BMP9经JNK激酶途径调控间充质干细胞C3H10T1/2成骨分化

为了证实JNK激酶在骨形态发生蛋白9(bone morphogenetic proteins 9,BMP9) 诱导间充质干细胞C3H10T1/2成骨分化中的作用,利用重组腺病毒将BMP9导入间充质干细胞C3H10T1/2. 通过碱性磷酸酶(ALP)活性测定、钙盐沉积实验、荧光素酶报告基因检测、Western印迹和组织化学染色等方法,检测BMP9是否可经JNK激酶途径调控间充质干细胞C3H10T1/2向成骨分化.动物实验验证在RNA沉默JNK蛋白激酶后,对BMP9诱导间充质干细胞C3H10T1/2向成骨分化的影响．结果发现,BMP9可以增强JNK 激酶的磷酸化;利用JNK抑制剂SP600125抑制JNK激酶活性后,BMP9诱导的间充质干细胞C3H10T1/2的早期成骨指标ALP活性和晚期指标钙盐沉积均受到抑制,而且经典SMAD信号的活化也相应受到抑制;RNA干扰沉默JNK基因表达后,同样也可抑制BMP9 诱导的C3H10T1/2细胞的ALP活性和裸鼠皮下异位成骨．因此表明,BMP9可活化JNK激酶途径从而诱导间充质干细胞C3H10T1/2向成骨分化．     

不同生境对藏东南地面生苔藓多样性和生物量的影响

为解析苔藓在藏东南森林生态系统中的重要生态作用, 以及森林干扰对林内地面生苔藓的影响, 该研究以藏东南色季拉山地面生苔藓植物为调查对象, 选取林分、坡向、坡度和地势组成等相似的7块100 m × 100 m的样地, 每块样地以林窗为中心, 在其东、南、西、北4个方向选取林窗、林缘和林下3种不同生境设置50 cm × 50 cm的样方, 每块样地共12个样方, 共计168个样方。通过对每个样方进行苔藓植物调查采集, 研究了西藏色季拉山苔藓多样性和不同生境条件下地面生苔藓单位面积生物量特征。主要结果: (1)研究区共有苔藓植物24科63属110种。其中, 优势科有8个, 分别是丛藓科、曲尾藓科、金发藓科、提灯藓科、真藓科、紫萼藓科、青藓科和灰藓科。苔藓各科分布规律明显, 曲尾藓科和真藓科广泛分布于各个海拔, 金发藓科、真藓科和提灯藓科分布在海拔3 700-4 300 m, 而丛藓科多分布在4 300 m以上。(2)林窗生境较林缘和林下复杂, 它干扰了苔藓物种组成和群落结构, 其苔藓种类最多、结构最复杂, 而林下的苔藓种类最少, 群落结构最简单。林窗地面生苔藓生物量最高, 其次为林缘, 林下苔藓生物量最低。(3)地面生苔藓生物量大小不仅受其物种组成、盖度、体形和群落结构的影响, 而且是众多因子共同作用的结果, 而非某一因子起主导作用。     

Two new species of Oxycera (Diptera, Stratiomyidae) from Ningxia, China

Two new speices, Oxycera rozkosnyisp. n. and Oxycera ningxiaensissp. n., are described from Liupanshan Nature Reserve, Ningxia Hui Autonomous Region, Northwest China. All essential diagnostic characters are figured and possible relationships of both taxa are briefly discussed, and a new key to species of Oxycera from China. The type specimens are deposited in the Institute of Entomology, Guizhou University, Guiyang (GUGC).     

MicroRNA expression profile of bronchioalveolar stem cells from mouse lung

Increasing evidence has suggested that bronchioalveolar stem cell (BASC) is the progenitor cells of lung cancer stem cells. However, the mechanisms by which self-renewal of BSACs is controlled and how BASCs turn into cancer stem cells still remains to be unknown. In the present study, we successfully isolated bronchioalveolar stem cells (BASCs) from mouse lung using FACS. These BASCs were characterized by clonal growth, self-renewal and high capacity for differentiation, suggesting that these BASCs are indeed stem cells. We investigated the microRNA (miRNA) expression profile of these BASCs using miRNA array and quantitative RT-PCR. We discovered that BASCs possessed a unique miRNA profile, with altered expression of several microRNAs, such as miR-142-3p, miR-451, miR-106a, miR-142-5p, miR-15b, miR-20a, miR-106b, miR-25, miR-486, in BASCs compared to control cells. Our results suggest that microRNAs might play important roles in maintaining the self-renewal capacity of BASCs, and suggest the intriguing possibility that aberrant expression of microRNAs could involved in turning BASCs into lung cancer stem cells.     

超声波对铜绿微囊藻超微结构和生理特性的影响

为了研究超声波对蓝藻细胞的影响,利用超声波（40W）处理200 mL铜绿微囊藻（Microcystis aeruginosa） 悬浮液20min,之后继续培养并于不同时间取样检测。检测悬浮藻细胞生物量发现其3d降低了97.84%;分别观察1、3、5d时沉降藻细胞超微结构变化,发现13d时细胞内脂质颗粒和藻青素颗粒增多、类囊体片层断裂、藻胆体脱落,5d时拟核区萎缩消失、细胞基础结构解体、胞质出现空洞、胞内结构颗粒降解;检测藻细胞光合放氧速率、叶绿素a （Chl.a）、超氧化物歧化酶（SOD）和过氧化氢酶（CAT）活性、膜透性以及跨膜ATP酶活性,发现光合放氧速率3d下降24.83%,Chl.a含量5d下降23.75%,超声组细胞SOD活性变化幅度比较大,但总体上活性降低,而CAT活性则表现为先增后减,活性始终大于对照组,同时胞内有机物渗出量增大,三种跨膜ATP酶活性（Na+/K+-ATPase、Mg2+-ATPase 和Ca2+-ATPase）均先升后降,并与膜透性变化相关。以上结果表明,超声波使铜绿微囊藻细胞沉降,并对其造成了胁迫,使部分藻细胞光合作用减弱,光合色素遭到损伤,细胞膜透性增大,甚至引起藻细胞程序性死亡。SOD活力的快速降低表明超声波使藻细胞内超氧离子（O2-）过量累积,从而对藻细胞造成氧化损伤,除此之外,超声波使藻细胞基础结构破坏、细胞内结构颗粒降解、细胞膜透性增大,这些都可能是致使部分铜绿微囊藻细胞死亡的重要原因。铜绿微囊藻细胞CAT以及跨膜ATP酶活性增大,表明藻细胞增强抗氧化酶活性以及离子调控和能量活动以抵御超声波的胁迫,而当胁迫随着时间减小后,细胞开始恢复生长和代谢,酶活力开始降低。       

脂肪酶非水相催化作用

从底物工程、介质工程、酶催化剂工程、构象工程等层面概述了提高非水相脂肪酶催化效率的方法.分别介绍了介质体系的优化与开发、脂肪酶催化剂的优化改良、催化过程的优化处理等新内容.指出在单层面优化的基础上,对非水相催化进行系统优化是必然趋势.     

The effect of the loading condition corresponding to functional shoulder activities on trabecular architecture of glenoid

There is little information on bone morphology as it relates to shoulder activities. This study investigated how loads corresponding to functional shoulder activities affect the trabecular architecture of the glenoid. Two different protocols were used. Protocol 1 investigated the material and morphological characteristics of the glenoid by analyzing digitized trabecular bone images obtained from 12 cadaver scapula specimens. Protocol 2 used a finite element analysis (FEA) to compute the principal stress trajectories acting within the glenoid. The principal stresses were derived for five loading conditions, which represent typical functional shoulder activities. The study showed that shoulder activity involved in carrying a light load makes the greatest contribution to the trabecular architecture compared with other shoulder activities considered in this study (p<0.05). With all of the activities considered in this study, the lateral region, particularly in the anterior and posterior portions, showed greater deviation and greater sensitivity to variation under loading conditions than did the other regions (p<0.05). These results suggest that owing to the extra sensitivity of the anterior and posterior parts of the lateral region, these regions may be more informative in the analysis of the trabecular architecture following shoulder musculoskeletal injuries. These results may provide essential design information for shoulder prostheses and contribute to an understanding of morphological changes resulting from injury.     

A post-burst after depolarization is mediated by group i metabotropic glutamate receptor-dependent upregulation of Ca(v)2.3 R-type calcium channels in CA1 pyramidal neurons

Activation of group I metabotropic glutamate receptors (subtypes mGluR1 and mGluR5) regulates neural activity in a variety of ways. In CA1 pyramidal neurons, activation of group I mGluRs eliminates the post-burst afterhyperpolarization (AHP) and produces an afterdepolarization (ADP) in its place. Here we show that upregulation of Ca(v)2.3 R-type calcium channels is responsible for a component of the ADP lasting several hundred milliseconds. This medium-duration ADP is rapidly and reversibly induced by activation of mGluR5 and requires activation of phospholipase C (PLC) and release of calcium from internal stores. Effects of mGluR activation on subthreshold membrane potential changes are negligible but are large following action potential firing. Furthermore, the medium ADP exhibits a biphasic activity dependence consisting of short-term facilitation and longer-term inhibition. These findings suggest that mGluRs may dramatically alter the firing of CA1 pyramidal neurons via a complex, activity-dependent modulation of Ca(v)2.3 R-type channels that are activated during spiking at physiologically relevant rates and patterns.