Reissner’s fiber formation depends on developmentally regulated factors extrinsic to the subcommissural organ

Reissners fiber (RF) is a threadlike structure present in the third and fourth ventricles and in the central canal of the spinal cord. RF develops by the assembly of glycoproteins released into the cerebrospinal fluid (CSF) by the subcommissural organ (SCO). SCO cells differentiate early during embryonic development. In chick embryos, the release into the CSF starts at embryonic day 7 (E7). However, RF does not form until E11, suggesting that a factor other than release is required for RF formation. The aim of the present investigation was to establish whether the factor(s) triggering RF formation is (are) intrinsic or extrinsic to the SCO itself. For this purpose, SCO explants from E13 chick embryos (a stage at which RF has formed) were grafted at two different developmental stages. After grafting, host embryos were allowed to survive for 6–7 days, reaching E9 (group 1) and E13 (group 2). In experimental group 1, the secretion released by the grafted SCOs never formed a RF; instead, it aggregated as a flocculent material. In experimental group 2, grafted SCO explants were able to develop an RF-like structure, similar to a control RF. These results suggest that the factor triggering RF formation is not present in the SCO itself, since E13 SCO secretion forms an RF in E13 brains but never develops RF-like structures when placed in earlier developmental environments. Furthermore, the glycoproteins released by implanted SCOs bind specifically to several structures: the apical portion of the mesencephalic floor plate and the choroid plexus of the third and fourth ventricles.C. Hoyo-Becerra and M. D. López-Avalos contributed equally to this study and should be considered as joint first authors. C. Hoyo-Becerra was the recipient of a predoctoral fellowship (PFPI) from the Ministerio de Ciencia y Tecnología (Spain). This work was supported by grants from DGICYT (BFI2003-03348; Spain) and FIS (01/0948; Spain), FIS (01–0948, PI021517; Spain) and ISCIII (red CIEN, nodo Fundación Carlos Haya).     

Optimization of theaflavin biosynthesis from tea polyphenols using an immobilized enzyme system and response surface methodology

Theaflavins were synthesized from tea polyphenols extracted from green tea using an immobilized polyphenol oxidase system. To optimize the production of theaflavins, response surface methodology was applied to determine the effects of five critical variables and their mutual interactions on theaflavin biosynthesis at five levels. A total of 52 individual experiments were performed and a statistical model predicted that the highest theaflavin concentration was 0.766mgml^–1 at optimized conditions. Using these optimal parameters under experimental conditions in three independent replicates, the average value of the biosynthesized theaflavin concentration reached 0.75±0.017mgml^–1 and matched the value predicted by the modelRevisions requested 03 November 2004; Revisions received 7 December 2004     

Phomapyrones from blackleg causing phytopathogenic fungi: isolation, structure determination, biosyntheses and biological activity

The isolation and structure determination of phomapyrones D-G, three 2-pyrones and a coumarin, from a group of isolates of the fungal pathogen Leptosphaeria maculans (Desm.) Ces. et de Not., asexual stage Phoma lingam (Tode ex Fr.) Desm, is reported. As well, phomenin B, infectopyrone, and polanrazines B and C were also obtained for the first time from these isolates. In addition, based on results of incorporations of 13C-labeled acetate and malonate, and deuterated methionine, a polyketide pathway is proposed for the biosyntheses of phomapyrones.     

Long-Term Changes in Shallow-Water Fouling Communities of the White Sea

The replacement of an ascidian (Styela rustica L.) fouling community by a blue mussel (Mytilus edulis L.) community was described for the White Sea. The alternation of populations of these two species takes place in fouling communities developing in the upper 3- to 5-m layer of water. The life span of each type of fouling probably depends on interannual climate fluctuations.     

酸提高绿茶提取物对脂肪酸合酶的抑制活性

脂肪酸合酶和肥胖、癌症等人类重大疾病相关.获取高活性脂肪酸合酶抑制剂有重要应用价值.50％乙醇的绿茶提取物具有抑制脂肪酸合酶和经口服降低大、小鼠体重的功能.该提取物在酸的作用下可明显地提高其抑制脂肪酸合酶的能力.采用1 mol/L硫酸或盐酸在100℃下处理绿茶提取物,发现该提取物对脂肪酸合酶的抑制活性随时间逐步提高.在25℃至120℃温度下,提高处理温度使抑制活性提高的速度加快和程度加大. 用1 mol/L盐酸120℃处理35 min或3 mol/L盐酸100℃处理30 min可使绿茶提取物抑制脂肪酸合酶的半抑制浓度下降20倍左右,达到1 μg/ml以下.用pKa值4.76至1.27的1 mol/L浓度的4种有机酸在100℃作用150 min使绿茶提取物抑制活性分别提高到1.48至5.84倍.提高酸的浓度也使被作用的提取物的抑制活性提高的更多.表现抑制活性提高的速度及程度和氢离子浓度正相关.判断绿茶提取物在酸作用下抑制活性的提高来源于其中所含儿茶素在氢离子作用下发生了化学变化.初步实验表明其变化过程比较复杂,确定其分子机制还需进一步的研究工作.     

MEK- 6318K 型血液分析仪对黄疸型肝病患者白细胞的检测

目的：探讨使用MEK-6318K血细胞分析仪时升高的胆红素对黄疸型肝病患者的白细胞结果影响程度及检测失败的原因,并提出解决方法。方法：对60例黄疸型肝病患者的标本分成两组：总胆红素在20—100umol／L范围30例,在100．1—250umol／L范围30例。均使用EDFA—K2抗凝真空采集病人静脉血2ml,分别用MEK-6318K血细胞分析仪和手工操作方法对同一标本进行血液细胞的分析测定。结果：总胆红素在20—100umol／L范围内30例患者的标本,两种方法测定白细胞结果经统计学处理P〉0．05无显著性差别;总胆红素在100．1—250umol／L范围内30例患者的标本,两种方法测定白细胞结果,经统计学处理P〈0．001有极显著性差别。结论：在使用MEK-6318K血细胞分析仪检测高黄疽标本时一定要注意白细胞结果,对报警标本,可以采用静脉血10ul测定模式,但最好采用手工操作来检测标本,这样才能为临床提供更准确结果。     

Coral disease dynamics at a subtropical location, Solitary Islands Marine Park, eastern Australia

Recent observations suggest that a spreading disease is increasingly contributing to hard coral mortality in the Solitary Islands Marine Park, NSW, Australia. This study determined coral disease prevalence and rate-of-spread through individual affected colonies and investigated the effect this epizootic had on coral populations at sites adjacent to South West Solitary Island. Quantitative data were collected between 2002 and 2004 using photographic and video methods, and visual census along radial arc belt transects. Disease similar to the reported white syndrome and white plague was apparent, spreading through hard coral species from the genera Turbinaria, Acropora, Goniastrea, Pocillopora, Stylophora and Porites. Coral disease prevalence varied between survey dates with mean prevalence increasing from 8.55% during March 2003 to 13.58% in June and declining to 7.75% in September and 6.21% during March 2004. There was a significant difference in mean prevalence between the affected species (p<0.001) and an overall difference between survey dates (p=0.001). Additionally, the rate-of-spread of coral disease through coral colonies determined using repeated, seasonal, still photographs followed similar patterns, with disease progression differing between affected species (p=0.004), and between survey dates (p<0.001). Analysis of the video-transects indicated significant difference in disease prevalence over larger spatial scales (100s of m). However, disease frequency did not vary significantly between 2002 and 2003.     

Noise-Induced Coherence and Network Oscillations in a Reduced Bursting Model

The dynamics of the Hindmarsh-Rose (HR) model of bursting thalamic neurons is reduced to a system of two linear differential equations that retains the subthreshold resonance properties of the HR model. Introducing a reset mechanism after a threshold crossing, we turn this system into a resonant integrate-and-fire (RIF) model. Using Monte-Carlo simulations and mathematical analysis, we examine the effects of noise and the subthreshold dynamic properties of the RIF model on the occurrence of coherence resonance (CR). Synchronized burst firing occurs in a network of such model neurons with excitatory pulse-coupling. The coherence level of the network oscillations shows a stochastic resonance-like dependence on the noise level. Stochastic analysis of the equations shows that the slow recovery from the spike-induced inhibition is crucial in determining the frequencies of the CR and the subthreshold resonance in the original HR model. In this particular type of CR, the oscillation frequency strongly depends on the intrinsic time scales but changes little with the noise intensity. We give analytical quantities to describe this CR mechanism and illustrate its influence on the emerging network oscillations. We discuss the profound physiological roles this kind of CR may have in information processing in neurons possessing a subthreshold resonant frequency and in generating synchronized network oscillations with a frequency that is determined by intrinsic properties of the neurons. PACS 05.45.-a, 05.40.Ca, 87.18.Sn, 87.19     

White spot syndrome virus (WSSV) interaction with crayfish haemocytes

WSSV particles were detected in separated granular cells (GCs) and semigranular cells (SGCs) by in situ hybridisation from WSSV-infected crayfish and the prevalence of WSSV-infected GCs was 5%, whereas it was 22% in SGCs. This indicates that SGCs are more susceptible to WSSV and that this virus replicated more rapidly in SGCs than in GCs and as a result the number of SGCs gradually decreased from the blood circulation. The effect of haemocyte lysate supernatant (HLS), containing the degranulation factor (peroxinectin), phorbol 12-myristate 13-acetate (PMA), the Ca(2+) ionophore A23187 on GCs from WSSV-infected and sham-injected crayfish was studied. The results showed that the percentage of degranulated GCs of WSSV-infected crayfish treated with HLS or PMA was significantly lower than that in the control, whereas no significant difference was observed when treated with the Ca(2+) ionophore. It was previously shown that peroxinectin and PMA have a degranulation effect via intracellular signalling involving protein kinase C (PKC), whereas the Ca(2+) ionophore uses an alternative pathway. HLS treatment of GCs and SGCs from WSSV-infected crayfish results in three different morphological types: non-spread, spread and degranulated cells. The non-spread cell group from both GCs and SGCs after treatment with HLS had more WSSV positive cells than degranulated cells, when detected by in situ hybridisation. Taken together, it is reasonable to speculate that the PKC pathway might be affected during WSSV infection. Another interesting phenomenon was that GCs from non-infected crayfish exhibited melanisation, when incubated in L-15 medium, while no melanisation was found in GCs of WSSV-infected crayfish. However, the phenoloxidase activities of both sham- and WSSV-injected crayfish in HLS were the same as well as proPO expression as detected by RT-PCR. This suggests that the WSSV inhibits the proPO system upstream of phenoloxidase or simply consumes the native substrate for the enzyme so that no activity is shown. The percentage of apoptotic haemocytes in WSSV-infected crayfish was very low, but it was significantly higher than that in the sham-injected crayfish on day 3 or 5 post-infection. The TEM observation in haematopoietic cells (hpt cells) suggests that WSSV infect specific cell types in haematopoietic tissue and non-granular hpt cells seem more favourable to WSSV infection.