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排序方式: 共有997条查询结果,搜索用时 15 毫秒
1.
Chromosome-specific subsets of human alphoid DNA identified by a chromosome 2-derived clone 总被引:3,自引:0,他引:3
Mariano Rocchi Antonio Baldini Nicoletta Archidiacono Shabnam Lainwala Orlando J. Miller Dorothy A. Miller 《Genomics》1990,8(4):705-709
We have cloned an alphoid DNA fragment, pBS4D, from the DNA of a human-hamster hybrid cell line containing chromosome 2 as its only cytologically detectable human component. Under high stringency conditions, pBS4D hybridized in situ mostly to chromosome 2 and to a lesser extent to chromosomes 18 and 20. Restriction analysis using the DNA from selected somatic hybrid cell lines revealed that the genomic organization of this alphoid DNA differs on each of these three chromosomes. 相似文献
2.
Maria Di Bello Valeria Lucchini Stefania Chiari Roberto Colleoni Nicoletta Colombo Alberto Mantovani Paola Allavena 《Cancer immunology, immunotherapy : CII》1988,27(1):63-68
Summary Expression of HLA-DR antigens by purified preparations of human ovarian carcinoma cells freshly isolated from surgical specimens was examined in parallel with the capacity of tumor cells to elicit a blastogenic response from autologous lymphocytes in mixed lymphocyte-tumor culture (MLTC) assay. Of 21 tumor preparations, 11 (52%) reacted with monoclonal antibodies 279 and/or 949 specific for a monomorphic determinant of HLA-DR antigens, with heterogeneous positivity, ranging between 30% and 95%. In this series of patients positive MLTC occurred in 8/21 individual experiments. The HLA-DR expression was proportionally similar in tumors giving positive MLTC (4/8=50%) and negative MLTC (7/13=53%). The lack of correlation between DR expression on tumor cells and stimulatory activity in autologous MLTC and the fact that DR-negative tumors could induce lymphocyte stimulation, support the hypothesis that blastogenesis occurs upon recognition of tumor-associated antigens, different from DR molecules, possibly tumor-specific antigens. 相似文献
3.
Nicoletta La Rocca Roberto Barbato Giorgio Casadoro Nicoletta Rascio 《Physiologia plantarum》1996,96(3):513-518
The assimilatory activity of cotyledons can play an essential role in the survival of seedlings with a slow and delayed development of primary leaves. Changes in the photosynthetic activity of the cotyledon, from the onset of greening through senescence, were studied in two such plants, carob and sunflower, in order to determine its efficiency and duration, also in connection with the achievement of assimilatory autonomy by the plantlet. Chlorophyll analyses showed that the cotyledon's chloroplasts reached maximal greening in plantlets with a pair of expanded leaves. In contrast, the cotyledon's photosynthetic activity, measured as the rate of oxygen release, started to decrease early, before expansion of primary leaves. The decrease was due to the inactivation of a number of photosystem II (PSII) units, as revealed by immunodetection of breackdown products of the reaction centre's D1 and D2 thylakoid proteins. No signals of PSII alteration were noticed in the primary leaf chloroplasts that differentiated under the same environmental conditions. The damage to the cotyledon PSII, occurring in a non-photoinhibitory situation, might be due to a slower rate of turnover of D1 polypeptide than in the leaf thylakoids. The differential turnover of this protein in cotyledons and in leaves might represent an organ-specific regulation of the photosynthetic activity. The peculiarity of the cotyledon thylakoids make these organs useful objects for studying the metabolic cycle of both D1 and D2 proteins in vivo, under non-photoinhibiting conditions. 相似文献
4.
The effects of the growth in a medium containing NH4NO3 as nitrogensource were studied on cell sap pH, cytoplasmic pH and malatecontent in chl1, an Arabidopsis thaliana mutant impaired inchlorate and nitrate transport. In all the conditions testedthe pH of the cytoplasm in chl1 was more alkaline, and thatof the vacuole was more acidic as compared with those measuredin wt. Treatment with bafilomycin A1, a specific inhibitor ofthe vacuolar H+-ATPase, induced a small alkalinization of thevacuole, and a significant acidification of the cytoplasm, theseeffects being greater in chl1 than in wt. The greater responseof the mutant to bafilomycin Al suggests that, in the absenceof the inhibitor, the activity of the tonoplast H+-ATPase inchl1 is higher than in wt, this diversity being a possible reasonfor the differences in intracellular pH detected between thetwo strains. A possible role for the vacuolar H+-ATPase in regulatingthe cytoplasmic pH is discussed. (Received August 2, 1995; Accepted February 1, 1996) 相似文献
5.
Nicoletta zini Patrizia Sabatelli Irene Faenza Andrea Ognibene Nadir M. Maraldi 《The Histochemical journal》1996,28(7):495-504
Summary Some key elements of signal transduction have been identified within the nucleus and demonstrated to be responsive to specific
agonists in numerous cell types. In particular, mitogenic stimuli have been reported to induce, a transient increase of the
nuclear phospholipase C β1 activity, causing the release of inositide-derived second messengers, whereas differentiating stimuli induced a decrease
of the enzyme activity and an increase of nuclear phosphatidylinositol 4,5-bisphosphate (PIP2). Recently, we reported evidence, in human osteosarcoma Saos-2 cell lines, on the presence of specific nuclear phospholipase
C isoforms and on the activation of phospholipase C β1 in the nucleus following the exposure to interleukin-1α. In this study we report immunocytochemical ultrastructural evidence on quantitative variations of PIP2 and phospholipase C β1 amounts in the nucleus of Saos-2 cells at different times of exposure to interleukin-1α. After short periods of culture in the presence of the agonist, the intranuclear amount of PIP2 is decreased, while a translocation of phospholipase C β1 occurs from the cytoplasm to the nucleus, in correspondence with the increased hydrolyzing activity of the enzyme. After
longer periods of incubation with interleukin-1α, on the other hand, the intranuclear amount of PIP2 is restored to initial level, while the amount of phospholipase C β1 is increased both at the nuclear and cytoplasmic level, when its activation is no longer effective. The results, compared
with those obtained in other cell types responsive to given agonists, account for a cell-specific modulation of signal transduction
based on polyphosphoinositide breakdown at the nuclear level. 相似文献
6.
7.
Nicoletta Zini Katia Scotlandi Nicola Baldini Giuseppe Nini Patrixia Sabatelli Nadir M Maraldi 《Biology of the cell / under the auspices of the European Cell Biology Organization》1995,84(3):195-204
Summary— Multidrug-resistant (MDR) variants of a human osteosarcoma cell line (U-2 OS) have been recently obtained by continuous exposure to doxorubicin (DX). The growth and phenotypic characteristics of these cell lines have been demonstrated to be related to the level of expression of P-glycoprotein. In this work, the morphological changes associated with MDR have been evaluated by quantitative image analysis and transmission electron microscopy. Resistant cells present morphological changes with respect to sensitive cells at both cytoplasmic and nuclear level. Some of these changes appear to be related to the degree of resistance but not to the direct presence of DX, since deprived cells maintain some modified characters, while others are partly lost. These findings suggest that DX exposure affects cell metabolism causing progressive changes of the cell morphotype. 相似文献
8.
Summary Research carried out into successively older sunflower leaves has allowed us to follow the different ontogenetic stages leading to the building up of a well-differentiated chloroplast. In all the intrathylakoid compartments of the young plastids there is very electron-dense material whose accumulation causes the dilatation of some thylakoid profiles and, consequently, the forming of roundish bodies. The thylakoid membranes appear as Lithtly Stained Membranes which, according to the most recent interpretation, are considered as incompletely organized ones. At a subsequent stage there is an increase of the thylakoid membrane staining along with a decrease of the electron-density of the intrathylakoid compartments that, at the end of the ontogenetic process, appear electrontransparent and flattened. Therefore, the intrathylakoid material appears to have been used up in the forming of well-organized membranes. This particular situation, present in the early ontogenetic stages of the plastids, may be attributed to an initial disequilibrium between the synthesis speed of membranal material and the capability to build up well-organized membranes. 相似文献
9.
D M Strong F Pandolfi R B Slease J E Budd J N Woody 《Journal of immunology (Baltimore, Md. : 1950)》1981,126(6):2205-2208
In a previous report, peripheral blood mononuclear T cells from a patient with T-chronic lymphocytic leukemia (T-CLL) were shown to bear receptors for the Fc portion of IgG (T gamma). Moreover, the ability of these cells to rosette with sheep erythrocytes was strongly inhibited by a preincubation of the cells with theophylline. These data indicated that they represent a highly purified subpopulation of Fc-IgG receptor-positive, low-affinity rosetting cells with in vitro suppressor activity on lectin-induced proliferation of normal lymphocytes. They also were reactive in antibody-dependent cell-mediated cytotoxicity but had no reactivity in natural killer cell assays. These cells were studied in this report with several heteroantisera and monoclonal antibodies. Results indicate that these T-CLL cells express a T cell antigenic pattern (OKT-3+) and the majority are Ia positive. They also react with the OKT-8 reagent (a reagent detecting the subset of T cells that contains the cytotoxic/suppressor cells), whereas they are negative with OKT-4 (which reacts with the subset of T cells that contains helper cells) and OKT-6 (thymocyte) antibodies. Heteroantisera also support the results obtained with monoclonal reagents. Despite some recent evidence showing that a high percentage of T gamma cells may belong to the monocyte-myeloid lineage, these T-CLL cells were negative with OKM-1, a monoclonal antibody reported to detect a monomyeloid antigen. These results suggest that a distinct subpopulation of suppressor T cells can be identified by membrane-marker phenotyping. 相似文献
10.
Franco Pandolfi Douglas M. Strong Guy D. Bonnard Ronald B. Herberman 《In vitro cellular & developmental biology. Plant》1980,16(9):754-760
Summary Four hematopoietic cell lines (CCRF-CEM, HSB-2, MOLT-4, and RPMI-8402), derived from acute lymphoblastic leukemia and expressing
T-cell surface markers (T-HCL), were studied with two specific anti-T-cell sera. The sera were raised in rabbits against human
thymocytes (anti-HTY) and against T-cells cultured in the presence of conditioned medium derived from lymphocytes stimulated
with PHA (anti-CTC). Both sera were absorbed to obtain a T-cell specific pattern of reaction and were further absorbed with
normal peripheral blood lymphocytes or with each of the four T-HCL. The anti-HTY sera absorbed with CEM, 8402, and HSB-2 still
reacted with MOLT-4. A similar pattern of reactivity was found only with the anti-CTC absorbed with 8402, whereas, after absorptions
with the other cell lines, this antiserum was unreactive against MOLT-4. After absorption with normal peripheral blood lymphocytes,
anti-HTY still reacted with thymocytes and MOLT-4 but was negative on CTC. In contrast, anti-CTC absorbed with peripheral
blood lymphocytes (PBL) was negative on thymocytes and MOLT-4 but still reacted against CTC. Our data confirm the existence
of a T-cell antigen (probably an early T-cell differentiation antigen) shared between thymus and MOLT-4. This antigen is not
expressed on CTC, although these cells express an antigenic pattern more complex than PBL. Antisera to CTC represents a source
of anti-T-cell sera free of contamination with antibodies to early thymus-related antigens but containing other T-cell-related
specificities.
Supported in part by Naval Medical Research and Development Command, Research Task No. ZF51.524.013.1025, and National Cancer
Institute Contract No. Y01-CB-00319. The opinions and assertions contained herein are the private ones of the writers and
are not to be construed as official or reflecting the views of the Navy Department or the naval service at large. The experiments
reported herein were conducted according to the principles set forth in the current edition of the “Guide for the Care and
Use of Laboratory Animals,” Institute of Laboratory Animal Resources, National Research Council. 相似文献