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Reverse cholesterol metabolism

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1. HDL is synthesized in the liver and intestine and transports cholesterol from tissues to the liver via reverse cholesterol transport. 2. The enzyme LCAT esterifies free cholesterol on HDL particles, forming a hydrophobic core and spherical HDL structure that can deliver cholesterol to the liver. 3. HDL accepts cholesterol from tissues via SR-B1 and transports it back to the liver for excretion, in a process called reverse cholesterol transport that removes excess cholesterol from the body.

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Reverse Cholesterol Metabolism PRESENTED BY: WAJEEHA AKRAM M-PHIL MOLECULAR MEDICINE DEPARTMENT OF BIOCHEMISTRY AND MOLECULAR MEDICINE AMC,NUMS
Synthesis of HDL HDL is synthesized and secreted from both liver and intestine. However, apo C and apo E are synthesized in the liver and transferred from liver HDL to intestinal HDL when the latter enters the plasma. A major function of HDL is to act as a repository for the apo C and apo E required in the metabolism of chylomicrons and VLDL. Nascent HDL consists of discoid phospholipid bilayer containing apo A and free cholesterol.
Metabolism of HDL LCAT and the LCAT activator apo A-Ibind to the discoidal particles, and the surface phospholipid and free cholesterol are converted into cholesteryl esters and lysolecithin . The nonpolar cholesteryl esters move into the hydrophobic interior of the bilayer, whereas lysolecithin is transferred to plasma albumin. Thus, a nonpolar core is generated, forming a spherical, pseudomicellar HDL covered by a surface film of polar lipids and apolipoproteins. This aids the removal of excess unesterified cholesterol from lipoproteins and tissues
Metabolism of HDL Role of LCAT LCAT( Lecithin Cholesterol Acyl Transferase) enzyme catalyzes the esterification of cholesterol to form Cholesteryl ester. The reaction can be represented as follows Lecithin + Cholesterol Lysolecithin + Cholesteryl Ester
Reverse Cholesterol Transport The cholesterol efflux is brought about by esterification of cholesterol under the effect of LCAT. The cholesteryl ester rich HDL (HDL2) gains entry through Scavenger receptor (SR-B1)
Reverse cholesterol transport The cholesterol efflux is brought about by esterification of cholesterol under the effect of LCAT. The cholesteryl ester rich HDL (HDL2) gains entry through Scavenger receptor (SR-B1) The class B scavenger receptor B1 (SR-B1) has been identified as an HDL receptor with a dual role in HDL metabolism.
In the liver and in steroidogenic tissues, it binds HDL via apo A-I, and cholesteryl ester is selectively delivered to the cells, although the particle itself, including apo A-I, is not taken up. In the tissues, on the other hand, SR-B1 mediates the acceptance of cholesterol from the cells by HDL, which then transports it to the liver for excretion via the bile (either as cholesterol or after conversion to bile acids) in the process known as reverse cholesterol transport
HDL- cycle HDL3, generated from discoidal HDL by the action of LCAT, accepts cholesterol from the tissues via the SRB1 and the cholesterol is then esterified by LCAT, increasing the size of the particles to form the less dense HDL2. HDL3 is then reformed, either after selective delivery of cholesteryl ester to the liver via the SR- B1 or by hydrolysis of HDL2 phospholipid and triacylglycerol by hepatic lipase. This interchange of HDL2 and HDL3 is called the HDL cycle. Free apo A-I is released by these processes and forms pre -HDL after associating with a minimum amount phospholipid and cholesterol
Metabolism of HDL A second important mechanism for reverse cholesterol transport involves the ATP-binding cassette transporter A1 (ABCA1). ABCA1 is a member of a family of transporter proteins that couple the hydrolysis of ATP to the binding of a substrate, enabling it to be transported across the membrane. ABCA1 preferentially transfer cholesterol from cells to poorly lipidated particles such as pre -HDL or apo A-1, which are then converted to HDL3 via discoidal HDL Pre -HDL is the most potent form of HDL inducing cholesterol efflux from the tissues
Scavenging action- HDL scavenges extra cholesterol from peripheral tissues by reverse cholesterol transport HDL, with the help of apo E competes with LDL for binding sites on the membranes and prevents internalization of LDL cholesterol in the smooth cells of the arterial walls HDL contributes its apo C and E to nascent VLDL and chylomicrons for receptor mediated endocytosis HDL stimulated prostacyclin synthesis by the endothelial cells, which prevent thrombus formation HDL also helps in the removal of macrophages from the arterial walls
Summary of formation and fate of lipoproteins Chylomicrons is a transporter of dietary lipids whereas VLDL is a transporter of endogenous lipids(mainly TGs). LDL transports cholesterol to peripheral cells while HDL transports cholesterol from peripheral cells back to liver.
Role of HDL in receptor mediated endocytosis HDL contributes its apo C and E to nascent VLDL and chylomicrons for receptor mediated endocytosis.

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Reverse cholesterol metabolism

  • 1. Reverse Cholesterol Metabolism PRESENTED BY: WAJEEHA AKRAM M-PHIL MOLECULAR MEDICINE DEPARTMENT OF BIOCHEMISTRY AND MOLECULAR MEDICINE AMC,NUMS
  • 2. Synthesis of HDL HDL is synthesized and secreted from both liver and intestine. However, apo C and apo E are synthesized in the liver and transferred from liver HDL to intestinal HDL when the latter enters the plasma. A major function of HDL is to act as a repository for the apo C and apo E required in the metabolism of chylomicrons and VLDL. Nascent HDL consists of discoid phospholipid bilayer containing apo A and free cholesterol.
  • 3. Metabolism of HDL LCAT and the LCAT activator apo A-Ibind to the discoidal particles, and the surface phospholipid and free cholesterol are converted into cholesteryl esters and lysolecithin . The nonpolar cholesteryl esters move into the hydrophobic interior of the bilayer, whereas lysolecithin is transferred to plasma albumin. Thus, a nonpolar core is generated, forming a spherical, pseudomicellar HDL covered by a surface film of polar lipids and apolipoproteins. This aids the removal of excess unesterified cholesterol from lipoproteins and tissues
  • 4. Metabolism of HDL Role of LCAT LCAT( Lecithin Cholesterol Acyl Transferase) enzyme catalyzes the esterification of cholesterol to form Cholesteryl ester. The reaction can be represented as follows Lecithin + Cholesterol Lysolecithin + Cholesteryl Ester
  • 5. Reverse Cholesterol Transport The cholesterol efflux is brought about by esterification of cholesterol under the effect of LCAT. The cholesteryl ester rich HDL (HDL2) gains entry through Scavenger receptor (SR-B1)
  • 6. Reverse cholesterol transport The cholesterol efflux is brought about by esterification of cholesterol under the effect of LCAT. The cholesteryl ester rich HDL (HDL2) gains entry through Scavenger receptor (SR-B1) The class B scavenger receptor B1 (SR-B1) has been identified as an HDL receptor with a dual role in HDL metabolism.
  • 7. In the liver and in steroidogenic tissues, it binds HDL via apo A-I, and cholesteryl ester is selectively delivered to the cells, although the particle itself, including apo A-I, is not taken up. In the tissues, on the other hand, SR-B1 mediates the acceptance of cholesterol from the cells by HDL, which then transports it to the liver for excretion via the bile (either as cholesterol or after conversion to bile acids) in the process known as reverse cholesterol transport
  • 8. HDL- cycle HDL3, generated from discoidal HDL by the action of LCAT, accepts cholesterol from the tissues via the SRB1 and the cholesterol is then esterified by LCAT, increasing the size of the particles to form the less dense HDL2. HDL3 is then reformed, either after selective delivery of cholesteryl ester to the liver via the SR- B1 or by hydrolysis of HDL2 phospholipid and triacylglycerol by hepatic lipase. This interchange of HDL2 and HDL3 is called the HDL cycle. Free apo A-I is released by these processes and forms pre -HDL after associating with a minimum amount phospholipid and cholesterol
  • 9. Metabolism of HDL A second important mechanism for reverse cholesterol transport involves the ATP-binding cassette transporter A1 (ABCA1). ABCA1 is a member of a family of transporter proteins that couple the hydrolysis of ATP to the binding of a substrate, enabling it to be transported across the membrane. ABCA1 preferentially transfer cholesterol from cells to poorly lipidated particles such as pre -HDL or apo A-1, which are then converted to HDL3 via discoidal HDL Pre -HDL is the most potent form of HDL inducing cholesterol efflux from the tissues
  • 10. Scavenging action- HDL scavenges extra cholesterol from peripheral tissues by reverse cholesterol transport HDL, with the help of apo E competes with LDL for binding sites on the membranes and prevents internalization of LDL cholesterol in the smooth cells of the arterial walls HDL contributes its apo C and E to nascent VLDL and chylomicrons for receptor mediated endocytosis HDL stimulated prostacyclin synthesis by the endothelial cells, which prevent thrombus formation HDL also helps in the removal of macrophages from the arterial walls
  • 11. Summary of formation and fate of lipoproteins Chylomicrons is a transporter of dietary lipids whereas VLDL is a transporter of endogenous lipids(mainly TGs). LDL transports cholesterol to peripheral cells while HDL transports cholesterol from peripheral cells back to liver.
  • 12. Role of HDL in receptor mediated endocytosis HDL contributes its apo C and E to nascent VLDL and chylomicrons for receptor mediated endocytosis.