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E. Ruiz L. Rodríguez J. Alonso-Azcárate J. Rincón 《International journal of phytoremediation》2009,11(4):360-384
In order to assess their practical capability for the absorption and accumulation of Pb, Zn, and Cu, five common crop plants, i.e. maize (Zea mays), sunflower (Helianthus annuus), canola (Brassica napus), barley (Hordeum vulgare) and White lupine (Lupinus albus) were tested in pot experiments using six soil samples taken from mine tailings, pasture and arable soils around an old Pb-Zn mine in Spain. Metal concentration ranges of the soils were 76.2–785 mg kg?1, 127–1652 mg kg?1, and 12.4–82.6 mg kg?1 for Zn, Pb, and Cu, respectively. With the exception of the highest polluted sample, soil total metal concentration did not influence significantly biomass yields of each crop for the different growth substrates. The order found for the total metal accumulation rate (TMAR) in the crops was Zn>>Pb > Cu, with maize reaching the highest metal concentrations. Pb root concentrations were markedly higher than those of shoots for all the crops, while Zn and Cu were translocated to shoots more efficiently. Concentrations of metals extracted by EDTA and BCR sequential extraction were well correlated, in general, with both root metal content and TMAR. CaCl2-extracted Zn was well correlated with root concentrations, TMAR and, in some cases, with shoot contents. Our study showed that the test crops were not feasible to remediate the heavily or moderately contaminated soils studied here in order to achieve the total metal soil concentrations required by the current European laws. 相似文献
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湘西河流表层沉积物重金属污染特征及其潜在生态毒性风险 总被引:14,自引:0,他引:14
花垣河和峒河是湘西地区受到锰矿和铅锌矿生产影响严重的两条河流。通过表层沉积物采样分析了Cd、Pb、Cu、Ni、Cr、Zn和Mn的总量,根据BCR连续提取程序分析沉积物样品中重金属的地球化学赋存形态,采用内梅罗指数法和地积累指数法评价了沉积物重金属污染特征,根据重金属的富集程度探讨了重金属污染来源,采用淡水生态系统沉积物质量基准(SQGs,TEL/PEL)和毒性单位评价了花垣河和峒河沉积物中重金属元素的生态毒性风险。结果表明,花垣河和峒河绝大多数位点的表层沉积物中Cd、Pb、Cu、Ni、Cr、Zn和Mn的总量高于参照点,形成严重的复合污染,花垣河沉积物中重金属的污染水平明显高于峒河,但沿程变化规律不明显,而峒河沉积物中重金属的沿程变化较有规律,即上游含量低,中下游含量较高。两条河流表层沉积物中富集程度居前列的均为Cd、Pb、Zn和Mn。花垣河和峒河沉积物重金属污染主要来源于矿业生产所产生废渣和废水的点排放。在花垣河和峒河的大多数位点,Cd、Pb和Mn的形态具有共同特征,其生物可利用态均较大程度地超过生物不可利用态,而且Mn和Cd的生物可直接利用态所占比例远高于其它重金属,而Cu和Cr的生物可直接利用态所占比例很低。花垣河沉积物中Cd、Pb和Zn在所有位点极大地超过PEL,在峒河中下游,Cd、Pb、Ni和Zn超过PEL,具有较大的潜在生物毒性。除上游S1位点外,花垣河的其余各位点都具有明显的急性毒性,峒河中下游各位点具有明显的急性毒性,这些河段需要重点治理。 相似文献
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《遗传学报》2020,47(1):27-35
B cells express B-cell receptors(BCRs) which recognize antigen to trigger signaling cascades for B-cell activation and subsequent antibody production. BCR activation has a crucial influence on B-cell fate. How BCR is activated upon encountering antigen remains to be solved, although tremendous progresses have been achieved in the past few years. Here, we summarize the models that have been proposed to explain BCR activation, including the cross-linking model, the conformation-induced oligomerization model, the dissociation activation model, and the conformational change model. Especially, we elucidate the partially resolved structures of antibodies and/or BCRs by far and discusse how these current structural and further immunogenomic messages and more importantly the future studies may shed light on the explanation of BCR activation and the relevant diseases in the case of dysregulation. 相似文献
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Liliana S. Mendonça João N. Moreira Maria C. Pedroso de Lima Sérgio Simões 《Biotechnology and bioengineering》2010,107(5):884-893
Chronic myeloid leukemia (CML) is triggered by the BCR‐ABL oncogene. Imatinib is the first‐line treatment of CML; however imatinib resistance and intolerance have been detected in many patients. Therefore, new therapeutic approaches are required. The present work aimed at the development and application of transferrin receptor (TrfR) targeted liposomes co‐encapsulating anti‐BCR‐ABL siRNA and imatinib at different molar ratios. The encapsulation yields and drug loading of each molecule was evaluated. Anti‐leukemia activity of the developed formulations co‐encapsulating siRNA and imatinib and of the combination of Trf‐liposomes carrying siRNA and free imatinib under two different treatment schedules of pre‐sensitization was assessed. The results obtained demonstrate that the presence of imatinib significantly decreases the encapsulation yields of siRNA, whereas imatinib encapsulation yields are increased by the presence of siRNA. Cytotoxicity assays demonstrate that the formulations co‐encapsulating siRNA and imatinib promote a 3.84‐fold reduction on the imatinib IC50 (from 3.49 to 0.91 µM), whereas a 8.71‐fold reduction was observed for the pre‐sensitization protocols (from 42.7 to 4.9 nM). It was also observed that the formulations with higher siRNA to imatinib molar ratios promote higher cell toxicity. Thus, the present work describes a novel triple targeting strategy with one single system: cellular targeting (through the targeting ligand, transferrin) and molecular targeting at the BCR‐ABL mRNA and Bcr‐Abl protein level. Biotechnol. Bioeng. 2010;107: 884–893. © 2010 Wiley Periodicals, Inc. 相似文献
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Activation of Bad trafficking is involved in the BCR-mediated apoptosis of immature B cells 总被引:1,自引:1,他引:0
Malissein E Verdier M Ratinaud MH Troutaud D 《Apoptosis : an international journal on programmed cell death》2006,11(6):1003-1012
The activity of Bad, a pro-apoptotic protein, is regulated by reversible phosphorylation. Moreover, sequestration of Bad within
subcellular compartments may be a new mechanism of apoptosis regulation. In this study, we report that Bad interacts with
14-3-3 protein in WEHI-231 immature B cells. This association is disrupted following BCR stimulation in correlation with Bad
translocation to mitochondria and apoptosis. Confocal microscopy was further used to examine the co-localization of Bad with
lipid rafts in WEHI-231 and murineex vivoB cells. Bad was found colocalized to lipid rafts in freshly isolated mature B lymphocytes, in contrast to immature cells.
Finally, co-immunoprecipitation experiments performed on WEHI-231 B cells revealed that PP1α interacts with Bcl-2 and Bad,
and dissociation of the complex was found correlated with appearance of apoptosis. Bcl-2 seemed to be required to assemble
the complex which may regulate Bad phosphorylation status and consequently cell survival. Collectively, present data outline
the role of Bad trafficking in the BCR-mediated apoptosis and suggest that differences in intracellular Bad trafficking may
be involved in the differential outcome of BCR signaling. 相似文献
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Watanabe K Ichinose S Hayashizaki K Tsubata T 《Biochemical and biophysical research communications》2008,374(2):274-281
Autophagy is a major pathway for degradation of cytoplasmic components, and is induced by some apoptotic stimuli mostly in cancer cells under the condition in which apoptosis is blocked. Ligation of the B cell antigen receptor (BCR) induces apoptosis and plays a crucial role in self-tolerance. However, whether BCR ligation induces autophagy is not clear. Here, we demonstrate that autophagosomes are extensively formed in normal mouse B cells as well as the WEHI-231 B cell line upon induction of BCR ligation-induced apoptosis regardless of whether apoptosis is blocked by overexpression of Bcl-2. In contrast, autophagosomes were not formed during apoptosis of spleen B cells cultured with medium alone or in BCR-ligated BAL17 cells which do not undergo apoptosis. Moreover, autophagy is not induced when apoptotic BCR signaling is abrogated by CD40 signaling. These results indicate that autophagy is induced specifically by apoptotic BCR signaling even in unmanipulated normal B cells. 相似文献
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FOXM1 Transcription Factor: A New Component of Chronic Myeloid Leukemia Stem Cell Proliferation Advantage
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Manuela Mancini Fausto Castagnetti Simona Soverini Elisa Leo Caterina De Benedittis Gabriele Gugliotta Gianantonio Rosti Luana Bavaro Sara De Santis Cecilia Monaldi Margherita Martelli Maria Alessandra Santucci Michele Cavo Giovanni Martinelli 《Journal of cellular biochemistry》2017,118(11):3968-3975