海洋酸化对微藻关键生理过程的调控机制及环境因素的影响

人类活动排放大量的CO₂通过海气界面进入海洋,打破原有海水碳酸盐平衡进而造成海洋酸化(OA)。OA会影响海水和海洋污染物的理化性质,进而对生活在海洋表层的浮游藻类生理过程产生显著调控作用。海洋微藻作为海洋中主要的初级生产者,其生理功能与过程的正常进行对于海洋生态系统具有重要作用。本文综述了OA对海洋微藻光合固碳、钙化过程、固氮作用3个关键生理过程的调控作用和具体机制,总结了OA条件下,环境因素(如太阳辐射、温度、营养元素)对微藻生理过程和生长的影响,以及OA通过改变典型海洋污染物(如有机污染物、重金属、微塑料)的环境行为而对微藻生理过程的调控作用。最后,结合研究现状,对未来需要开展的研究方向进行展望。本文为进一步了解OA对海洋生态系统的潜在影响提供了重要信息。     

鄂西南木林子常绿落叶阔叶混交林2014~2019年主要物种动态变化

为了明确鄂西南木林子亚热带山地常绿落叶阔叶混交林的短期群落动态,为该区森林生态的保护、恢复与可持续经营提供科学依据。该研究基于木林子自然保护区2.2 hm²动态监测样地,以2014和2019年样地内所有胸径(DBH)≥1 cm的木本植物为研究对象,从物种组成与多样性、重要值、死亡率、补员率及胸径等方面分析了其动态变化。结果表明：(1)5年间2.2 hm²样地内木本植物个体从17 308株减少到16 533株,降幅为4.48%,胸高断面积31.42 m²·hm^-2增长到35.53 m²·hm^-2,物种增加了1科6属18种,消失1属7种。 乔木、亚乔木、灌木及藤本4类生长型物种的Margalef丰富度指数均上升,而Pielou均匀度指数均下降;除乔木外其他3种生长型的Shannon Wiener多样性指数和Simpson指数均上升。(2)补员个体1 269株,平均胸径2.44 cm,胸高断面积为0.32 m²·hm^-2,平均新增115.36 株·hm^-2·a^-1,隶属39科59属99种;死亡个体2 044株,平均胸径3.32 cm,胸高段面积为1.31 m²·hm^-2,平均死亡185.82 株·hm^-2·a^-1,隶属51科90属146种;不同径级补员与死亡个体数差异明显,总体上随着径级的增大而减少。(3)46个主要物种中有15种重要值增大,有31种降低,增加与降低的变化幅度为乔木层>灌木层>亚乔木层;平均胸径从4.70 cm上升为5.12 cm,除锥栗(Castanea henryi)平均胸径有所下降外其他物种均上升。(4)主要树种中有44个为增长型种群,另外2个物种种群增长率不变,主要物种年补员率大于年死亡率,不同生长型物种及其不同径级的死亡率与补员率不同,不同径级补员率总体大于死亡率;随着径级的增大,补员率与死亡率的差值逐渐降低趋于平缓。研究认为,该群落物种组成与多样性及主要物种的重要值、平均胸径变化幅度较小,未发生明显波动,主要物种不同径级的更新动态有所差别,但不剧烈,因此整个群落外貌基本保持不变,发展较为稳定。     

中老铁路经济廊带生态质量及其与人类活动的关系

区域生态质量很大程度上受人类活动强度影响,制约着区域经济可持续发展。以中老铁路经济廊带为对象,重点研究区内人类活动强度对区域生态环境的影响。选取1999、2009、2019年遥感影像计算遥感生态指数(RSEI),采用空间自相关及局域G统计量探测研究区生态质量的时空演变规律,并结合同期人口密度构建地理加权回归模型,定量分析区内人类活动强度引起的生态效应。研究表明: 1999—2019年,区内生态质量经历了先升后降的变化,RSEI均值由1999年的0.645升为2009年的0.738,随后又降为2019年的0.721,中部地区生态质量波动较大;基于地理加权回归模型(GWR)拟合人口密度与生态质量的效果明显好于最小二乘法,基于GWR的不同时期R²均高于0.7且拟合效果稳定,2019年拟合度最好(R²为0.785),1999、2009年R²分别为0.726、0.754;中老铁路沿线南部万象一带的生态质量对人类活动较敏感,以中度敏感区为主。对高、中、低度敏感区而言,人口密度每增长10、100、1000倍将相应导致RSEI均值降低0.2、0.4、0.6。经济廊带发展会导致人口密度增加,在规划布局过程中应控制人类活动,防止潜在敏感区及现有敏感区生态质量进一步恶化。     

左旋卡尼汀对脂多糖诱导小鼠肺微血管内皮细胞自噬和凋亡的影响*

目的:探讨左旋卡尼汀(LC)对脂多糖(LPS)损伤的小鼠肺微血管内皮细胞(PMVECs)的保护作用及自噬、凋亡的影响。方法:采用体外培养的小鼠PMVECs,分为对照组(Control组)、LPS组(10 μg/ ml,3、6、12、24 h)、LPS(10 μg/ ml,24 h)+LC(终浓度为2.5、5、10 μg/ml)(LC组)。Annexin V-FITC/PI双标记法检测细胞凋亡,细胞免疫荧光染色法检测自噬小体,Western blot法检测自噬相关蛋白LC3及凋亡蛋白Caspase-3的含量,CCK-8法检测细胞活力。结果:① 与Control组比较,LPS 6 h、12 h、24 h组PMVECs细胞活力显著受到抑制,细胞凋亡率、自噬蛋白LC3Ⅱ表达显著增高(P均＜0.01),LC3蛋白阳性表达。②与LPS 24 h组比较,各浓度LC组PMVECs细胞活力显著提高、自噬蛋白LC3II表达水平显著升高(P均＜0.01),而PMVECs凋亡率和凋亡蛋白Caspase-3表达水平均明显降低 (P＜0.05)。结论:LC具有提高LPS刺激的小鼠PMVECs活性、促进PMVECs自噬、抑制凋亡的作用。     

表达透明颤菌血红蛋白基因对酿酒酵母生长及细胞内氧化状态的影响*

透明颤菌血红蛋白基因vgb在多种研究和工业发酵菌中异源表达很好的解决了高密度发酵中的溶氧率问题。酿酒酵母是经典的真核模型,且在发酵工业中具有重要的应用价值,但vgb在酿酒酵母中异源表达对细胞生长的影响并不清楚。以ADH1为启动子构建了含透明颤菌(Vistreoscilla)血红蛋白基因vgb的异源表达质粒YEplac195-ADH1pr-vgb,并转化至酿酒酵母BY4741。通过生长敏感性实验,发现在发酵碳源和非发酵碳源中,vgb的异源表达均抑制了菌株生长。接着,通过2',7'-二氯荧光黄双乙酸盐和PI染色和脂质过氧化产物检测分析,发现过表达vgb的酿酒酵母细胞中活性氧(ROS)的积累、细胞膜通透性改变以及脂质过氧化。结果表明,酿酒酵母中过表达vgb改变细胞的氧化状态促进活性氧的累积,氧化应激导致菌株的生长抑制。     

血清DCN、NRG-1、MIF水平与首发未服药精神分裂症患者临床症状和认知功能的相关性分析

目的:探讨血清核心蛋白多糖(DCN)、神经调节蛋白-1(NRG-1)、巨噬细胞迁移抑制因子(MIF)水平与首发未服药精神分裂症患者临床症状和认知功能的相关性。方法:选择2018年1月~2020年11月期间长江大学附属第一医院收治的首发未服药精神分裂症患者80例作为精神分裂症组,同期于长江大学附属第一医院进行体检的健康志愿者80例作为对照组。应用阳性和阴性症状量表(PANSS)评估患者精神病理症状,应用MATRICS共识认知成套测验(MCCB)评估所有受试者认知功能。根据PANSS评分将精神分裂症组分为PANSS评分高分组和低分组,比较两组血清DCN、NRG-1、MIF水平,并分析以上指标水平与PANSS总分、MCCB各项评分的相关性。结果:精神分裂症组患者PANSS总分为(77.18±13.57)分。精神分裂症组MCCB各项评分均低于对照组(P<0.05)。精神分裂症组血清DCN、NRG-1水平低于对照组,MIF水平高于对照组(P<0.05)。PANSS高分组血清DCN、NRG-1水平低于PANSS低分组,MIF水平高于PANSS低分组(P<0.05)。Pearson相关性分析显示,首发未服药精神分裂症患者血清DCN、NRG-1水平与PANSS总分呈负相关,与MCCB各项评分呈正相关,MIF水平与PANSS总分呈正相关,与MCCB各项评分呈负相关(均P<0.05)。结论:首发未服药精神分裂症患者血清DCN、NRG-1、MIF水平异常,且以上指标水平与患者临床症状和认知功能受损有一定联系,提示检测以上指标水平可能为该病患者认知功能及临床症状的评估提供参考。     

Knockout of Akt1/2 suppresses the metastasis of human prostate cancer cells CWR22rv1 in vitro and in vivo

Although primary androgen deprivation therapy resulted in tumour regression, unfortunately, majority of prostate cancer progress to a lethal castration-resistant prostate cancer, finally die to metastasis. The mutual feedback between AKT and AR pathways plays a vital role in the progression and metastasis of prostate cancer. Therefore, the treatment of a single factor will eventually inevitably lead to failure. Therefore, better understanding of the molecular mechanisms underlying metastasis is critical to the development of new and more effective therapeutic agents. In this study, we created prostate cancer CWR22rv1 cells with the double knockout of Akt1 and Akt2 genes through CRISPR/Cas9 method to investigate the effect of Akt in metastasis of prostate cancer. It was found that knockout of Akt1/2 resulted in markedly reduced metastasis in vitro and in vivo, and appeared to interfere AR nuclear translocation through regulating downstream regulatory factor, FOXO proteins. It suggests that some downstream regulatory factors in the AKT and AR interaction network play a vital role in prostate cancer metastasis and are potential targeting molecules for prostate cancer metastasis treatment.     

Methyl-compounds driven benthic carbon cycling in the sulfate-reducing sediments of South China Sea

Methane is a potent greenhouse gas; methane production and consumption within seafloor sediments has generated intense interest. Anaerobic oxidation of methane (AOM) and methanogenesis (MOG) primarily occur at the depth of the sulfate–methane transition zone or underlying sediment respectively. Methanogenesis can also occur in the sulfate-reducing sediments through the utilization of non-competitive methylated compounds; however, the occurrence and importance of this process are not fully understood. Here, we combined a variety of data, including geochemical measurements, rate measurements and molecular analyses to demonstrate the presence of a cryptic methane cycle in sulfate-reducing sediments from the continental shelf of the northern South China Sea. The abundance of methanogenic substrates as well as the high MOG rates from methylated compounds indicated that methylotrophic methanogenesis was the dominant methanogenic pathway; this conclusion was further supported by the presence of the methylotrophic genus Methanococcoides. High potential rates of AOM were observed in the sediments, indicating that methane produced in situ could be oxidized simultaneously by AOM, presumably by ANME-2a/b as indicated by 16S rRNA gene analysis. A significant correlation between the relative abundance of methanogens and methanotrophs was observed over sediment depth, indicating that methylotrophic methanogenesis could potentially fuel AOM in this environment. In addition, higher potential rates of AOM than sulfate reduction rates at in situ methane conditions were observed, making alternative electron acceptors important to support AOM in sulfate-reducing sediment. AOM rates were stimulated by the addition of Fe/Mn oxides, suggesting AOM could be partially coupled to metal oxide reduction. These results suggest that methyl-compounds driven methane production drives a cryptic methane cycling and fuels AOM coupled to the reduction of sulfate and other electron acceptors.