Chapter 12 - Laurel County Schools
Download
Report
Transcript Chapter 12 - Laurel County Schools
THE CELL CYCLE IS PRECISELY REGULATED
The timing and rate of cell division is crucial to
normal growth, development, and maintenance
of multicellular organisms.
CELL CYCLE
FREQUENCY OF CELL DIVISION
Frequency of cell division varies with cell type
skin
cells sustain a lot of damage - divide
frequently throughout life
liver cells retain ability to divide, but keep it in
reserve
mature nerve & muscle cells are highly specialized
- do not divide at all after maturity
HOW DO CELLS KNOW WHEN TO DIVIDE?
cell communication = signals
chemical signals in cytoplasm give cue
signals usually mean proteins
activators
inhibitors
experimental evidence: Can
you explain this?http://bio.kimunity.com
HOW DO CELLS KNOW WHEN TO DIVIDE?
Evidence of cytoplasmic signals
Fuse M phase with G1 cell – cell immediately
condenses DNA and builds spindle
Fuse S phase with G1 cell – cell enters S phase
CHECKPOINT CONTROL SYSTEM
Checkpoints
Control
points where stop
and go signals regulate
the cycle
Check if key cellular
processes have been
completed correctly
Signals
may be internal or
external
Generally STOP that must
be over ridden by GO
CHECKPOINT CONTROL SYSTEM
3
major checkpoints:
G1
can
DNA synthesis begin?
G2
has
M
DNA synthesis been completed correctly?
phase
can
sister chromatids separate correctly?
G1 CHECKPOINT
G1 checkpoint is most
critical
restriction
point
if cells receives go-ahead
signal, completes cell cycle
& divides
if does not receive go-ahead
signal, cell exits cycle &
switches to a non-dividing
state called G0 phase
Most cells are in G0 phase
HOW DOES THE CELL “TELL TIME”?
Rhythmic fluctuations of key molecules
function as the cell cycle “clock”
2 main types: kinases and cyclins
Kinases
- enzymes that activate or deactivate
other proteins by phosphorylating them
Cyclins are proteins that combine with kinases
HOW DOES THE CELL “TELL TIME”?
cyclin and Cdks combine to form MPF, M-phase
promoting factor; MPF phosphorylates a variety of
proteins and initiates many events of mitosis
such as destruction of the nuclear envelope and
condensation of chromosomes
Cdk levels are constant throughout the cell cycle
but cyclin synthesis rises during S and G2 phases
MPF activity peaks at metaphase – MPF activates
a molecule that destroys cyclin
HOW DOES THE CELL “TELL TIME”?
cyclin and Cdks combine to form MPF,
M-phase promoting factor
MPF phosphorylates a variety of proteins which
initiates many events of mitosis , ex. destruction of
nuclear envelope and condensation of chromosomes
Cdk levels are constant throughout the cell cycle
but cyclin synthesis rises during S and G2 phases
MPF activity peaks at metaphase – MPF activates
a molecule that destroys cyclin
CDK ALWAYS PRESENT – RISE IN CYCLIN MEANS
RISE IN MPF – TRIGGERS MITOSIS
DESTRUCTION OF CYCLIN ENDS MITOSIS
“GO-AHEAD” SIGNALS
Signals
that promote cell growth &
division
proteins
internal
signals
“promoting
external
factors”
signals
“growth
factors”
PROTEIN SIGNALS
Promoting
factors
Cyclins
proteins
whose concentrations fluctuate in the cell
CDKs
cyclin-dependent
kinases
MPF
maturation
(mitosis) promoting factor
APC
anaphase
promoting complex
PROTEIN SIGNALS
Growth
factors
external
signals
protein signals released by body cells that
stimulate other cells to divide
density-dependent
crowded
anchorage
to
inhibition
cells stop dividing
dependence
divide cells must be attached to a substrate
GROWTH FACTORS
EXAMPLE: Platelet derived growth factor (PDGF)
made by platelets (blood cells)
binding of PDGF to cell receptors stimulates division and
wound begins to heal
CANCER CELLS
Cancer cells have escaped cell cycle controls
cancer cells are free of both density-dependent
inhibition & anchorage dependence
Noncancerous cells grown in culture stop dividing
when they touch each other and the sides of the
container
CANCER OVERRIDES CHECKPOINTS
Cancer cells divide excessively & invade other
tissues
free
of body’s control mechanisms
breakdown in cell cycle control system
breakdown in signaling pathway
cancer cells manufacture their own growth factors
stimulate
cell division
stimulate blood vessel growth
CANCER CELLS DIVIDE INDEFINITELY
Cancer cells divide indefinitely if have continual
supply of nutrients
nearly
all normal mammalian cells divide 20-50
times under culture conditions before they stop,
age & die
cancer cells may be “immortal”
HeLa
cells from a tumor removed from a woman
(Henrietta Lacks) in 1951 are still reproducing in culture
CANCER
The abnormal behavior of cancer cells begins
when a single cell in a tissue undergoes a
transformation that converts it from a normal
cell to a cancer cell
usually
immune system recognizes & destroys
transformed cells
cells that evade destruction proliferate to form a
tumor, a mass of abnormal cells
BENIGN TUMORS
Benign tumor
abnormal
cells remain at originating site as a lump
most do not cause serious problems and can be
removed by surgery
MALIGNANT TUMORS
Malignant tumors
cells
leave the original site
impair the functions of one or more organs
chromosomal & metabolic abnormalities
lose attachment to nearby cells & are carried by the
blood & lymph system to other tissues
start
more tumors = metastasis
TREATMENT FOR CANCERS
Treatments
target rapidly dividing
cells
high-energy
radiation &
chemotherapy with toxic drugs
WHAT CAN CAUSES THE GENETIC
CHANGES THAT LEAD TO LOSS OF
CONTROL OF THE CELL CYCLE
CHEMICALS
HIGH
ENERGY RADIATION
VIRUSES
INHERITED DEFECTS