Cell Injury 4B Intracellular Accumulations...The Cellular Basis of Disease Cell Injury 4B...
Transcript of Cell Injury 4B Intracellular Accumulations...The Cellular Basis of Disease Cell Injury 4B...
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The Cellular Basis of Disease Cell Injury 4B
Intracellular Accumulations
Christine Hulette MD
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Objectives
• Identify sub lethal cell injury caused by lysosomal accumulation of endogenous and exogenous material.
• Explain the etiology, pathologic and clinical manifestations of lysosomal storage diseases.
• Describe and understand the pathophysiology and clinical implications of intracellular accumulations including Lipids, Proteins, Glycogen, Pigments
• Describe and understand Pathologic Calcification and differentiate between dystrophic and metastatic calcification.
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Intracellular accumulations
• Lipids • Steatosis
• Cholesterol and Cholesterol Esters
• Proteins
• Glycogen
• Pigments
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• Abnormal metabolism – Steatosis (Fatty change)
• Abnormal protein folding – Alpha 1 antitrypsin deficiency
• Lack of enzyme – Lysosomal storage disease
• Indigestible material – Carbon or heme
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Causes of Steatosis (Fatty Liver )
• Alcohol is a hepatotoxin that leads to increased synthesis and reduced breakdown of lipids.
• Nonalcoholic fatty liver disease is associated with diabetes and obesity.
• CCl4 and protein malnutrition cause reduced synthesis of apoproteins.
• Hypoxia inhibits fatty acid oxidation.
• Starvation increases mobilization of fatty acids from peripheral stores.
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85.1.pg.fattyliver
85-Fatty Liver (Gross)
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Intracellular Lipid Accumulation Cholesterol and cholesterol esters
• Atherosclerosis
• Xanthomas
• Cholesterolosis
• Niemann-Pick Disease Type C
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Atherosclerotic Plaque
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Xanthoma
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Cholesterolosis
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Intracellular Protein
Accumulations • Excessive amounts of normal proteins
(Multiple myeloma -Russell Bodies)
• Defective intracellular transport and secretion
(Cystic fibrosis)
• Aggregation of abnormal proteins (Alpha-1
Antitrypsin deficiency; Systemic Amyloidosis)
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Excessive normal proteins (Russell bodies) PathGuy
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Defective intracellular transport
and secretion (Cystic fibrosis)
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Aggregation of abnormal proteins
(Amyloid in Liver)
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Indigestible material Pigments
Exogenous Pigment – Carbon in lung =
anthracosis
Endogenous Pigments
Hemosiderin- multiple transfusions
Lipofuscin- aging pigment
Melanin- skin and neurotransmission
Bilirubin-hepatocytes
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Exogenous pigment Anthracotic pigment in Lung
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Endogenous pigment Hemosiderin in Liver
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Pathologic Calcification
• Dystrophic Calcification – occurs in areas
of necrosis and atherosclerosis.
• Metastatic Calcification – occurs in normal
tissues when there is hypercalcemia.
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Metastatic Calcification
• Excess Parathyroid hormone
• Destruction of bone
• Vitamin D disorders
• Renal failure
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A 22 year-old woman has congenital anemia
that has required multiple transfusions of
RBCs for many years. Which of the following
findings would most likely appear in a liver
biopsy specimen?
A. Steatosis in hepatocytes
B. Bilirubin in canaliculi
C. Glycogen in hepatocytes
D. Amyloid in the liver
E. Hemosiderin in hepatocytes
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A 22 year-old woman has congenital anemia
that has required multiple transfusions of
RBCs for many years. Which of the following
findings would most likely appear in a liver
biopsy specimen?
A. Steatosis in hepatocytes
B. Bilirubin in canaliculi
C. Glycogen in hepatocytes
D. Amyloid in the liver
E. Hemosiderin in hepatocytes
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Summary
• Intracellular accumulations
• Lipids
• Proteins
• Glycogen
• Pigments
• Pathologic Calcification
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Conclusions • Cell injury may occur by a variety of mechanisms and sources -
endogenous (ischemia/inflammation) or exogenous (drugs/toxins)
• Cell injury can be reversible or irreversible.
• Reversible cell injury can result in changes which may recover when the cause is removed, or which may persist.
• Irreversible (lethal) cell injury may cause only transient functional impairment if the dead cells can be replaced.
• Alternatively, lethal cell injury may lead to permanent functional impairment if the dead cells can not be replaced.
• Cell death (apoptosis) is a normal mechanism to remove damaged cells which can be activated in pathologic conditions.
• Substances may be deposited within cells in response to cell injury.
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All clinical disease
arises from abnormal
cell structure and
function.