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Tissue Hemostasis
done through the regulation of cell count and size. Done by creating new cells, Growth arrest and cell loss.
mitogens
signaling molecules that stimulate cell replication
growth factors
cells that stimulate cell growth
survival factors
protect the cell against apoptosis.
G0 phase
normal state of the cell what it is not undergoing cell division. cells have to be driven to leave this stage
apoptosis
programed cell death. happens to cells lacking survival factors. plays an important role in regulating cells and removing unnecessary material, why we don’t have webbed hands.
caspase cascade
molecular mechanism of apoptosis. apoptosis signal triggers the initiator caspase. this activates the executioner caspases which destroy over 1k cell proteins which destroys the cell. one of the nucleases released chops up DNA
ECM and growth facors
the extra cellular matrix interacts with growth factors. when cells are suspended, they rarely leave g-phase, sometimes do when perched and frequently do when placed on a large patch.
cell size control
mechanism is very much a mystery, but there is very large variation in cell size and shape across the body.
size control clues from yeast
in yeast cell division is normally regulated by the amount of nutrients present btu if you inhibit the m-Tor gene the cell will continue to divide in an environment without sufficient nutrients resulting in smaller and smaller cells.
cytoplasm to dna ratio
can be a regulator of cell size. if there is too much cytoplasm and not enough things to put in it the cell shrinks and vise versa.
growth factors and cell size
secreted growth factors can also control cell size. why inhibiting myostatin makes really muscular animals
Fluorescence activated Cell sorting
cells are given a fluorescent die indicating their amount of double stranded DNA, then the cell is dropped through a laser beam to check for fluorescence. After this the cell is given a charge based on whether or not it has fluorescence. After that the cells are sorted based off of charge. let’s researchers isolate cells at certain states in the cell cycle.
G1 checkpoint
gateway into the S phase, checks if the dna is intact and if the environment is favorable for replication.
G2 checkpoint
controls entrance into mitosis. ensures that all the dna is still intact and that it all has been replicated
frog egg division
frog eggs divide into smaller cells simultaneously every 30 or so minutes. experimental model showing cell replication regulation
maturation promoting factor
multi protein complex of m-cyclin and mdk. increased my-cylin presence increases mdk ativity which starts mitosis. m-cdk concentration is constant
cyclins cyclin dependent kinases and cell division checkpoints
when the two combine to form an active complex cell replication will pass the relevant checkpoint. This is deactivated when the complex is flagged with ubiquitin which flags the cyclin for digestion.
m-cdk and kinases
kinases can both activate and inactivate m-cdk regulated by positive feedback
cyclins for different steps
m-cyclin used for mitosis s-cyclin used for s-phase act as molecular switches for the different steps in the cell cycle
checkpoints and signaling
cell signaling helps the cell coordinate its cycle movement with internal and external factors
mitosis
the process of dividing the cell dna into two identical daughter cells.
cytokinesis
when the dividing cell splits the cytoplasm proteins and organelles between the two new cells.
prophase
first phase of mitosis. when the sister chromatids align and are condensed, the mitotic spindle starts to form and the nuclear envelope is still intact.
kinetochore
molecular complex, allows spindle to attach to the chromatin. the microtubule enters the kinetochore then depolarizes causing it to fan out locking it in place.
condensin
molecular complex condenses compacts and configures dna ring strucure hinges around a strand of dna dna
cohesion
molecular complex holds sister chromatids together at the end of s-phase ring ring structure singes around two strands of dna.
mitotic spindle
long strands of microtubules centered at centrosomes. begin formation in prophase. grab chromatids during cell division and help the cell maintain its shape
prometaphase
second part of cell division. starts with the break down of the nuclear envelope. then the microtubules attach to the kinetochores.
role of the cytoskeleton in cell division
the cytoskeleton segregates sister chromosomes and aligns the microtubules.
metaphase
third part of mitosis, mitotic spindle aligns the sister chromatids in the center of the cell. done by kinesin proteins on the microtubules.
anaphase
fourth part of mitosis, starts when the sister chromatids separate happens because of motor proteins pulling the spindle apart.
Anaphase A
shortening of the kinetochore microtubules. force is mainly generated at the kinetochores.
Anaphase B
microtubules expand, sliding force at the overlap is used to push the poles apart.
telophase
last part of mitosis. the daughter chromatids assemble at the respective poles and the nuclear envelope beings to re-form. the contractile ring also assembles and begins to contract.
nuclear Lamins
form a network of proteins under the inner membrane of the nuclear envelope which provides support to the nucleus. in prophase they are phosphorylated leading to the degradation of the nuclear envelope but in telophase they are dephosphorylated letting the envelope re-form.
nuclear vesicles
vesicles containing important parts of the nuclear membrane which assemble around chromatins in telophase
actomyosin contractile ring
during cytokinesis it circles the parent cell and constricts separating it into two daughter cells.
sister chromatins
bound together identical copies of chromosomes.
advantages of sexual reproduction
production of gametes, recombination, and the resulting mix of parental dna
meiosis
cellular division which forms haploid cells that are genetically distinct.
haploid cells
cells that only have one set of chromosomes
s-phase
part of the cell cycle where dna is replicated