Isomer-specific effects of conjugated linoleic acid on proliferative activity of cultured neural progenitor cells

We used forebrain-specific conditional presenilin 1 (PS1) and presenilin 2 (PS2) double knockout mice (dKO mice), which exhibit neurodegenerative disease-like symptoms, including inflammation of the brain and periphery, to investigate whether periodontal and salivary tissues display alterations. Mandibles were dissected for alveolar bone height analysis. Maxillae were fixed and decalcified for histological observation and osteoclast detection. Submandibular glands were fixed for histological observation. The submandibular gland and the gingiva of the mandibular incisor teeth were used to assay inflammatory mediators. At 9 months, the number of osteoclasts had significantly increased in the periodontal ligament and the periodontal tissues exhibited obvious histomorphological abnormalities in the dKO mice compared to the control mice at the same age. Alveolar bone loss in dKO mice increased with age. The salivary tissues in dKO mice exhibited obvious age-dependent histomorphological abnormalities. The levels of the inflammatory mediators IL-1β, TNF-α, and GM-CSF in the submandibular gland and gingiva also increased in an age-dependent manner. These findings suggest that inflammation in the dKO brain could expand to the periphery, including the oral tissue, which could ultimately induce abnormalities in the periodontal and salivary tissues.     

Hsp20 functions as a novel cardiokine in promoting angiogenesis via activation of VEGFR2

Heat shock proteins (Hsps) are well appreciated as intrinsic protectors of cardiomyocytes against numerous stresses. Recent studies have indicated that Hsp20 (HspB6), a small heat shock protein, was increased in blood from cardiomyopathic hamsters. However, the exact source of the increased circulating Hsp20 and its potential role remain obscure. In this study, we observed that the circulating Hsp20 was increased in a transgenic mouse model with cardiac-specific overexpression of Hsp20, compared with wild-type mice, suggesting its origin from cardiomyocytes. Consistently, culture media harvested from Hsp20-overexpressing cardiomyocytes by Ad.Hsp20 infection contained an increased amount of Hsp20, compared to control media. Furthermore, we identified that Hsp20 was secreted through exosomes, independent of the endoplasmic reticulum-Golgi pathway. To investigate whether extracellular Hsp20 promotes angiogenesis, we treated human umbilical vein endothelial cells (HUVECs) with recombinant human Hsp20 protein, and observed that Hsp20 dose-dependently promoted HUVEC proliferation, migration and tube formation. Moreover, a protein binding assay and immunostaining revealed an interaction between Hsp20 and VEGFR2. Accordingly, stimulatory effects of Hsp20 on HUVECs were blocked by a VEGFR2 neutralizing antibody and CBO-P11 (a VEGFR inhibitor). These in vitro data are consistent with the in vivo findings that capillary density was significantly enhanced in Hsp20-overexpressing hearts, compared to non-transgenic hearts. Collectively, our findings demonstrate that Hsp20 serves as a novel cardiokine in regulating myocardial angiogenesis through activation of the VEGFR signaling cascade.     

高度城市化地区既有建筑屋顶绿化建设潜力评析——以上海中心城区为例

广泛的屋顶绿化是改善城市生态环境的重要举措。为探求中国高度城市化地区屋顶绿化建设推广的可行途径,综述了国外先进国家的屋顶绿化建设历程以及针对既有建筑的拓展型屋顶绿化的建设难点,并以中国屋顶绿化发展较早的上海为例,对其中心城区（即上海市外环线以内的区域,总面积约667.80km2）既有建筑的屋顶绿化进行了适建性评估。国外屋顶绿化建设领先的国家大多经历了从鼓励到强制、从新建建筑到既有建筑的历程;针对既有建筑的拓展型屋顶绿化的建设更具技术挑战性,必须进行构造创新、基质优化、植物精选和成本控制;上海已率先发布屋顶绿化建设的强制性政策,相关技术研发已有相当基础,但推广建设类型仍有局限,拓展型屋顶绿化极具建设潜力。     

Endothelial nitric-oxide synthase enhances lipopolysaccharide-stimulated tumor necrosis factor-alpha expression via cAMP-mediated p38 MAPK pathway in cardiomyocytes

The purpose of this study was to investigate the role of endothelial nitric-oxide synthase (eNOS), cAMP, and p38 MAPK in tumor necrosis factor-alpha (TNF-alpha) expression induced by lipopolysaccharide (LPS). LPS dose- and time-dependently induced phosphorylation of p38 MAPK and TNF-alpha expression in neonatal mouse cardiomyocytes. TNF-alpha expression was preceded by p38 MAPK phosphorylation, and selective inhibition of p38 MAPK abrogated LPS-induced TNF-alpha expression. Deficiency in eNOS decreased basal and LPS-stimulated TNF-alpha expression in cardiomyocytes. NOS inhibitor l-NAME attenuated LPS-induced p38 MAPK phosphorylation and TNF-alpha production in wild-type cardiomyocytes, whereas NO donor 2,2'-(hydroxynitrosohydrazono)bis-ethanamine (DETA-NO) (2 microm) or overexpression of eNOS by adenoviral gene transfer restored the response of eNOS(-/-) cardiomyocytes to LPS. These effects of NO were mediated through cAMP-dependent pathway based on the following facts. First, deficiency in eNOS decreased basal levels of intracellular cAMP, and DETA-NO elevated intracellular cAMP levels in eNOS(-/-) cardiomyocytes. Second, a cAMP analogue 8-Br-cAMP mimicked the effect of NO in eNOS(-/-) cardiomyocytes. Third, either inhibition of cAMP or cAMP-dependent protein kinase attenuated LPS-stimulated p38 MAPK phosphorylation and TNF-alpha production in wild-type cardiomyocytes. In conclusion, eNOS enhances LPS-stimulated TNF-alpha expression in cardiomyocytes. Activation of p38 MAPK is essential in LPS-stimulated TNF-alpha expression. Moreover, the effects of NO on LPS-stimulated TNF-alpha expression are mediated through cAMP/cAMP-dependent protein kinase-dependent p38 MAPK pathway in neonatal cardiomyocytes.     

Identification and Characterization of an Oocyte Factor Required for Porcine Nuclear Reprogramming

Nuclear reprogramming of somatic cells can be induced by oocyte factors. Despite numerous attempts, the factors responsible for successful nuclear reprogramming remain elusive. In the present study, we found that porcine oocytes with the first polar body collected at 42 h of in vitro maturation had a stronger ability to support early development of cloned embryos than porcine oocytes with the first polar body collected at 33 h of in vitro maturation. To explore the key reprogramming factors responsible for the difference, we compared proteome signatures of the two groups of oocytes. 18 differentially expressed proteins between these two groups of oocytes were discovered by mass spectrometry (MS). Among these proteins, we especially focused on vimentin (VIM). A certain amount of VIM protein was stored in oocytes and accumulated during oocyte maturation, and maternal VIM was specifically incorporated into transferred somatic nuclei during nuclear reprogramming. When maternal VIM function was inhibited by anti-VIM antibody, the rate of cloned embryos developing to blastocysts was significantly lower than that of IgG antibody-injected embryos and non-injected embryos (12.24 versus 22.57 and 21.10%; p < 0.05), but the development of in vitro fertilization and parthenogenetic activation embryos was not affected. Furthermore, we found that DNA double strand breaks dramatically increased and that the p53 pathway was activated in cloned embryos when VIM function was inhibited. This study demonstrates that maternal VIM, as a genomic protector, is crucial for nuclear reprogramming in porcine cloned embryos.     

用组合模型综合比较的方法分析气候变化对朱鹮潜在生境的影响

气候变化的不确定性和物种与环境关系的不确定性使气候变化生物学的研究充满变数。为了降低不确定性,人们开始用组合模型综合比较的方法研究物种对气候变化的响应。以朱鹮(Nipponia nippon)为研究对象,介绍组合模型综合比较方法的特点。朱鹮曾经高度濒危,目前种群大小在迅速恢复中;然而其分布区依旧狭小,气候变化可能是朱鹮面临的新威胁。应用BIOMOD模型中的9种模型,选择了每年的最低温和最高温、温度的季节性变异、每年的总降水量和降水的季节性变异共5个气候因子,依据WorldClim气候数据的CGCM2气候模型的A2a排放情形,计算了朱鹮当前(1950—2000年)的适宜生境和2020年、2050年、2080年3个阶段的潜在生境范围。结果表明朱鹮潜在生境将逐渐北移,生境中心脱离现在的保护区。因此,制定朱鹮的长期保护策略是必要的。9个模型在预测结果上、变量权重上和拟合优度的指标上都有差异,反映了模型本身的不确定性。气候变化的生物学效应比较复杂,应用多个模型进行综合比较,可以尽可能地减少模型所导致的误差。     

1-磷酸鞘氨醇促进间充质干细胞向心肌分化

为研究1-磷酸鞘氨醇 (Sphingosine-1-phosphate,S1P) 对脐带间充质干细胞 (Umbilical cord mesenchymal stem cells,UC-MSCs) 和脂肪间充质干细胞 (Adipose derived mesenchymal stem cells,AD-MSCs) 向心肌分化的影响,探索其适宜的作用时间和浓度,将UC-MSCs和AD-MSCs接种到培养板,用添加不同浓度S1P的心肌细胞培养液诱导两种干细胞向心肌分化,诱导时间分为7 d、14 d和28 d。采用免疫荧光染色检测心肌特异性蛋白,α-肌动蛋白 (α-actin)、缝隙连接蛋白 (Connexin-43) 以及肌球蛋白重链 (MYH-6) 的表达,并通过共聚焦显微镜和荧光显微镜进行观察;采用MTT分析细胞的活性;膜片钳检测分化细胞的钙瞬变 (此为心肌细胞的功能性指标)。结果表明,S1P与心肌细胞培养液协同作用,能够促进UC-MSCs和AD-MSCs向心肌细胞的分化。并且,随着S1P浓度的增加,促分化作用增强,但细胞活性降低。S1P在心肌细胞培养液中的适宜作用时间为14 d,适宜作用浓度为0.5 μmol/L。而且联合心肌细胞培养液可以使UC-MSCs和AD-MSCs的心肌分化细胞产生钙瞬变,具有类似心肌细胞的功能性。S1P能够与心肌细胞培养液协同作用,促进UC-MSCs和AD-MSCs的心肌功能性分化。     

氨基酸配方有机肥对胡麻生长和籽粒产量及品质的影响

通过田间试验,以不施肥为对照(CK),研究了单施化肥(T0)、不同比例氨基酸配方有机肥与化肥配施和单施氨基酸配方有机肥(T100)对胡麻干物质积累分配规律、产量、品质及氮肥利用效率的影响。结果表明:(1)氨基酸配方有机肥对胡麻出苗率具有明显促进作用,且随着氨基酸配方有机肥施用量的增加胡麻出苗率提高。(2)氨基酸配方有机肥促进了胡麻干物质积累进程,增加了干物质积累总量,如在成熟期时,30%氨基酸配方有机肥与70%化肥配施(T30)处理的干物质积累总量最大,比不施肥、单施化肥和单施有机肥处理分别显著增加60.52%、37.01%和29.97%;且T30处理的产量与不施肥(CK)、单施化肥(T0)、单施生物有机肥(T100)相比分别增加了72.07%、16.47%、13.30%。(3)不同比例氨基酸配方有机肥与化肥配施的处理下均可改善胡麻的品质,提高胡麻氮肥利用效率,其中在30%氨基酸配方有机肥替代化肥(T30)的情况下胡麻干物质积累、产量及亚麻酸含量最高,60%氨基酸配方有机肥替代化肥(T60)的情况下胡麻亚油酸含量较高。研究认为,30%氨基酸配方有机肥与70%化肥配施对当地胡麻生产的影响效果最佳。