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41.
Antibodies directed against tumor-associated antigens are emerging as effective treatments for a number of cancers, although the mechanism(s) of action for some are unclear and still under investigation. We have previously examined a chimeric IgE antibody (MOv18 IgE), against the ovarian tumor-specific antigen, folate binding protein (FBP), and showed that it can direct human PBMC to kill ovarian cancer cells. We have developed a three-color flow cytometric assay to investigate the mechanism by which IgE receptors on U937 monocytes target and kill ovarian tumor cells. U937 monocytes express three IgE receptors, the high-affinity receptor, FcεRI, the low-affinity receptor, CD23, and galectin-3, and mediate tumor cell killing in vitro by two mechanisms, cytotoxicity, and phagocytosis. Our results suggest that CD23 mediates phagocytosis, which is enhanced by upregulation of CD23 on U937 cells with IL-4, whereas FcεRI mediates cytotoxicity. We show that effector : tumor cell bridging is associated with both activities. Galectin-3 does not appear to be involved in tumor cell killing. U937 cells and IgE exerted ovarian tumor cell killing in vivo in our xenograft model in nude mice. Harnessing IgE receptors to target tumor cells suggests the potential of tumor-specific IgE antibodies to activate effector cells in immunotherapy of ovarian cancer. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   
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In situ mesocosm experiments were performed under summer (1997) and winter (1999) conditions in the littoral zone of a subtropical lake in Florida, USA. The objective was to quantify phosphorus (P) accumulation by various components of the community after adding pulsed doses of dissolved inorganic P. A short-term experiment also was done to quantify the rate of P loss from the water column, with simultaneous use of an inert tracer to confirm that P depletion was not due to leakage of the tanks. In the experiments, added P was rapidly removed from the water; samples collected 3–4 days after adding spikes of near 100 μg l?1 P contained little or no soluble reactive P. In the short-term experiment, we documented that the half-life of added P was approximately 6–8 h in the water column, and that the tanks were not exchanging water with the surrounding lake. Little of the added P ended up in plankton, rooted vascular plants, or sediments. The main sink for P was periphyton, including surface algal mats, benthic algal mats and detritus, and epiphyton. In the summer 1997 experiment, the periphyton was intimately associated with a non-rooted plant (Utricularia), which also may have sequestered P from the water. Structure of the littoral community varied between summer and winter, and this influenced which periphyton component accounted for most of the P removal. In regard to P mass balances, we accounted for 54% of the added P in 1997, when coarse sampling was done. In 1999, when there was more detailed sampling of the community, 92% of the added P was located in various community components. Subtropical littoral periphyton can be a large sink for P, as long as depth and underwater irradiance conditions favor its growth.  相似文献   
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本文综述了生物陶瓷材料研制发展的历史和现状,介绍了生物陶瓷材料在当前临床应用的情况,展望了其应用前景。  相似文献   
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Mouse spermatozoa were exposed in vitro for 1 h to 27- or 2,450-MHz CW RF radiation at SARs of 0 to 90 W/kg under isothermal (37 +/- 0.2 degrees C) conditions. Exposure at either frequency to RF radiation at SARs of 50 W/kg or greater resulted in a statistically significant reduction in the ability of irradiated sperm to fertilize mouse ova in vitro (P less than .05). Over the range of SARs there was no apparent difference in the effects of 27- vs. 2,450-MHz RF radiation. There were no readily detectable exposure effects on spermatozoan morphology, ultrastructure, or capacitation. The reduction of in vitro fertilization is attributed to a direct effect of RF radiation on spermatozoa rather than to heating.  相似文献   
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J M East  D Melville  A G Lee 《Biochemistry》1985,24(11):2615-2623
A spin-labeled phospholipid is used to study lipid-protein interactions in the (Ca2+,Mg2+)-ATPase of sarcoplasmic reticulum from muscle. A novel null method is used to decompose composite electron spin resonance spectra into two components, characteristic of immobilized and mobile environments. Calculations based on a random mixing model suggest that protein-protein interactions will be relatively rare in these systems and that the immobilized lipid does not represent lipid trapped between proteins but rather represents annular phospholipid at the lipid-protein interface of the adenosinetriphosphatase. The apparent decrease in the amount of immobilized lipid with increasing temperature is shown to be consistent with lipid exchange between bulk and annulus, characterized by an exchange time of 10(-7) s at 37 degrees C. A minimum number of annular phospholipid sites of 32 and 22 are calculated at 0 and 37 degrees C, respectively.  相似文献   
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