Lecture 8 2/18/14 Flashcards

1
Q

Eosinophils

A

they pick up the eosinophil stains or basophilic stain. Part of the granulocytes. Granule Stains. Stain reddish-orange

Account for 2-4% of the WBC count

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2
Q

N L M E B

A

Never = Neutrophils - 60%

Let = Lymphocytes - 30%

Monkeys = Monocytes - 8%

Eat = Eosinophils - 3%

Bananas = Basophils - 0%

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3
Q

Major Role of Eosinophils

A

Combat irritants caused by allergic reactions and fight parasitic infections.

They engulf antibodies that mark various antigenic substances.

Bi-Lobed nucleus cell.

Produces histamine

3 Molecules: Histamine, Seratonin, and Bradykinins

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4
Q

Basophil

A

Picks up the basophilic stain

Don’t have a cytoplasm.

Big Guns for allergic reactions

Produces the bradykinin for inflammatory response. Small, darkly stained granules that fill up the cytoplasm to obscure the nucleus.

Account for .5% of the WBC’s. They enter the tissue and release heparin, which heparin is a blood thinner.

Involved in the anti-flammatory response. Histamine and seratonin to prevent blood clotting and increase local inflammation. 2-3 lobed nuclei. You will find in the blood stream.

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5
Q

Mast Cell

A

is nothing more than a resident basophil. Won’t be found in the blood stream. Derived from basophil cell line. Some small percentage of basophils end up in the cell tissue.

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6
Q

Hypovolumic

A

lowered blood volume, could cause death.

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7
Q

Granulocyte Development

A

Hemocytoblasts -> Myeloid Stem Cell -> Progenitor Cells -> Myeloblast (Precursor cell to all granulocytes) -> Myelocytes -> Band Cells (WBC that has not matured, no segmented nuclei) -> WBC’s to become segmented.

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8
Q

Agranular Leukocytes

A

Leukocytes are white blood cells

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9
Q

Lymphocytes

A

account for 25-30% of the WBC population. These cells have a large nucleus surrounded by a thin halo of cytoplasm.

Major role responsible for specific immunity, which is the ability to attack different types of microbes on an individual basis.

B-Lymphocytes it develops, and develops or mature in bone marrow. T-Lymphocytes - mature in the thymus.

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10
Q

T-Lymphocytes

A

Responsible for cellular immunity by attacking the cells directly. Killer T cells.

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11
Q

T-Killer Cells

A

Punch holes in bacterial cell walls. The cell then can’t maintain.

General immunity

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12
Q

Complement System

A

Part of immune system. Destroys bacterium. Destroys cell walls

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13
Q

B-Cells or B-Lymphocytes

A

responsible for humoral immunity, more of a specific immunity.

Divide wildly and split to become memory B Cell and Plasma Cell, involved in making antibodies.

Plasma Cells which secrete antibodies that attack a specific antigenic substance. antibodies will bind to antigens to make an antigen/antibody complex.

This complex is heavier, it has a tendency to precipitate out solution and roll along the endothelium, where the WBC’s can get a hold of it, and then we can start our immuno response.

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14
Q

Memory Cells

A

“remember” a specific antigen, and when re-exposed to that antigen divide wildly to make plasma cells that will produce specific antibodies to that antigen.

They may live months to years within the body. The basis for vaccinations or immunizations.

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15
Q

Lymphocyte Development

A

Hemocytoblast -> lymphoid stem cell (lymphatic tissue) -> Lymphoplast -> Prolymphocyte -> Lymphocyte

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16
Q

Monocytes

A

account for 3-8% of the WBC population. Take longer to reach the infection site .

Utilize phagocytic action to engulf the foreign invader. Prevalent in chronic infections (i.e. tuberculosis).

A relatively large WBC. The nucleus is oval or kidney-bean shaped. When it stains, faint pink cytoplasm, washed out kidney shape nucleus.

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17
Q

What are resident monocytes called?

A

Macrophages and they flow around in the blood stream

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18
Q

They are also resident macrophages in what?

A

In all of the tissue in the body.

The first cell that will be involved in fighting the infection immediately will be the resident macrophages, the cell that is already there.

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19
Q

Monocyte Development

A

Hemocytoblast -> Myeloid Stem Cell -> Monoblast -> Promonocyte -> Monocyte

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20
Q

Thrombocytes Platelets

A

Comes from thrombin. Not more than cytoplasmic packets or another cell called a megakaryocyte(marrow) - a large cell with a large nucleus, this cell never leaves the bone marrow.

Between 250,000-400,000/mm3. Function to initiate and carry out the clotting process of blood. Life span- approximately 1 week.

21
Q

Thrombocyte Development

A

Hemocytoblast -> Myeloid Stem Cell -> Megakaryocyte (Marrow) -> Platelets

22
Q

Plasma

A

The liquid-like component of blood remaining when the formed elements are removed.

Approx. 55% of total blood volume. Made up of water, electrolytes nutrients, waste products and proteins.

23
Q

3 Types of Proteins

A

Albumins

Globular Proteins

Fibrinogens

24
Q

Albumins

A

serves as an osmotic agent for blood. Egg Proteins. Represent approx. 60% of blood proteins.

Job is to maintain blood fluid volume. Can act as a osmotic agent. To keep the water in the capillaries.

25
Q

Globular Proteins

A

globs of protein flowing in the blood stream. Most of these are carrier proteins for other molecules like hormones.

Represent 35% of blood proteins. Function as blood transporters and immune proteins.

26
Q

Fibrinogens

A

also made by the liver. Involved in the clotting mechanism.

27
Q

Differences between plasma and interstitial fluid

A

Plasmid will have Greater O2 Greater CO2, increased dissolved proteins and decreased proteins. Greater number of proteins in the blood.

28
Q

The Clotting Process

A

The process of clotting is known as coagulation or hemostasis (the prevention of blood loss)

29
Q

5 Phases of Blood Clotting

A

Stage 1 The Vascular Phase

Stage 2 The Platelet Phase

Stage 3 The Coagulation Phase

Stage 4 Clot Retraction Phase

Stage 5 Fibrinolysis

30
Q

Stage 1 The Vascular Phase

A

When we cut the vessel, we create a vascular spasm. 1st step in the clotting process.

31
Q

Stage 2 The Platelet Phase

A

involved in platelet adhesion. The injured cells become sticky, then the platelets adhere to that stickiness and then start their process.

32
Q

Stage 3 Coagulation Phase

A

a cascade of effects involving 11 different factors called procoagulants.

33
Q

Two Pathways of the Coagulation Phase

A

Extrinsic Pathway

Intrinsic Pathway

34
Q

Extrinsic Pathway

A

1st part and reacts quickly but it’s affect are short lived; When we damage the tissue, there is a release of tissue release of PF-3 thromboplastin

35
Q

Intrinsic Pathway

A

releases PF-3, Platelet Factory 3. Activate the platelet thromboplastin.

36
Q

Both Extrinsic and Intrinsic Pathway Merge into what?

A

Common Pathway

37
Q

Prothrombin Converts to

A

Thrombin

38
Q

Thrombin Converts to

A

Fibrinogen

39
Q

Fibrinogen Converts to

A

Fibrin

40
Q

Common Pathway Conversion

A

Will convert Prothrombin to Thrombin, then thrombin converts Fibrinogen into Fibrin

41
Q

Procoagulants (Clotting Factors)

A

made in the liver, are the intermediates in the clotting pathway. 11 of these. Every single step requires calcium. Don’t have calcium you can’t clot.

42
Q

Classic Hemophilia

A

absence of clotting factor 8. Part of the intrinsic pathway. Without it, we don’t have a robust response. Sex linked. So it travels more on the X Chromosome. More common in males.

43
Q

Stage IV Clot Retraction Phase

A

also known as Syneresis. Tightening of the clot. Reduces the size of the damaged area. Then scar tissue cells, part of the healing process. Many cells have actin and myosin. Clathrin has actin and myosin.

44
Q

Stage V Fibrinolysis

A

clot dissolution. Start out with Plasminogen which then converts to Plasmin. Plasmin is an enzyme that breaks down clot.

45
Q

Plasminogen converts to what?

A

Plasmin

46
Q

Name 3 Unwanted Clotting

A

Thrombosis

Embolus

Embolism

47
Q

Thrombosis

A

clot in an unbroken vessel that is stationary.

48
Q

Embolus

A

dislodged clot moving through a vessel.

49
Q

Embolism

A

condition of embolus of the dislodged clot moving through the vessel. can also be air bubble, or fat globule.