Using niche modelling and human influence index to indicate conservation priorities for Atlantic forest deer species

To prioritise conservation actions and management strategies for threatened forest deer species at the Atlantic forest, we aimed to identify and describe the most suitable habitat areas for forest deer species and to indicate conservation measures for state agents and local communities. We adopt an approach based on ecological niche modelling, key variable thresholds and spatial analyses. In addition, we associated our approach with a human influence index, an invasive species dataset of occurrences, protected area cover and IUCN category. We indicate 2 % (484 km²) of the Atlantic forest cover as conservation priority areas (CPAs). Of these, 56.8 % are outside protected areas, 20.7 % are inside IUCN categories i, ii and iii protected areas, 19.9 % are inside IUCN categories iv, v, and vi protected areas, and 2.6 % are inside indigenous areas. Also, we indicate the most relevant protected areas for deer conservation in the Atlantic forest. The CPAs were classified into more human-influenced areas (MHIA) and less human-influenced areas (LHIA), and we identified 21 significant (greater than120 km²) continuous CPAs outside protected areas. We highlight actions in several perspectives of human influence, governance levels and law protection that would rationalise the use of funds and human resources.     

西洛他唑在急性脑梗死患者rt-PA溶栓治疗后的作用及对血清CD62p、CD63、PAF的作用分析

摘要 目的：探讨西洛他唑在急性脑梗死患者重组人组织型纤溶酶原激活物（rt-PA）溶栓治疗后的作用及对血清血小板溶酶体膜蛋白（CD63）、α颗粒膜糖蛋白（CD62p）、血小板活化因子（PAF）的作用分析。方法：选择2020年2月至2022年2月我院接诊的90例急性脑梗死患者,按照随机数表法分为观察组及对照组,各45例。两组均接受rt-PA溶栓治疗,对照组溶栓后使用阿司匹林治疗,观察组在对照组基础上,联合西洛他唑治疗,均连续治疗14 d。比较两组临床疗效、血清CD62p、CD63、PAF、全血粘度、血浆粘度和红细胞比容（HCT）及美国国立卫生院卒中量表（NIHSS）评分、巴氏量表（Barthel指数）评分的变化及出血事件发生率。结果：观察组患者的临床疗效总有效率为91.11%,高于对照组的73.33%,有统计学意义（P＜0.05）;观察组血清CD62p、CD63、PAF均比对照组低,有统计学意义（P＜0.05）;观察组全血粘度、血浆粘度、HCT均比对照组低,有统计学意义（P＜0.05）;观察组的NIHSS评分均低于对照组,Barthel指数高于对照组,有统计学意义（P＜0.05）;两组出血事件总发生率比较,无统计学意义（P＞0.05）。结论：西洛他唑在急性脑梗死患者rt-PA溶栓治疗后的作用明显,可有效降低血清CD62p、CD63、PAF的表达,改善血小板功能,安全性较好,值得临床推广。     

研究报告: EIF2B5表达下调的人星形胶质细胞与人神经元在内质网应激后细胞存活及miRNA表达的差异

目的 探讨白质消融性白质脑病中胶质细胞选择性受累而神经元受累轻微的原因。方法 将EIF2B5-RNAi表达载体转染至人星形胶质细胞和人神经元,检测基础状态下及内质网应激（endoplasmic reticulum stress,ERS）后细胞凋亡和活力,检测参与ERS调控的已知和未知miRNA,筛选EIF2B5-RNAi人星形胶质细胞在ERS后miRNA变化。结果 与EIF2B5-RNAi人神经元相比,星形胶质细胞自发凋亡及细胞活力下降。较之神经元,更多miRNA参与星形胶质细胞ERS刺激后的调控,EIF2B5-RNAi组参与调控的miRNA数目显著减少。聚类分析发现,5条已知miRNA是通路连接的关键组分。结论 人星形胶质细胞在ERS后可能更加依赖众多促细胞增殖分化的miRNA修复,而EIF2B5-RNAi人星形胶质细胞存在自发凋亡,ERS后严重减少的miRNA可能导致细胞无法存活。     

近20年内蒙古鄂托克旗草地降水利用效率时空演变的驱动力量化

降水利用效率(PUE)是评价干旱半干旱地区草地生产力与降水关系的有效指标。为进一步探究气候变化和人类活动对草地PUE的驱动机理,本研究采用改进的CASA模型估算了2001—2020年鄂托克旗草地净初级生产力(NPP),结合同期降水量的空间插值数据获取了研究区草地PUE,利用简单线性回归和分段线性回归分析了PUE的时空演变特征及其空间格局对6类气候因子的响应,并引入基于偏导数的量化分析方法定量评估了气候变化和人类活动对PUE动态的相对贡献。结果表明: 鄂托克旗草地PUE多年均值为0.748 g C·m^-2·mm^-1,年际波动呈显著下降趋势,下降速率为0.014 g C·m^-2·mm^-1·a^-1;PUE在空间上西低东高,沿气温、降水、相对湿度、日照时数和ET₀的增长梯度呈显著的单峰分段线性模式,而沿风速梯度表现为先快后慢的持续显著增长模式;研究区94.3%的草地表现为PUE衰减态势,且有43.6%为严重衰减,这一突出问题是气候变化和人类活动共同作用导致的,二者的贡献分别为-1.162×10^-2和-0.240×10^-2 g C·m^-2·mm^-1·a^-1,而气候变化是首要驱动力,其中降水是关键气候驱动因子。     

沿海养殖池塘对红树林生态系统影响的时空变化监测与分析

随着沿海人类活动的日益加剧, 其对红树林生态系统健康和可持续发展的影响也逐渐凸显, 实现红树林周边典型人类活动时空动态变化监测对红树林生态系统的保护与修复意义重大。该研究基于Landsat多时相遥感数据和Google Earth Engine平台, 通过面向对象的机器学习方法, 融入水体季节波动信息作为分类特征, 获取了1990、2000、2010和2020年4个不同时期中国沿海红树林分布省区(包括广东、福建、浙江、台湾、广西及海南) 30 m分辨率的养殖池塘空间格局及其变化特征, 并进一步解析养殖池塘对红树林生态系统的影响。研究结果表明: (1)研究区域内4个时间节点的沿海养殖池塘面积总量分别为2 963、5 200、5 377及4 805 km², 呈先增加后减少的趋势, 于2010-2020年间达到峰值。沿海养殖池塘面积变化趋势和达峰时间存在明显区域差异性, 其主要原因是红树林保护政策、养殖池塘规范管理和阶段性经济目标的区域差异化。(2)我国沿海养殖池塘集中分布在21°-24° N区域(广东和广西), 与红树林沿纬度的分布格局呈错峰分布。其中, 红树林与沿海养殖池塘集中分布区(21°-22° N)存在大量养殖池塘堤边生长红树林的特色格局, 此区域内两者交互作用最为紧密, 是探究人类活动对红树林生态系统影响的典型热点地区。(3)养殖池塘侵占红树林是造成红树林损失的最直接原因, 并导致红树林空间分布格局呈现局部破碎化或聚集化的极端发展趋势。该研究通过解析沿海养殖池塘的空间格局, 为精准评估红树林周边典型人类活动变化提供数据支撑, 为进一步监测红树林空间格局动态变化趋势和红树林优先修复区识别提供参考依据。     

古人类对赭石的利用行为在其演化中的意义

长期以来赭石利用行为被视为人类行为现代性的标志之一,受到国内外考古学界的普遍关注。本文回溯和梳理了全球背景下赭石利用的起源、发展及其与人类演化史的关系。在现代人广泛分布于全球之后,赭石利用行为更加丰富和多样化地出现在各地,然而现有考古证据表明该行为并不是解剖学意义上的现代人突变性的发明。赭石利用不能被单纯地定义为现代人行为,而应是有着长久演化积累的现代性行为之一。在长期传播与演化过程中,赭石的功能从意识形态、艺术表达等逐渐扩展到作为矿物成分被用于实际生产生活。赭石的利用历史可追溯到中更新世中期,但其广泛分布仍与晚更新世以来现代人的广泛扩散直接相关,对于理解现代人的意识形态、社会组织方式以及艺术表达、精神文化发展都具有重要的意义。国内目前所发表的相关考古学证据相对较少,以下马碑遗址为代表的材料,也恰处于现代人在全球广泛扩散的窗口期,并伴有进步的细小石器镶嵌使用的证据,成为认识东亚现代人行为的关键性考古证据。     

Downregulation of tripartite motif protein 11 attenuates cardiomyocyte apoptosis after ischemia/reperfusion injury via DUSP1-JNK1/2

Currently, the prevention of ischemic diseases such as myocardial infarction associated with ischemia/reperfusion (I/R) injury remains to be a challenge. Thus, this study was designed to explore the effects of tripartite motif protein 11 (TRIM11) on cardiomyocytes I/R injury and its underlying mechanism. Cardiomyocytes AC16 were used to establish an I/R injury cell model. After TRIM11 downregulation in I/R cells, cell proliferation (0, 12, 24, and 48 h) and apoptosis at 48 h as well as the related molecular changes in oxidative stress-related pathways was detected. Further, after the treatment of TRIM11 overexpression, SP600125, or DUSP1 overexpression, cell proliferation, apoptosis, and related genes were detected again. As per our findings, it was determined that TRIM11 was highly expressed in the cardiomyocytes AC16 after I/R injury. Downregulation of TRIM11 was determined to have significantly reduced I/R-induced proliferation suppression and apoptosis. Besides, I/R-activated c-Jun N-terminal kinase (JNK) signaling and cleaved caspase 3 and Bax expression were significantly inhibited by TRIM11 downregulation. In addition, the overexpression of TRIM11 significantly promoted apoptosis in AC16 cells, and JNK1/2 inhibition and DUSP1 overexpression potently counteracted the induction of TRIM11 overexpression in AC16 cells. These suggested that the downregulation of TRIM11 attenuates apoptosis in AC16 cells after I/R injury probably through the DUSP1-JNK1/2 pathways.     

Engineering nucleotide sugar synthesis pathways for independent and simultaneous modulation of N-glycan galactosylation and fucosylation in CHO cells

Glycosylation of recombinant therapeutics like monoclonal antibodies (mAbs) is a critical quality attribute. N-glycans in mAbs are known to affect various effector functions, and thereby therapeutic use of such glycoproteins can depend on a particular glycoform profile to achieve desired efficacy. However, there are currently limited options for modulating the glycoform profile, which depend mainly on over-expression or knock-out of glycosyltransferase enzymes that can introduce or eliminate specific glycans but do not allow predictable glycoform modulation over a range of values. In this study, we demonstrate the ability to predictably modulate the glycoform profile of recombinant IgG. Using CRISPR/Cas9, we have engineered nucleotide sugar synthesis pathways in CHO cells expressing recombinant IgG for combinatorial modulation of galactosylation and fucosylation. Knocking out the enzymes UDP-galactose 4′-epimerase (Gale) and GDP-L-fucose synthase (Fx) resulted in ablation of de novo synthesis of UDP-Gal and GDP-Fuc. With Gale knock-out, the array of N-glycans on recombinantly expressed IgG is narrowed to agalactosylated glycans, mainly A2F glycan (89%). In the Gale and Fx double knock-out cell line, agalactosylated and afucosylated A2 glycan is predominant (88%). In the double knock-out cell line, galactosylation and fucosylation was entirely dependent on the salvage pathway, which allowed for modulation of UDP-Gal and GDP-Fuc synthesis and intracellular nucleotide sugar availability by controlling the availability of extracellular galactose and fucose. We demonstrate that the glycoform profile of recombinant IgG can be modulated from containing predominantly agalactosylated and afucosylated glycans to up to 42% and 96% galactosylation and fucosylation, respectively, by extracellular feeding of sugars in a dose-dependent manner. By simply varying the availability of extracellular galactose and/or fucose, galactosylation and fucosylation levels can be simultaneously and independently modulated. In addition to achieving the production of tailored glycoforms, this engineered CHO host platform can cater to the rapid synthesis of variably glycoengineered proteins for evaluation of biological activity.     

Genotype distribution and evolutionary analysis of rotavirus associated with acute diarrhea outpatients in Hubei,China, 2013–2016

Group A human rotaviruses (RVAs) annually cause the deaths of 215,000 infants and young children. To understand the epidemiological characteristics and genetic evolution of RVAs, we performed sentinel surveillance on RVA prevalence in a rotavirus-surveillance network in Hubei, China. From 2013 to 2016, a total of 2007 fecal samples from hospital outpatients with acute gastroenteritis were collected from four cities of Hubei Province. Of the 2007 samples, 153 (7.62%) were identified positive for RVA by real-time RT-PCR. RVA infection in Hubei mainly occurred in autumn and winter. The highest detection rate of RVA infection was in 1–2 years old of outpatients (16.97%). No significant difference of RVA positive rate was observed between females and males. We performed a phylogenetic analysis of the G/P genotypes based on the partial VP7/VP4 gene sequences of RVAs. G9P[8] was the most predominant strain in all four years but the prevalence of G2P[4] genotype increased rapidly since 2014. We reconstructed the evolutionary time scale of RVAs in Hubei, and found that the evolutionary rates of the G9, G2, P[8], and P[4] genotypes of RVA were 1.069×10^-3, 1.029×10^-3, 1.283×10^-3 and 1.172×10^-3 nucleotide substitutions/site/year, respectively. Importantly, using a molecular clock model, we showed that most G9, G2, P[8], and P[4] genotype strains dated from the recent ancestor in 2005, 2005, 1993, and 2013, respectively. The finding of the distribution of RVAs in infants and young children in Hubei Province will contribute to the understanding of the epidemiological characteristics and genetic evolution of RVAs in China.