甲状腺癌中彩色多普勒超声诊断价值探析

目的探讨甲状腺癌中彩色多普勒超声的诊断价值。方法选择2015年8月~2016年8月我院收治的甲状腺癌患者50例为观察组,并选择同期收治的甲状腺良性疾病患者50例为对照组,分析两组患者彩色多普勒超声检查图像特征,并比较其血流动力学参数。结果观察组的影像学特征多为边缘不清晰,形态不规整,呈低回声,内部微小钙化,血流分布杂乱,血流阻力指数高于0.7;对照组的影像学特征多为边缘清晰,形态规整,呈低回声和中等偏高回声,血流分布规则,血流阻力指数低于0.7。相较于对照组,观察组患者的血流速度和血流阻力指数均明显升高(均P0.05)。结论彩色多普勒超声在甲状腺癌诊断中能显示较为典型的声像图特征和血流动力学成像特点,可为临床早期诊断和治疗提供可靠的依据和指导,具有较高临床应用价值。     

EMAP-II sensitize U87MG and glioma stem-like cells to temozolomide via induction of autophagy-mediated cell death and G2/M arrest

Despite the fact that temozolomide (TMZ) has been widely accepted as the key chemotherapeutic agent to prolong the survival of patients with glioblastoma, failure and recurrence cases can still be observed in clinics. Glioma stem-like cells (GSCs) are thought to be responsible for the drug resistance. In this study, we investigate whether endothelial monocyte-activating polypeptide-II (EMAP-II), a pro-inflammatory cytokine, can enhance TMZ cytotoxicity on U87MG and GSCs or not. As described in prior research, GSCs have been isolated from U87MG and maintained in the serum-free DMEM/F12 medium containing EGF, b-FGF, and B27. TMZ and/or EMAP-II administration were performed for 72 h, respectively. The results showed that TMZ combined with EMAP-II inhibit the proliferation of U87MG and GSCs by a larger measure than TMZ single treatment by decreasing the IC₅₀. EMAP-II also enhanced TMZ-induced autophagy-mediated cell death and G2/M arrest. Moreover, we found that EMAP-II functioned a targeted suppression on mTOR, which may involve in the anti-neoplasm mechanism. The results suggest that EMAP-II could be considered as a combined chemotherapeutic agent against glioblastoma by sensitizing U87MG and GSCs to TMZ.     

Structural Insight of a Trimodular Halophilic Cellulase with a Family 46 Carbohydrate-Binding Module

Cellulases are the key enzymes used in the biofuel industry. A typical cellulase contains a catalytic domain connected to a carbohydrate-binding module (CBM) through a flexible linker. Here we report the structure of an atypical trimodular cellulase which harbors a catalytic domain, a CBM46 domain and a rigid CBM_X domain between them. The catalytic domain shows the features of GH5 family, while the CBM46 domain has a sandwich-like structure. The catalytic domain and the CBM46 domain form an extended substrate binding cleft, within which several tryptophan residues are well exposed. Mutagenesis assays indicate that these residues are essential for the enzymatic activities. Gel affinity electrophoresis shows that these tryptophan residues are involved in the polysaccharide substrate binding. Also, electrostatic potential analysis indicates that almost the entire solvent accessible surface of CelB is negatively charged, which is consistent with the halophilic nature of this enzyme.     

Head group specificity in the requirement of phosphatidylcholine biosynthesis for very low density lipoprotein secretion from cultured hepatocytes

We have demonstrated that hepatic very low density lipoprotein (VLDL) secretion requires active phosphatidylcholine (PC) synthesis via either the CDP-choline pathway or phosphatidylethanolamine (PE) methylation pathway (Yao, Z., and Vance, D.E. (1988) J. Biol. Chem. 263, 2998-3004). In the present work, the head group specificity of phospholipid synthesis required for lipoprotein secretion was investigated in cultured hepatocytes isolated from choline-deficient rats. When N-monomethylethanolamine (0.1 mM) or N,N-dimethylethanolamine (0.1 mM) was added to the culture medium, the cells synthesized correspondingly phosphatidylmonomethylethanolamine (PMME) or phosphatidyldimethylethanolamine (PDME). However, the synthesis of PDME could correct the impaired VLDL secretion only to a limited extent, whereas the synthesis of PMME inhibited VLDL secretion. Although dimethylethanolamine did not promote VLDL secretion as well as choline, dimethylethanolamine altered the increased triacylglycerol synthesis in the choline-deficient cells as effectively as choline. Supplementation of the culture medium with ethanolamine (0.1 mM) had little effect on cellular PE or PC levels, nor was normal VLDL secretion resumed. However, the amounts of cellular PC and PE were both decreased when the medium was supplemented with N-monomethylethanolamine or N,N-dimethylethanolamine. These results suggest that the choline head group moiety of PC is specifically required for normal VLDL secretion and cannot be replaced with ethanolamine, monomethylethanolamine, or dimethylethanolamine. In addition, the impaired VLDL secretion from the choline-deficient hepatocytes could also be corrected by supplementation of betaine (0.2 mM) and homocysteine (0.2 mM), indicating the utilization of a methyl group from betaine for PC formation via methylation of PE.     

新疆伊犁河不同河段鱼类的物种多样性和优势种

为了了解伊犁河鱼类群落结构和多样性特征, 于2012—2014年连续3年对我国境内新疆伊犁河上、中和下游不同河段进行鱼类资源调查。获得27种鱼类样本, 隶属于6目9科23属。伊犁河中、上游河段主要以斯氏高原鳅、新疆裸重唇鱼、新疆高原鳅和伊犁裂腹鱼等土著鱼类为优势种, 下游河段的优势种主要有鲤、草鱼和鲫等外来种。伊犁河中、上游河段鱼类种类稀少, 大中型鱼类资源稀少, 鱼类群落多样性低。梯级水电站的开发、过度捕捞以及外来种入侵对伊犁河鱼类鱼类群落造成了很大的影响。     

干旱条件下钙离子对一氧化氮诱导黄瓜不定根发生的影响

以黄瓜品种‘新春4号’为材料,研究干旱胁迫下一氧化氮(NO)和钙离子(Ca²⁺)处理下黄瓜的生根指标、内源Ca²⁺荧光强度以及抗氧化酶(超氧化物歧化酶SOD、过氧化氢酶CAT、抗坏血酸过氧化物酶APX)活性,分析干旱条件下黄瓜不定根发生过程中NO和Ca²⁺之间的关系.结果表明: 200 μmol·L^-1 氯化钙(CaCl₂)和0.05%聚乙二醇(PEG)共处理显著提高了干旱条件下黄瓜不定根的根长和根数;添加Ca²⁺螯合剂(EGTA)和通道抑制剂(BAPTA/AM)处理显著降低了干旱条件下NO诱导的不定根根数和根长.干旱条件下,NO和CaCl₂处理提高了黄瓜下胚轴内源Ca²⁺荧光强度;而NO清除剂(cPTIO)处理的Ca²⁺荧光强度显著低于NO处理.干旱条件下,NO和CaCl₂处理显著提高了黄瓜下胚轴抗氧化酶活性;而Ca²⁺抑制剂或螯合剂处理显著降低了NO诱导的抗氧化酶活性.由此可见,干旱条件下Ca²⁺参与了NO调控黄瓜抗氧化酶活性,缓解了干旱胁迫对不定根形成产生的伤害,进而促进了不定根的发生.