家兔精子膜蛋白rsp10基因的克隆和特征分析

 sp10基因在精卵识别过程中起着重要作用 .从家兔睾丸cDNA文库中克隆了家兔的sp10基因 (rsp10 ) ,cDNA序列全长 12 82bp ,包含 10 0 5bp开放阅读框 .由开放阅读框推测出的氨基酸序列与人、狒狒、狐和小鼠的SP10氨基酸序列之间存在较高水平的同源性 ,同源性分别为 70 %、69%、68%和 61% .在大肠杆菌中表达rsp10基因 ,获得重组rSP10 .用重组rSP10免疫雌性母兔 ,得到rSP10专一性多抗 .对精子膜蛋白进行免疫印迹分析发现 ,rsp10基因在家兔睾丸中的表达呈现多态性 .rsp10基因在GenBank的登录号为 :AF2 51558.     

一个可能引起歧义的概念——“条件致病菌”辨析

"条件致病菌"是国内医学微生物学教材中普遍应用的一个基本概念,但此概念在建立与应用中都存在明显缺陷,其使用可能对医学学生理解"人体共生微生物群落"与"机会性感染"等重要的医学基础理念造成误解与歧义。谨就此提出一些粗浅的认识与观点,希望通过同行间切磋,就此建立更完善的概念与更合理的表述。     

Use of silicone fluids in studies of cellular amino acids

In numerous cellular studies, cells labeled with radioisotopes have been separated from the labeling medium by an aqueous solution in order to determine the quantity of internalized labels; however, the aqueous wash tends to remove significant labeling from the cells. Therefore, in order to preserve all of the internalized labels, non-aqueous medium such as silicone fluids may be used. The termination of the labeling is achieved in the silicone method when, upon centrifugation, the cells separate from the medium and enter the silicone fluid to sediment to the tube bottom. This sedimentation of cells placed above a layer of silicone fluid exhibits a critical dependence on the centrifugal force, and gives rise to an uncertainty of only 2 s in determining the time of separation of cells from the medium using General Electric F-50 silicone fluid and a modified Beckman J2-21 centrifuge. It is therefore possible to determine the kinetics of incorporation of labeled amino acids into intracellular pools and proteins. In particular, since this silicone wash method determines the size of the total pool and the aqueous wash method determines the size of the acid-extractable pool, the simultaneous measurements of the size of both pools leads to the determination of the kinetics of labeling of the free amino acid pool. Among many possible applications and extensions of these methods, the studies of formation of intracellular pools and relations among different pools of transported molecules, such as water and amino acids, appear promising.     

贵州六盘水发现东阳江麝鼩

在贵州省六盘水市杨梅乡慕尼克村,利用陷阱法捕捉到3号麝鼩属(Crocidura)标本。本次采集标本的体形较小,头体长(49.0 ± 0.8)mm,尾长[(41.8 ± 4.2)mm]略短于头体长(尾长/头体长为85%)。背毛呈浅灰褐色,腹毛颜色浅于背毛,呈灰色。尾部双色,背侧黑褐色,腹侧淡于背侧。前足背部白色,后足则为淡灰色。尾近乎裸露,尾基约1/3着生稀疏白色长毛。颅全长(15.92 ± 0.55)mm,脑颅高(4.75 ± 0.18)mm。上门齿1枚,有一长而大的前尖和一小而矮的后尖。上单尖齿3枚,第1单尖齿最大,第2单尖齿略大于第3单尖齿,1枚第四前臼齿(P4),3枚臼齿。上述特征与东阳江麝鼩(C. dongyangjiangensis)模式标本的描述和鉴定特征基本一致,因此将3号采集标本鉴定为东阳江麝鼩。基于Cyt b基因进行分子系统发育分析,采集标本与麝鼩属物种中的东阳江麝鼩遗传距离最近,在0.004 ~ 0.027之间。系统发生树显示,3号标本与东阳江麝鼩构成一个单系进化分支,进一步证实本次采集的3号标本是东阳江麝鼩,为贵州省分布新记录种。     

串叶松香草的核型研究

串叶松香草Silphiura perfoliatum L.系菊科(Compositae)松香草属(SilphiumL.)多年生宿根草本植物,原产北美洲。1979年由中国科学院植物研究所北京植物园首次从朝鲜引进我国,1980年引种我所栽培,通过几年的试验观察表明:串叶松香草是一种高产、质优、适应性强的饲料作物,近年来,我省广泛发展和应用。据文献报     

海南省常见植物根围巨孢霉目丛枝菌根真菌

报道了从海南岛常见植物根围土壤中分离获得的巨孢霉目丛枝菌根真菌23种,分别属于Gigaspora、Scutellospora、Dentiscutata、Racocetra、Quatunica、Cetraspora等6个属,其中Dentiscutata hawaiiensis和Dentiscutata nigerita为中国新记录种。     

蚁蛉生物学研究进展

蚁蛉科Myrmeleontidae昆虫的幼虫俗称蚁狮,我国古人很早就将其入药,是一种具有良好开发利用前景的药用昆虫。文章对蚁蛉分类学、生物学、人工饲养、药用价值和杀虫活性物质分离等方面的研究进行综述,以期较全面了解蚁蛉的研究进展,为进一步研究、开发和利用蚁蛉提供参考。     

近自然化改造对马尾松和杉木人工林生物量及其分配的影响

近自然化改造作为森林新增碳汇的最有希望的选择之一,将如何通过改变林分结构影响林分生物量和生产力进而影响林分固碳能力和潜力目前尚不清楚,因此,了解近自然化改造对人工林生物量及其分配的影响,对人工林生态系统碳管理具有重要意义。以马尾松近自然化改造林(P(CN))、马尾松未改造纯林(P(CK))、杉木近自然改造林(C(CN))和杉木未改造纯林(C(CK))4种人工林为研究对象,采用样方调查和生物量实测的方法,分析4种林分生物量差异,旨在揭示近自然化改造对马尾松和杉木人工林生物量及其分配的影响。结果表明:马尾松杉木人工林近自然化改造通过调整林分结构显著提升马尾松和杉木人工林生物量和生产力,8a后马尾松和杉木林分生物量分别增加46.71%和37.24%。乔木层生物量在林分生物量总量中占主导地位(95.48%-98.82%),并对林分生态系统总生物量变化起决定性作用。林分生物量和生产力的增加主要因为近自然化改造改变了林分群落结构,进而提高了乔木层生产力。研究结果表明,合理的经营措施不仅可以改善林分结构,提升林分生产力,并可为增强植被固碳能力创造有利条件。     

CCL5/CCR5 axis promotes the motility of human oral cancer cells

CCL5 (previously called RANTES) is in the CC‐chemokine family and plays a crucial role in the migration and metastasis of human cancer cells. On the other hand, the effect of CCL5 is mediated via CCR receptor. RT‐PCR and flow cytometry studies demonstrated CCR5 but not CCR1 and CCR3 mRNA in oral cancer cell lines, especially higher in those with high invasiveness (SCC4) as compared with lower levels in HSC3 cells and SCC9 cells. Stimulation of oral cancer cells with CCL5 directly increased the migration and metalloproteinase‐9 (MMP‐9) production. MMP‐9 small interfering RNA inhibited the CCL5‐induced MMP‐9 expression and thereby significantly inhibited the CCL5‐induced cell migration. Activations of phospholipase C (PLC), protein kinase Cδ (PKCδ), and NF‐κB pathways after CCL5 treatment was demonstrated, and CCL5‐induced expression of MMP‐9 and migration activity was inhibited by the specific inhibitor of PLC, PKCδ, and NF‐κB cascades. In addition, migration‐prone sublines demonstrate that cells with increasing migration ability had more expression of MMP‐9, CCL5, and CCR5. Taken together, these results indicate that CCL5/CCR5 axis enhanced migration of oral cancer cells through the increase of MMP‐9 production. J. Cell. Physiol. 220: 418–426, 2009. © 2009 Wiley‐Liss, Inc.     

PML/RARalpha fusion protein mediates the unique sensitivity to arsenic cytotoxicity in acute promyelocytic leukemia cells: Mechanisms involve the impairment of cAMP signaling and the aberrant regulation of NADPH oxidase

Acute promyelocytic leukemia (APL) cells are characterized by PML/RARalpha fusion protein, high responsiveness to arsenic trioxide (ATO)-induced cytotoxicity and an abundant generation of reactive oxygen species (ROS). In this study we investigated the association among these three features in APL-derived NB4 cells. We found that NADPH oxidase-derived ROS generation was more abundant in NB4 cells compared with monocytic leukemia U937 cells. By using PR9, a sub-line of U937 stably transduced with the inducible PML/RARalpha expression vectors, we attributed disparities on ROS generation and ATO sensitivity to the occurrence of PML/RARalpha fusion protein, since PML/RARalpha-expressing cells appeared higher NADPH oxidase activity, higher ROS level and higher sensitivity to ATO. On the other hand, the basal intensity of cAMP signaling pathway was compared between NB4 and U937 as well as between PR9 cells with or without PML/RARalpha, demonstrating that PML/RARalpha-expressing cells had an impaired cAMP signaling pathway which relieved its inhibitory effect on NADPH oxidase derived ROS generation. In summary, the present study demonstrated the correlation of PML/RARalpha with cAMP signaling pathway, NADPH oxidase and ROS generation in APL cells. PML/RARalpha that bestows NB4 cells various pathological features, paradoxically also endows these cells with the basis for susceptibility to ATO-induced cytotoxcity.