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Cells growth and division

Electron micrographs of freeze-etched preparations clearly demonstrated that S-layers completely cover the cell surface during all stages of cell growth and division [5,56,57]. [Pg.338]

Figure 9.3 Activation of T-cells by interaction with macrophage-displayed antigen. Activation results in IL-2 production, which acts in an autocrine manner to stimulate further T-cell growth and division. IL-2 thus represents the major regulatory molecule responsible for stimulation of cell-mediated immunity. Note that it was initially believed that binding of presented antigen alone was insufficient to trigger T-cell activation. It was thought that co-stimulation with IL-1 was reguired. However, the assay used to detect the co-stimulation was found not to be specific for IL-1 alone. The role of IL-1 as a co-stimulator of T-cell activation is now believed to be minimal at most... Figure 9.3 Activation of T-cells by interaction with macrophage-displayed antigen. Activation results in IL-2 production, which acts in an autocrine manner to stimulate further T-cell growth and division. IL-2 thus represents the major regulatory molecule responsible for stimulation of cell-mediated immunity. Note that it was initially believed that binding of presented antigen alone was insufficient to trigger T-cell activation. It was thought that co-stimulation with IL-1 was reguired. However, the assay used to detect the co-stimulation was found not to be specific for IL-1 alone. The role of IL-1 as a co-stimulator of T-cell activation is now believed to be minimal at most...
Because HMG CoA reductase occurs before a branch point in the biosynthetic pathway, complete inhibition of the enzyme by cholesterol would necessarily deprive the cell of many other intermediates, some of which are important in cell growth and division. A group of drugs known as statins are widely used to reduce plasma cholesterol concentration by inhibiting HMG CoA reductase. Interest is now rising in the possible use of statins as anticancer drugs due to their impact on reducing the production of mediators of cell proliferation. [Pg.191]

TFIF is formed from the vitamin folate through two reductions catalyzed by dihydrofolate reductase shown in Figure 1-17-4. It picks up a one-carbon unit from a variety of donors and enters the active one-carbon pool. Important pathways lequirii forms of THF from this pool include the synthesis of all purines and thymidine, wfakh in turn are used for DNA and RNA synthesis during cell growth and division. [Pg.249]

Given this structural similarity, it should not be surprising to learn that sulfanilamide competes with p-aminobenzoic acid for a binding site on the surface of dihydropteroate synthetase. Put another way, sulfanilamide binds to the enzyme where p-aminobenzoic acid should bind but no reaction occurs. The consequence is that a step in folic acid biosynthesis is disrupted and the bacterial cell is deprived of adequate folic acid. Nucleic acid synthesis, among other things, is disrupted, leading to a cessation of cell growth and division. The human immune system can mop up what remains. No similar consequences befall the human host since it cannot make folic acid in the first place and must get an adequate supply of this vitamin in the diet. [Pg.322]

B. Oxaloacetate synthesis is also needed when mitochondria are formed during cell growth and division. [Pg.95]

Tentative thesis Cancer cells do not respond to the body s ordinary controls on cell growth and division as normal cells do. Thus, a cure for cancer must prevent cancer cells from dividing uncontrollably while allowing normal cells to divide normally. Finding a way to stop cell growth and division in cancer cells without interfering in normal cell division has proved a difficult task for cancer researchers. [Pg.45]

Figure 11-15 The cell cycle, which depicts the relative lengths of time for each stage of cell growth and division. After mitosis (M) the cell grows during the Gj (gap) period. At the Gj checkpoint the cell prepares to divide, with DNA synthesis occurring during the S-phase. After a second gap (G2) mitosis takes place to complete the cycle. Figure 11-15 The cell cycle, which depicts the relative lengths of time for each stage of cell growth and division. After mitosis (M) the cell grows during the Gj (gap) period. At the Gj checkpoint the cell prepares to divide, with DNA synthesis occurring during the S-phase. After a second gap (G2) mitosis takes place to complete the cycle.
M Matsuhashi. Utilization of lipid-linked precursors and the formation of peptidoglycan in the process of cell growth and division membrane enzymes involved in the final steps of peptidoglycan synthesis and the mechanism of their regulation. In JM Ghuysen, R Hakenbeck, eds. Bacterial Cell Wall. Amsterdam, The Netherlands Elsevier Science, 1994, pp 55-72. [Pg.279]

Rheinwald JG (1989), Methods for clonal growth and serial cultivation of normal human epidermal keratinocytes and mesothelial cells, In Baserga R (Ed.), Cell Growth and Division A Practical Approach, IRL Press, Oxford, pp. 81-94. [Pg.37]

A lot of effort as regards phenomena identification is based on specific growth rate analysis. In Chapter 2, cell growth and division were proposed in three phases, based on values of specific growth rates. The number of steps observed in a culture depends on each system, that is, some steps may not exist or have an insignificant duration under some conditions. [Pg.191]

Baserga, R. (1989). Cell Growth and Division, p. 91, IRL Press, Oxford. [Pg.328]

Additional examples of substances synthesized by cell culture are listed in review articles and books [1-8,14,15, 21]. It is important to note that many of these compounds are secondary metabolites that is, their production is not related to cell growth and division. Indeed, high rates of production of secondary metabolites usually occur during low rates of growth, often under conditions of significant physiological or biochemical stress on the cells [4]. [Pg.29]

Before a cell can divide, it must essentially double its mass and duplicate all of its contents, so that the two new daughter cells have all the components to initiate their own cycles of cell growth and division. Because the events of nuclear division (mitosis) and cytoplasmic division (cytokinesis) produced dramatic morphologic changes readily seen with the light microscope, earlier studies focused on these relatively brief events. In the time between divisions (interphase), little seemed to be happening. We now know that most of the biochemical events in preparation for division occur continuously throughout interphase. [Pg.358]

Ras activates several pathways, of which the mitogen-activated protein (MAP) kinase cascade has been most well studied. This cascade transmits signals downstream and results in the transcription of genes involved in cell growth and division. [Pg.306]

The nucleic acids, deoxyrribonucleic aciti (DNA) and ribonucleic acid iRNA), are the chemical carriers of a ccU s genetic information. Coded In a cell s DNA is a 3 the inrormation that deterroineti the nature of the cell, controls cell growth and division, and directs bitwynthests of the enzyenes and other pnrt in rc[Pg.1158]

Cell regulation allows cells to respond to their environment and control and coordinate cell growth and division. [Pg.134]

The mode of action of this class of drugs is related to the inhibition of cell growth and division. [Pg.55]


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See also in sourсe #XX -- [ Pg.420 , Pg.421 , Pg.422 ]

See also in sourсe #XX -- [ Pg.375 , Pg.376 , Pg.377 ]




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