Fundamentals of Biology
Lesson 29
The Lymphatic and Excretory Systems
I. Structure.
A. Lymph: the fluid contained in the lymphatic
system.
B. Lymph capillaries.
1. Located almost everywhere in the
body.
2. Dead-end, one-way tubes.
3. Extracellular fluid is under
greater pressure than fluid in the lymph capillaries.
4. Walls of capillaries allow fluid
to enter easily, but prevent fluid leaving.
C. Lymph vessels.
1. Similar to veins.
2. Muscle fibers in the walls pump
the fluid along.
3. Movement of skeletal muscles
assist the flow of lymph.
4. Valves prevent back-flow.
D. Lymph nodes: filter out and destroy foreign
matter.
E. Thoracic duct and right lymph duct: empty into veins
near the heart.
II. Purpose.
A. Drain excess water from the extracellular fluid back
into the circulatory system.
B. Temporary reservoir for fluids taken into the body.
C. Carry large molecules (e.g. proteins and hormones too
large to cross the capillary wall) to the blood.
D. Transport some food molecules (e.g. fats) from the
intestine to the blood.
E. Fight disease at the lymph nodes.
III. Development of Types of Blood Cells.
A. All arise from hematopoietic stem cells in the bone
marrow.
B. Erythroids develop into erythrocytes.
C. Myeloids develop into monocytes and granulocytes.
1. Monocytes develop into macrophages.
a. Large
phagocytic cells.
b. Engulf
virtually any substance foreign to the body.
c. Wandering:
travel through the blood and lymph.
d. Fixed:
embedded in lymph tissue.
2. Granulocytes.
a. The most
common leukocytes.
b. Develop
into neutrophils: small phagocytic cells.
D. Lymphocytes.
1. Small cells with varying shapes.
2. The most important leukocytes.
3. Circulate throughout the body in
the blood and lymph.
4. Perform several immune functions.
a. Recognize
antigens.
b. Produce
antibodies.
c. Control
the immune response.
d. Remember
the immune response somehow.
5. 2 major types.
a. T
lymphocytes: undergo further differentiation in the thymus gland.
b. B
lymphocytes.
i. Named for the bursa of Fabricius in birds where they undergo further
differentiation.
ii. This differentiation in mammals takes place in the bone marrow.
c. Look
alike, but bear different surface markers and perform different functions.
6. Both types come in 1000's of
different varieties, one for each antigen.
IV. Lymph Nodes.
A. A network of sinuses lined with lymphocytes and fixed
macrophages.
B. As the lymph passes through, the macrophages engulf
bacteria, viruses, etc. and digest them in vacuoles.
V. Immunity.
A. The ability of the body to destroy a pathogen or render
it harmless.
B. Antigen: any foreign substance against which the
body reacts.
1. Usually a protein.
2. E.g. part of a viral capsid, or a
chemical released by a bacteria.
C. Antibody: a protein which travels through the
body in the blood and lymph to aid in destroying an antigen.
VI. Humoral Immunity.
A. Destruction of antigens by antibodies in the body
humors.
B. Each person has 1000's of different B lymphocytes, each
recognizing a different antigen.
C. An antigen stimulates a specific B lymphocyte to divide
and produce plasma cells and memory B cells.
D. Plasma cells produce antibodies.
1. Live 4-5 days.
2. Produce up to 2,000 antibodies per
second.
E. These antibodies travel throughout the body to find and
react with their specific antigen.
1. Block a receptor site on a viral
capsid.
2. Precipitate the antigen: cause it
to clump together.
3. Cause agglutination: cause
infected cells to clump together.
4. Immobilize flagella.
F. The neutralized antigen can then be removed by
phagocytosis or another means.
G. Memory B cells may live for several dozen years.
1. A second infection will trigger
them to divide and make antibodies much faster.
2. The antigen can be eliminated
before the person notices any disease symptoms.
VII. Cell-mediated Immunity.
A. Destruction of cells infected by an antigen.
B. Certain parts of certain antigens become bonded to the
surface of a macrophage attempting to engulf them.
C. This may stimulate the division and differentiation of
a helper T cell.
1. Helper T cells: provide more cells
from which to make the other T cells.
2. Killer T cells: attack body
cells joined to an antigen.
a. Attach to
the affected cell.
b. Release a
membrane lysing enzyme.
c. The cell
membrane ruptures, killing the cell.
3. Suppressor T cells: stop
the activity of the other lymphocytes when the infection has been arrested.
4. Memory T cells: will
circulate in the blood for dozens of years, ready to respond rapidly to another
infection.
VIII. Kinds of Immunity.
A. Active: the antibodies or T cells are made by the
person infected.
1. Natural: he got the disease.
2. Artificial: he received a vaccine.
B. Passive: the antibodies are supplied to the person.
1. Natural: obtained from his mother,
either through the placenta or by nursing.
2. Artificial: obtained from the
blood serum of other humans or animals.
The Excretory System
I. Organs.
A. Kidneys.
1. Filter metabolic wastes from the
blood.
2. Excrete these wastes as urine.
B. Ureters.
1. Muscular tubes connecting kidneys
to the urinary bladder.
2. Urine is moved by peristalsis.
C. Urinary Bladder.
1. Urine reservoir.
2. Muscular wall, lining.
D. Urethra.
1. Tube leading from the bladder to
the outside.
2. Two sphincters at the exit.
3. Operation.
a. Muscles of
bladder contract.
b. Pressure
forces one sphincter open.
c. Other
sphincter must be opened voluntarily.
II. Kidneys.
A. Structure.
1. Connective tissue: a thin layer
surrounds and holds the kidneys in place.
2. Cortex: contains the outer
part of the nephrons.
3. Medulla.
a. Pyramids:
cone-shaped masses of tissue.
b. Contains
the inner part of the nephrons.
4. Pelvis: collects urine.
B. Flow volume.
1. Out of 5.6 l total of
blood, 1.2 l pass through the kidneys each minute.
2. All the blood passes through the
kidneys 280 times per day.
C. Nephrons.
1. General.
a. This is
the functional part of the kidney.
b. 1million
per kidney.
2. Renal corpuscle.
a. Located in
the cortex.
b. Glomerulus:
a capillary bed
c. Bowman’s
capsule: cup-shaped end to the tubule of the nephron.
d. Blood
enters the glomerulus under pressure.
e. Much of
the blood fluid filters into the capsule, including glucose and amino acids.
f. Large
proteins and whole cells are left behind.
3. Proximal convoluted tubule.
a. Located in
the cortex.
b. Na+
and glucose are returned to the blood by active transport.
c. Cl-
follows the sodium passively
d. H2O
follows the Cl- by osmosis.
e. 100% of
glucose and 75% of salt and H2O return to the blood.
4. Loop of Henle.
a. Extends
down into the medulla.
b. Purpose is
to set up a high concentration of NaCl in the medulla.
i. There is no known carrier that can transport H2O molecules.
ii. Cells move water across a membrane by setting up a concentration gradient so
H2O will move by osmosis.
c. Later, H2O
will diffuse out from the collecting duct which also passes through the medulla.
d. Cl-
is pumped out of the ascending part of the loop, and Na+ follows.
e. H2O
would follow, too, but this part of the loop is impermeable to H2O.
f. Since
there is more Cl- in the lower part of the loop, more Cl-
will be pumped out here.
g. Thus the
lower part of the medulla has a higher concentration of NaCl.
h. As fluid
descends the loop, water diffuses out because of this high concentration of NaCl.
i. (The
descending part of the loop is permeable to water.)
j. Cl-
and Na+ also diffuse into the descending part of the loop.
k. Thus the
NaCl are constantly recycled.
l. The point
of all this is to set up a concentration gradient in the medulla so that water
will diffuse out of the collecting duct.
m. This
system is called a countercurrent multiplier.
5. Distal convoluted tubule.
a. Located in
the cortex.
b. Na+
is returned to the blood by active transport.
c. H2O
follows the Na+ by osmosis.
d. K+
and H+ enter the tubule by active transport.
e. NH3
follows by diffusion.
f. Secretion
of H+ helps regulate the pH of the blood.
6. Collecting duct.
a. Passes
through the medulla and empties into the pelvis.
b. Urine is
concentrated.
c. H2O
exits the duct by osmosis as it passes through the increasing NaCl gradient.
d. The Na+,
Cl-, and H2O diffuse back into the capillaries or the
lymphatic system.
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