慢性缺氧对大鼠膈肌组织化学和超微结构影响的研究

研究慢性缺氧和参麦注射液治疗对大鼠膈肌组织化学和超微结构的影响,结果显示：缺氧使膈肌ＳＤＨ活性降低,Ⅰ类纤维极显著减少,运动终板ＣｈＥ活性极显著降低,线粒体肿胀变性,神经肌肉运动终板突触前部囊泡减少,突触间隙模糊,终板模电子密度降低;参麦治疗可恢复缺氧膈肌的ＳＤＨ活性及Ⅰ类纤维数目,显著提高终板ＣｈＥ活性,线粒体结构恢复正常,运动终板突触前部囊泡丰富,突触间隙清晰,终板膜电子密度正常。表明慢性缺氧降低膈肌有氧氧化能力,影响其能量代谢及神经冲动的传递,从而减弱其收缩力,而参安治疗可改善缺氧造成的上述损害,为其临床应用提供了实验医学依据。     

Crystal Structures of the Human G3BP1 NTF2-Like Domain Visualize FxFG Nup Repeat Specificity

Ras GTPase Activating Protein SH3 Domain Binding Protein (G3BP) is a potential anti-cancer drug target implicated in several cellular functions. We have used protein crystallography to solve crystal structures of the human G3BP1 NTF2-like domain both alone and in complex with an FxFG Nup repeat peptide. Despite high structural similarity, the FxFG binding site is located between two alpha helices in the G3BP1 NTF2-like domain and not at the dimer interface as observed for nuclear transport factor 2. ITC studies showed specificity towards the FxFG motif but not FG and GLFG motifs. The unliganded form of the G3BP1 NTF2-like domain was solved in two crystal forms to resolutions of 1.6 and 3.3 Å in space groups P2₁2₁2₁ and P6₃22 based on two different constructs, residues 1–139 and 11–139, respectively. Crystal packing of the N-terminal residues against a symmetry related molecule in the P2₁2₁2₁ crystal form might indicate a novel ligand binding site that, however, remains to be validated. The crystal structures give insight into the nuclear transportation mechanisms of G3BP and provide a basis for future structure based drug design.     

Identification of potential miRNA biomarkers for traumatic osteonecrosis of femoral head

Traumatic osteonecrosis of femoral head (TONFH) is a common orthopedic disease caused by physical injury in hip. However, the unclear pathogenesis mechanism of TONFH and lacking of simple noninvasive early diagnosis method cause the necessity of hip replacement for most patients with TONFH. In this study, we aimed to identify circulating microRNAs (miRNAs) by integrated bioinformatics analyses as potential biomarker of TONFH. mRNA expression profiles were downloaded from the Gene Expression Omnibus database. Then we combined two miRNA screen methods: Weighted gene co-expression network analysis and fold change based differentially expressed miRNAs analysis. As a result, we identified 14 key miRNAs as potential biomarkers for TONFH. Besides, 302 target genes of these miRNAs were obtained and the miRNA–mRNA interaction network was constructed. Furthermore, the results of Kyoto Encyclopedia of Gene and Genome pathway analysis, Gene Ontology function analysis, protein–protein interaction (PPI) network analysis and PPI network module analysis showed close correlation between these 14 key miRNAs and TONFH. Then we established receiver operating characteristic curves and identified 6-miRNA signature with highly diagnosis value including miR-93-5p (area under the curve [AUC] = 0.93), miR-1324 (AUC = 0.92), miR-4666a-3p (AUC = 0.92), miR-5011-3p (AUC = 0.92), and miR-320a (AUC = 0.89), miR-185-5p (AUC = 0.89). Finally, the results of quantitative real-time polymerase chain reaction confirmed the significantly higher expression of miR-93-5p and miR-320a in the serum of patients with ONFH. These circulating miRNAs could serve as candidate early diagnosis markers and potential treatment targets of TONFH.     

蚂蚁筑巢对西双版纳热带森林土壤易氧化有机碳时空动态的影响

蚂蚁筑巢定居能够形成与巢穴周围显著不同的微生境和土壤养分环境,从而对土壤易氧化有机碳(EOC)产生重要影响.本研究以中国科学院西双版纳勐仑热带植物园白背桐群落为研究对象,比较蚂蚁巢地与非巢地土壤EOC时空分布特征,并分析蚂蚁筑巢引起土壤理化性质的改变对土壤EOC时空动态的影响.结果表明: 研究区蚁巢和非蚁巢地土壤EOC随月份均呈明显的单峰型变化规律,表现为6月>9月>3月>12月;土壤EOC沿土层呈逐渐降低的变化趋势,在0～5 cm土层,蚁巢土壤EOC显著大于非巢地,在5～10和10～15 cm土层的差异不显著.蚂蚁筑巢显著提高了土壤温度、土壤有机碳、土壤易氧化有机碳、土壤微生物生物量碳、全氮、硝态氮和水解氮含量,显著降低了土壤含水率和容重,但对铵态氮、pH值的影响不显著.土壤有机碳、土壤微生物生物量碳是调控蚁巢和非巢地土壤EOC时空变化的主要因子,土壤温度、含水率、全氮和硝态氮等土壤指标对土壤EOC的影响次之.蚂蚁筑巢主要通过改变微生境(土壤温度和水分)及土壤养分(主要是土壤有机碳和微生物生物量碳)的状况,进而调控热带森林土壤易氧化有机碳的时空动态.     

逆境胁迫下向日葵的耐受机制

向日葵作为我国五大油料作物之一,具有极高的食用价值和油用价值。向日葵在我国的种植分布集中在东北、西北和华北地区,时常面临着干旱、盐碱、温度和重金属胁迫的问题。主要综述了近年来向日葵面临的几种主要逆境胁迫的最新研究进展,以及在不同逆境胁迫下向日葵的耐受机制,并根据不同逆境胁迫筛选出了相应的抗逆向日葵品种,同时进行了生理差异和基因信息分析。通过阐明向日葵在逆境胁迫下的耐受机制,以期对向日葵高产育种及耐逆育种提供理论依据和指导方向。     

小细胞肺癌患者外周血淋巴细胞亚群分析

目的探究化疗对小细胞肺癌(small cell lung cancer,SCLC)患者免疫功能的影响。方法选择2013年1月到2018年12月我院收治的95例小细胞肺癌患者为研究对象。患者第一周期、第二周期化疗前采用流式细胞术检测患者外周血淋巴细胞亚群水平,分别按照不同疗效及不同化疗方案对患者外周血淋巴细胞亚群进行比较。结果(1)化疗后,95例患者CD3⁺、CD4⁺、CD8⁺细胞平均值增加,CD19⁺、γδT细胞平均值减少,差异均有统计学意义(均P<0.05)。(2)化疗后,部分缓解组患者CD3⁺、CD8⁺细胞平均值增加,CD19⁺细胞减少,差异有统计学意义(均P<0.05);病情稳定组和病情进展组患者各细胞水平无显著变化(均P>0.05)。(3)依托泊苷联合顺铂(EP)方案组化疗后患者CD3⁺、CD8⁺细胞平均值增多,CD19⁺细胞减少,差异均有统计学意义(均P<0.05);伊立替康联合顺铂(IP)方案和依托泊苷联合卡铂(EC)方案组化疗后患者各细胞水平无显著变化(均P>0.05)。结论化疗可以调节小细胞肺癌患者的免疫功能,增强细胞免疫,降低体液免疫,其中EC方案对患者细胞免疫的增强作用较为显著。     

RAB31 marks and controls an ESCRT-independent exosome pathway

Exosomes are generated within the multivesicular endosomes (MVEs) as intraluminal vesicles (ILVs) and secreted during the fusion of MVEs with the cell membrane. The mechanisms of exosome biogenesis remain poorly explored. Here we identify that RAB31 marks and controls an ESCRT-independent exosome pathway. Active RAB31, phosphorylated by epidermal growth factor receptor (EGFR), engages flotillin proteins in lipid raft microdomains to drive EGFR entry into MVEs to form ILVs, which is independent of the ESCRT (endosomal sorting complex required for transport) machinery. Active RAB31 interacts with the SPFH domain and drives ILV formation via the Flotillin domain of flotillin proteins. Meanwhile, RAB31 recruits GTPase-activating protein TBC1D2B to inactivate RAB7, thereby preventing the fusion of MVEs with lysosomes and enabling the secretion of ILVs as exosomes. These findings establish that RAB31 has dual functions in the biogenesis of exosomes: driving ILVs formation and suppressing MVEs degradation, providing an exquisite framework to better understand exosome biogenesis.Subject terms: Small GTPases, Endosomes, Multivesicular bodies, Lysosomes, ESCRT