腺苷和乙酰胆碱后适应诱导的心肌保护作用

近年来缺血后适应的提出成为抗再灌注损伤的里程碑,其良好的临床可控性和可靠的保护效应引起人们广泛关注。缺血后适应即在心肌长时间缺血后再灌注之前,进行数次短暂的再灌注,缺血的循环处理,诱导产生心肌保护效应,其循环次数和间隔时间存在种属差异。研究证实后适应不仅限制急性期梗死面积,还可以减轻长期损伤,其是否与保护血管内皮、抑制中性粒细胞介导的氧化损伤相关还存在争议。上调再灌注损伤补救激酶（reperfusion injury salvageHnase,RISK）通路是后适应保护的重要机制之一,即激活磷脂酰肌醇一3激酶（phosphatidy linositol3-kinase,P13K）-Akt途径和,或细胞外信号调节激酶（extracellular signal-regulatedkinase,ERK）途径,抑制线粒体通透性转换孔的开放,减少细胞凋亡和坏死。但是这两条途径的地位和关系还有待于进一步研究。为了更加适用于临床,研究者将机械调控转变为药物干预,观察药物能否模拟缺血后适应发挥保护作用,即药物后适应。腺苷是研究最广泛,也是最有希望成为临床正式用药的一种药物。我们实验室首先提出了乙酰胆碱可以模拟缺血后适应,通过线粒体ATP敏感钾通道发挥心肌保护效应。本文着重阐述缺血后适应保护缺血,再灌注损伤的效应和信号转导通路,尤其是腺苷和乙酰胆碱模拟药物后适应的可能机制和临床应用。     

高密度中心城区蓝绿空间冷岛效应及其影响因素——以北京五环路以内地区为例

蓝绿空间作为城市绿色基础设施的重要组成部分,对促进城市热环境健康、改善局地微气候具有重要作用。利用Landsat 8遥感影像、土地利用等数据,基于辐射传输方程算法、K均值聚类算法、相关性分析等方法,量化了典型的高密度中心城区--北京五环快速路以内地区的1199块1hm²以上的蓝绿空间冷岛效应的表征指标,并分析与蓝绿空间规模、形状复杂度、景观组成、环境组成、植被覆盖等要素的相关关系,还根据蓝绿空间的不同降温特性进行分类,探讨每类蓝绿空间在缓解高密度中心城区热岛效应中的独特作用、优势与机制。结果表明：（1）蓝绿空间的规模、形状复杂度、景观组成等景观要素与冷岛效应的关系显著,如总面积、绿地面积和水体面积与降温幅度、降温范围、降温服务呈显著正相关,与降温效率和降温速率呈显著负相关;周长与降温范围、降温服务呈显著正相关,与降温效率和速率呈显著负相关;周长面积比与降温幅度和降温服务呈显著负相关,与降温效率和蓝绿空间自身温度呈显著正相关,而形状指数则与降温范围和降温服务呈显著正相关。（2）蓝绿空间的环境要素与冷岛效应也存在相关关系。蓝绿空间之间会产生冷岛效应的协同与促进现象,蓝绿空间降温范围内的其他蓝绿空间的总面积与该蓝绿空间的降温幅度、降温范围、降温服务和辐射距离呈显著正相关,与蓝绿空间自身温度呈显著负相关。（3）蓝绿空间的总面积、水体面积、周长与降温幅度之间,周长面积比与降温效率之间存在阈值,为节约土地资源、保证降温效果,建议不应过多超过阈值。（4）基于蓝绿空间在降温幅度、效率、辐射距离等方面的差异,将蓝绿空间划分为4类。高密度中心城区蓝绿空间规划建设应充分评估区域降温需求,了解蓝绿空间降温现状,合理配置具有不同降温特性和优势的蓝绿空间,在土地和资金有限的情况下,充分发挥各类蓝绿空间的冷岛效应。本研究有助于政府和规划师摸清当前蓝绿空间冷岛效应的现状、问题和发展潜力,对理论和实践具有一定参考意义。     

真核生物DNA复制起始调控

复制起始调控是真核生物复制调控机制的重要环节,也是细胞生长调控的核心问题．对SV40病毒和酵母体系的研究为阐明真核生物的复制起始机制及其与细胞周期的关系提供了线索．目前,与DNA复制起始有关的多种蛋白质因子（如核蛋白P₁,DNA单链结合蛋白,DNA聚合酶α,增殖细胞核抗原等）的作用机理逐渐明朗,周期依赖的调控特点得到了证实文章着重介绍了DNA复制起始在细胞周期中的两个调控点及各种周期蛋白在该点的作用,文中还涉及复制起始异常与肿瘤发生的关系.     

Genetic Analysis of Human Adenovirus Type 7 Strains Circulating in Different Parts of China

To investigate the molecular epidemiology and genetic variation of human adenovirus type 7(HAdV-7) in children with acute respiratory infections(ARI) in China. HAdV-7-positive respiratory samples collected from children with ARI in Beijing, Shijiazhuang, Wenzhou and Guangzhou from 2014–2018 were selected for gene amplification and sequence analysis. Fifty-seven HAdV-7 clinical strains with hexon, penton base and fiber gene sequences were obtained. Meanwhile17 strains were selected randomly from different cities for whole genome sequencing. Phylogenetic and variation analyses were performed based on the obtained sequences, HAdV-7 prototype strain Gomen(AY594255), vaccine strains(AY495969 and AY594256) and representative sequences of strains. The phylogenetic trees constructed based on whole genome sequences, major capsid protein genes(hexon, penton base and fiber) and the early genes(E1, E2, E3 and E4) were not completely consistent. The HAdV-7 strains obtained in this study always clustered with most of the circulating strains worldwide from the 1980 s to the present. Compared with the HAdV-7 prototype strain Gomen(AY594255), some amino acid mutations in loop1 and loop2 of hexon and the RGD loop region of the penton base gene were observed. Recombination analysis showed that partial regions of 55 k Da protein and 100 kDa hexon-assembly associated protein genes among all HAdV-7 strains in this study were from HAdV-16 and HAdV-3, respectively. Our study demonstrated the molecular evolution characteristics of HAdV-7 strains circulating in China and provided basic reference data for the prevention, control and vaccine development of HAdV-7.     

林隙（gap）更新动态研究进展

林隙（ｇａｐ）更新动态研究进展臧润国（中国林业科学研究院生态环境研究所,北京１０００９３）ＲｅｓｅａｒｃｈＡｄｖａｎｃｅｓｏｆＧａｐＲｅｇｅｎｅｒａｔｉｏｎＤｙｎａｍｉｃｓ．ＺａｎｇＲｕｎｇｕｏ（ＩｎｓｔｉｔｕｔｅｏｆＥｃｏｌｏｇｙａｎｄＥｎｖｉｒ...     

混合生物结皮对土壤养分的影响与群落结构之关联——以黄土丘陵区的生物结皮为例

自然条件下生物结皮是藻、藓及地衣等结皮类型以不同比例组成的混合群落,显著影响土壤养分含量,目前混合生物结皮对土壤养分的影响与其群落结构的关系尚不清楚,限制了混合生物结皮土壤养分的评估。为此,研究通过测定单一组成的藻结皮、藓结皮以及80%藻+20%藓、60%藻+40%藓、40%藻+60%藓和20%藻+80%藓4个不同藻藓比例的混合生物结皮土壤有机碳、全氮、全磷、速效磷、铵态氮和硝态氮含量,研究了混合生物结皮土壤养分与其群落结构之间的关联。结果显示：(1)藓结皮层土壤有机碳、全氮、速效磷、铵态氮和硝态氮含量显著高于藻结皮,分别高出166.4%、77.2%、55.1%、56.2%和42.2%。(2)藻藓混合生物结皮土壤有机碳、全氮、速效磷和铵态氮含量与组成和盖度等结构特征有关,可以通过单一类型生物结皮土壤养分含量与盖度加权预测混合生物结皮土壤养分储量。(3)混合生物结皮土壤有机碳、全氮、速效磷和铵态氮储量实测值(x)与预测值(y)拟合的线性函数分别为y=0.97x、y=0.96x、y=1.18x和y=0.92x。(4)混合生物结皮对全磷和硝态氮含量的影响与群落结构无关。生物结皮对下层0—5 ...     

博莱霉素同系物对癌基因表达的影响

应用快速酶联免疫法（ELISA）及Northern印迹杂交法研究了博莱霉素（BLM）同系物诱导癌基因表达的作用．通过检测P21和c－myc蛋白表达的改变和药物在RNA的转录水平上对癌基因表达的影响,证明BLM能够抑制c－myc基因的表达．这种抑制作用不仅发生在蛋白质的翻译水平,而且可能发生在RNA的转录水平上．BLMA6及A2对Ras基因亦有极显著的抑制,提示其亦为以p21蛋白为靶点的抗癌抗生素．A6、A2与A5之间的区别提示在同系物之间可能存在不同的抗癌机理     

Comparative triplet-state properties of the three tryptophan residues in bacteriophage T4 lysozyme and in the enzyme complex with methylmercury(II)

Triplet-state energies, zero-field splittings (ZFS), and total decay rate constants of the individual triplet-state sublevels of the tryptophan (Trp) residues located at positions 126, 138, and 158 in bacteriophage T4 lysozyme have been determined by using low-temperature phosphorescence and optical detection of magnetic resonance spectroscopy in zero applied magnetic field. An investigation of spectral and kinetic properties of individual Trp residues was facilitated by measurements on point-mutated proteins containing two Trp----Tyr substitutions. We find that the phosphorescence lifetime of the buried Trp-138 is considerably shorter than those of the solvent-exposed Trp residues. CH3HgII binding to cysteine residues in T4 lysozyme selectively perturbs the triplet state of Trp-158 by means of an external heavy-atom effect. In contrast with the previous observation of selective x-sublevel perturbation in the Trp-CH3Hg complex, the radiative character of the z sublevel (z is the out-of-plane axis) is selectively enhanced due to the heavy-atom perturbation of Trp-158. The observed pattern of radiative and total sublevel decay constants of the perturbed Trp is attributed to a special orientation of the Hg atom with respect to the indole plane.     

重组人干细胞因子在昆虫细胞中的高效表达

含信号肽的可溶性人干细胞因子（ｈＳＣＦ）ｃＤＮＡ 基因重组于杆状病毒转移载体ｐＶＬ９４１ 中,重组转移载体ｐＶＬ９４１ＳＣＦ与野生型苜蓿夜蛾核型多角体病毒（ＡｃＮＰＶ）ＤＮＡ 共转染草地夜蛾细胞Ｓｆ９ 后,通过体内同源重组构建了重组病毒ＡｃＮＰＶＳＣＦ。Ｓｏｕｔｈｅｒｎ 杂交表明重组病毒基因组中含有ｈＳＣＦ基因片段。重组病毒感染单层Ｓｆ９ 细胞后,表达产物分泌到胞外培养液中。用ＭＴＴ 比色法和ＴＦ１ 细胞株测定表达产物与ＩＬ３ 的协同效应,测得感染重组病毒的培养细胞第三天表达量为１９７０ ｕｎｉｔｓ／ｍ Ｌ培养液。Ｗｅｓｔｅｒｎｂｌｏｔｔｉｎｇ 分析可见分子量为１８ ×１０３ 、２０ ×１０３ 和２２ ×１０３ 三条带。     

LPCAT1 reprogramming cholesterol metabolism promotes the progression of esophageal squamous cell carcinoma

Tumor cells require high levels of cholesterol for membrane biogenesis for rapid proliferation during development. Beyond the acquired cholesterol from low-density lipoprotein (LDL) taken up from circulation, tumor cells can also biosynthesize cholesterol. The molecular mechanism underlying cholesterol anabolism in esophageal squamous cell carcinoma (ESCC) and its effect on patient prognosis are unclear. Dysregulation of lipid metabolism is common in cancer. Lysophosphatidylcholine acyltransferase 1 (LPCAT1) has been implicated in various cancer types; however, its role in esophageal squamous cell carcinoma (ESCC) remains unclear. In this study, we identified that LPCAT1 is highly expressed in ESCC and that LPCAT1 reprograms cholesterol metabolism in ESCC. LPCAT1 expression was negatively correlated with patient prognosis. Cholesterol synthesis in ESCC cells was significantly inhibited following LPCAT1 knockdown; cell proliferation, invasion, and migration were significantly reduced, along with the growth of xenograft subcutaneous tumors. LPCAT1 could regulate the expression of the cholesterol synthesis enzyme, SQLE, by promoting the activation of PI3K, thereby regulating the entry of SP1/SREBPF2 into the nucleus. LPCAT1 also activates EGFR leading to the downregulation of INSIG-1 expression, facilitating the entry of SREBP-1 into the nucleus to promote cholesterol synthesis. Taken together, LPCAT1 reprograms tumor cell cholesterol metabolism in ESCC and can be used as a potential treatment target against ESCC.Subject terms: Cancer metabolism, Cancer prevention