Vander’s Human Physiology The Mechanisms of Body Function Tenth Edition by Widmaier Raff Strang © The McGraw-Hill Companies, Inc. Figures and tables from.

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Presentation transcript:

Vander’s Human Physiology The Mechanisms of Body Function Tenth Edition by Widmaier Raff Strang © The McGraw-Hill Companies, Inc. Figures and tables from the book, with additional comments by: John J. Lepri, Ph. D., The University of North Carolina at Greensboro Chapter 4

Diffusion: solute moves down its concentration gradient: simple diffusion: small (e.g., oxygen, carbon dioxide) lipid soluble (e.g., steroids) facilitated diffusion: requires transporter (e.g., glucose) Chapter 4 Movement of Molecules Across Cell Membranes = Trans-Membrane Traffic

Active transport: solute moves against its concentration gradient: primary active transport: ATP directly consumed (e.g., Na+ K+ATPase) secondary active transport: energy of ion gradient (usually Na+) used to move second solute (e.g., nutrient absorption in gut) Exo- and endo- cytosis: large scale movements of molecules Chapter 4 Movement of Molecules Across Cell Membranes = Trans-Membrane Traffic (cont.)

Diffusion of ions across the membrane concentration difference across the membrane solubility in the membrane lipids presence of the ion channels area of the membrane presence of electrical forces acting upon the ions

Over time, solute molecules placed in a solvent will evenly distribute themselves. START: Initially higher concentration of molecules randomly move toward lower concentration. Diffusional equilibrium is the result (Part b). Figure 4-1

At time B, some glucose has crossed into side 2 as some cross into side 1. Figure 4-2

Note: the partition between the two compartments is a membrane that allows this solute to move through it. Figure 4-3 Net flux accounts for solute movements in both directions.

Figure cartoon models of integral membrane proteins that function as ion channels; the regulated opening and closing of these channels is the basis of how neurons function.

Figure 4-6 A thin shell of positive (outside) and negative (inside) charge provides the electrical gradient that drives ion movement across the membranes of excitable cells.

The opening and closing of ion channels results from conformational changes in integral proteins. Discovering the factors that cause these changes is key to understanding excitable cells. Figure 4-7

The solute acts as a ligand that binds to the transporter protein…. Figure 4-8 A cartoon model of carrier-mediated transport. … and then a subsequent shape change in the protein releases the solute on the other side of the membrane.

Channel gating Ligand-gated channels Voltage-gated channels Mechanically-gated channels

Cystic Fibrosis A defective membrane channel through which chloride ions move from cells into extracellular fluid. Mucus buildup leads to eventual obstruction of the airways and pancreatic ducts.

In simple diffusion, flux rate is limited only by the concentration gradient. In carrier- mediated transport, the number of available carriers places an upper limit on the flux rate. Figure 4-9

Two types of mediated(by way of transporter) transport can be distinguished : Facilitated diffusion : proceeds from higher to lower concentration Active transport : uphill transport at the expenses of energy

The most important facilitated diffusion Glucose transporter Diabetes mellitus is due to an insufficient transport of glucose into tissue cells

In both simple and facilitated diffusion, solutes move in the direction predicted by the concentration gradient. In active transport, solutes move opposite to the direction predicted by the concentration gradient. membrane Figure 4-10

Active transport Primary active transport : the transporter itself is an ATPase that cause the breakdown of ATP and phosphorylate itself. Therefore, change the affinity of the transporters solute binding site. Secondary active transport : use of an ion concentration gradient across a membrane as the energy source. The flow of the ion provides energy for the uphill movement of the actively transported solutes.

Models showing how active transport might operate. The transported solute binds to the protein as it is phosphorylated (ATP expense).

Figure 4-12 Here, in the operation of the Na + -K + -ATPase, also known as the “sodium pump,” each ATP hydrolysis moves three sodium ions out of, and two potassium ions into, the cell.

Ca-ATPase In the plasma membrane, the active transport of Ca is from cytosol into extracellular fluid. In the organelle membranes, the active transport of Ca is from cytosol into organelle. The extracellular [Ca] is 1 mM, while the intracellular [Ca] is 0.1 uM.

Secondary active transport uses the energy in an ion gradient to move a second solute. Figure 4-13

Cotransport: the ion and the second solute cross the membrane in the same direction. Countertransport: the ion and the second solute move in opposite directions. Figure 4-14

Figure 4-15 Diverse examples of carrier-mediated transport.

Here, water is the solvent. The addition of solute lowers the water concentration. Addition of more solute would increase the solute concentration and further reduce the water concentration. Solvent + Solute = Solution Figure 4-16

Begin: The partition between the compartments is permeable to water and to the solute. After diffusional equilibrium has occurred: Movement of water and solutes has equalized solute and water concentrations on both sides of the partition. Figure 4-17

Begin: The partition between the compartments is permeable to water only. After diffusional equilibrium has occurred: Movement of water only has equalized solute concentration. Figure 4-18

Figure 4-19

Figure 4-20

Alternative functions of endocytosis: 1.Transcellular transport 2.Endosomal processing 3.Recycling the membrane 4.Destroying engulfed materials Figure 4-21

Endocytosis Fluid endocyosis (pinocytosis) Phagocytosis Receptor mediated endocytosis clathrin-coated pit, endosome fuses with lysosome Potocytosis formaion of caveolae and deliver their contents directly to the cytosol

Figure 4-22

Figure 4-23

Figure 4-24

Figure 4-25

The End.