells give rise to plasma cells, which produce antibodies
22
Q

Describe Monocytes

A

Monocytes

  • Monocytes account for 4–8% of leukocytes
    • They are the largest leukocytes
    • They have abundant pale-blue cytoplasms
    • They have purple-staining, U- or kidney-shaped nuclei
    • They leave the circulation, enter tissue, and differentiate into macrophages
23
Q

Describe Macrophages

A

Macrophages

  • Are highly mobile and actively phagocytic
  • Activate lymphocytes to mount an immune response

Phagocytes are cells that protect the body by ingesting (phagocytosing) harmful foreign particles, bacteria, and dead or dying cells.

24
Q

Explain Platelets

A

Platelets
Pluripotent stem cells also differentiate into cells that produce
platelets (see Figure 14.2a). Some myeloid stem cells
develop into cells called megakaryoblasts, which in turn transform into megakaryocytes, huge cells that splinter into
2000–3000 fragments in the red bone marrow and then enter
the bloodstream. Each fragment, enclosed by a piece of the
megakaryocyte cell membrane, is a platelet. Between 150,000
and 400,000 platelets are present in each L of blood.
Platelets are disc-shaped, have a diameter of 2–4 m, and exhibit
many vesicles but no nucleus. When blood vessels are
damaged, platelets help stop blood loss by forming a platelet
plug. Their vesicles also contain chemicals that promote
blood clotting (both processes are described shortly). After
their short life span of 5–9 days, platelets are removed by
macrophages in the spleen and liver.

25
Q

Explain Formation of Leukocytes

A

Formation of Leukocytes

  • myelopoesis* = the production of bone marrow and of all cells that arise from it, namely, all blood cells. But in a narrower sense that is also commonly used, myelopoiesis is the regulated formation specifically of myeloid leukocytes (myelocytes), including eosinophilic granulocytes, basophilic granulocytes, neutrophilic granulocytes, and monocytes.
  • lymphopoesis* = the generation of lymphocytes, one of the five types of white blood cell (WBC). It is more formally known as lymphoid hematopoiesis. Pathosis in lymphopoiesis leads to any of various lymphoproliferative disorders, such as the lymphomas and lymphoid leukemias.
26
Q

Explain Leukemias

A

Leukocytes Disorders: Leukemias

  • Leukemia refers to cancerous conditions involving WBCs
  • Leukemias are named according to the abnormal WBCs involved
    • Myelocytic leukemia – involves myeloblasts
    • Lymphocytic leukemia – involves lymphocytes
  • Acute leukemia involves blast-type cells and primarily affects children
  • Chronic leukemia is more prevalent in older people
27
Q

Explain Platelets

A

Platelets

  • Platelets are fragments of megakaryocytes with a bluestaining outer region and a purple granular center
  • Their granules contain serotonin, Ca2+, enzymes, ADP, and platelet-derived growth factor (PDGF)
  • Platelets function in the clotting mechanism by forming a temporary plug that helps seal breaks in blood vessels
  • Platelets not involved in clotting are kept inactive by NO and prostacyclin
28
Q

Explain Genesis of Platelets

A

Genesis of Platelets

The stem cell for platelets is the hemocytoblast

29
Q

Explain Hemostasis

A

Hemostasis

  • A series of reactions for stoppage of bleeding
  • During hemostasis, three phases occur in rapid sequence
    • Vascular spasms – immediate vasoconstriction in response to injury
    • Platelet plug formation
    • Coagulation (blood clotting)
30
Q

Explain the Coagulation Process

A

Coagulation Process

31
Q

Explain Thromboembolytic Conditions

A

Hemostasis Disorders: Thromboembolytic Conditions

  • Thrombus – a clot that develops and persists in an unbroken blood vessel
    • Thrombi can block circulation, resulting in tissue death (e.g. heart attack)
  • Embolus – a thrombus freely floating in the blood stream
    • Pulmonary emboli can impair the ability of the body to obtain oxygen
    • Cerebral emboli can cause strokes
32
Q

Explain Thrombocytopenia

A

Hemostasis Disorders: Bleeding Disorders

Thrombocytopenia – condition where the number of circulating platelets is deficient

  • Patients show petechiae due to spontaneous, widespread hemorrhage
  • Caused by suppression or destruction of bone marrow (e.g., malignancy, radiation)
33
Q

Explain Hemophilia

A

Hemostasis Disorders: Bleeding Disorders

  • Inability to synthesize procoagulants by the liver results in severe bleeding disorders; causes can range from vitamin K deficiency to hepatitis and cirrhosis
  • Hemophilias – hereditary bleeding disorders caused by lack of clotting factors
    • Hemophilia A – most common type (83% of all cases) due to a deficiency of factor VIII
    • Hemophilia B – due to a deficiency of factor IX
    • Hemophilia C – mild type, due to a deficiency of factor XI
34
Q

Explain how blood groups are classified

A

Human Blood Groups

  • RBC membranes have glycoprotein antigens on their external surfaces
  • These antigens are:
    • Unique to the individual
    • Recognized as foreign if transfused into another individual
    • Promoters of agglutination and are referred to as agglutinogens
  • Presence or absence of these antigens is used to classify blood groups
35
Q

How many natural varities of RBC antigens are there?

A

Humans have 30 varieties of naturally occurring RBC antigens

36
Q

Which antigens cause vigorous transfusion reactions if improperly transfused?

A

The antigens of the ABO and Rh blood groups cause vigorous transfusion reactions when they are improperly transfused

37
Q

What are the other blood groups antigens than ABO and Rh?

A

Other blood groups (M, N, Dufy, Kell, and Lewis) are mainly used for legalities

38
Q

Describe the ABO blood groups

A

ABO Blood Groups

  • The ABO blood groups consists of:
    • Two antigens (A and B) on the surface of the RBCs
    • Two antibodies in the plasma (anti-A and anti-B)
  • ABO blood groups may have various types of antigens and preformed antibodies
  • Agglutinogens and their corresponding antibodies cannot be mixed without serious hemolytic reactions
39
Q

Explain Rh Blood Groups

A

Rh Blood Groups

  • There are eight different Rh agglutinogens, three of which (C, D, and E) are common
  • Presence of the Rh agglutinogens on RBCs is indicated as Rh +
  • Anti-Rh antibodies are not spontaneously formed in Rh – individuals
  • However, if an Rh – individual receives Rh + blood, anti-Rh antibodies form
  • A second exposure to Rh + blood will result in a typical transfusion reaction
40
Q

Explain Transfusion Reactions

A

Transfusion Reactions

  • Transfusion reactions occur when mismatched blood is infused
  • Donor’s cells are attacked by the recipient’s plasma agglutinins causing:
    • Diminished oxygen-carrying capacity
    • Clumped cells that impede blood flow
    • Ruptured RBCs that release free hemoglobin into the bloodstream
41
Q

Explain Agglutinin

A

An agglutinin is a substance that causes particles to coagulate to form a thickened mass

42
Q

Explain how Blood is being tested

A

Blood Types

  • When serum containing anti-A or anti-B agglutinins is added to blood, agglutination will occur between the agglutinin and the corresponding agglutinogens
  • Positive reactions indicate agglutination
43
Q

Explain how the reaction looks like when testing for Blood types ABO

A

ABO - blood testing

44
Q
A