咸淡交替灌溉对克隆植物大米草生长繁殖和生物量分配的影响

通过温室模拟控制实验,研究了咸淡交替灌溉处理对外来克隆植物大米草(Spartina anglica)形态性状、克隆生长、生物量积累及分配格局的影响。实验共设6种浇灌处理:单一淡水灌溉(D)、单一咸水浇灌(X)、淡咸交替灌溉(DX)、咸淡交替灌溉(XD)、淡咸淡交替灌溉(DXD)和咸淡咸交替灌溉(XDX)。结果表明:DX处理条件下,大米草株高、叶片数及根长均达到最高;克隆数最多,且显著高于X、DXD和XDX处理;芽数及根状茎总长均显著大于XDX处理;在DX和D处理下,地上生物量、根系生物量、地下生物量和总生物量均显著高于其它处理。这表明作为滨海盐沼植物,大米草种群比较适应淡咸水交替环境,单一的咸水,以及过度的咸淡转换均不利于大米草的生长繁殖与生物量积累,而淡咸水交替过程的失序可能是引起我国大米草种群衰退的重要原因。     

不同火烧强度迹地林下灌草层物种多样性及其与土壤因子的关系

为揭示胶东丘陵区麻栎黑松混交林过火后林下灌丛群落结构和多样性变化,探究群落物种分布和多样性指数与土壤因子之间的相互关系,该研究以威海仙姑顶中度、轻度、未过火林地为研究对象,对不同火烧强度林地进行土壤的定量分析和植物物种多样性调查,并运用典范对应分析法(CCA)和冗余分析法(RDA)进行排序,以明确影响不同火烧迹地林下灌丛群落物种多样性的关键土壤因子。结果表明:(1)各林地丰富度、多样性、均匀度指数在群落垂直方向上均表现为草本层大于灌木层。灌木层丰富度、多样性、均匀度指数均随火烧强度的增加先升后降,轻度火烧达到最大值,是灌丛群落特征变化的关键转折期;草本层Patrick、Shannon-Wiener和Simpson指数逐渐降低,Margalef指数先降低后微弱上升,均在未过火林地达到最大值,均匀度指数各林地无显著差别(P0.05)。(2)未过火与中度火烧地之间的Morista-Horn指数在灌木层、草本层和灌草层中均为最小,β多样性最高,林下物种组成差别迥异;轻度与中度火烧地在灌木层次上物种异质性较高,未过火与轻度火烧地在草本层次上拥有较高异质性的物种更替。(3)中度和轻度火烧地林下灌丛群落大致均可分为3个类群,未过火林下灌丛植物疏离分散,则未形成类群;中度火烧影响植物物种多样性的正向主要因子为碳氮比(C/N),逆向主要因子为全磷(TP)、全钾(TK);轻度火烧正向因子为氮磷比(N/P),逆向因子为pH;未过火林地物种多样性受多种土壤因子的共同作用。(4)火烧提高了林下灌丛群落物种更替速率,增加了灌木层物种多样性,降低了草本层物种多样性,轻度火烧地的物种丰富度水平较高,火烧迹地影响群落物种多样性的因子既有相似性又存在差异性,TK和TP是火烧迹地物种多样性的共同影响因子,磷(P)是火烧迹地物种多样性的共同限制性元素。     

STIM／SOCE通路参与细胞功能调控的研究进展

钙库操作性钙离子通道（store-operated calcium entry,SOCE）是介导胞外Ca^2＋进入细胞内的重要通道之一,其核心蛋白由位于内质网上的基质相互作用分子（stromalinteractionmolecule,STIM）和位于细胞膜上的Orai蛋白构成。目前研究发现,STIM蛋白存在STIM1和STIM2两种亚型,其主要功能略有不同。当内质网内钙库中Ca^2＋消耗之后,STIM蛋白通过其特殊的结构能够感受内质网内钙库中Ca^2＋浓度的变化,发生快速的转位和聚合化等激活反应,与质膜上的Orai蛋白偶联。实现SOCE通路的功能开放,引起Ca^2＋内流。当钙库中Ca^2＋得到补充之后,STIM蛋白与Orai蛋白缓慢解离即失活,通路关闭。目前对STIM蛋白结构的研究提示,通过其激活和失活机制不仅能够参与调节SOCE通路的开放与关闭,也参与对细胞内重要的细胞增殖、分化等功能活动调控。STIM蛋白可能成为治疗多种疾病的潜在的新靶点。     

内蒙古三个民族舌运动类型的遗传学研究

调查了内蒙古汉、蒙古、回族舌运动类型(卷舌、翻舌、叠舌、三叶舌与尖舌),共716例。研究结果显示:各种舌运动类型出现率性别间均无显著性差异;卷舌基因分别与叠、翻、尖、三叶舌基因间存在着互相作用关系,卷舌基因对叠舌基因是隐性上位基因,对翻舌、尖舌、三叶舌基因是修饰基因;内蒙古3个民族间卷、叠、尖舌出现率接近。本文首次调查并研究了尖舌性状。尖舌在过去国内外文献中未见报道。 Abstract:The tongue moving types(including tongue rolling,tongue twisting,tongue folding,clover-leaf tongue and pointed tongue)of 716 cases of Han,Mongol and Hui nationalities in Inner Mongolia were investigated.The results showed that no difference in the frequencies of various tongue moving types between male and female and that the frequencies of rolling,folding and pointed tongue were close to each other among the three nationalities of Inner Mongolia.However,some interactions between genes were revealed,that the rolling gene is a recessive epistatic gene to folding gene and a modifier gene to twisting,pointed and clover-leaf gene respectively.The research on pointed tongue in this paper has never been reported in China and abroad.     

Secretory delivery of recombinant proteins in attenuated Salmonella strains: potential and limitations of Type I protein transporters

Live attenuated Salmonella strains have been extensively explored as oral delivery systems for recombinant vaccine antigens and effector proteins with immunoadjuvant and immunomodulatory potential. The feasibility of this approach was demonstrated in human vaccination trials for various antigens. However, immunization efficiencies with live vaccines are generally significantly lower compared to those monitored in parenteral immunizations with the same vaccine antigen. This is, at least partly, due to the lack of secretory expression systems, enabling large-scale extracellular delivery of vaccine and effector proteins by these strains. Because of their low complexity and the terminal location of the secretion signal in the secreted protein, Type I (ATP-binding cassette) secretion systems appear to be particularly suited for development of such recombinant extracellular expression systems. So far, the Escherichia coli hemolysin system is the only Type I secretion system, which has been adapted to recombinant protein secretion in Salmonella. However, this system has a number of disadvantages, including low secretion capacity, complex genetic regulation, and structural restriction to the secreted protein, which eventually hinder high-level in vivo delivery of recombinant vaccines and effector proteins. Thus, the development of more efficient recombinant protein secretion systems, based on Type I exporters can help to improve efficacies of live recombinant Salmonella vaccines. Type I secretion systems, mediating secretion of bacterial surface layer proteins, such as RsaA in Caulobacter crescentus, are discussed as promising candidates for improved secretory delivery systems.     

Humoral immune response against proteophosphoglycan surface antigens of Entamoeba histolytica elicited by immunization with synthetic mimotope peptides

The protozoan parasite Entamoeba histolytica, which is responsible for intestinal amebiasis and amebic liver abscess, is causing significant morbidity and mortality worldwide. Proteophosphoglycans (PPGs, also known as lipophosphoglycans, LPGs, or lipopeptidophosphoglycans, LPPGs) are major surface components of E. histolytica. Passive immunization with a monoclonal antibody (EH5) directed against the PPGs protected severe combined immune-deficient mice from amebic liver abscess. The structure of the PPGs is very complex and only known in part. To find peptide mimics of E. histolytica PPG antigens, we had screened phage-displayed random peptide libraries with the antibody EH5. We identified various peptide mimics of E. histolytica PPGs, all sharing a consensus sequence Gly-Thr-His-Pro-X-Leu. Several of the phage clones induced a significant, specific IgG response against membrane antigens of E. histolytica after immunization of mice with whole phage particles. In the present work, in order to avoid the use of phage particles for immunization, we coupled two selected chemically synthesized peptides to keyhole limpet hemocyanin (KLH). The two KLH-conjugated peptides were immunogenic in mice and induced the production of high titers of anti-peptide antibodies, and one of the two peptides was also able to induce significant titers of antibodies against E. histolytica PPGs. Our results demonstrate that the KLH-conjugated peptides are able to mimic the EH5 epitope without the M13 phage sequences flanking the peptide inserts and independent of the structural framework of the phage.     

Lymphatic endothelial murine chloride channel calcium-activated 1 is a ligand for leukocyte LFA-1 and Mac-1

The lymphatic circulation mediates drainage of fluid and cells from the periphery through lymph nodes, facilitating immune detection of lymph-borne foreign Ags. The 10.1.1 mAb recognizes a lymphatic endothelial Ag, in this study purified by Ab-affinity chromatography. SDS-PAGE and mass spectrometry identified murine chloride channel calcium-activated 1 (mCLCA1) as the 10.1.1 Ag, a 90-kDa cell-surface protein expressed in lymphatic endothelium and stromal cells of spleen and thymus. The 10.1.1 Ab-affinity chromatography also purified LFA-1, an integrin that mediates leukocyte adhesion to endothelium. This mCLCA1-LFA-1 interaction has functional consequences, as lymphocyte adhesion to lymphatic endothelium was blocked by 10.1.1 Ab bound to endotheliumor by LFA-1 Ab bound to lymphocytes. Lymphocyte adhesion was increased by cytokine treatment of lymphatic endothelium in association with increased expression of ICAM-1, an endothelial surface protein that is also a ligand for LFA-1. By contrast, mCLCA1 expression and the relative contribution of mCLCA1 to lymphocyte adhesion were unaffected by cytokine activation, demonstrating that mCLCA1 and ICAM-1 interactions with LFA-1 are differentially regulated. mCLCA1 also bound to the LFA-1-related Mac-1 integrin that is preferentially expressed on leukocytes. mCLCA1-mediated adhesion of Mac-1- or LFA-1-expressing leukocytes to lymphatic vessels and lymph node lymphatic sinuses provides a target for investigation of lymphatic involvement in leukocyte adhesion and trafficking during the immune response.     

Biomechanical and clinical alterations of the hip joint following femoral neck fracture and implantation of bipolar hip endoprosthesis

The implantation of a bipolar partial hip endoprosthesis is a treatment of choice for displaced medial femoral neck fracture. We present an experimental study which asses and compare biomechanical and clinical status through period before and after hip fracture and implantation of bipolar partial hip endoprosthesis. This study encompassed 75 patients who suffered from an acute medial femoral neck fracture and were treated with the implantation of a bipolar partial hip endoprosthesis. Their biomechanical status (stress distribution on the hip joint weight bearing area) and clinical status (Harris Hip Score) were estimated for the time prior to the injury and assessed at the follow-up examination that was, on average, carried out 40 months after the operation. Despite ageing, the observed Harris Hip Score at the follow-up examination was higher than that estimated prior to the injury (77.9 > 69.6; p = 0.006). Similarly, the hip stress distribution was reduced (2.7 MPa < 2.3 MPa; p = 0.001). While this reduction can be attributed to a loss of weight due to late ageing, the principal improvement came from the operative treatment and corresponding restoration of the biomechanical properties of the hip joint. The implantation of a bipolar partial hip endoprosthesis for patients with displaced medial femoral neck fractures improves the biomechanical and clinical features of the hip, what should have on mind during making decision about treatment.     

Apoptosis and cell cycle progression in an acidic environment after irradiation

Apoptosis and cell cycle progression in HL60 cells irradiated in an acidic environment were investigated. Apoptosis was determined by TUNEL staining, PARP cleavage, DNA fragmentation, and flow cytometry. The majority of the apoptosis that occurred in HL60 cells after 4 Gy irradiation took place after G(2)/M-phase arrest. When irradiated with 12 Gy, a fraction of the cells underwent apoptosis in G(1) and S phases while the rest of the cells underwent apoptosis in G(2)/M phase. The apoptosis caused by 4 and 12 Gy irradiation was transiently suppressed in medium at pH 7.1 or lower. An acidic environment was found to perturb progression of irradiated cells through the cell cycle, including progression through G(2)/ M phase. Thus it was concluded that the suppression of apoptosis in the cells after 4-12 Gy irradiation in acidic medium was due at least in part to a delay in cell cycle progression, particularly the prolongation of G(2)/M-phase arrest. Irradiation with 20 Gy indiscriminately caused apoptosis in all cell cycle phases, i.e. G(1), S and G(2)/M phases, rapidly in neutral pH medium and relatively slowly in acidic pH medium. The delay in apoptosis in acidic medium after 20 Gy irradiation appeared to result from mechanisms other than prolonged G(2)/ M-phase arrest.     

Chromium(III)-mediated structural modification of glycoprotein: impact of the ligand and the oxidants

The interaction of three types of chromium(III) complexes, [Cr(salen) (H2O2]+, [Cr(en)3]3+, and [Cr(EDTA) (H2O)]- with AGP has been investigated. [Cr(salen) (H2O2]+, [Cr(en)3]3+ and [Cr(EDTA) (H2O]- bind to Human alpha1-acid glycoprotein with a protein:metal ratio of 1:8, 1:6, and 1:4, respectively. The binding constant, K(b) was estimated to be 1.37 +/- 0.12 x 10(5) M(-1), 1.089 +/- 0.05 x 10(5) M(-1) and 5.3 +/- 0.05 x 10(4) M(-1) for [Cr(salen) (H2O2]+, [Cr(en)3]3+, and [Cr(EDTA) (H2O)]-, respectively. [Cr(en)3]3+ has been found to induce structural transition of AGP from the native twisted beta sheet to a more compact alpha-helix. The complexes, [Cr(salen) (H2O2]+ and [Cr(EDTA) (H2O]-, in the presence of H2O2, have been found to bring about nonspecific cleavage of AGP, whereas [Cr(en)3]3+ does not bring about any protein damage. Treatment of [Cr(salen) (H2O)2]+-protein adduct with iodosyl benzene on the other hand led to site specific cleavage of the protein. These results clearly demonstrate that protein damage brought about by chromium(III) complexes depends on the nature of the coordinated ligand, nature of the metal complex, and the nature of the oxidant.