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Cell survival

Modulation of the Killing of Mammalian Cells by Thiols. Important aspects of the effects of exogenous thiols on clonogenic cell survival following exposure to low linear energy transfer (LET) radiations include the following. [Pg.487]

Thiols must be added before or within a very short time after irradiation to protect against ceU killing. This is apparent from conventional cell survival data (9) but is even better illustrated by kinetic studies showing that 2-mercaptoethanol (see Table 1) protects oxic V79 cells when added just before but not 7 milliseconds after irradiation (5). [Pg.488]

There are numerous reports of the effects of antioxidant vitamins on transformation. Vitamin C suppresses x-ray-induced transformation when CSHlOTy cells are treated daily for one week following irradiation (97), suppresses transformation by y-rays or neutrons, and prevents the promotion of radiation-induced transformation by 12-0-tetradecanoylphorbol 13-acetate (TPA), but has no effect on cell survival (98). In these studies, the continuous presence of vitamin C for a critical period appears to be necessary for suppression of transformation. Vitamin C may act on the promotion stage of... [Pg.491]

Simple Seeds and Stable Patterns First, because live cells survive only if surrounded by 2 or 3 other live cells and dead cells become alive only if surrounded by exactly three live cells, initial states consisting of either single or neighboring live cells immediately yield the null state. Survival in Life therefore requires a minimum of three live cells. Figures 3,66 and 3.67 show the fates of all starting configurations consisting of three and four live cells. [Pg.133]

The supply of oxygen and nutrients is a critical determinant for mammalian cell survival. Therefore, cells are located within a distance of 100 pm to maximally 150 pm of blood vessels. Multicellular... [Pg.81]

Antimetabolites compete with and possibly oust naturally occurring metabolites required for normal biochemical reactions and lead either to the synthesis of malfunctioning macromolecules and/or blockade of necessary intermediate or final metabolic products that are vital to cell survival. Both processes interfere with DNA synthesis and therefore antimetabolites can be used in cancer treatment, as they inhibit cell division and the growth of tumors. [Pg.147]

NGF family-NGF, BDNF, NT-3, and NT-4 TRK - TRK-A, B, C Promotes neu rite outgrowth and neural cell survival... [Pg.566]

Neurotrophins are peptides or protein molecules that regulate both cell survival and cell death of specific neuronal phenotypes and thus serve to influence development, maintenance, function, and plasticity of the nervous system. [Pg.845]

Phosphorylation is the reversible process of introducing a phosphate group onto a protein. Phosphorylation occurs on the hydroxyamino acids serine and threonine or on tyrosine residues targeted by Ser/Thr kinases and tyrosine kinases respectively. Dephosphorylation is catalyzed by phosphatases. Phosphorylation is a key mechanism for rapid posttranslational modulation of protein function. It is widely exploited in cellular processes to control various aspects of cell signaling, cell proliferation, cell differentiation, cell survival, cell metabolism, cell motility, and gene transcription. [Pg.976]

Nevertheless, SDM showed a maximum decrease in the cell survival rate of approximately 12% and 27% at the lowest and highest concentrations of microparticles, respectively (Figure 14). The massive cytotoxicity induced by CLM may be explained by the presence of remaining molecules of terephthaloyl chloride, which plays the role of cross-linking agent during the formation of CLM and is well known as a toxic substance. [Pg.78]

Poly(DL-lactide) was used as the excipient in microspheres of CCNU, a nitrosourea, prepared by a solvent evaporation procedure (96,97). PLA-CCNU microspheres 3.0 pm in diameter were injected i.v. and leukemia cell survival was determined by spleen colony assay. A 100-fold decrease in leukemia cell survival was observed with the microspheres in both spleen and liver compared to untreated controls. Promising results were also obtained with Lewis lung carcinoma in mice. These studies showed that 2- to 4-ym microspheres were preferentially targeted to the lungs. [Pg.21]

Increased nonconjugated (indirect) bilirubin Shortened red cell survival time as measured by injection of autologous Cr-labeled red cells... [Pg.620]

The first is cell injury (cytotoxicity), which can be severe enough to result in cell death. There are many mechanisms by which xenobiotics injure cells. The one considered here is covalent binding to cell macromol-ecules of reactive species of xenobiotics produced by metabolism. These macromolecular targets include DNA, RNA, and protein. If the macromolecule to which the reactive xenobiotic binds is essential for short-term cell survival, eg, a protein or enzyme involved in some critical cellular function such as oxidative phosphorylation or regulation of the permeability of the plasma membrane, then severe effects on cellular function could become evident quite rapidly. [Pg.631]

Bacellar H, Munoz A et al (1994) Temporal trends in the incidence of HIV-l-related neurologic diseases Multicenter AIDS Cohort Study, 1985-1992. Neurology 44(10) 1892-1900 Banki K, Hutter E et al (1998) Molecular ordering in HIV-induced apoptosis. Oxidative stress, activation of caspases, and cell survival are regulated by transaldolase. . J Biol Chem 273(19) 11944-11953... [Pg.77]

Booth V Keizer DW, Kamphuis MB et al (2002) The CXCR3 binding chemokine IP-IO/CXCLIO structure and receptor interactions. Biochemistry 41 10418-10425 Burns JM, Summers BC, Wang Y et al (2006) A novel chemokine receptor for SDF-1 and I-TAC involved in cell survival, cell adhesion, and tumor development. J Exp Med 203 2201-2213 Callebaut C, Krust B, Jacotot E et al (1993) T cell activation antigen, CD26, as a cofactor for entry of HIV in CD4+ cells. Science 262 2045-2050... [Pg.166]

Jones G, Power C (2006) Regulation of neural cell survival by HIV-1 infection. Neurobiol Dis 21 1-17... [Pg.168]

Johnson Z, Proudfoot AE, Handel TM (2005) Interaction of chemokines and glycosaminoglycans a new twist in the regulation of chemokine function with opportunities for therapeutic intervention. Cytokine Growth Factor Rev 16 625-636 Jones G, Power C (2006) Regulation of neural cell survival by HIV-1 infection. Neurobiol Dis 21 1-17... [Pg.244]

Knapp PE, Itkis OS, Zhang L, Spruce BA, BakaUdn G, Hauser KF (2001) Endogenous opioids and oligodendroglial function possible autocrine/paracrine effects on cell survival and development. Glia 35 156-165... [Pg.371]

The phage lambda (X) ofE. coll is the temperate phage that has been most extensively studied. When any particular strain oiE. coli, say K12, is infected with A, the cells surviving the infection are designated E. coli K 12(A) to indicate that they are carrying the /1-prophage. [Pg.60]


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See also in sourсe #XX -- [ Pg.575 ]

See also in sourсe #XX -- [ Pg.98 , Pg.99 ]

See also in sourсe #XX -- [ Pg.42 , Pg.122 ]

See also in sourсe #XX -- [ Pg.278 ]




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Cell survival and growth

Cell survival development

Cell survival measurements

Cell survival molecules

Cell survival pathways

Cell survival pathways ancient

Cell survival pathways primordial

Cell survival tyrosine phosphorylation

Cell surviving fractions

Genetics cell survival

Growth and Survival of CD4 T Cell Subsets

Neural precursor cell survival

Red cell survival

Schwann cells survival

Survival

Survive

Surviving

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