Chapter 7 and 17 The Immune system and Development and
Aging
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IMMUNE SYSTEM
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l FIGHTS OFF DISEASES l 2 TYPES OF DEFENSES 1. NON-SPECIFIC-
GENERAL INFLAMMATION AND ATTACK 2. SPECIFIC- HIGHLY ACCURATE-
ANTIBODIES AND T-CELLS
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ANTIGEN l ANY FOREIGN SUBSTANCE THAT IS CAPABLE OF ACTIVATING
THE IMMUNE SYSTEM l USUALLY SMALL PARTICLES ON THE SURFACES OF
INVADING CELLS AND VIRUSES l POLLEN AND MOLD CAN BE ANITGENS FOR
THOSE WITH ALLERGIES
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LYMPHATIC SYSTEM l LYMPHOID VESSELS AND ORGANS 1. COLLECT
EXCESS CLEAR FLUID (plasma that leaks out of blood vessels) AND
RETURN IT TO BLOODSTREAM 2. TINY LYMPH VESSELS ABSORB FATS IN THE
SMALL INTESTINE 3. HELPS FIGHT DISEASE
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LYMPH VESSELS l FOUND THROUGHOUT THE BODY l CONTAIN ONE WAY
VALVES, MUSCULAR CONTRACTION PUMPS FLUID EDEMA= TOO MUCH FLUID l
LYMPH IN VESSELS EVENTUALLY DRAINS INTO 2 LARGE VEINS IN THE BASE
OF THE NECK
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LYMPHOID ORGANS Lymph NODES- A CAPSULE LINED WITH IMMUNE CELLS
SPLEEN- CAPSULE FILLED WITH BLOOD AND IMMUNE CELLS THYMUS- where T
LYMPHOCYTES MATURE RED BONE MARROW- MAKES ALL BLOOD CELLS
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NON-SPECIFIC DEFENSES l FIGHTS CANCER CELLS AND PATHOGENS-
VIRUSES AND OTHER ORGANISMS THAT CAUSE DISEASE l SKIN, MUCOUS
MEMB., STOMACH- PREVENTS ENTRY l INTERFERON- A CHEMICAL THAT IS
PRODUCED BY A VIRAL INFECTED CELL- TELLS OTHER CELLS TO MAKE
ANTIVIRAL CHEMICALS
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BROKEN SKIN l INFLAMMATORY Reaction BRADYKININS from damaged
cells l STIMULATE PAIN RECEPTORS l STIMULATE MAST CELLS which make
HISTAMINES which dilate capillaries and make them leaky l
MACROPHAGES crawl out of the dilated capillaries and destroy
invaders
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SPECIFIC DEFENSES l B- CELLS l T- CELLS
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B-CELLS l MATURE IN RED BONE MARROW l PRODUCE SPECIFIC
PROTEINNS CALLED ANTIBODIES WHICH BIND TO ANTIGENS- this either
KILLS the PATHOGEN OR MARKS IT FOR ATTACK by T-cells l PLASMA CELLS
MAKE ANTIBODIES MEMORY CELLS ARE DORMANT but CAN BE
REACTIVATED
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SPECIFICITY l THOUSANDS OF DIFFERENT TYPES OF B-CELLS l EACH
TYPE HAS A SPECIAL ANTIGEN RECEPTOR l WHEN A CELLS ANTIGEN BINDS-
IT DIVIDES INTO PLASMA CELLS (which make antibodies) AND MEMORY B
CELLS
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T CELLS l MATURE IN THE THYMUS l SOME DIRECTLY ATTACK CELLS
THAT BEAR ANTIGENS, OTHERS STIMULATE B CELLS l ALSO HAVE SPECIFIC
RECEPTORS l Must be presented with the antigen by an antigen
presenting cell (APC) l CLONAL SELECTION PRODUCES KILLER T CELLS
AND MEMORY T
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ACTIVE IMMUNITY to DISEASE l FROM INFECTION OR VACCINATION l
TRIGGERS IMMUNE RESPONSE BY B AND T CELLS- MAKES MEMORY B, T l NEXT
EXPOSURE= secondary exposure MEMORY B AND T CELLS DIVIDE VERY
QUICKLY AND AN INFECTION CAN BE FOUGHT OFF QUICKLY l Most of the
time you dont ever feel sick
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IMMUNIZATION l VACCINES CONTAIN PARTICLES OF THE PATHOGEN OR A
WEAKENED OR KILLED PATHOGEN= ANTIGEN l SMALL POX- ERADICATED by
vaccine in 1970s, but possible terrorist weapon l TETANUS,
DIPHTHERIA, HEP. B, FLU, MEASLES, MUMPS, RUBELLA, POLIO
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PASSIVE IMMUNITY l ANTIBODIES FROM ANOTHER SOURCE ARE GIVEN TO
A PERSON l FOUND IN MOTHERS MILK OR MADE BY ANOTHER ORGANISM AND
INJECTED l NO MEMORY CELLS= SHORT TERM IMMUNITY
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ALLERGIES l OVERACTIVE IMMUNE SYSTEM l SPECIAL BAD TYPE E
ANTIBODIES ARE SOMETIMES PRESENT ON CERTAIN MAST CELLS l IF AN
ALLERGEN MATCHES THE E ANTIBODIES THEN THE MAST CELL RELEASES
HISTAMINE- WHICH CAUSES LEAKY CAPILLARIES- RUNNY NOSE itching
etc.
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ALLERGY RELIEF l SHOTS- INJECT SMALL AMOUNTS OF ALLERGEN l
TRIGGERS GOOD ANTIBODIES TO BE MADE l GOOD ANTIBODIES NEUTRALIZE
ALLERGEN BEFORE IT CAN ATTACH TO BAD TYPE E ANTIBODIES
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TRANSPLANT REJECTION l FOREIGN TISSUES OR ORGANS HAVE FOREIGN
CHEMICALS ON SURFACES OF THE CELLS l THE BODY NATURALLY ATTACKS
THESE ANTIGENS l IMMUNOSUPPRESSIVE DRUGS MUST BE GIVEN IN ORDER TO
PREVENT REJECTION
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AUTOIMMUNE DISEASES l The immune system attacks your own cells
l MULTIPLE SCLEROSIS- BODY ATTACKS ITS OWN NERVE CELL COVERINGS l
LUPUS BODY ATTACKS ITS OWN DNA l RHEUMATOID ARTHRITIS- JOINTS l
TYPE 1 DIABETES- CHILDS BODY DESTROYS INSULIN MAKING CELLS IN THE
PANCREAS
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DEVELOPMENT AND AGING
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FERTILIZATION l THE UNION OF THE SPERM NUCLEUS AND THE EGG
NUCLEUS l PRODUCES A DIPLOID CELL CALLED A ZYGOTE l TAKES PLACE IN
THE OVIDUCTS
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STEPS 1. SPERM COME IN CONTACT WITH THE OUTSIDE LAYER OF THE
EGG 2. ACROSOMAL ENZYMES ARE RELEASED- EATS THROUGH OUTER LAYER of
egg 3. SPERM NUCLEUS ENTERS EGG CELL 4. SPERM & EGG NUCLEI
FUSE
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AFTER FERT. l ZYGOTE BEGINS TO DIVIDE l CELLS GROW (INCREASE IN
SIZE) l CELLS DIFFERENTIATE- CELL SHAPE CHANGES ACCORDING TO THE
FUNCTION IT IS ASSIGNED
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PLACENTA l TISSUE THROUGH WHICH THE EMBRYO RECEIVES NUTRIENTS
AND GETS RID OF WASTES l NO BLOOD TO BLOOD CONTACT- EMBRYO HAS ITS
OWN BLOOD AND HEART UMBILICAL CORD- PIPE THAT CONNECTS EMBRYO TO
PLACENTA
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EMBRYONIC DEVELOPMENT l 0-2 MONTHS (60 DAYS) l END OF 1ST
MONTH- TAIL, LIMB PADDLES, HEART BEATS, LIVER PRODUCES BLOOD CELLS
l END OF 2ND MONTH- TAIL GONE, ALL ORGANS ARE PRESENT FETAL
DEVELOPMENT- 3-9 MONTHS (61+ DAYS)
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BIRTH l FETUS PRODUCES ANDROGENS l PLACENTA CONVERTS ANDROGENS
INTO ESTROGEN WHICH CAUSES THE UTERUS TO CONTRACT l 3 STAGES
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STAGE 1 l MUCOUS PLUG PUSHED OUT OF CERVICAL CANAL l AMNIONIC
MEMBRANE BREAKS (water breaks) l CERVIX DILATES
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STAGE 2 l STRONG CONTRACTIONS l BABY USUALLY COMES OUT HEAD
FIRST EPISIOTOMY- AN INCISION THAT ENLARGES THE VAGINA l UMBILICAL
CORD IS CUT l BABYS FIRST BREATH
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STAGE 3 l AFTER SEVERAL MINUTES THE PLACENTA (afterbirth) IS
EXPELLED
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LACTATION l AFTER DELIVERY THE MOTHERS PITUITARY PRODUCES
PROLACTIN l 1ST FEW DAYS- COLOSTRUM IS PRODUCED- THIN YELLOW MILKY
FLUID THAT IS RICH IN PROTEINS AND ANTIBODIES l IF CHILD IS BREAST
FED- TRUE MILK WILL BE PRODUCED NEXT
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AGING l PROGRESSIVE CHANGES FROM AGE 20 THAT CONTRIBUTE TO
INFIRMITY, DISEASE AND DEATH (a depressing definition isnt
it?)
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THEORIES GENETIC- CELLS CAN ONLY DIVIDE 50 TIMES, MUTATIONS,
FREE RADICALS GENERAL WEARING OUT- EX. TYPE 2 DIABETES EXTERNAL
FACTORS- DIET, HARMFUL CHEMICALS LEAD TO CELL DEATH
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EFFECTS l SKIN- LESS ELASTIC, FAT CONTENT DECREASES, LOOSE and
WRINKLED l DECREASED ELASTICITY- OF SKIN, BLOOD VESSELS, LUNGS l
FATTY PLAQUES- PARTIALLY CLOG BLOOD VESSELS l POOR CIRCULATION=
LESS BLOOD AND NUTRIENTS TO ALL OTHER ORGANS (EX. LIVER,
KIDNEYS)
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NERVOUS SYSTEM l REACTION TIME INCREASES l DECREASED BLOOD FLOW
CAN STARVE NEURONS WHICH DIE EASILY
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REPRODUCTIVE SYSTEM FEMALES- AFTER MENOPAUSE- NON FERTILE
MALES- SPERM ARE PRODUCED UNTIL DEATH