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U N I T I
GUYTON & HALL
Copyright © 2006 by Elsevier, Inc.
Textbook of Medical Physiology, 11th Edition
Chapter 2:
The Cell and its Functions
Slides by John E. Hall, Ph.D. and Louise C. Nuttle, Ph.D.
Organization of the Cell
Figure 2-1
Copyright © 2006 by Elsevier, Inc.
Cell Composition
Copyright © 2006 by Elsevier, Inc.
Water
Ions
...70-85% of cell mass
Proteins ...10-20%
Lipids ...2-95%
Carbohydrates ...1-6%
Membrane Components:
hydrophilic
“head”
hydrophobic
FA “tail”
ions
CO2
H2O
urea
Copyright © 2006 by Elsevier, Inc.
LIPIDS:
• barrier to water and water-soluble substances
• organized in a bilayer of phospholipid molecules
O2
N2
halothane
glucose
Cell Membrane:
Copyright © 2006 by Elsevier, Inc.
Bilayer of Phospholipids with Proteins
Figure 2-3
• provide “specificity” to a membrane
• defined by mode of association with the lipid bilayer
– integral: channels, pores, carriers, enzymes, etc.
– peripheral: enzymes, intracellular signal mediators
K+
Proteins:
Copyright © 2006 by Elsevier, Inc.
• glycolipids (approx. 10%)
• glycoproteins (majority of integral proteins)
• proteoglycans
GLYCOCAL
YX
Copyright © 2006 by Elsevier, Inc.
Carbohydrates:
• negative charge of the carbo chains repels other
negative charges
• involved in cell-cell attachments/interactions
• play a role in immune reactions
GLYCOCAL
YX
Copyright © 2006 by Elsevier, Inc.
(-) (-) (-)
(-)
(-)
(-)
(-)
Carbohydrates (Cont.):
• present in membranes in varying amounts
• generally decreases membrane FLUIDITY and
PERMEABILITY (except in plasma membrane)
• increases membrane FLEXIBILITY and STABILITY
(-) (-)
(-) (-)
(-)
(-)
(-)
Cholesterol:
Copyright © 2006 by Elsevier, Inc.
Figure 2-2
Copyright © 2006 by Elsevier, Inc.
Cell Organelles
The Endoplasmic Reticulum:
• Network of tubular and flat vesicular structures
• Membrane is similar to (and contiguous with) the plasma membrane
• Space inside the tubules is called the endoplasmic matrix
Figure 2-4
Copyright © 2006 by Elsevier, Inc.
•outer membrane surface
covered with ribosomes
•newly synthesized
proteins are extruded into
the ER matrix
•proteins are “processed”
inside the matrix
- crosslinked
- folded
- glycosylated (N-linked)
- cleaved
Rough or Granular ER
Figure 2-13
Copyright © 2006 by Elsevier, Inc.
• site of lipid synthesis
- phospholipids
- cholesterol
•growing ER membrane
buds continuously
forming transport
vesicles, most of which
migrate to the Golgi
apparatus
Smooth ER
Figure 2-13
Copyright © 2006 by Elsevier, Inc.
The Golgi Apparatus:
•Membrane
composition similar
to that of the smooth
ER and plasma
membrane
•Composed of 4 or
more stacked layers
of flat vesicular
structures
Figure 2-5
Copyright © 2006 by Elsevier, Inc.
•Receives transport vesicles
from smooth ER
•Substances formed in the ER
are “processed”
- phosphorylated
- glycosylated
•Substances are concentrated,
sorted and packaged for
secretion.
Copyright © 2006 by Elsevier, Inc.
Exocytosis:
Secretory vesicles diffuse
through the cytosol and
fuse to the plasma
membrane
Lysosomes fuse with
internal endocytotic
vesicles
Copyright © 2006 by Elsevier, Inc.
Secretion:
•secretory vesicles
containing proteins
synthesized in the RER bud
from the Golgi apparatus
•fuse with plasma membrane
to release contents
-constitutive secretion -
happens randomly
-stimulated secretion -
requires trigger
Copyright © 2006 by Elsevier, Inc.
Lysosomes:
• vesicular organelle formed from budding Golgi
• contain hydrolytic enzymes (acid hydrolases)
- phosphatases
- nucleases
- proteases
- lipid-degrading enzymes
- lysozymes digest bacteria
•fuse with pinocytotic or
phagocytotic vesicles to form
digestive vesicles
Figure 2-12
Copyright © 2006 by Elsevier, Inc.
Lysosomal Storage Diseases
Copyright © 2006 by Elsevier, Inc.
Absence of one or more hydrolases
• not synthesized
• inactive
• not properly sorted and packaged
Result: Lysosomes become engorged with undigested substrate
Examples:
• Acid lipase A deficiency
• I-cell disease (non-specific)
• Tay-Sachs disease (HEX A)
Peroxisomes:
Copyright © 2006 by Elsevier, Inc.
• similar physically to lysosomes
• two major differences:
• formed by self-replication
• they contain oxidases
Function: oxidize substances (e.g. alcohol) that
may be otherwise poisonous
Secretory Granules
Copyright © 2006 by Elsevier, Inc.
Figure 2-6
Copyright © 2006 by Elsevier, Inc.
Mitochondria
:Primary function: extraction of energy from nutrients
Figure 2-7
Copyright © 2006 by Elsevier, Inc.
The Nucleus: “Control Center” of the Cell
The double nuclear membrane and matrix are
contiguous with the endoplasmic reticulum
Figure 2-9
• 100 nm in diameter
• functional diameter
is ~9 nm
• (selectively)
permeable to
molecules of up to
44,000 MW
The nuclear membrane is permeated by
thousands of nuclear pores
Figure 2-9
Copyright © 2006 by Elsevier, Inc.
Chromatin (condensed DNA) is found in the nucleoplasm
Nucleolus
• one or more per nucleus
• contains RNA and proteins
• not membrane delimited
• functions to form the granular “subunits” of ribosomes
Copyright © 2006 by Elsevier, Inc.
•molecules attach to cell-
surface receptors
concentrated in clathrin-
coated pits
•receptor binding induces
invagination
•also ATP-dependent and
involves recruitment of
actin and myosin
Receptor-mediated endocytosis:
Figure 2-11
Copyright © 2006 by Elsevier, Inc.
Digestion of Substances in
Pinocytotic or Phagocytic Vesicles
Copyright © 2006 by Elsevier, Inc.
Figure 2-12
Step 1.
• Carbohydrates are converted
into glucose
• Proteins are converted into
amino acids
• Fats are converted into
fatty acids
Step 2.
• Glucose, AA, and FA are
processed into AcetylCoA
Step 3.
•AcetylCoA reacts with O2 to
produce ATP
A maximum of 38 molecules of
ATP are formed per molecule of
glucose degraded.
ATP production
(More in Chapter 67)
The Use of ATP for Cellular Function
• under “standard” conditions G° is only -7.3 kcal/mole
• ATP concentration is ~10x that of ADP, the G is -12 kcal/mole
1. Membrane
transport
2. Synthesis of
chemical
compounds
3. Mechanical
work
Figure 2-15
The Cytoskeleton
Copyright © 2006 by Elsevier, Inc.
Intermediate Filaments:
• Comprised of cell-specific fibrillar monomers
(e.g. vimentin, neurofilament proteins, keratins, nuclear
lamins)
Microtubules:
• Heterodimers of  and  tubulin
• Make up spindle fibers, core of axoneme structure
Thin Filaments:
• F-Actin
• Make up “stress fibers” in non-muscle cells
Thick Filaments:
• Myosin (types I and II)
•Together with actin support cellular locomotion and
subcellular transport
Cilia and Ciliary Movements:
• Occurs only on the inside surfaces
of the human airway and fallopian
tubes
• Each cilium is comprised of
11 microtubules
• 9 double tubules
• 2 single tubules axoneme
Figure 2-17
Copyright © 2006 by Elsevier, Inc.
• Each cilium is an outgrowth of
the basal body and is covered by
an outcropping of the plasma
membrane.
• Ciliary movement
is ATP-dependent
(also requires Ca2+ and Mg2+)
Copyright © 2006 by Elsevier, Inc.
Ameboid Locomotion:
•continual endocytosis at the “tail”and exocytosis at the leading edge of
the pseudopodium
•attachment of the pseudopodium is facilitated by receptor proteins carried
by vesicles
•forward movement
results through interaction
of actin and myosin
(ATP-dependent)
Figure 2-16
Cell movement is influenced by
chemical substances…
high
concentrati
on
(positive)
Low
concentrati
on
(negative)
Chemotaxis
Copyright © 2006 by Elsevier, Inc.
THANKS

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cell and its function.pptx

  • 1. U N I T I GUYTON & HALL Copyright © 2006 by Elsevier, Inc. Textbook of Medical Physiology, 11th Edition Chapter 2: The Cell and its Functions Slides by John E. Hall, Ph.D. and Louise C. Nuttle, Ph.D.
  • 2. Organization of the Cell Figure 2-1 Copyright © 2006 by Elsevier, Inc.
  • 3. Cell Composition Copyright © 2006 by Elsevier, Inc. Water Ions ...70-85% of cell mass Proteins ...10-20% Lipids ...2-95% Carbohydrates ...1-6%
  • 4. Membrane Components: hydrophilic “head” hydrophobic FA “tail” ions CO2 H2O urea Copyright © 2006 by Elsevier, Inc. LIPIDS: • barrier to water and water-soluble substances • organized in a bilayer of phospholipid molecules O2 N2 halothane glucose
  • 5. Cell Membrane: Copyright © 2006 by Elsevier, Inc. Bilayer of Phospholipids with Proteins Figure 2-3
  • 6. • provide “specificity” to a membrane • defined by mode of association with the lipid bilayer – integral: channels, pores, carriers, enzymes, etc. – peripheral: enzymes, intracellular signal mediators K+ Proteins: Copyright © 2006 by Elsevier, Inc.
  • 7. • glycolipids (approx. 10%) • glycoproteins (majority of integral proteins) • proteoglycans GLYCOCAL YX Copyright © 2006 by Elsevier, Inc. Carbohydrates:
  • 8. • negative charge of the carbo chains repels other negative charges • involved in cell-cell attachments/interactions • play a role in immune reactions GLYCOCAL YX Copyright © 2006 by Elsevier, Inc. (-) (-) (-) (-) (-) (-) (-) Carbohydrates (Cont.):
  • 9. • present in membranes in varying amounts • generally decreases membrane FLUIDITY and PERMEABILITY (except in plasma membrane) • increases membrane FLEXIBILITY and STABILITY (-) (-) (-) (-) (-) (-) (-) Cholesterol: Copyright © 2006 by Elsevier, Inc.
  • 10. Figure 2-2 Copyright © 2006 by Elsevier, Inc. Cell Organelles
  • 11. The Endoplasmic Reticulum: • Network of tubular and flat vesicular structures • Membrane is similar to (and contiguous with) the plasma membrane • Space inside the tubules is called the endoplasmic matrix Figure 2-4 Copyright © 2006 by Elsevier, Inc.
  • 12. •outer membrane surface covered with ribosomes •newly synthesized proteins are extruded into the ER matrix •proteins are “processed” inside the matrix - crosslinked - folded - glycosylated (N-linked) - cleaved Rough or Granular ER Figure 2-13 Copyright © 2006 by Elsevier, Inc.
  • 13. • site of lipid synthesis - phospholipids - cholesterol •growing ER membrane buds continuously forming transport vesicles, most of which migrate to the Golgi apparatus Smooth ER Figure 2-13 Copyright © 2006 by Elsevier, Inc.
  • 14. The Golgi Apparatus: •Membrane composition similar to that of the smooth ER and plasma membrane •Composed of 4 or more stacked layers of flat vesicular structures Figure 2-5 Copyright © 2006 by Elsevier, Inc.
  • 15. •Receives transport vesicles from smooth ER •Substances formed in the ER are “processed” - phosphorylated - glycosylated •Substances are concentrated, sorted and packaged for secretion. Copyright © 2006 by Elsevier, Inc.
  • 16. Exocytosis: Secretory vesicles diffuse through the cytosol and fuse to the plasma membrane Lysosomes fuse with internal endocytotic vesicles Copyright © 2006 by Elsevier, Inc.
  • 17. Secretion: •secretory vesicles containing proteins synthesized in the RER bud from the Golgi apparatus •fuse with plasma membrane to release contents -constitutive secretion - happens randomly -stimulated secretion - requires trigger Copyright © 2006 by Elsevier, Inc.
  • 18. Lysosomes: • vesicular organelle formed from budding Golgi • contain hydrolytic enzymes (acid hydrolases) - phosphatases - nucleases - proteases - lipid-degrading enzymes - lysozymes digest bacteria •fuse with pinocytotic or phagocytotic vesicles to form digestive vesicles Figure 2-12 Copyright © 2006 by Elsevier, Inc.
  • 19. Lysosomal Storage Diseases Copyright © 2006 by Elsevier, Inc. Absence of one or more hydrolases • not synthesized • inactive • not properly sorted and packaged Result: Lysosomes become engorged with undigested substrate Examples: • Acid lipase A deficiency • I-cell disease (non-specific) • Tay-Sachs disease (HEX A)
  • 20. Peroxisomes: Copyright © 2006 by Elsevier, Inc. • similar physically to lysosomes • two major differences: • formed by self-replication • they contain oxidases Function: oxidize substances (e.g. alcohol) that may be otherwise poisonous
  • 21. Secretory Granules Copyright © 2006 by Elsevier, Inc. Figure 2-6
  • 22. Copyright © 2006 by Elsevier, Inc. Mitochondria :Primary function: extraction of energy from nutrients Figure 2-7
  • 23. Copyright © 2006 by Elsevier, Inc. The Nucleus: “Control Center” of the Cell The double nuclear membrane and matrix are contiguous with the endoplasmic reticulum Figure 2-9
  • 24. • 100 nm in diameter • functional diameter is ~9 nm • (selectively) permeable to molecules of up to 44,000 MW The nuclear membrane is permeated by thousands of nuclear pores Figure 2-9 Copyright © 2006 by Elsevier, Inc.
  • 25. Chromatin (condensed DNA) is found in the nucleoplasm Nucleolus • one or more per nucleus • contains RNA and proteins • not membrane delimited • functions to form the granular “subunits” of ribosomes Copyright © 2006 by Elsevier, Inc.
  • 26. •molecules attach to cell- surface receptors concentrated in clathrin- coated pits •receptor binding induces invagination •also ATP-dependent and involves recruitment of actin and myosin Receptor-mediated endocytosis: Figure 2-11 Copyright © 2006 by Elsevier, Inc.
  • 27. Digestion of Substances in Pinocytotic or Phagocytic Vesicles Copyright © 2006 by Elsevier, Inc. Figure 2-12
  • 28. Step 1. • Carbohydrates are converted into glucose • Proteins are converted into amino acids • Fats are converted into fatty acids Step 2. • Glucose, AA, and FA are processed into AcetylCoA Step 3. •AcetylCoA reacts with O2 to produce ATP A maximum of 38 molecules of ATP are formed per molecule of glucose degraded. ATP production (More in Chapter 67)
  • 29. The Use of ATP for Cellular Function • under “standard” conditions G° is only -7.3 kcal/mole • ATP concentration is ~10x that of ADP, the G is -12 kcal/mole 1. Membrane transport 2. Synthesis of chemical compounds 3. Mechanical work Figure 2-15
  • 30. The Cytoskeleton Copyright © 2006 by Elsevier, Inc. Intermediate Filaments: • Comprised of cell-specific fibrillar monomers (e.g. vimentin, neurofilament proteins, keratins, nuclear lamins) Microtubules: • Heterodimers of  and  tubulin • Make up spindle fibers, core of axoneme structure Thin Filaments: • F-Actin • Make up “stress fibers” in non-muscle cells Thick Filaments: • Myosin (types I and II) •Together with actin support cellular locomotion and subcellular transport
  • 31. Cilia and Ciliary Movements: • Occurs only on the inside surfaces of the human airway and fallopian tubes • Each cilium is comprised of 11 microtubules • 9 double tubules • 2 single tubules axoneme Figure 2-17 Copyright © 2006 by Elsevier, Inc. • Each cilium is an outgrowth of the basal body and is covered by an outcropping of the plasma membrane. • Ciliary movement is ATP-dependent (also requires Ca2+ and Mg2+)
  • 32. Copyright © 2006 by Elsevier, Inc. Ameboid Locomotion: •continual endocytosis at the “tail”and exocytosis at the leading edge of the pseudopodium •attachment of the pseudopodium is facilitated by receptor proteins carried by vesicles •forward movement results through interaction of actin and myosin (ATP-dependent) Figure 2-16
  • 33. Cell movement is influenced by chemical substances… high concentrati on (positive) Low concentrati on (negative) Chemotaxis Copyright © 2006 by Elsevier, Inc.