中国新疆博格达山周边地区大型地衣物种多样性及分布特征

本研究对中国新疆博格达山周边地区大型地衣进行地衣分类学和生态学结合的综合研究,通过分析大型地衣物种多样性和分布特征,探讨影响地衣分布的环境变量与生态因子。研究结果表明:(1)分布在博格达山周边地区的大型地衣共有43种,隶属于6目、11科、15属,其中茶渍目和黄枝衣目大型地衣占优势,分别占该地区大型地衣科、属、种总数的55%、67%、81%。(2)博格达山周边地区的大型地衣组成5个样点组,分别是蓝灰蜈蚣衣+裂片石黄衣组、细片石黄衣+亚灰大孢蜈蚣衣组、长缘毛蜈蚣衣+菊叶黄梅组、地卷+暗裂芽黑蜈蚣衣组、黑蜈蚣衣+枪石蕊组,样点组的分布与环境因子密切相关。(3)在影响大型地衣分布的环境因素中海拔对地衣种类分布的影响较显著。本研究为更准确地确定博格达山区大型地衣分布规律提供科学依据。     

新疆阿勒泰地区草地螟成虫发生特征

【目的】明确草地螟Loxostege sticticalis成虫在新疆阿勒泰地区发生消长规律以及卵巢发育与种群动态和迁飞之间的关系。【方法】采用高空探照灯诱集草地螟成虫并解剖卵巢,观察卵巢发育进度。【结果】研究区域存在草地螟成虫数量突增突减现象; 2015年发生量比2016年多,2015年草地螟8月30日消失,2016年草地螟8月22日消失。2015和2016年草地螟成虫夜间在第2时段(00:10-01:50)、第3时段(01:50-03:30)出现次数多。2015年第一代草地螟成虫数量突然增加时,65. 5%的雌蛾卵巢发育处于Ⅲ级;自7月下旬第一代草地螟成虫数量呈现下降趋势,此时69. 1%的雌蛾卵巢发育处于Ⅱ级。2016年第一代草地螟成虫数量突然增加时,71. 25%的雌蛾卵巢发育处于Ⅳ级。2015和2016年第一代草地螟雌蛾中各级别卵巢均能解剖到,但是Ⅲ和Ⅳ级卵巢的比例仍然最高。【结论】2015和2016年新疆阿勒泰地区草地螟属于外地虫源迁入和本地虫源形成的混合种群。     

新疆石人沟山区岩面生地衣群落分布格局的环境解释

地衣作为真菌和绿藻/蓝绿藻的成功共生体,广泛分布在陆地生态中的各种栖息地。岩面生地衣作为陆地生态系统的主要组成部分,在干旱和半干旱地区陆地食物链中具有重要地位,同时对岩石的生物腐蚀和土壤的形成有重要作用。岩面生地衣的多样性和分布格局强烈地受到海拔、湿度、温度、降水量、太阳辐射强度和基物的特征(岩石类型、岩石大小、岩石的化学成分和营养成分)等多种因素的影响。为了研究乌鲁木齐县石人沟山区岩面生地衣群落与基物间的关系,该研究在乌鲁木齐县石人沟山区设立16个样地,计测样地中岩面生地衣的盖度,包括坡度、坡向、光照强度等7个环境因子,采用典范对应分析法(CCA)对各群落的物种分布格局与环境因子的关系进行了探讨。结果表明:石人沟山区的岩面生地衣共有27种,隶属于7目9科15属。其中,黄枝衣目、茶渍目和鸡皮衣目的种类较多,占该地区岩面生地衣总数的74.07%。CCA排序结果显示坡度、坡向、光照强度、湿度、岩石pH值是5个影响岩面生地衣种类分布格局的主要环境因子,并显示了岩面生地衣与样地间的对应性。     

甲状腺激素对适应性免疫细胞的作用

摘要：甲状腺激素（Thyroid hormones,THs）参与免疫功能的调节,在固有免疫和适应性免疫中发挥着重要作用。THs异常分泌所致的免疫功能失调被认为参与了格雷夫斯病和桥本甲状腺炎等自身免疫性疾病的发生发展。目前,THs在固有免疫细胞（中性粒细胞、巨噬细胞、树突状细胞、自然杀伤细胞、肥大细胞）中的作用已得到了较好的阐明,但THs对适应性免疫细胞（T淋巴细胞与B淋巴细胞）的影响等方面的研究仍未引起足够的重视。因此,本研究从适应性免疫细胞的角度出发,重点讨论了THs对这些细胞的发育、分化及功能等方面的影响,为进一步理解THs调节免疫功能的作用提供新视角。     

The porcine chloride channel calcium-activated family member pCLCA4a mirrors lung expression of the human hCLCA4

Pig models of cystic fibrosis (CF) have recently been established that are expected to mimic the human disease closer than mouse models do. The human CLCA (originally named chloride channels, calcium-activated) member hCLCA4 is considered a potential modifier of disease severity in CF, but its murine ortholog, mCLCA6, is not expressed in the mouse lung. Here, we have characterized the genomic structure, protein processing, and tissue expression patterns of the porcine ortholog to hCLCA4, pCLCA4a. The genomic structure and cellular protein processing of pCLCA4a were found to closely mirror those of hCLCA4 and mCLCA6. Similar to human lung, pCLCA4a mRNA was strongly expressed in porcine lungs, and the pCLCA4a protein was immunohistochemically detected on the apical membranes of tracheal and bronchial epithelial cells. This stands in sharp contrast to mouse mCLCA6, which has been detected exclusively in intestinal epithelia but not the murine lung. The results may add to the understanding of species-specific differences in the CF phenotype and support the notion that the CF pig model may be more suitable than murine models to study the role of hCLCA4.     

Binding of trastuzumab to ErbB2 is inhibited by a high pericellular density of hyaluronan

Although trastuzumab is an efficient drug, primary and acquired resistance is a challenging problem. The authors have previously shown in mouse xenograft experiments that masking ErbB2 by hyaluronan leads to diminished binding of the antibody and consequent resistance. In the current work, they correlated trastuzumab binding with the pericellular density of hyaluronan in ErbB2-overexpressing human breast cancer samples. A method for quantifying the relative binding of trastuzumab was developed involving constant and low-frequency background subtraction, segmenting the image to membrane and background pixels followed by evaluation of trastuzumab fluorescence, normalized with the expression level of ErbB2, only in the membrane. The normalized binding of trastuzumab showed a negative correlation with the pericellular density of hyaluronan (r = -0.52) with the effect being the most pronounced in the extreme cases (i.e., low and high hyaluronan densities predicted strong and weak binding of trastuzumab, respectively). Removal of hyaluronan by hyaluronidase digestion unmasked the trastuzumab binding epitope of ErbB2 demonstrated by a significantly increased normalized binding of the antibody. The results show that the accumulation of pericellular hyaluronan plays a crucial role in masking ErbB2.     

YKL-40 is differentially expressed in human embryonic stem cells and in cell progeny of the three germ layers

The secreted glycoprotein YKL-40 participates in cell differentiation, inflammation, and cancer progression. High YKL-40 expression is reported during early human development, but its functions are unknown. Six human embryonic stem cell (hESC) lines were cultured in an atmosphere of low or high oxygen tension, in culture medium with or without basic fibroblast growth factor, and on feeder layers comprising mouse embryonic fibroblasts or human foreskin fibroblasts to evaluate whether hESCs and their progeny produced YKL-40 and to characterize YKL-40 expression during differentiation. Secreted YKL-40 protein and YKL-40 mRNA expression were measured by enzyme-linked immunosorbent assay (ELISA) and quantitative RT-PCR. Serial-sectioned colonies were stained for YKL-40 protein and for pluripotent hESC (OCT4, NANOG) and germ layer (HNF-3β, PDX1, CD34, p63, nestin, PAX6) markers. Double-labeling showed YKL-40 expression in OCT4-positive hESCs, PAX6-positive neuroectodermal cells, and HNF-3β-positive endodermal cells. The differentiating progeny showed strong YKL-40 expression. Abrupt transition between YKL-40 and OCT4-positive hESCs and YKL-40-positive ecto- and neuroectodermal lineages was observed within the same epithelial-like layer. YKL-40-positive cells within deeper layers lacked contact with OCT4-positive cells. YKL-40 may be important in initial cell differentiation from hESCs toward ectoderm and neuroectoderm, with retained epithelial morphology, whereas later differentiation into endoderm and mesoderm involves a transition into the deeper layers of the colony.     

Effect of reactivity on cellular accumulation and cytotoxicity of oxaliplatin analogues

The purpose of this study was to systematically investigate the relationships between reactivity, cellular accumulation, and cytotoxicity of a panel of oxaliplatin analogues with different leaving groups in human carcinoma cells. The reactivity of the complexes towards the nucleotides 2'-deoxyguanosine 5'-monophosphate and 2'-deoxyadenosine 5'-monophosphate was studied using capillary electrophoresis. Cellular accumulation and cytotoxicity were measured in an oxaliplatin-sensitive and oxaliplatin-resistant ileocecal colorectal adenocarcinoma cell line pair (HCT-8/HCT-8ox). Platinum concentrations were determined by flameless atomic absorption spectrometry. The 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay was used to assess cytotoxicity. Early cellular platinum accumulation was predominantly affected by lipophilicity. A relationship between reactivity and cellular accumulation was observed for three of four platinum complexes investigated, whereas the most lipophilic oxaliplatin analogue was an exception. Increased reactivity and reduced lipophilicity were associated with high cytotoxic activity. Resistance was influenced by lipophilicity but not by reactivity. The observed relationships may help in the design of analogues with high antitumoral activity in oxaliplatin-sensitive as well as oxaliplatin-resistant cells.     

Combination of chemometrically assisted voltammetry, calorimetry, and circular dichroism as a new method for the study of bioinorganic substances: application to selenocystine metal complexes

Selenium-containing compounds play an important role in antioxidant defense systems, binding to toxic metals, preventing their uptake into cells, and thus protecting cells from metal-induced formation of reactive oxygen species. Here, we present a proposal for a relatively new method as a complement to the more usual methods used in selenium studies. A systematic study of the metal-binding properties of selenocystine (SeCyst) in the presence of divalent metal cations (Cd, Co, Hg, Ni, and Zn) is reported. Isothermal titration calorimetry provides thermodynamic parameters of the systems. Titrations produced curves that could be fit reasonably well to the one set of sites model. The data clearly demonstrate that one M²⁺ binds one SeCyst molecule, and the stable M(SeCyst) complex is formed under these conditions. The order of the SeCyst binding constant for the metal ions is Hg²⁺ > Cd²⁺ ~ Zn²⁺ > Ni²⁺> Co²⁺. Cadmium ion was selected as a modulator for the behavior of SeCyst in the presence of a nonessential metal, and zinc was selected for the case of an essential element. These interactions of SeCyst with Cd²⁺ and Zn²⁺, either individually or combined, were studied in aqueous buffered solutions at physiological pH by differential pulse polarography and circular dichroism spectroscopy. Furthermore, recently developed chemometric tools were applied to differential pulse polarography data obtained in mixtures of SeCyst and glutathione in the presence of Cd²⁺ at physiological pH.     

The alkenyl migration mechanism catalyzed by extradiol dioxygenases: a hybrid DFT study

6-Hydroxymethyl-6-methylcyclohexa-2,4-dienone is a mechanistic probe which when incubated with an extradiol dioxygenase yields a 2-tropolone product. This observation was originally interpreted as evidence supporting a direct heterolytic 1,2-alkenyl migration mechanism for a ring expansion reaction catalyzed by this class of Fe(II)-dependent nonheme enzymes (Xin and Bugg in J Am Chem Soc 130:10422-10430, 2008). In the work reported in this contribution we used quantum chemical methods to test whether such a mechanism is energetically possible and we found that it is not, neither for the mechanistic probe nor for the native catalytic cycle intermediate. Models of increasing complexity were used to calculate energy barriers to the heterolytic 1,2-alkenyl migration and alternative radical mechanisms. It was found that the former involves substantially higher barriers than the latter. A tentative radical mechanism that accounts for the transformation of the probe substrate to 2-tropolone was also proposed, and it involves acceptable barriers.