GC–MS explores health care components in the extract of Pterocarpus Macarocarpus Kurz

Pterocarpus is often used to make high-grade furniture, with beneficial health functions on the human body. Therefore, this article with large fruit red sandalwood as an example, to explore its extract on the human body beneficial health care ingredients. FT-IR analysis, in the 2855–3421?cm^?1 wave segment, ethyl acetate after extraction of large fruit red sandalwood powder infrared transmittance increased the maximum value; GC–MS analysis, large fruit red sandalwood in the human body with a cough and phlegm, detoxification and enhance human immunity and other effects. Among them, Homopterocarpin in the inhibition and killing of cancer cell activity outstanding performance. Cryptomeridiol is a natural product with anti-Alzheimer's disease and antispasmodic properties, with significant medicinal value.     

雷公藤AP2/ERF转录因子基因的克隆与分析

该研究以雷公藤发状根为材料,根据雷公藤根转录组数据设计引物,采用RT-PCR方法克隆得到2个雷公藤AP2/ERF转录因子,分别命名为TwAP2/ERF1基因(GenBank登录号:GAVZ01042389.1)和TwAP2/ERF2基因(GenBank登录号:GAVZ01016765.1)。TwAP2/ERF1基因含有一个525bp开放阅读框(ORF),编码186个氨基酸;TwAP2/ERF2基因的ORF为789bp,编码262个氨基酸;2个基因编码的蛋白质均为亲水性蛋白质。系统进化分析表明,TwAP2/ERF1与油桐(Vernicia fordii)AP2/ERF(APQ47444.1)和木油桐(Vernicia montana)AP2/ERF(APQ47365.1)相似性较高,TwAP2/ERF2与毛果杨(Populus trichocarpa)AP2/ERF(XP_002304640.1)和樱桃(Prunus pseudocerasus)AP2/ERF(ALD84477.1)相似性较高。雷公藤发状根经MeJA诱导后,TwAP2/ERF1基因的相对表达量明显提高,并于处理后9h达到最高值,为对照表达量的16.77倍;而MeJA处理对TwAP2/ERF2基因的表达表现出抑制作用,但于处理后48h相对表达量有所提高。研究表明,雷公藤TwAP2/ERF1转录因子响应MeJA早期诱导正调控,推测其可能参与调控雷公藤植物次生代谢产物的生物合成,该研究结果为阐明雷公藤次生代谢物质的生物合成调控与利用现代生物技术提高雷公藤植物细胞中次生代谢物质的含量奠定了基础。     

MNS16A Tandem Repeats Minisatellite of Human Telomerase Gene and Cancer Risk: A Meta-Analysis

Background

Researchers have provided evidence that telomere dysfunction play an important role in cancer development. MNS16A is a polymorphic tandem repeats minisatellite of human telomerase (hTERT) gene that influences promoter activity of hTERT and thus implicates to relate with risk of several malignancies. However, results on association between MNS16A and cancer risk remain controversial. We therefore conduct a meta-analysis to derive a more precise estimation of association between MNS16A and cancer risk.

Methods

A systematic literature search was conducted by searching PubMed, ISI Web of Knowledge, Human Genome and Epidemiology Network Navigator and Google Scholar digital database for publications on associations between MNS16A and cancer risk. Variants with statistically significant associations by meta-analysis were assessed using Venice criteria.

Results

10 case-control articles enrolling 6101 cases and 10521 controls were brought into our meta-analysis. The relationships were strong epidemiological credibility in cerebral cancer and breast cancer population (P for heterogeneity > 0.1). The cumulative analysis in chronologic order suggested a clear tendency towards a significant association with additional study samples.

Conclusions

The results provided a more accurate depiction of the role of MNS16A in cerebral cancer and breast cancer susceptibility. Additional larger studies were warranted to validate our findings.     

昆仑山北坡4种优势灌木的气体交换特征

在自然条件下对昆仑山北坡四种灌木塔里木沙拐枣（Calligonum roborowasikii）、驼绒藜（Ceratoides latens）、合头草(Sympegma regelii)和昆仑绢蒿(Seriphidium korovinii)的气体交换、水势的季节变化特征及生长季末δ13C值进行了比较研究。结果表明：驼绒藜、塔里木沙拐枣和合头草气体交换日变化为单峰曲线,昆仑绢蒿为双峰曲线;其中塔里木沙拐枣属高光合高蒸腾型,水分利用效率最高,合头草属低光合低蒸腾型,驼绒藜属高光合低蒸腾型,昆仑绢蒿属低光合高蒸腾,水分利用效率最低。驼绒藜光合速率8月日变化,10：00-12：00,16：00-20：00两个时段,Pn下降,主要决定因素均为非气孔因素。沙拐枣6月光合速率日变化,12：00-14：00时,Pn下降,主要受气孔导度因素影响;16：00-20：00时,Pn下降,可能是同时受气孔和非气孔因素的影响。从耐旱机理可以将4种灌木归类：塔里木沙拐枣和昆仑绢蒿属于高水势延迟脱水耐旱机理;驼绒藜和合头草属于低水势忍耐脱水机理。用δ13C表征植物水分利用效率时,只有部分物种有很好的一致性。     

Role of IL-18 in transplant biology

Since pro-inflammatory cytokine IL-18 and its receptor (IL-18R) are closely involved in regulating both adaptive and innate immune responses, it is conceivable that they might play an important role in organ transplantation. IL-18 can stimulate lymphocytes to produce the IFN-γ and regulate macrophage activity, thereby increasing the expression of proinflammatory cytokines including IL-1β, IL-6, CCL4 (macrophage inflammatory protein-1β), CXCL2 (macrophage inflammatory protein-2), and CCL2 (monocyte chemotactic protein-1). Nevertheless, the IL-18 signaling pathway and its underlying mechanisms remain obscure in transplant biology. This review is to summarize recent advances in our knowledge about the IL-18 signaling pathway and to analyze their functions in transplant-related biology. It was found that IL-18/IL-18R signaling pathway contributed to vascular transplantation, ischemmia/reperfusion, acute kidney injury, and acute rejection of kidney/liver/heart transplantation. IL-18 was a potential CYP3A expression modulator and was capable of affecting tacrolimus pharmacokinetics. Neutralizing IL-18 by its inhibitor IL-18 binding protein could efficiently suppress the production of injury-associated cytokines such as IL-6, TNF-α, IFN-γ, CXCL10 (IFN-γ-inducible protein10), and CX₃CL1 (fractalkine) and improve allograft function. Blockade of IL-18 signaling could regulate cardiomyocyte apoptosis and inhibit Th17 cells differentiation. Alteration of IL-18 levels was suggested as a biomarker for predicting ongoing allograft outcome. All these activities could deepen our understanding of immunobiological role of IL-18 and its receptor in the field of organ transplantation. Intervention of IL-18 signaling pathway might be utilized as a therapeutic strategy in clinic.     

Detection and quantification of protein biomarkers from fewer than 10 cells

The use of antibody microarrays continues to grow rapidly due to the recent advances in proteomics and automation and the opportunity this combination creates for high throughput multiplexed analysis of protein biomarkers. However, a primary limitation of this technology is the lack of PCR-like amplification methods for proteins. Therefore, to realize the full potential of array-based protein biomarker screening it is necessary to construct assays that can detect and quantify protein biomarkers with very high sensitivity, in the femtomolar range, and from limited sample quantities. We describe here the construction of ultramicroarrays, combining the advantages of microarraying including multiplexing capabilities, higher throughput, and cost savings with the ability to screen very small sample volumes. Antibody ultramicroarrays for the detection of interleukin-6 and prostate-specific antigen (PSA), a widely used biomarker for prostate cancer screening, were constructed. These ultramicroarrays were found to have a high specificity and sensitivity with detection levels using purified proteins in the attomole range. Using these ultramicroarrays, we were able to detect PSA secreted from 100 LNCaP cells in 3 h and from just four LNCaP cells in 24 h. Cellular PSA could also be detected from the lysate of an average of just six cells. This strategy should enable proteomic analysis of materials that are available in very limited quantities such as those collected by laser capture microdissection, neonatal biopsy microspecimens, and forensic samples.