人肌型特异烯醇化酶放免分析法及初步应用

建立了人肌型特异烯醇化酶(hMSE)的放免分析法,抗血清的亲和常数为5.1×10⁹L/mol,采用改良的BHR法制备了 ¹²⁵I-hMSE,后者非特异结合率为3%,与抗血清(1∶10³)结合率达50.16%;批内和批间CV分别为8.6%和13%.回收率为95%-105%.标准曲线范围为5-320μg/L.最小检出率为5μg/L.最佳反应条件:0.1mol/LpH7.4PBS(含5mmol/L MgSO₄,0.1%吐温-20,0.1%NaN₃);反应温度和时间:37℃反应0.5h和4℃,0.5h,作为快速测定;或选用4℃反应24h.65例健康人血清hMSE浓度为23.9±10.9μg/L(x±s).hMSE超过57μg/L(x+3s).为阳性值.测定了AMI和肌病患者,血清hMSE明显升高.     

寄主经历对稻褐飞虱致害特性的影响

对寄主经历不同的稻褐飞虱Nilaparvata lugens 3龄若虫致害特性的研究结果表明：在抗虫品种Mudgo上的生活经历显著提高试虫在含Bphl基因的Mudeo、IR26、IR28、IR34上的蜜露排泄量、存活率及试虫对Mudgo的选择性：而ASD7上的经历仅显著提高试虫在ASD7上的蜜露量和存活率。不同品种上的经历对试虫的影响有所不同。同时,各经历试虫 在抗虫品种上的蜜露排泄量显著小于在TNl上的排泄量。     

Proteomic Analysis of Clinical Isolate of Stenotrophomonas maltophilia with bla(NDM-1,)bla(L1) and bla(L2) β-Lactamase Genes under Imipenem Treatment

The co-occurrence of L1 and AmpR-L2 with bla(NDM-1) gene with an upstream 250-bp promoter was detected in a clinical isolate of Stenotrophomonas maltophilia DCPS-01, which was resistant to all β-lactams and sensitive only to colistin and fluoroquinolones. To investigate expression of resistance genes and the molecular mechanisms of bacteria resistance to carbapenems, proteomic profiles of the isolate was passaged with and without the drug by using 2D-PAGE. The results showed that 33 genes exhibiting a ≥3-fold change were identified as candidates that may help S. maltophilia survive drug selection. Strikingly, L1 was expressed more highly in cells grown with imipenem, and the abundant NDM-1 further increased, while very little L2 was detected even following induction. Specific activities for β-lactamase revealed that L2 remained at constitutive low levels (10.6 U/mg), while L1 and NDM-1 showed clear activity (69.8 U/mg). Our data support that imipenem could specifically and reversibly induce L1 and NDM-1, which together played key roles in drug resistance in DCPS-01. Although NDM-1 mediated resistance to carbapenems has been found in very few cases, to our knowledge, this is the first proteomics research of S. maltophilia with NDM-1, giving very broad-spectrum antibiotic resistance profiles.     

澜沧江流域北部中华蜜蜂食源和营养生态位随海拔梯度的变化特征

为了解澜沧江流域北部中华蜜蜂(Apis cerana cerana)的分布,探究中华蜜蜂的食源和营养生态位沿海拔梯度的变化特征,调查了澜沧江流域北部各海拔区域中华蜜蜂的种群分布,运用蜂蜜孢粉学(melissopalynology)分析了各海拔区域中华蜜蜂蜂蜜中花粉的组成特征和变化规律,并综合分析了海拔、中华蜜蜂营养生态位和蜂蜜中花粉的相关性,探讨了自然环境与中华蜜蜂的分布,海拔梯度与蜜粉源植物、中华蜜蜂的食源和营养生态位的关系。结果表明:澜沧江流域北部中华蜜蜂的食源种类丰富,中华蜜蜂种群主要分布于2200—2800 m海拔区域。不同海拔区域中华蜜蜂采食花粉的种类和数量不同,中华蜜蜂种群分布多的海拔区域,蜂蜜中花粉的种类较多,但花粉数量相对少。随着海拔梯度升高,中华蜜蜂蜂蜜中花粉的数量表现为先降后增,而花粉的种类则表现为先增后降。不同海拔区域的中华蜜蜂营养生态位存在差异,推测各海拔区域蜜粉源植物分布、中华蜜蜂种内和种间授粉昆虫及食草动物等竞争因素不同,但各海拔梯度间的变化差异不显著。海拔与中华蜜蜂营养生态位呈正相关(r=0.051),相关性不显著;海拔与蜂蜜中花粉数量呈正相关(r=0.047),与蜂蜜中花粉种类呈正相关(r=0.144),相关性都不显著;中华蜜蜂营养生态位与蜂蜜中花粉的种类呈负相关(r=-0.305),相关性显著(P!0.05);与花粉的数量呈负相关(r=-0.064),相关性不显著。蜂蜜中花粉的数量与种类呈正相关(r=-0.303),且相关性显著(P!0.05)。     

A novel dual Ca2+ sensor system regulates Ca2+-dependent neurotransmitter release

Ca²⁺-dependent neurotransmitter release requires synaptotagmins as Ca²⁺ sensors to trigger synaptic vesicle (SV) exocytosis via binding of their tandem C2 domains—C2A and C2B—to Ca²⁺. We have previously demonstrated that SNT-1, a mouse synaptotagmin-1 (Syt1) homologue, functions as the fast Ca²⁺ sensor in Caenorhabditis elegans. Here, we report a new Ca²⁺ sensor, SNT-3, which triggers delayed Ca²⁺-dependent neurotransmitter release. snt-1;snt-3 double mutants abolish evoked synaptic transmission, demonstrating that C. elegans NMJs use a dual Ca²⁺ sensor system. SNT-3 possesses canonical aspartate residues in both C2 domains, but lacks an N-terminal transmembrane (TM) domain. Biochemical evidence demonstrates that SNT-3 binds both Ca²⁺ and the plasma membrane. Functional analysis shows that SNT-3 is activated when SNT-1 function is impaired, triggering SV release that is loosely coupled to Ca²⁺ entry. Compared with SNT-1, which is tethered to SVs, SNT-3 is not associated with SV. Eliminating the SV tethering of SNT-1 by removing the TM domain or the whole N terminus rescues fast release kinetics, demonstrating that cytoplasmic SNT-1 is still functional and triggers fast neurotransmitter release, but also exhibits decreased evoked amplitude and release probability. These results suggest that the fast and slow properties of SV release are determined by the intrinsically different C2 domains in SNT-1 and SNT-3, rather than their N-termini–mediated membrane tethering. Our findings therefore reveal a novel dual Ca²⁺ sensor system in C. elegans and provide significant insights into Ca²⁺-regulated exocytosis.     

LncRNA FOXD2‐AS1 as a competitive endogenous RNA against miR‐150‐5p reverses resistance to sorafenib in hepatocellular carcinoma

The current study elucidated the role of a long non‐coding RNA (lncRNA), FOXD2‐AS1, in the pathogenesis of hepatocellular carcinoma (HCC) and the regulatory mechanism underlying FOXD2‐AS1/miR‐150‐5p/transmembrane protein 9 (TMEM9) signalling in HCC. Microarray analysis was used for preliminary screening of candidate lncRNAs in HCC tissues. qRT‐PCR and Western blot analyses were used to detect the expression of FOXD2‐AS1. Cell proliferation assays, luciferase assay and RNA immunoprecipitation were performed to examine the mechanism by which FOXD2‐AS1 mediates sorafenib resistance in HCC cells. FOXD2‐AS1 and TMEM9 were significantly decreased and miR‐150‐5p was increased in SR‐HepG2 and SR‐HUH7 cells compared with control parental cells. Overexpression of FOXD2‐AS1 increased TMEM9 expression and overcame the resistance of SR‐HepG2 and SR‐HUH7 cells. Conversely, knockdown of FOXD2‐AS1 decreased TMEM9 expression and increased the sensitivity of HepG2 and Huh7 cells to sorafenib. Our data also demonstrated that FOXD2‐AS1 functioned as a sponge for miR‐150‐5p to modulate TMEM9 expression. Taken together, our findings revealed that FOXD2‐AS1 is an important regulator of TMEM9 and contributed to sorafenib resistance. Thus, FOXD2‐AS1 may serve as a therapeutic target against sorafenib resistance in HCC.     

Potential Role of Cyr61 Induced Degeneration of Human Müller Cells in Diabetic Retinopathy

The degeneration of Müller cells has been recognized to involve in the pathogenesis of diabetic retinopathy. However, the mechanism is not yet clear. This study is to explore the potential role of Cyr61, a secreted signaling protein in extracellular matrix, in inducing human Müller cell degeneration in diabetic retinopathy (DR). Twenty patients with proliferative diabetic retinopathy (PDR) and twelve non-diabetic patients were recruited for this study. Vitreous fluid was collected during vitrectomy surgery for Cyr61 ELISA. Human Müller cell line MIO-M1 were cultured to be subconfluent, and then treated with glucose (0–20 mM) or Cyr61 (0–300 ng/ml). Cyr61 expression induced by increasing concentrations of glucose was evaluated by RT-qPCR and Western blot. Effects of Cyr61 on Müller cells viability, migration and apoptosis were observed by MTT assay, Transwell assay, and TUNEL assay. Vitreous Cyr61 levels were observed to be 8-fold higher in patients with PDR (3576.92±1574.58 pg/mL), compared with non-diabetic controls (436.14±130.69 pg/mL). Interestingly, the active PDR group was significantly higher than the quiescent PDR group (P<0.01). In retinal Müller cells culture, high glucose significantly and dose-dependently elevated Cyr61 expression at both mRNA and protein levels. Cyr61 at high concentrations dose-dependently inhibited the viability and migration of Müller cells. TUNEL assay further revealed that high concentration of Cyr61 significantly promoted the cell apoptosis. In conclusion, these findings demonstrated for the first time that the expression of Cyr61 was elevated by high glucose in Müller cells, and Cyr61 inhibited cell viability and migration while induced apoptosis, suggesting the potential role of Cyr61 in Müller cell degeneration. The elevated Cyr61 levels in vitreous fluid of PDR patients further support its role in diabetic retinopathy (DR).     

现代生物声学的学科发展趋势及中国机遇

随着数字录音技术、电子学和微电子学、人工智能、信息科学等跨学科领域的技术革新,现代生物声学逐渐与生物学、生态学等学科及关联学科之间形成了广泛的交叉前沿领域。现阶段,现代生物声学主要以生物学、生态学等基础学科的理论方法为指导,着重于揭示环境中各类声音在生物之间以及生物与人类、环境之间的相互作用及相关科学规律,为人类认识、保护和利用生物声学资源提供理论基础和解决方案。本文重点阐述了现代生物声学的学科内涵和学科特征,介绍了动物生物声学、生态声学、水下生物声学、环境生物声学、保护生物声学、计算生物声学以及现代生物声学研究的技术框架等前沿热点和发展趋势,评估了中国生物声学研究的学科现状与发展机遇,并对未来学科建设进行了展望。     

The Diel Rhythms of Biosonar Behavior in the Yangtze Finless Porpoise (Neophocaena asiaeorientalis asiaeorientalis) in the Port of the Yangtze River: The Correlation between Prey Availability and Boat Traffic

Information on the habitat use of the critically endangered Yangtze finless porpoise (Neophocaena asiaeorientalis asiaeorientalis) is critical for its conservation. The diel biosonar behavior of the porpoise in the port areas of the Yangtze River was examined along with simultaneous observations of fish density and boat traffic. Biosonar pulses from the porpoises were detected for 1233 min (5.77%) over a 21,380 min duration of effective observations. In total, 190 (5.63%) buzzes (an indication of prey capture attempts) were recorded among the 3372 identified click trains. Of the 168 echolocation encounters (bouts of click trains less than eight min apart), 150 (89.3%) involved single animals, indicating that solitary porpoises were frequently present and feeding in the port areas. Significant diel patterns were evident involving the biosonar behavior of the porpoises (including click trains and buzzes), fish density and boat traffic. The frequencies of the click trains and buzzes were significantly lower during the day than in the evening and at night, which suggests that porpoises in this region are primarily engaged in crepuscular and nocturnal foraging. The lack of a significant diel pattern in the echolocation encounters indicates the importance of the port in porpoise conservation. A forced feeding schedule may be associated with the lack of a significant correlation between porpoise acoustics and boat traffic. Overall, prey availability appears to be the primary factor that attracts porpoises. Additionally, porpoises tend to migrate or remain downstream in the morning and migrate or remain upstream in the evening, most likely to follow their prey. The findings of this study can be used to improve the conservation of the Yangtze finless porpoise.