Impact of biofilm matrix components on interaction of commensal Escherichia coli with the gastrointestinal cell line HT-29

Commensal Escherichia coli form biofilms at body temperature by expressing the extracellular matrix components curli fimbriae and cellulose. The role of curli fimbriae and cellulose in the interaction of commensal E. coli with the intestinal epithelial cell line HT-29 was investigated. Expression of curli fimbriae by the typical commensal isolate E. coli TOB1 caused adherence and internalization of the bacteria and triggered IL-8 production in HT-29 cells. In particular, induction of IL-8 production was complex and involved curli-bound flagellin. While cellulose alone had no effect on the interaction of TOB1 with HT-29 cells, co-expression of cellulose with curli fimbriae decreased adherence to, internalization and IL-8 induction of HT-29 cells. Investigation of a panel of commensal isolates showed a partial correlation between expression of curli fimbriae and enhanced internalization and IL-8 production. In addition, a high immunostimulatory flagellin was identified. Thus, the consequences of expression of extracellular matrix components on commensal bacterial-host interactions are complex.     

Interferon-alpha and transforming growth factor-β co-induce growth inhibition of human tumor cells

A hallmark of resistance to type I interferons (IFNs) is the lack of antiproliferative responses. We show here that costimulation with IFN-alpha and transforming growth factor beta-1 (TGF-beta) potentiates antiproliferative activity in a sensitive (ME15) and resistant (D10) human melanoma cell line. A DNA microarray-based search for proliferation control genes involved that are cooperatively activated by IFN-alpha and TGF-beta, yielded 28 genes. Among these are the insulin-like growth factor-binding protein 3 (IGFBP3) and the calcium-binding protein S100A2; we demonstrate, that recombinant IGFBP3 protein is a potent growth inhibitor requiring TGF-beta activity. The antiproliferative activity of S100A2 is significantly enhanced by IFN-alpha in stably transfected ME15 or D10 cell lines. We show for the first time that IFN-alpha is a potent inducer of intracellular calcium release required for activation of S100A2. Our study provides a functional link between IFN-alpha and TGF-beta signaling and extends the function of IFN signaling to calcium-sensitive processes.     

诱发核部件裂变探测技术仿真研究

寻求科学有效的核物质核查技术与方法,对防止核扩散、处理核材料具有重要意义。在分析核部件属性、探测原理及相关探测方法的基础上,利用模拟数据通过Matlab软件仿真比较了不同形式的平均修正算法,即:Bartlett法、Welch法和Nuttall法,结果表明:结合了平均和平滑特性的Nuttall法的方差性能、分辨率较好、运算量较小,更能准确、有效地反映核裂变信号的相关特征参数。     

Highly homologous HERC proteins localize to endosomes and exhibit specific interactions with hPLIC and Nm23B

Small HERC proteins are defined by the presence of one RCC1-like domain and a HECT domain. Having evolved out of one common ancestor, the four members of the family exhibit a high degree of homology in genomic organization and amino acid sequence, thus it seems possible that they might accomplish similar functions. Here we show that small HERC proteins interact with each other and localize to the same cellular structures, which we identify as late endosomes and lysosomes. We demonstrate interaction of HERC3 with the ubiquitin-like proteins hPLIC-1 and hPLIC-2 and we establish interaction of HERC5 with the metastasis suppressor Nm23B. While hPLIC proteins are not ubiquitinated by HERC3, HERC5 plays an important role in ubiquitination of Nm23B. In summary, although small HERC proteins are highly homologous showing the same subcellular distribution, they undergo different molecular interactions.     

SO_2两转两吸流程中“ⅢⅠ-ⅣⅡ”和“ⅢⅡ-ⅣⅠ”换热情况浅析

通过工艺计算，定量分析比较 Ｓ Ｏ２ 转化中“ⅢⅠ－ ⅣⅡ”和“ⅢⅡ－ ⅣⅠ”两种换热流程的差异，论证了就换热情况而言，“ⅢⅠ－ ⅣⅡ”流程优于“ⅢⅡ－ ⅣⅠ”流程     

用柱层析和TLC分离小麦PGIP和植保素

植物抗病能力大小的测定需要比较准确可靠且相对简便的办法。采用接种病菌于植物上观察染菌情况虽然直观，但受病菌本身的生理状态及外界环境影响很大，且不便于定量的表述。因此，选择合适的生理生化指标作为植物抗性大小的衡量标准，对于植物病理的研究具有重要的意义。选择了小麦体系的两种抗性物质－ 小麦植保素和 Ｐ Ｇ Ｉ Ｐ作为小麦的抗性指标来分离分析     

水蓄冷空调系统蓄冷槽中斜温层厚度的数值计算

介绍了水蓄冷空调系统蓄冷槽中温度场与斜温层厚度的数值求解及影响斜温层厚度的因素。     

中腔胞壁比值法测定棉纤维成熟度系数的讨论

用中腔胞壁比值法测定棉纤维成熟度系数有明确的标准规定,但这些规定有些令人费解.为此作者用折射率跟棉纤维折射率相近的厚壁玻璃管模拟棉纤维在放大镜和高倍显微镜下观察,证实了标准规定的合理和必要性.中腔胞壁比值的理论计算值与实验值准确地符合.     

Mechanical and biochemical characterization of the contraction elicited by a calcium-independent myosin light chain kinase in chemically skinned smooth muscle

Summary The contraction induced by a Ca²⁺-independent myosin light chain kinase (MLCK-) was characterized in terms of isometric force (F_o), immediate elastic recoil (SE), unloaded shortening velocity (V_us), shortening under a constant load and ATPase activity of chemically skinned smooth muscle preparations. These parameters were compared to those measured in a Ca²⁺-induced contraction to assess the nature of cross bridge interaction in the MLCK-induced contraction. F_o developed in chicken gizzard fibers as well as SE were similar in contractions elicited by either agent. V_us in the contraction induced by MLCK-(0.36 mg/ml) was similar though averaged 39.3±8.9% less than V_us induced by Ca²⁺ (1.6x10^–6M) in the control fibers. Addition of Ca²⁺ (1.6x10^–6M) to a contraction induced by MLCK-resulted in small increases in both F_o and V_us. Shortening under a constant load was similar for both types of contractions. The contraction induced by MLCK-was accompanied by an increased rate of ATP hydrolysis. The MLCK-induced contraction is thus kinetically similar though not identical to a contraction induced by Ca²⁺. We conclude that with respect to actin-myosin interaction, MLCK- and Ca²⁺-induced contractions are similar.