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Chapter 18 - Metabolism and Movement of Lipids

18.1: Phospholipids and Sphingolipids: Synthesis and Intracellular Movement

  • Fatty acids are composed of:

    • Phospholipids

    • Sphingolipids

    • Triglycerides

  • The synthesizing of fatty acids occurs through water-soluble enzymes which are modified through the endoplasmic reticulum

  • The synthesizing final steps are catalyzed by membrane associations in the ER, Golgi, mitochondria, and peroxisomes

  • Pre-existing membranes have each type of membrane initially incorporated into it

  • The exoplasmic and cytosolic leaflets distribute membrane phospholipids

18.2: Cholesterol: A Multifunctional Membrane Lipid

  • The cytosol is the main base for the initial steps in cholesterol biosynthesis, and the last steps take place in the ER membrane

  • HMG-CoA reductase catalyzes the rate-controlling step required for cholesterol biosynthesis

  • HMG-CoA has transmembrane segments embedded into the ER

  • The biosynthetic precursors of steroid hormones are intermediated by cholesterol and isoprenoid, and lipid-soluble vitamins, bioactive molecules, and bile acids also helped

  • There is evidence that indicates that cholesterol and phospholipid membrane movement is not highly dependent on the Golgi complex

  • Systems that help with cholesterol and phospholipid transport:

    • Golgi independent vesicular transport

    • Direct protein-mediated contacts that travel between different membranes

    • Soluble protein carriers

  • StAR proteins move cholesterol through the mitochondria for the function of steroid hormone synthesis

  • StAR proteins have a hydrophobic cholesterol building pocket

  • NPC1 is needed for cholesterol to move normally into intracellular compartments

18.3: Lipid Movement into and out of Cells

  • Proteins needed for lipid movement in and out of cells

  • Cell surface transport proteins and water-soluble binding proteins; or

  • Lipoprotein secretion and lipoprotein receptor facilitated uptake

  • Fatty acids are transported in the plasma membrane through fatty acid transporters such as FATPs and CD36, and these fatty acids are moved between intracellular binding proteins and extracellular carriers

  • The ABC superfamily, which is made of ATP hydrolyzing small molecule pumps, controls ABC proteins which control the export of lipids in the cells

  • Lipids in lipoprotein cores:

    • Cholesterol

    • Esters

    • Triglycerides

  • Lipoproteins all have a unique characteristic protein and a different function in the cellular export system

18.4: Feedback Regulation of Cellular Lipid Metabolism

  • Enzymes, transporters, receptors, and proteins are controlled by two key transcription control pathways

  • The active nSREBP transcription factor is released from the Golgi in the insig-1(2)/SCAP/SREBP pathway by intramembrane proteolysis, which occurs when the cholesterol levels are low

  • It then acts like a gene expression containing sterol regulatory elements (SREs)

  • Membrane proteins in the lipid metabolism can have homologous transmembrane sterol sensing domains in them

  • Domains like this can help with detection and responses to changes in levels of both lipids and sterols

18.5: The Cell Biology of Atherosclerosis, Heart Attacks, and Strokes

  • Atherosclerosis progressively accumulates cholesterol, the extracellular matrix, and inflammatory and other cells

  • If the atherosclerotic plaques cause partial or complete blockage of the coronary arteries then the heart cannot get its needed nutrients, which can ultimately cause a heart attack (similarly, this happening to the brain causes a stroke)

  • Infection or injury can cause inflammatory responses in the artery wall, which cause foam cells that show atherosclerosis

  • Plasma LDL (bad cholesterol) causes the formation of foam cells

  • Plasma HDL (good cholesterol) reverses the transport of cholesterol, lessening the risk of atherosclerosis

  • Two drugs used to treat atherosclerosis:

    • Statins (reduces cholesterol biosynthesis)

    • Bile acid sequestrants (prevent enterohepatic recycling of bile acids)

C

Chapter 18 - Metabolism and Movement of Lipids

18.1: Phospholipids and Sphingolipids: Synthesis and Intracellular Movement

  • Fatty acids are composed of:

    • Phospholipids

    • Sphingolipids

    • Triglycerides

  • The synthesizing of fatty acids occurs through water-soluble enzymes which are modified through the endoplasmic reticulum

  • The synthesizing final steps are catalyzed by membrane associations in the ER, Golgi, mitochondria, and peroxisomes

  • Pre-existing membranes have each type of membrane initially incorporated into it

  • The exoplasmic and cytosolic leaflets distribute membrane phospholipids

18.2: Cholesterol: A Multifunctional Membrane Lipid

  • The cytosol is the main base for the initial steps in cholesterol biosynthesis, and the last steps take place in the ER membrane

  • HMG-CoA reductase catalyzes the rate-controlling step required for cholesterol biosynthesis

  • HMG-CoA has transmembrane segments embedded into the ER

  • The biosynthetic precursors of steroid hormones are intermediated by cholesterol and isoprenoid, and lipid-soluble vitamins, bioactive molecules, and bile acids also helped

  • There is evidence that indicates that cholesterol and phospholipid membrane movement is not highly dependent on the Golgi complex

  • Systems that help with cholesterol and phospholipid transport:

    • Golgi independent vesicular transport

    • Direct protein-mediated contacts that travel between different membranes

    • Soluble protein carriers

  • StAR proteins move cholesterol through the mitochondria for the function of steroid hormone synthesis

  • StAR proteins have a hydrophobic cholesterol building pocket

  • NPC1 is needed for cholesterol to move normally into intracellular compartments

18.3: Lipid Movement into and out of Cells

  • Proteins needed for lipid movement in and out of cells

  • Cell surface transport proteins and water-soluble binding proteins; or

  • Lipoprotein secretion and lipoprotein receptor facilitated uptake

  • Fatty acids are transported in the plasma membrane through fatty acid transporters such as FATPs and CD36, and these fatty acids are moved between intracellular binding proteins and extracellular carriers

  • The ABC superfamily, which is made of ATP hydrolyzing small molecule pumps, controls ABC proteins which control the export of lipids in the cells

  • Lipids in lipoprotein cores:

    • Cholesterol

    • Esters

    • Triglycerides

  • Lipoproteins all have a unique characteristic protein and a different function in the cellular export system

18.4: Feedback Regulation of Cellular Lipid Metabolism

  • Enzymes, transporters, receptors, and proteins are controlled by two key transcription control pathways

  • The active nSREBP transcription factor is released from the Golgi in the insig-1(2)/SCAP/SREBP pathway by intramembrane proteolysis, which occurs when the cholesterol levels are low

  • It then acts like a gene expression containing sterol regulatory elements (SREs)

  • Membrane proteins in the lipid metabolism can have homologous transmembrane sterol sensing domains in them

  • Domains like this can help with detection and responses to changes in levels of both lipids and sterols

18.5: The Cell Biology of Atherosclerosis, Heart Attacks, and Strokes

  • Atherosclerosis progressively accumulates cholesterol, the extracellular matrix, and inflammatory and other cells

  • If the atherosclerotic plaques cause partial or complete blockage of the coronary arteries then the heart cannot get its needed nutrients, which can ultimately cause a heart attack (similarly, this happening to the brain causes a stroke)

  • Infection or injury can cause inflammatory responses in the artery wall, which cause foam cells that show atherosclerosis

  • Plasma LDL (bad cholesterol) causes the formation of foam cells

  • Plasma HDL (good cholesterol) reverses the transport of cholesterol, lessening the risk of atherosclerosis

  • Two drugs used to treat atherosclerosis:

    • Statins (reduces cholesterol biosynthesis)

    • Bile acid sequestrants (prevent enterohepatic recycling of bile acids)