A&P I Exam 2 Review Slides Lectures 5-8 Ch. 2, 3, and...
Transcript of A&P I Exam 2 Review Slides Lectures 5-8 Ch. 2, 3, and...
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A&P I Exam 2 Review Slides
Lectures 5-8
Ch. 2, 3, and 24 (cell resp.)
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A Closer Look at Mitochondria
Strategically
placed in cell
where ATP
demand is high
Concentration of enzymes in the matrix is so high that there is
virtually no hydrating water. Enzyme-linked reactions and
pathways are so crowded that normal rules of diffusion do not apply!
Figure from: Martini, Anatomy & Physiology, Prentice Hall, 2001
(Impermeable to charged or polar molecules)
Mitochondria
• membranous sacs with
inner partitions
• contain their own DNA
• generate energy
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Overview of Cellular RespirationFigure from: Martini, Anatomy & Physiology, Prentice Hall, 2001
Cellular
respiration
(aerobic)
AnaerobicATP
*Most ATP from here
ATP
• Structural – Functional Relationship - Inner membrane:
• Contains Matrix where TCA cycle takes place
• Has enzymes and molecules that allow Electron Transport System to be carried out
e-
+ e-
ETS
e-
e-
2
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Overview of Glucose Breakdown
Figure from: Hole’s Human A&P, 12th edition, 2010
NAD+
NAD+
NAD+, FAD
NADH
NADH
FADH2
NADH
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Anaerobic Glycolysis & Lactic Acid
During glycolysis, if O2 is not
present in sufficient quantity,
lactic acid is generated to keep
glycolysis going so it continues
to generate ATP (even without
mitochondria)
NOTE what happens with and
without O2 being available…
Figure from: Hole’s Human A&P, 12th edition, 2010
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GLYCOLYSIS TCA ETC
Where it takes
place
Cytoplasm Mitochondria Mitochondria
Products Produced ATP
NADH
Pyruvate
ATP
NADH,FADH2
CO2
ATP
NAD+,FAD
H2O
Purpose Breakdown of glucose
(6 carbons) to 2
molecules of pyruvate
(3 carbons)
Generation of energy
intermediates (NADH,
FADH2, ATP) and CO2
Generation of ATP and reduction
of O2 to H2O (Recall that
reduction is the addition of
electrons)
What goes on 1. Glucose is
converted to pyruvate,
which is converted to
acetyl CoA when there is sufficient O2
present.
2. Acetyl CoA enters
the TCA cycle.
3. If O2 is not present,
pyruvate is converted
to lactic acid to
replenish the supply of
NAD+ so glycolysis
can continue to make ATP
1. The energy in acetyl CoA
is trapped in activated
carriers of electrons (NADH,
FADH2) and activated carriers of phosphate groups
(ATP).
2. The carriers of electrons
that trap the energy from
acetyl CoA bring their high
energy electrons to the
electron transport chain.
1. Chemiosmosis (that drives
oxidative phosphorylation) uses
the electrons donated by NADH
and FADH2 to eject H+ from the matrix of the mitochondria to the
intermembrane space.
2. These H+ then flow down
their concentration gradient
through a protein (ATP synthase)
that makes ATP from ADP and
phosphate.
3. During this process, the H+
that come through the channel in ATP synthase are combined with
O2 to make H2O.
Summary Table of Cell Respiration
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Some Definitions…
Gene – segment of DNA that codes for a protein or RNA
- About 30,000 protein-encoding genes in humans
- DNA’s instructions are ultimately responsible for the
ability of the cell to make ALL its components
*Chromatin – combination of DNA plus histone proteins
used to pack DNA in the cell nucleus
Genome – complete set of genes of an organism
- Human Genome Project was complete in 2001
- Genomes of other organisms are important also
Genetic Code – method used to translate a sequence of
nucleotides of DNA into a sequence of amino acids
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Structure of Nucleic Acids
Figure from: Alberts et al., Essential Cell Biology, Garland Press, 1998
Purines: Adenine and Guanine (double ring)
Pyrimidines: Cytosine, Thymine, and Uracil (single ring)
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Structure of DNA
A double-stranded
DNA molecule is
created by BASE-
PAIRING of the
nitrogenous bases
via HYDROGEN
bonds.
Notice the
orientation of the
sugars on each
stand.
*DNA is an antiparallel, double-stranded polynucleotide helix
5'3'
5'3'
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Structure of DNA
Base pairing in DNA is VERY specific.
- Adenine only pairs with Thymine (A-T)
- Guanine only pairs with Cytosine (G-C)
Note that there are:
- THREE hydrogen bonds in G-C pairs
- TWO hydrogen bonds in A-T pairs
- A purine (two rings)base hydrogen
bonds with a pyrimidine base (one ring)
Figure from: Martini, “Human Anatomy & Physiology”, Prentice Hall, 2001
Complementary base pairing…
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DNA Replication
Figure from: Martini, “Human Anatomy &
Physiology”, Prentice Hall, 2001
THINGS TO NOTE:
1. DNA is replicated in the
S phase of the cell cycle
2. New strands are
synthesized in a 5’ to 3’
direction
3. DNA polymerase has a
proofreading function
(1 mistake in 109
nucleotides copied!)
4. Semi-conservative
replication describes
pairing of post-
replication strands of
DNA (1 new, 1 old)
5’
5’
5’
5’
3’
3’
5’
3’
3’
3’
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RNA
• RNA is a polynucleotide with important
differences from DNA
– Uses Uracil (U) rather than Thymine (T)
– Uses the pentose sugar, ribose
– Usually single-stranded
• There are three important types of RNA
– mRNA (carries code for proteins)
– tRNA (the adapter for translation)
– rRNA (forms ribosomes, for protein synthesis)
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Transciption/Translation
• Transcription
– generates mRNA from DNA
– Occurs in nucleus of the cell
– Uses ribonucleotides and RNA polymerase to synthesize mRNA
• Translation
– generates polypeptides (proteins) from mRNA
– Occurs in the cytoplasm of the cell
– Uses 3 components: mRNA, tRNA w/aa, and ribosomes
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The Genetic Code
1. Codon – group of three ribonucleotides found in mRNA that specifies an aa
2. Anticodon – group of three ribonucleotides found in tRNA that allows specific
hydrogen bonding with mRNA
3. AUG is a start codon and also codes for MET. UAA, UAG, and UGA are stop codons
that terminate the translation of the mRNA strand.
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tRNAs
Transfer RNAs (tRNA) function as
‘adapters’ to allow instructions in the
form of nucleic acid to be converted
to amino acids.
Figures from:
Martini,
Anatomy &
Physiology,
Prentice Hall,
2001
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Eukaryotic Genes
Figure from: Alberts et al., Essential Cell Biology, Garland Publishing, 1998
The template strand of DNA is the one that’s transcribed.
The coding strand of DNA is used as the complementary
strand for the template strand in DNA and looks like the
codons.
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Eukaryotic mRNA Modification
Figure from: Alberts et al., Essential Cell Biology, Garland Publishing, 1998
Newly made eukaryotic
mRNA molecules
(primary transcripts)
undergo modification in
the nucleus prior to
being exported to the
cytoplasm.
1. Introns removed
2. 5' guanine cap added
3. Poly-A tail added
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The Fate of Proteins in the Cell
• Breakdown of proteins regulates the amount of a given
protein that exists at any time.
• Each protein has unique lifetime, but the lifetimes of
different proteins varies tremendously.
• Proteins with short life-spans, that are misfolded, or that
become oxidized must be destroyed and recycled by the cell.
Enzymes that degrade proteins are
called proteases. They are hydrolytic
enzymes.
Most large cytosolic proteins in
eukaryotes are degraded by enzyme
complexes called proteasomes.
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Cell Membranes
Figure from: Martini, Anatomy & Physiology, Prentice Hall, 2001
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Passage of Materials through the Cell Membrane
oxygen, carbon
dioxide and other
lipid-soluble
substances diffuse
freely through the
membrane
Carrier/channel
proteins required
for all but fat-
soluble molecules
and small
uncharged
molecules
Cellular Transport ReviewTRANSPORT
PROCESS
IS
ENERGY
NEEDED?
CONCEN-
TRATION
GRADIENT
GENERAL
DESCRIPTION
EXAMPLE
IN
HUMANS
SIGNIFICANCE
SIMPLE
DIFFUSION
NO [HIGH]
TO
[LOW]
spreading out of
molecules to
equilibrium
O2 into cells; CO2
out of cells.
Cellular
Respiration
FACILITATED
DIFFUSION
NO [HIGH]
TO
[LOW]
Using a special carrier
protein to move
something through the
cell membrane (cm)
Process by which
glucose enters
cells
OSMOSIS NO [HIGH]
TO
[LOW]
water (solvent) moving
through the cell
membrane to dilute a
solute
maintenance
of osmotic
pressure.
Same
FILTRATION NO [HIGH]
TO
[LOW]
using pressure to push
something through a cell
mmembrane (sprinkler
hose)
manner in which
the kidney filters
things from blood
Separates small
from large
molecules using
hydrostatic pressure
ACTIVE
TRANSPORT
YES [LOW]
TO
[HIGH]
opposite of diffusion at
the expense of energy
K+-Na+-ATPase
pump
maintenance of the
resting
membrane
potential
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Cellular Transport Review
TRANSPORT
PROCESS
IS
ENERGY
NEEDED?
CONCEN-
TRATION
GRADIENT
GENERAL
DESCRIPTION
EXAMPLE
IN
HUMANS
SIGNIFICANCE
ENDOCYTOSIS YES [LOW]
TO
[HIGH]
bringing a
substance
into the cell
that is too
large to
enter by
any of the
above
ways;
Phagocytosi: cell
eating;
Pinocytosis: cell
drinking.
Phagocytosed
(foreign)
particles
fuse with
lysosomes
to be
destroyed
help fight infection
EXOCYTOSIS YES [LOW]
TO
[HIGH]
expelling a
substance
from the
cell into
ECF
Exporting
proteins;
dumping
waste
Same
Osmotic Pressure/Tonicity
Osmotic Pressure (Osmolarity) – ability of solute to generate
enough pressure to move a volume of water by osmosis
*Osmotic pressure increases as the number of nonpermeable
solutes particles increases
• isotonic – same
osmotic pressure as a
second solution
• hypertonic – higher
osmotic pressure
• hypOtonic – lower
osmotic pressure
0.9% NaCl
5.0% Glucose
Crenation
The O in
hypotonic
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Cell Nucleus
• control center of cell
• nuclear envelope
(membrane)• porous double membrane
• separates nucleoplasm from
cytoplasm (*eukaryotes only)
• nucleolus• dense collection of RNA and
proteins
• site of ribosome production
• chromatin• fibers of DNA and proteins
• stores information for synthesis
of proteinsFigure From: Marieb & Hoehn, Human Anatomy & Physiology, 9th ed., Pearson
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Cellular Organelles
CELL COMPONENT DESCRIPTION/
STRUCTURE
FUNCTION(S)
CELL MEMBRANE Bilayer of phospholipids with proteins
dispersed throughout
cell boundary; selectively permeable
(i.e. controls what enters and
leaves the cell; membrane
transport)
CYTOPLASM jelly-like fluid (70% water) suspends organelles in cell
NUCLEUS Central control center of cell; bound
by lipid bilayer membrane;
contains chromatin (loosely
colied DNA and proteins)
controls all cellular activity by
directing protein synthesis (i.e.
instructing the cell what
proteins/enzymes to make.
NUCLEOLUS dense spherical body(ies) within
nucleus; RNA & protein
Ribosome synthesis
RIBOSOMES RNA & protein; dispersed throughout
cytoplasm or studded on ER
protein synthesis
ROUGH ER Membranous network studded with
ribosomes
protein synthesis
SMOOTH ER Membranous network lacking
ribosomes
lipid & cholesterol synthesis
GOLGI “Stack of Pancakes”; cisternae modification, transport, and packaging
of proteins
Table 1 of 2
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Cellular Organelles
CELL COMPONENT DESCRIPTION/
STRUCTURE
FUNCTION(S)
LYSOSOMES Membranous sac of digestive enzymes destruction of worn cell parts
(“autolysis) and foreign particles
PEROXISOMES Membranous sacs filled with oxidase
enzymes (catalase)
detoxification of harmful substances
(i.e. ethanol, drugs, etc.)
MITOCHONDRIA Kidney shaped organelles whose inner
membrane is folded into “cristae”.
Site of Cellular Respiration;
“Powerhouse of Cell”
FLAGELLA long, tail-like extension; human sperm locomotion
CILIA short, eyelash extensions;
human trachea & fallopian tube
to allow for passage of substances
through passageways
MICROVILLI microscopic ruffling of cell membrane increase surface area
CENTRIOLES paired cylinders of microtubules at
right angles near nucleus
aid in chromosome alignment and
movement during metaphase,
anaphase, and telophase of mitosis
Table 2 of 2
The Cell Cycle
• series of changes a cell
undergoes from the time it
forms until the time it divides
• stages
• interphase
• mitosis
• cytoplasmic division
• differentiation
Differentiated cells may spend all their time in ‘G0’ (neurons, skeletal muscle, red
blood cells). Stem cells may never enter G0
Figure From: Marieb & Hoehn, Human Anatomy & Physiology, 9th ed., Pearson
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Why the Cell Cycle Must Have Controls
1. DNA/Cell replication must not proceed unless a ‘signal to proceed’ is received
2. DNA must be completely and correctly replicate before mitosis takes place otherwise it should not occur.
3. Chromosomes must be correctly positioned during mitosis so they are separated correctly
What are the Controls of the Cell Cycle?
• cell division capacities vary greatly among cell types• skin and bone marrow cells divide often
• liver cells divide a specific number of times then cease
• chromosome tips (telomeres) that shorten with each mitosis
provide a mitotic clock (cell senescence)
• cells divide to provide a more favorable surface area to
volume relationship
• growth factors and hormones stimulate cell division• hormones stimulate mitosis of smooth muscle cells in uterus
• epidermal growth factor stimulates growth of new skin
• tumors are the consequence of a loss of cell cycle control
• contact inhibition
• Cyclins and Cyclin-dependent kinases provide central control
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Mitosis and MeiosisFigures from: Martini, Anatomy & Physiology, Prentice Hall, 2001
Mitosis – production of two identical diploid daughter cells
Meiosis – production of four genetically varied, haploid gametes
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The Cell Cycle and Mitosis
• I (INTERPHASE)
• PASSED (PROPHASE)
• MY (METAPHASE)
• ANATOMY (ANAPHASE)
• TEST (TELOPHASE/CYTOKINESIS)
Interphase and Mitosis (IPMAT)
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Interphase Early Prophase Late Prophase
Metaphase Anaphase Telophase/Cytokinesis
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Cell Death
• Two mechanisms of cell death
– Necrosis
– Programmed cell death (PCD or apoptosis)
• Necrosis
– Tissue degeneration following cellular injury or destruction
– Cellular contents released into the environment causing an inflammatory response
• Programmed Cell Death (Apoptosis)
– Orderly, contained cell disintegration
– Cellular contents are contained and cell is immediately phagocytosed – no inflammation
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Stem and Progenitor Cells
Stem cell
• can divide to form two new stem cells
• can divide to form a stem cell and a progenitor cell
• totipotent – can give rise to any cell type (Embryonic stem
cells)
• pluripotent – can give rise to a restricted number of cell
types
Progenitor cell
• committed cell further along differentiation pathway
• can divide to become only a restricted number of cells
• pluripotent
• *not self-renewing, like stem cells