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TRANSPORT ACROSS CELL
MEMBRANES
•Cell membrane maintains
a constant and distinctive
intracellular environment
which is essential for
functioning of the
organelles
•There are several mechanisms of transport across cell
membranes.
•They may be grouped as under the headings:
1) Passive transport
2) Active transport
3) Vesicular transport
4) Transport across epithelia
5) Transport across capillaries
PASSIVE TRANSPORT
• It refers to the mechanism of transport of substances
along the gradient without expenditure of any energy.
• It depends on physical factors like concentration
gradient, electrical gradient and pressure gradient
• It is also called downhill movement
• Passive transport mechanism operating at cell
membrane level are
 Diffusion
 Osmosis
1. DIFFUSION
• Diffusion refers to passive transport of molecules
from areas of higher concentration to areas of lower
concentration
• Diffusion through cell membrane is divided into 2
subtypes
 Simple diffusion
Facilitated diffusion
Carrier
protein
SIMPLE DIFFUSION
 Movement of molecules or ions occurs through a
membrane due to their random movement.
 In this process, there occurs a net flux of molecules
from areas of high to areas of low concentration until
diffusional equilibrium is reached.
This can be expressed by Fick’s law of diffusion
Fick’s law of diffusion
J = D A (C1 - C2)
T
J  Rate of diffusion
D Diffusion co-efficient
A Area of membrane
T Thickness of membrane
C1-C2 Concentration gradient
• Simple diffusion can occur through 2 pathways
i. Direct passage without involvement of carrier
molecules
ii. Passage through protein channel molecules
i. Simple diffusion of lipid soluble substances
• Lipid soluble substances diffuse very rapidly through the
bilipid layer.
 O2, CO2, N2
 Fatty acids
 Alcohol
 Ketone bodies, Aldehydes
 Small uncharged molecules
• The rate of diffusion is directly proportional to the lipid
solubility of the substances and concentration gradient across
the membrane
ii. Simple diffusion through protein channels
•Water and other lipid insoluble substances pass
through cell membrane due to the presence of protein
channels
 Water
 Electrolytes or Ions
Eg: Sodium channels, Potassium channels, Chloride
channels, Calcium channels, Aquaporin channels
• Passage of substances through the protein channels is
regulated by selective permeability and gating of the
channels
• Permeability of such substances depends upon their
molecular size, shape and charge
• Some protein channels are continuously open (non
gated) while most are gated on either side of the
channel that can open or close as per requirement
• The opening and closing of gates are controlled by 3
principal ways
1. Voltage gated channels
Eg: Voltage gated sodium channels
2. Ligand gated channels
Eg: Acetyl choline channels
3. Mechanically gated channels
Eg: Stretch sensitive channels in ventricles, hair
cells
FACILITATED DIFFUSION
• Water soluble substances having larger molecular size
which cannot diffuse through protein channels
• They are transported across the cell membrane down their
concentration gradient with help of carrier proteins
without expenditure of energy.
• This type of diffusion is called facilitated or carrier
mediated diffusion
 Glucose
 Amino acids
•Mechanism of facilitated diffusion:
A conformational change occurs in the carrier
protein after the molecule to be transported is bound
at the receptor site.
As a result, the binding site is switched to the
opposite side of the cell membrane and the diffusing
molecule is released.
FACTORS AFFECTING NET RATE OF DIFFUSION
I. Concentration gradient
II. Electrical potential across the membrane
III. Permeability coefficient of the substance for the membrane
IV. Pressure difference across the membrane
V. Temperature
VI. Distance across which diffusion is occurring(thickness of
membrane)
VII. Area of membrane
2. OSMOSIS
• It refers to the diffusion of water or any other solvent
molecules through a semipermeable membrane from
a solution containing lower concentration of solutes
towards the solution containing higher concentration
of solutes.
• Osmotic pressure refers to the minimum pressure
which when applied on the side of higher solute
concentration prevents the osmosis
• The osmotic pressure exerted by the colloidal
substances in the body is called colloidal osmotic
pressure
• The colloidal osmotic pressure due to plasma proteins
is called oncotic pressure
• Osmole is the unit to express the concentration of osmotically active
particles in a given solution (Osm)
• One osmole = Molecular weight (g)
Number of freely moving particles that each mol liberates in
solution.
• Osmolality of a solution refers to the number of osmotically active
particles per kilogram of a solution (Osm/kg)
• Osmolarity refers to number of osmoles per litre of a solution
(Osm/L)
Plasma Osmolality(mOsm/L)
=2[Na+ (mEq/L) ]+0.055[Glucose (mg/dL) ] + 0.36[BUN(mg/dL)]
• Normal plasma osmolality is 290 mOsm/kg
270 mOsm is contributed by Na+, Cl-, HCO3-
20 mOsm is contributed by glucose and urea
Plasma proteins contribute only 2 mOsm due to large
molecular weight and lesser number of particles
• Tonicity refers to the osmolality of a solution in relation plasma(290
mOsm)
• Isotonic fluids – solutions having osmolality similar to plasma
Eg: 0.9 % NaCl solution, 5% Glucose solution
• Hypertonic fluids - solutions having osmolality higher than plasma
• Hypotonic fluids - solutions having osmolality lower than plasma
• It is the RBC membrane across which the tonicity is tested
In Isotonic solution In Hypotonic solution In Hypertonic solution
RBCs do not change
the shape or size
Cells swell due to
endosmosis
Cells shrink due to
exosmosis
ACTIVE TRANSPORT
• Active transport is also carrier mediated like facilitated
diffusion
• It refers to the mechanism of transport of substances
against the chemical or electrical gradient
• It is also called uphill movement
• It involves expenditure of energy which is liberated by
breakdown of high energy compounds like ATP
Mechanism of active transport
• The substance to be transported combines with a
specific carrier protein on the cell membrane
• The complex undergoes conformational change and is
actively pumped towards the inner/outer surface of
the cell membrane
• Hence, it is also called as active pump mechanism
• The carrier protein then moves back to its original
position
• Active transport is of two types
Primary active transport
Secondary active transport
PRIMARY ACTIVE TRANSPORT
• Energy derived directly from breakdown of ATP or
some other high energy phosphate compound
Eg: Na⁺-K⁺ ATPase pump
H⁺-K⁺ ATPase pump
Calcium ATPase pump
SECONDARY ACTIVE TRANSPORT
• Energy is derived secondarily from the ionic
differences created by primary active transport
• At many areas in body, transport of some other
substances such as glucose, amino acid, chloride,
iodine is coupled with active transport of sodium
• It may occur as:
 Co-transport
 Counter transport
CO-TRANSPORT
• Examples :
Sodium- Glucose co-transport in intestine and
renal tubule
Sodium-Glucose-Amino acid cotransport
Sodium-Potassium-Chloride cotransport in renal
tubule
CO-TRANSPORT
COUNTER TRANSPORT
• Examples:
Sodium-Calcium counter transport in all cell membranes
Sodium-Hydrogen counter transport seen in Proximal
tubule in kidney
Anion exchangers: Chloride bicarbonate exchanger
VESICULAR TRANSPORT
• It involves the transport of macromolecules which can
neither pass through the cell membrane by diffusion nor by
active transport mechanisms
• In vesicular transport, formation and transport of vesicles are
facilitated by
 Clathrin
 Coating proteins
 Dynamin
 Docking proteins
Eg: Neurotransmitters, Hormones, Waste products of
metabolism
• Vesicular transport is of three types
Endocytosis
Exocytosis
Transcytosis
ENDOCYTOSIS
• It is the process in which substance to be transported
into the cell by in-folding of the cell membrane
around the substance and internalizing it in the form
of endocytic vesicle.
• The vesicle may contain fluid and dissolved solutes or
particulate material
• This includes:
 Pinocytosis(cell drinking)
 Phagocytosis(cell eating)
 Receptor mediated endocytosis
Constitutive endocytosis (Non clathrin/non caveolae)
Clathrin mediated endocytosis
Caveolae mediated endocytosis
• Pinocytosis – refers to the process of engulfing liquid
substances by the enfolding of the cell membrane
Eg: Reabsorption by renal tubular epithelial cells
• Phagocytosis – is the process of engulfing solid
particles consisting of 3 steps – attachment,
engulfment and killing
Eg: Bacteria, dead tissue and foreign particles
• Receptor mediated endocytosis – the substance to be
transported binds with a special receptor protein
present on the cell surface and the complex is
engulfed
Eg: Transport of iron, cholesterol into the cells
• Endocytosis takes place by 2 mechanisms:
1. Constitutive endocytosis
The substance first makes contact with the
cell membrane, the cell membrane invaginates to form
endocytic vesicle and is pinched off
2. Clathrin mediated endocytosis
It occurs at the specific sites(coated pits)
on the cell membrane where clathrin accumulates
Eg: Uptake of nerve growth factor , low density
lipoprotein
• In Caveolar mediated endocytosis, caveolae bud off
from the plasma membrane and fuse back with the
plasma membrane
EXOCYTOSIS
• It is reverse of endocytosis and by this process the
substances are expelled from the cell without passing
through cell membrane.
• The substances which are to be extruded are collected in the
form of vesicles which move towards the cell membrane,
fuses with cell membrane.
• The area of fusion breaks down releasing the contents to
the exterior
• The process of exocytosis requires Ca2+ and energy along
with docking proteins.
• Substances like digestive enzymes, hormones,
neurotransmitters, mucus are secreted out of the cell
• Exocytosis occurs by 2 pathways:
1. Non constitutive or regulated pathway
Proteins secreted initially enters the
secretory granules where processing occur before
exocytosis
2. Constitutive pathway
Prompt transport of proteins to the cell
membrane in vesicle with little or no processing
TRANSCYTOSIS
• Vesicular transport within the cell is called transcytosis
or cytopempsis
• Vesicles are formed within the cell and transported in
the cytoplasm
• It involves 3 steps – vesicle formation, vesicle
transportation, docking in the cell
TRANSPORT ACROSS EPITHELIA
• There are two mechanisms
a. Transcellular transport or transport through the cell
Substance enters the cell from one side and exit through
other side
Eg: Reabsorption of sodium and glucose in kidney tubule
and in intestine
b. Paracellular transport
Transport through the tight junctions
Eg: Movement of sodium chloride in epithelia of small
intestine, gall bladder, proximal renal tubule
TRANSPORT ACROSS THE CAPILLARY WALL
• Capillary wall acts like impermeable membrane to colloids &
exert an osmotic pressure.
• Filtration:
Fluid is forced through a membrane or barrier because of a
difference in pressure on the two sides.
Eg: Ultrafiltration through glomerular capillary endothelium
and Bowman’s capsule epithelium
APPLIED PHYSIOLOGY
• Channelopathies:
-Single ion channel mutations resulting in various
diseases
-Affects both excitable & non excitable cells
Example for excitable cells
• Periodic paralysis due to defective one subunit of K+ channel
• Long QT syndrome due to defect in both Na+ & K+ channel
subunit
• Myasthenia occurs due to defective nicotinic acetylcholine
receptor
• Malignant hyperthermia due to defect in ryanodine receptor
of Ca2+ channel
Examples for non excitable cells:
• Cystic fibrosis due to defect in Chloride channel
• Bartter’s syndrome due to defect in K⁺ channel subunit
Plasma osmolality & diseases
• The total plasma osmolality may increase in patients having
severe dehydration
• In diabetes, Increased plasma glucose concentration
Increased Plasma osmolality
Shrinkage of cells mainly brain cells
Hyperosmolar coma
• In renal disease, raised plasma levels of urea causes
hyperosmolality
REFERENCES
• William F. Ganong - Review of Medical Physiology - Twenty
sixth edition
• Guyton & Hall - Textbook of Medical Physiology -Thirteenth
edition
• G K Pal – Comprehensive textbook of Medical Physiology –
First edition
• Indu Khurana – Textbook of Medical Physiology –Third
edition

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Transport across cell membranes

  • 2. •Cell membrane maintains a constant and distinctive intracellular environment which is essential for functioning of the organelles
  • 3. •There are several mechanisms of transport across cell membranes. •They may be grouped as under the headings: 1) Passive transport 2) Active transport 3) Vesicular transport 4) Transport across epithelia 5) Transport across capillaries
  • 4. PASSIVE TRANSPORT • It refers to the mechanism of transport of substances along the gradient without expenditure of any energy. • It depends on physical factors like concentration gradient, electrical gradient and pressure gradient • It is also called downhill movement
  • 5. • Passive transport mechanism operating at cell membrane level are  Diffusion  Osmosis
  • 6. 1. DIFFUSION • Diffusion refers to passive transport of molecules from areas of higher concentration to areas of lower concentration • Diffusion through cell membrane is divided into 2 subtypes  Simple diffusion Facilitated diffusion
  • 8. SIMPLE DIFFUSION  Movement of molecules or ions occurs through a membrane due to their random movement.  In this process, there occurs a net flux of molecules from areas of high to areas of low concentration until diffusional equilibrium is reached. This can be expressed by Fick’s law of diffusion
  • 9. Fick’s law of diffusion J = D A (C1 - C2) T J  Rate of diffusion D Diffusion co-efficient A Area of membrane T Thickness of membrane C1-C2 Concentration gradient
  • 10. • Simple diffusion can occur through 2 pathways i. Direct passage without involvement of carrier molecules ii. Passage through protein channel molecules
  • 11. i. Simple diffusion of lipid soluble substances • Lipid soluble substances diffuse very rapidly through the bilipid layer.  O2, CO2, N2  Fatty acids  Alcohol  Ketone bodies, Aldehydes  Small uncharged molecules • The rate of diffusion is directly proportional to the lipid solubility of the substances and concentration gradient across the membrane
  • 12.
  • 13. ii. Simple diffusion through protein channels •Water and other lipid insoluble substances pass through cell membrane due to the presence of protein channels  Water  Electrolytes or Ions Eg: Sodium channels, Potassium channels, Chloride channels, Calcium channels, Aquaporin channels
  • 14. • Passage of substances through the protein channels is regulated by selective permeability and gating of the channels • Permeability of such substances depends upon their molecular size, shape and charge • Some protein channels are continuously open (non gated) while most are gated on either side of the channel that can open or close as per requirement
  • 15.
  • 16. • The opening and closing of gates are controlled by 3 principal ways 1. Voltage gated channels Eg: Voltage gated sodium channels 2. Ligand gated channels Eg: Acetyl choline channels 3. Mechanically gated channels Eg: Stretch sensitive channels in ventricles, hair cells
  • 17.
  • 18.
  • 19. FACILITATED DIFFUSION • Water soluble substances having larger molecular size which cannot diffuse through protein channels • They are transported across the cell membrane down their concentration gradient with help of carrier proteins without expenditure of energy. • This type of diffusion is called facilitated or carrier mediated diffusion  Glucose  Amino acids
  • 20. •Mechanism of facilitated diffusion: A conformational change occurs in the carrier protein after the molecule to be transported is bound at the receptor site. As a result, the binding site is switched to the opposite side of the cell membrane and the diffusing molecule is released.
  • 21.
  • 22. FACTORS AFFECTING NET RATE OF DIFFUSION I. Concentration gradient II. Electrical potential across the membrane III. Permeability coefficient of the substance for the membrane IV. Pressure difference across the membrane V. Temperature VI. Distance across which diffusion is occurring(thickness of membrane) VII. Area of membrane
  • 23. 2. OSMOSIS • It refers to the diffusion of water or any other solvent molecules through a semipermeable membrane from a solution containing lower concentration of solutes towards the solution containing higher concentration of solutes.
  • 24.
  • 25.
  • 26. • Osmotic pressure refers to the minimum pressure which when applied on the side of higher solute concentration prevents the osmosis • The osmotic pressure exerted by the colloidal substances in the body is called colloidal osmotic pressure • The colloidal osmotic pressure due to plasma proteins is called oncotic pressure
  • 27. • Osmole is the unit to express the concentration of osmotically active particles in a given solution (Osm) • One osmole = Molecular weight (g) Number of freely moving particles that each mol liberates in solution. • Osmolality of a solution refers to the number of osmotically active particles per kilogram of a solution (Osm/kg) • Osmolarity refers to number of osmoles per litre of a solution (Osm/L)
  • 28. Plasma Osmolality(mOsm/L) =2[Na+ (mEq/L) ]+0.055[Glucose (mg/dL) ] + 0.36[BUN(mg/dL)] • Normal plasma osmolality is 290 mOsm/kg 270 mOsm is contributed by Na+, Cl-, HCO3- 20 mOsm is contributed by glucose and urea Plasma proteins contribute only 2 mOsm due to large molecular weight and lesser number of particles
  • 29. • Tonicity refers to the osmolality of a solution in relation plasma(290 mOsm) • Isotonic fluids – solutions having osmolality similar to plasma Eg: 0.9 % NaCl solution, 5% Glucose solution • Hypertonic fluids - solutions having osmolality higher than plasma • Hypotonic fluids - solutions having osmolality lower than plasma • It is the RBC membrane across which the tonicity is tested In Isotonic solution In Hypotonic solution In Hypertonic solution RBCs do not change the shape or size Cells swell due to endosmosis Cells shrink due to exosmosis
  • 30.
  • 31. ACTIVE TRANSPORT • Active transport is also carrier mediated like facilitated diffusion • It refers to the mechanism of transport of substances against the chemical or electrical gradient • It is also called uphill movement • It involves expenditure of energy which is liberated by breakdown of high energy compounds like ATP
  • 32. Mechanism of active transport • The substance to be transported combines with a specific carrier protein on the cell membrane • The complex undergoes conformational change and is actively pumped towards the inner/outer surface of the cell membrane • Hence, it is also called as active pump mechanism • The carrier protein then moves back to its original position
  • 33. • Active transport is of two types Primary active transport Secondary active transport
  • 34. PRIMARY ACTIVE TRANSPORT • Energy derived directly from breakdown of ATP or some other high energy phosphate compound Eg: Na⁺-K⁺ ATPase pump H⁺-K⁺ ATPase pump Calcium ATPase pump
  • 35.
  • 36. SECONDARY ACTIVE TRANSPORT • Energy is derived secondarily from the ionic differences created by primary active transport • At many areas in body, transport of some other substances such as glucose, amino acid, chloride, iodine is coupled with active transport of sodium • It may occur as:  Co-transport  Counter transport
  • 37. CO-TRANSPORT • Examples : Sodium- Glucose co-transport in intestine and renal tubule Sodium-Glucose-Amino acid cotransport Sodium-Potassium-Chloride cotransport in renal tubule
  • 38.
  • 40. COUNTER TRANSPORT • Examples: Sodium-Calcium counter transport in all cell membranes Sodium-Hydrogen counter transport seen in Proximal tubule in kidney Anion exchangers: Chloride bicarbonate exchanger
  • 41.
  • 42. VESICULAR TRANSPORT • It involves the transport of macromolecules which can neither pass through the cell membrane by diffusion nor by active transport mechanisms • In vesicular transport, formation and transport of vesicles are facilitated by  Clathrin  Coating proteins  Dynamin  Docking proteins
  • 43. Eg: Neurotransmitters, Hormones, Waste products of metabolism • Vesicular transport is of three types Endocytosis Exocytosis Transcytosis
  • 44. ENDOCYTOSIS • It is the process in which substance to be transported into the cell by in-folding of the cell membrane around the substance and internalizing it in the form of endocytic vesicle. • The vesicle may contain fluid and dissolved solutes or particulate material
  • 45. • This includes:  Pinocytosis(cell drinking)  Phagocytosis(cell eating)  Receptor mediated endocytosis Constitutive endocytosis (Non clathrin/non caveolae) Clathrin mediated endocytosis Caveolae mediated endocytosis
  • 46. • Pinocytosis – refers to the process of engulfing liquid substances by the enfolding of the cell membrane Eg: Reabsorption by renal tubular epithelial cells
  • 47. • Phagocytosis – is the process of engulfing solid particles consisting of 3 steps – attachment, engulfment and killing Eg: Bacteria, dead tissue and foreign particles
  • 48. • Receptor mediated endocytosis – the substance to be transported binds with a special receptor protein present on the cell surface and the complex is engulfed Eg: Transport of iron, cholesterol into the cells
  • 49. • Endocytosis takes place by 2 mechanisms: 1. Constitutive endocytosis The substance first makes contact with the cell membrane, the cell membrane invaginates to form endocytic vesicle and is pinched off 2. Clathrin mediated endocytosis It occurs at the specific sites(coated pits) on the cell membrane where clathrin accumulates Eg: Uptake of nerve growth factor , low density lipoprotein
  • 50. • In Caveolar mediated endocytosis, caveolae bud off from the plasma membrane and fuse back with the plasma membrane
  • 51.
  • 52. EXOCYTOSIS • It is reverse of endocytosis and by this process the substances are expelled from the cell without passing through cell membrane. • The substances which are to be extruded are collected in the form of vesicles which move towards the cell membrane, fuses with cell membrane.
  • 53. • The area of fusion breaks down releasing the contents to the exterior • The process of exocytosis requires Ca2+ and energy along with docking proteins. • Substances like digestive enzymes, hormones, neurotransmitters, mucus are secreted out of the cell
  • 54. • Exocytosis occurs by 2 pathways: 1. Non constitutive or regulated pathway Proteins secreted initially enters the secretory granules where processing occur before exocytosis 2. Constitutive pathway Prompt transport of proteins to the cell membrane in vesicle with little or no processing
  • 55.
  • 56.
  • 57.
  • 58. TRANSCYTOSIS • Vesicular transport within the cell is called transcytosis or cytopempsis • Vesicles are formed within the cell and transported in the cytoplasm • It involves 3 steps – vesicle formation, vesicle transportation, docking in the cell
  • 59.
  • 60. TRANSPORT ACROSS EPITHELIA • There are two mechanisms a. Transcellular transport or transport through the cell Substance enters the cell from one side and exit through other side Eg: Reabsorption of sodium and glucose in kidney tubule and in intestine b. Paracellular transport Transport through the tight junctions Eg: Movement of sodium chloride in epithelia of small intestine, gall bladder, proximal renal tubule
  • 61.
  • 62.
  • 63. TRANSPORT ACROSS THE CAPILLARY WALL • Capillary wall acts like impermeable membrane to colloids & exert an osmotic pressure. • Filtration: Fluid is forced through a membrane or barrier because of a difference in pressure on the two sides. Eg: Ultrafiltration through glomerular capillary endothelium and Bowman’s capsule epithelium
  • 64.
  • 65. APPLIED PHYSIOLOGY • Channelopathies: -Single ion channel mutations resulting in various diseases -Affects both excitable & non excitable cells
  • 66. Example for excitable cells • Periodic paralysis due to defective one subunit of K+ channel • Long QT syndrome due to defect in both Na+ & K+ channel subunit • Myasthenia occurs due to defective nicotinic acetylcholine receptor • Malignant hyperthermia due to defect in ryanodine receptor of Ca2+ channel
  • 67. Examples for non excitable cells: • Cystic fibrosis due to defect in Chloride channel • Bartter’s syndrome due to defect in K⁺ channel subunit
  • 68. Plasma osmolality & diseases • The total plasma osmolality may increase in patients having severe dehydration • In diabetes, Increased plasma glucose concentration Increased Plasma osmolality Shrinkage of cells mainly brain cells Hyperosmolar coma • In renal disease, raised plasma levels of urea causes hyperosmolality
  • 69. REFERENCES • William F. Ganong - Review of Medical Physiology - Twenty sixth edition • Guyton & Hall - Textbook of Medical Physiology -Thirteenth edition • G K Pal – Comprehensive textbook of Medical Physiology – First edition • Indu Khurana – Textbook of Medical Physiology –Third edition