Hepatobiliary System Flashcards

1
Q

Identify the basis for the anatomic subdivision of the liver and the specifics of its blood supply

A

Anatomic divisions:
o Divided into right and left lobe
o Subdivided into 8 functional segments

Dual blood supply to liver
o Portal vein (~1300 ml/min)
o Hepatic artery (~500 ml/min)
o Result: infarcts are rare

Single blood supply to biliary tree
o Hepatic artery
o So with obstruction → necrosis and stricture formation (ischemic cholangitis)
o If bile escapes → biloma formation (bile accumulation in liver parenchyma outside of bile ducts) → infection → abscess formation within liver

Blood drainage:
o 3 hepatic veins (right, middle, left)
NOTE: Caudate lobe (segment 1) = functionally separate
• Has own venous drainage directly to vena cava; partly through middle hepatic vein
• Result: compensatory hypertrophy when hepatic outflow obstruction at level of main hepatic veins (“Budd-Chiari Syndrome”)

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2
Q

Identify the basis for the anatomic subdivision of the liver and the specifics of its blood supply

A

Anatomic divisions:
o Divided into right and left lobe
o Subdivided into 8 functional segments

Dual blood supply to liver
o Portal vein (~1300 ml/min)
o Hepatic artery (~500 ml/min)
o Result: infarcts are rare

Single blood supply to biliary tree
o Hepatic artery
o So with obstruction → necrosis and stricture formation (ischemic cholangitis)
o If bile escapes → biloma formation (bile accumulation in liver parenchyma outside of bile ducts) → infection → abscess formation within liver

Blood drainage:
o 3 hepatic veins (right, middle, left)
NOTE: Caudate lobe (segment 1) = functionally separate
• Has own venous drainage directly to vena cava; partly through middle hepatic vein
• Result: compensatory hypertrophy when hepatic outflow obstruction at level of main hepatic veins (“Budd-Chiari Syndrome”)

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3
Q

Identify the basis for the anatomic subdivision of the liver and the specifics of its blood supply

A

Anatomic divisions:
o Divided into right and left lobe
o Subdivided into 8 functional segments

Dual blood supply to liver
o Portal vein (~1300 ml/min)
o Hepatic artery (~500 ml/min)
o Result: infarcts are rare

Single blood supply to biliary tree
o Hepatic artery
o So with obstruction → necrosis and stricture formation (ischemic cholangitis)
o If bile escapes → biloma formation (bile accumulation in liver parenchyma outside of bile ducts) → infection → abscess formation within liver

Blood drainage:
o 3 hepatic veins (right, middle, left)
NOTE: Caudate lobe (segment 1) = functionally separate
• Has own venous drainage directly to vena cava; partly through middle hepatic vein
• Result: compensatory hypertrophy when hepatic outflow obstruction at level of main hepatic veins (“Budd-Chiari Syndrome”)

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4
Q

Compare and contrast the morpho-functional unit of the liver and the distinction between the liver lobule and the portal acinus.

A

Portal acinus
o Smallest functional unit
o Cluster of hepatocytes supplied by terminal portal vein → through liver sinusoids → collected in terminal hepatic venule
Hepatocytes in acinus occupy 3 zones:
• Zone 1: closest to terminal portal vein, receive highest O2 and nutrient concentration
• Zone 2: between 1 & 3
• Zone 3: closest to the terminal hepatic vein; exposed to lowest O2 concentration and most susceptible to hypoxic injury

Hepatic lobule
o Morphological liver lobule
o Cluster of hepatocytes centered by central vein (terminal hepatic venule)

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5
Q

Space of Disse

A

o Space between sinusoid and hepatocytes; contains Stellate cells
o No true basement membrane

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6
Q

Endothelial Cells in the liver

A
  • Form the sinusoids
  • Have fenestrae = regulation of traffic of macromolecules
  • Pathologic states (alcoholic liver disease = fenestrae get shut off)
  • No true basement membrane
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7
Q

Kupffer cells

A
  • 90% of tissue-bound macrophages in body
  • Located in sinusoids
  • Clear portal blood of endotoxins from gut; general defense and clearance of bacteremia
  • With cirrhosis = less blood flow to liver → Kupffer cells can work on pathogens → more prone to infection
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8
Q

Stellate cells (Ito or lipocytes)

A
  • Storage of vitamin A
  • Activation = lose vitamin A and become myofibroblasts

Able to:
• Contract → obliterate sinusoid → portal HT
• Secrete collagen = deposited in space of Disse → barrier formation; impair blood flow

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9
Q

Pit Cells

A
  • Large granular lymphocytes with natural killer ability
  • Located in sinusoids
  • Hyperplasia → hepatomegaly and liver dysfunction
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10
Q

Compare the drainage of the lymph (lymphatic system) and of the bile (biliary tree) from the liver.

A

Bile canaliculi
Created by plasma membrane domains of 2 adjacent hepatocytes
• From apical membrane of other epithelial cells
Drain into bile ducts (in portal triad) → ductules (“Canals of Hering”)
• Ductule cells = stem cells of liver

Lymph
o Formed in space of Disse
o Drains into space of Mall (in periphery of portal triad between limiting plate and CT in portal space)
o Drains into lymphatic vessels → cysterna chhyli

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11
Q

Contrast apoptosis vs. necrosis

A
Apoptosis
o	 Cell shrinkage 
o	Endonucleases cleave DNA 
o	Fragmentation → small condensed bodies with intact organelles (apoptotic bodies)
o	No inflammation 
Necrosis 
o	Cell swelling
o	Formation of plasma membrane blebs → rupture (cytolysis)
o	Rupture and release of cell organelles
o	Non-specific DNA hydrolysis
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12
Q

Identify the two main mechanisms of new hepatocyte formation in liver regeneration.

A

Compensatory hyperplasia
o Decrease in hepatocyte mass (up to 70%) → stimulates hepatocyte division
o Chronic liver disease: fibrous tissue may be deposited = distorts liver architecture → cirrhosis (fibrosis encircles regenerative nodules destroying acinar architecture)

Stem cell regeneration
o Sudden diffuse hepatocyte necrosis (ex: acute liver failure) → division and differentiation of cells in Canal of Hering (stem cells forming the ductule)
o Potential of becoming bile duct cells and hepatocytes
o Process takes months to occur (so may still need a transplant)

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13
Q

Compare and contrast the morpho-functional unit of the liver and the distinction between the liver lobule and the portal acinus.

A

Portal acinus
o Smallest functional unit
o Cluster of hepatocytes supplied by terminal portal vein → through liver sinusoids → collected in terminal hepatic venule
Hepatocytes in acinus occupy 3 zones:
• Zone 1: closest to terminal portal vein, receive highest O2 and nutrient concentration
• Zone 2: between 1 & 3
• Zone 3: closest to the terminal hepatic vein; exposed to lowest O2 concentration and most susceptible to hypoxic injury

Hepatic lobule
o Morphological liver lobule
o Cluster of hepatocytes centered by central vein (terminal hepatic venule)

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14
Q

Space of Disse

A

o Space between sinusoid and hepatocytes; contains Stellate cells
o No true basement membrane

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15
Q

Endothelial Cells in the liver

A
  • Form the sinusoids
  • Have fenestrae = regulation of traffic of macromolecules
  • Pathologic states (alcoholic liver disease = fenestrae get shut off)
  • No true basement membrane
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16
Q

Kupffer cells

A
  • 90% of tissue-bound macrophages in body
  • Located in sinusoids
  • Clear portal blood of endotoxins from gut; general defense and clearance of bacteremia
  • With cirrhosis = less blood flow to liver → Kupffer cells can work on pathogens → more prone to infection
17
Q

Stellate cells (Ito or lipocytes)

A
  • Storage of vitamin A
  • Activation = lose vitamin A and become myofibroblasts

Able to:
• Contract → obliterate sinusoid → portal HT
• Secrete collagen = deposited in space of Disse → barrier formation; impair blood flow

18
Q

Pit Cells

A
  • Large granular lymphocytes with natural killer ability
  • Located in sinusoids
  • Hyperplasia → hepatomegaly and liver dysfunction
19
Q

Compare the drainage of the lymph (lymphatic system) and of the bile (biliary tree) from the liver.

A

Bile canaliculi
Created by plasma membrane domains of 2 adjacent hepatocytes
• From apical membrane of other epithelial cells
Drain into bile ducts (in portal triad) → ductules (“Canals of Hering”)
• Ductule cells = stem cells of liver

Lymph
o Formed in space of Disse
o Drains into space of Mall (in periphery of portal triad between limiting plate and CT in portal space)
o Drains into lymphatic vessels → cysterna chhyli

20
Q

Contrast apoptosis vs. necrosis

A
Apoptosis
o	 Cell shrinkage 
o	Endonucleases cleave DNA 
o	Fragmentation → small condensed bodies with intact organelles (apoptotic bodies)
o	No inflammation 
Necrosis 
o	Cell swelling
o	Formation of plasma membrane blebs → rupture (cytolysis)
o	Rupture and release of cell organelles
o	Non-specific DNA hydrolysis
21
Q

Identify the two main mechanisms of new hepatocyte formation in liver regeneration.

A

Compensatory hyperplasia
o Decrease in hepatocyte mass (up to 70%) → stimulates hepatocyte division
o Chronic liver disease: fibrous tissue may be deposited = distorts liver architecture → cirrhosis (fibrosis encircles regenerative nodules destroying acinar architecture)

Stem cell regeneration
o Sudden diffuse hepatocyte necrosis (ex: acute liver failure) → division and differentiation of cells in Canal of Hering (stem cells forming the ductule)
o Potential of becoming bile duct cells and hepatocytes
o Process takes months to occur (so may still need a transplant)

22
Q

Compare and contrast the morpho-functional unit of the liver and the distinction between the liver lobule and the portal acinus.

A

Portal acinus
o Smallest functional unit
o Cluster of hepatocytes supplied by terminal portal vein → through liver sinusoids → collected in terminal hepatic venule
Hepatocytes in acinus occupy 3 zones:
• Zone 1: closest to terminal portal vein, receive highest O2 and nutrient concentration
• Zone 2: between 1 & 3
• Zone 3: closest to the terminal hepatic vein; exposed to lowest O2 concentration and most susceptible to hypoxic injury

Hepatic lobule
o Morphological liver lobule
o Cluster of hepatocytes centered by central vein (terminal hepatic venule)

23
Q

Space of Disse

A

o Space between sinusoid and hepatocytes; contains Stellate cells
o No true basement membrane

24
Q

Endothelial Cells in the liver

A
  • Form the sinusoids
  • Have fenestrae = regulation of traffic of macromolecules
  • Pathologic states (alcoholic liver disease = fenestrae get shut off)
  • No true basement membrane
25
Q

Kupffer cells

A
  • 90% of tissue-bound macrophages in body
  • Located in sinusoids
  • Clear portal blood of endotoxins from gut; general defense and clearance of bacteremia
  • With cirrhosis = less blood flow to liver → Kupffer cells can work on pathogens → more prone to infection
26
Q

Stellate cells (Ito or lipocytes)

A
  • Storage of vitamin A
  • Activation = lose vitamin A and become myofibroblasts

Able to:
• Contract → obliterate sinusoid → portal HT
• Secrete collagen = deposited in space of Disse → barrier formation; impair blood flow

27
Q

Pit Cells

A
  • Large granular lymphocytes with natural killer ability
  • Located in sinusoids
  • Hyperplasia → hepatomegaly and liver dysfunction
28
Q

Compare the drainage of the lymph (lymphatic system) and of the bile (biliary tree) from the liver.

A

Bile canaliculi
Created by plasma membrane domains of 2 adjacent hepatocytes
• From apical membrane of other epithelial cells
Drain into bile ducts (in portal triad) → ductules (“Canals of Hering”)
• Ductule cells = stem cells of liver

Lymph
o Formed in space of Disse
o Drains into space of Mall (in periphery of portal triad between limiting plate and CT in portal space)
o Drains into lymphatic vessels → cysterna chhyli

29
Q

Contrast apoptosis vs. necrosis

A
Apoptosis
o	 Cell shrinkage 
o	Endonucleases cleave DNA 
o	Fragmentation → small condensed bodies with intact organelles (apoptotic bodies)
o	No inflammation 
Necrosis 
o	Cell swelling
o	Formation of plasma membrane blebs → rupture (cytolysis)
o	Rupture and release of cell organelles
o	Non-specific DNA hydrolysis
30
Q

Identify the two main mechanisms of new hepatocyte formation in liver regeneration.

A

Compensatory hyperplasia
o Decrease in hepatocyte mass (up to 70%) → stimulates hepatocyte division
o Chronic liver disease: fibrous tissue may be deposited = distorts liver architecture → cirrhosis (fibrosis encircles regenerative nodules destroying acinar architecture)

Stem cell regeneration
o Sudden diffuse hepatocyte necrosis (ex: acute liver failure) → division and differentiation of cells in Canal of Hering (stem cells forming the ductule)
o Potential of becoming bile duct cells and hepatocytes
o Process takes months to occur (so may still need a transplant)