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Cell Transport

Each component of blood has a function ia the body. Red cells transport oxygen and carbon dioxide between the lungs and cells ia the tissues. White cells function as defense of the body. Platelets are important for hemostasis, ie, the maintenance of vascular iategrity. Plasma, an aqueous solution containing various proteias and fatty acids, transports cells, food, and hormones throughout the body. Some proteias ia plasma play a role ia clotting, others are messengers between cells. [Pg.520]

Ren, X. Springer, T. E. and Gottesfeld, S. (1998). Direct Methanol Fuel Cell Transport Properties of the Polymer Electrolyte Membrane and Cell Performance. Vol. 98-27. Proc. 2nd International Symposium on Proton Conducting Membrane Euel Cells. Pennington, NJ Electrochemical Society. [Pg.644]

Hematopoietic (blood) cells transport oxygen and carbon dioxide, contribute to host immunity, and facilitate blood clotting [1], A complex, interrelated, and multistep process, called hematopoiesis, controls the production as well as the development of specific marrow cells from immature precursor cells to functional mature blood cells. This well-regulated process also allows for replacement of cells lost through daily physiologic activities. The proliferation of precursor cells, the maturation of these into mature cells, and the survival of hematopoietic cells require the presence of specific growth factors. [Pg.579]

Cells Transport Certain Macromolecules Across the Plasma Membrane... [Pg.428]

The entry rate of glucose into red blood cells is far greater than would be calculated for simple diffusion. Rather, it is an example of facilitated diffiision (Chapter 41). The specific protein involved in this process is called the glucose transporter or glucose permease. Some of its properties are summarized in Table 52-3-The process of entry of glucose into red blood cells is of major importance because it is the major fuel supply for these cells. About seven different but related glucose transporters have been isolated from various tissues unlike the red cell transporter, some of these are insidin-dependent (eg, in muscle and adipose tissue). There is considerable interest in the latter types of transporter because defects in their recruitment from intracellular sites to the surface of skeletal muscle cells may help explain the insulin resistance displayed by patients with type 2 diabetes mellitus. [Pg.611]

At least seven similar but distinct glucose transporters have been detected to date in mammalian tissues, of which the red cell transporter is one. [Pg.612]

Microbial cells transported with the stream of fluid above the surface interact with conditioning films. Immediately after attachment, microorganisms initiate production of slimy adhesive substances, predominantly exopolysaccharides (EPS) that assist the formation of microcolonies and microbial films. EPS create bridges for microbial cells to the substratum and permit negatively charged bacteria to adhere to both negatively and positively charged surfaces. EPS may also control interfacial chemistry at the mineral/biofilm interface. [Pg.206]

Mezzit LA, Lucas WJ 1996 Plasmodesmatal cell transport of proteins and nucleic acids. Plant Mol Biol 32 251-273... [Pg.247]

Precellular solute ionization dictates membrane permeability dependence on mucosal pH. Therefore, lumenal or cellular events that affect mucosal microclimate pH may alter the membrane transport of ionizable solutes. The mucosal microclimate pH is defined by a region in the neighborhood of the mucosal membrane in which pH is lower than in the lumenal fluid. This is the result of proton secretion by the enterocytes, for which outward diffusion is slowed by intestinal mucus. (In fact, mucosal secretion of any ion coupled with mucus-restricted diffusion will provide an ionic microclimate.) Important differences in solute transport between experimental systems may be due to differences in intestinal ions and mucus secretion. It might be anticipated that microclimate pH effects would be less pronounced in epithelial cell culture (devoid of goblet cells) transport studies than in whole intestinal tissue. [Pg.174]

JPF Bai, GL Amidon. Structural specificity of mucosal-cell transport and metabolism of peptide drugs. J Pharm Sci 9 969-978, 1992. [Pg.199]

Shepherd VA, Orlovich DA, Ashford AE. Cell-to-cell transport via motile tubules in growing hyphae of a fungus. J Cell Sci 1993 105 1173-1178. [Pg.90]

The simplest numerical implementation of inter-cell transport in an Eulerian PDF code consists of the following steps. [Pg.354]

J. P. F. Bai, G. L. Amidon, Structural Specificity of Mucosal-Cell Transport and Metabolism of Peptide Drugs Implication for Oral Peptide Drug Delivery , Pharm. Res. 1992, 9, 969-978. [Pg.370]

The 02Fib molecule is called oxyhemoglobin and has a bright red color. The red blood cells transport 02Fib to all cells of the body, where 02Fib dissociates, yielding up the needed O2 molecules. [Pg.113]

Synthesis of those proteins that are destined for incorporation into cellnlar membranes or for export from the cell. Transport of those proteins that are destined for cell membranes or for release from the cell is achieved throngh vesicles that pinch off from the endoplasmic reticnlnm and fnse with membranes of the Golgi (see below). [Pg.5]

Flow near the interface that is influenced by gradients of interface tension is called Marangoni convection. It may have further modes [27]. Thus, a low Marangoni convection in an interface, which results from small concentration differences, may be increased to a strong flow in the shape of rolling cells by mass transfer. These rolling cells transport liquid out of the... [Pg.407]

Transport Studies with Intact Cells Transport of glutathione, glutathione disulfide, and glutathione conjugates across the hepato-cyte plasma membrane, 173, 523 Ca fluxes and phosphoinosi-... [Pg.450]

The thyroid follicular cells transport I across the cell and secrete the precursor protein, Tg, into the follicular lumen. In addition, these cells contain an apical membrane-bound enzyme, thyroperoxidase (TPO), and the enzymatic machinery to produce hydrogen peroxide (H2O2). In the presence of H2O2, TPO catalyzes the incorporation of L into tyrosyl residues of Tg to form monoiodotyrosine (MIT) and diiodotyrosine (DIT) and the coupling of these iodotyrosyl residues to form T4 and Tj. [Pg.743]

It has been emphasized in the previous paragraphs that effecting the through-membrane transport of artificial antiviral nucleotide analogs would be beneficial in that it might allow the direct into-cytoplasm entry of species that would be otherwise inactive in vivo (due to an inability to cross hydrophobic cell membranes). Within the overall scope of this problem, finding ways to effect the into-cell transport of nucleotide di- and triphosphates is deemed particularly important. This is because it is often these forms that are the most potent. [Pg.124]

A solid state galvanic cell consists of electrodes and the electrolyte. Solid electrolytes are available for many different mobile ions (see Section 15.3). Their ionic conductivities compare with those of liquid electrolytes (see Fig. 15-8). Under load, galvanic cells transport a known amount of component from one electrode to the other. Therefore, we can predetermine the kinetic boundary condition for transport into a solid (i.e., the electrode). By using a reference electrode we can simultaneously determine the component activity. The combination of component transfer and potential determination is called coulometric titration. It is a most useful method for the thermodynamic and kinetic investigation of compounds with narrow homogeneity ranges. For example, it has been possible to measure in a... [Pg.399]

Our first goal in this chapter is to explain how biological membranes can be, on the one hand, thin and flexible, and on the other, durable and functional. We start by examining the constituents of membranes with the aim of developing a general model for membrane structure. Then we turn to the question of how cells transport polar materials across membranes. [Pg.383]

Long-term side effects of lithium treatment include weight gain. The treatment is associated with development of hypothyroidism in about 10-15% of cases. There is an association with kidney disease. Birch has expressed the general view that Li may interact with magnesium-dependent processes, and theoretical chemistry supports this view. Despite the widespread clinical significance of Li, there is presently no consensus on its mode of action. One postulate for the mechanism is termed hyperpolarization . Li affects the conductivity in cell transport channels. Other explanations include modulation of neurotransmitter concentrations and inhibition of Na+/K+/Mg2+/ Ca2+ ATPases. [Pg.772]

Facilitated transport is not energy dependent, and therefore, cannot move a substance against a concentration gradient, as in active transport. The direction in which the substance moves across the membrane depends upon the difference in the substance s concentration between the exterior and interior of the cell transport across the membrane occurs in the direction of higher to lower concentration of substance. Facilitated transport is stereospecific. [Pg.288]

Yuan, J. and Sunden, B. Analysis of Intermediate Temperature Solid Oxide Fuel Cell Transport Processes and Performance, ASME Journal of Heat Transfer, 127,1380 (2005). [Pg.134]


See other pages where Cell Transport is mentioned: [Pg.388]    [Pg.206]    [Pg.89]    [Pg.509]    [Pg.246]    [Pg.326]    [Pg.263]    [Pg.388]    [Pg.140]    [Pg.82]    [Pg.83]    [Pg.322]    [Pg.8]    [Pg.239]    [Pg.243]    [Pg.451]    [Pg.586]    [Pg.190]    [Pg.44]    [Pg.44]    [Pg.539]    [Pg.304]    [Pg.1005]    [Pg.222]    [Pg.400]   
See also in sourсe #XX -- [ Pg.206 ]




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Transporter cell

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