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Eukaryote epithelium

An idealised eukaryotic epithelium is represented in Figure 1. This might, for example, be the gut mucosa, the reabsorbing portion of a renal tubule system, or a gill epithelium. The solute must move from the bulk solution (e.g. the external environment, or a body fluid such as urine) into an unstirred layer... [Pg.339]

Figure 1. Solute transfer across an idealised eukaryote epithelium. The solute must move from the bulk solution (e.g. the external environment, or a body fluid) into an unstirred layer comprising water/mucus secretions, prior to binding to membrane-spanning carrier proteins (and the glycocalyx) which enable solute import. Solutes may then move across the cell by diffusion, or via specific cytosolic carriers, prior to export from the cell. Thus the overall process involves 1. Adsorption 2. Import 3. Solute transfer 4. Export. Some electrolytes may move between the cells (paracellular) by diffusion. The driving force for transport is often an energy-requiring pump (primary transport) located on the basolateral or serosal membrane (blood side), such as an ATPase. Outward electrochemical gradients for other solutes (X+) may drive import of the required solute (M+, metal ion) at the mucosal membrane by an antiporter (AP). Alternatively, the movement of X+ down its electrochemical gradient could enable M+ transport in the same direction across the membrane on a symporter (SP). A, diffusive anion such as chloride. Kl-6 refers to the equilibrium constants for each step in the metal transfer process, Kn indicates that there may be more than one intracellular compartment involved in storage. See the text for details... Figure 1. Solute transfer across an idealised eukaryote epithelium. The solute must move from the bulk solution (e.g. the external environment, or a body fluid) into an unstirred layer comprising water/mucus secretions, prior to binding to membrane-spanning carrier proteins (and the glycocalyx) which enable solute import. Solutes may then move across the cell by diffusion, or via specific cytosolic carriers, prior to export from the cell. Thus the overall process involves 1. Adsorption 2. Import 3. Solute transfer 4. Export. Some electrolytes may move between the cells (paracellular) by diffusion. The driving force for transport is often an energy-requiring pump (primary transport) located on the basolateral or serosal membrane (blood side), such as an ATPase. Outward electrochemical gradients for other solutes (X+) may drive import of the required solute (M+, metal ion) at the mucosal membrane by an antiporter (AP). Alternatively, the movement of X+ down its electrochemical gradient could enable M+ transport in the same direction across the membrane on a symporter (SP). A, diffusive anion such as chloride. Kl-6 refers to the equilibrium constants for each step in the metal transfer process, Kn indicates that there may be more than one intracellular compartment involved in storage. See the text for details...
Figure 2. Sodium and chloride uptake across an idealised freshwater-adapted gill epithelium (chloride cell), which has the typical characteristics of ion-transporting epithelia in eukaryotes. In the example, the abundance of fixed negative charges (muco-proteins) in the unstirred layer may generate a Donnan potential (mucus positive with respect to the water) which is a major part of the net transepithelial potential (serosal positive with respect to water). Mucus also contains carbonic anhydrase (CA) which facilitates dissipation of the [H+] and [HCO(] to CO2, thus maintaining the concentration gradients for these counter ions which partly contribute to Na+ import (secondary transport), whilst the main driving force is derived from the electrogenic sodium pump (see the text for details). Large arrow indicates water flow... Figure 2. Sodium and chloride uptake across an idealised freshwater-adapted gill epithelium (chloride cell), which has the typical characteristics of ion-transporting epithelia in eukaryotes. In the example, the abundance of fixed negative charges (muco-proteins) in the unstirred layer may generate a Donnan potential (mucus positive with respect to the water) which is a major part of the net transepithelial potential (serosal positive with respect to water). Mucus also contains carbonic anhydrase (CA) which facilitates dissipation of the [H+] and [HCO(] to CO2, thus maintaining the concentration gradients for these counter ions which partly contribute to Na+ import (secondary transport), whilst the main driving force is derived from the electrogenic sodium pump (see the text for details). Large arrow indicates water flow...
Pearse and Bretscher (1981) have discussed the role of coated vesicles in membrane synthesis and function. Eukaryotic cells are able to specifically take up macromolecules by absorptive endocytosis. The macromolecules are usually transferred to lyso-somes where they may be degraded. The first stage of the process involves the binding of macromolecules to receptors which are localized in coated pits. The latter are indented sites on the plasma membrane and the coated pit buds into the cytoplasm to form a coated vesicle in which lie the endocytosed macromolecules. The coated vesicle sheds its coat rapidly and the endocytic vesicles fuse with each other. This allows receptors to be returned to the plasma membrane while the contents are transferred to the lyso-somes. In order to explain how lysosomal and plasma membranes remain different, it was suggested that the coated pits are able to accept certain macromolecules while excluding others. The accepted proteins enter the coated pit and were presumed to bind directly or indirectly to clathrin. Clathrin, a 180000-dalton protein on the cytoplasmic face of coated pits, provides the polyhedron skeleton for the coated vesicles. Examples of the use of coated vesicles for mediated endocytosis are in the uptake of low-density lipoprotein from the blood and in humans for the transport of immunoglobulins from the mother to the child. For other mammals such as the rat the antibodies are selectively absorbed from the mother s milk by the intestinal epithelium. Coated vesicles also provide a mechanism for virus transport into cells. [Pg.383]


See other pages where Eukaryote epithelium is mentioned: [Pg.348]    [Pg.348]    [Pg.338]    [Pg.15]    [Pg.1884]    [Pg.166]    [Pg.652]    [Pg.1710]    [Pg.15]    [Pg.217]    [Pg.219]    [Pg.971]    [Pg.950]    [Pg.126]    [Pg.165]   
See also in sourсe #XX -- [ Pg.339 , Pg.340 ]




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