Regulation of fibronectin and laminin binding activity in cultured human lymphoblastic cell lines

The current study shows that a clonal derivative of the Jurkat cell line up-regulates both the avidity and density of the α 6/β1 receptor in response to phorbol 12-myristate 13-acetate (PMA). This derivative attaches to fibronectin and, to a lesser degree, laminin constitutively. Adhesion and spreading are dramatically up-regulated following treatment with PMA. The response on fibronectin peaks within 4 hours, is insensitive to cyclohexaminde, can be blocked by monoclonal antibodies (Mabs) to the β1 and α 5 subunits of the β1 family of integrins, and is not associated with increased expression of the α 5 or β1 epitopes at the cell surface. In contrast, the response on laminin is biphasic. The early phase parallels the response on fibronectin. The second phase peaks after 48–72 hours of treatment with PMA, is sensitive to cycloheximide, can be blocked by Mabs to the β1 and α 6 subunits, and is associated with increased expression of the α 6 epitope. Both the density independent and dependent responses to PMA in Jurkat cells are blocked by the protein kinase inhibitor staurosporine. The HSB-2, CEM, Molt-4, and HPB-ALL T-lymphoblastic cell lines also up-regulate attachment to fibronectin and laminin following treatment with PMA. All four lines constitutively attach to fibronectin and show rapid up-regulation of attachment following treatment with PMA. None of the lines attach to laminin prior to PMA treatment; however, specific adhesion developed after 4–120 hours of treatment. The most mature lines (Jurkat and HPB-ALL) up-regulated adhesion on laminin more rapidly than the less phenotypically mature lines (CEM, Molt-4, and HSB-2). In summary, clonal derivatives of the Jurkat cell line up-regulated attachment to laminin through protein kinase dependent increases in α /β1 receptor avidity and density. In addition, the expression of functional receptors for laminin is linked to developmental maturity in a series of T-lymphoblastic cell lines. © 1993 Wiley-Liss, Inc.     

异色瓢虫若虫对麦三叉蚜的捕食作用

研究表明,异色瓢虫高龄若虫捕食麦二叉蚜的功能反应为ＨｏｌｌｉｎｇⅡ型反应,喜好捕食低龄若蚜;在４０℃下捕食率最低,１０℃次之,２５℃最高．在１０～２５℃内捕食率ｙ与温度ｘ的关系为ｙ＝２８．１３０３＋２．６６６５ｘ,在２５～４０℃内为ｙ＝１９９．９２７５－３．６４２ｘ;在种内干扰条件下,其捕食作用率Ｅ与开敌密度Ｐ的关系为Ｅ＝０．６８９７Ｐ－０．７９３０,搜索常数Ｑ为０．６８９７,干扰系数ｍ为０．７９３０;其分摊竞争强度Ｉ与异色瓢虫密度Ｐ的关系为Ｉ＝０．０４００＋１．０３８３ｌｏｇＰ．     

聚羟基脂肪酸酯的应用展望

聚羟基脂肪酸酯(Polyhydroxyalkanoates,简称PHA)是由微生物合成的天然高分子基材料,作为微生物碳源和能源的储备物质。目前,PHA的单体种类有150多种,致使PHA的品种繁多、材料学性质各不相同。PHA具有材料多变性、非线性光学性能、压电性能、气体阻隔性能、热塑性、生物可降解性、良好的生物相容性等特点,使其在塑料包装、化工、医药、农业、生物能源等诸多领域的具有很大的应用前景。文中系统介绍了目前PHA的应用和未来的发展。     

棉田动物群落动态及天敌与害虫种群之间的关系

通过对棉田动物群落动态及天敌与害虫种群之间关系的系统研究,得出：l）棉田生物多样性指数越大,群落稳定性越高;2）龟纹瓢虫与棉蚜种群数量之间极相关,草间小黑株与棉蚜种群之间有相关关系,棉蚜及龟纹瓢虫种群增长为指数增长;3）棉蚜及其多种天敌在水平分布上均为聚集格局;4）棉蚜、龟纹瓢虫及草间小黑蛛在垂直分布上均为聚集格局,龟纹瓢虫对棉蚜聚集场所具有追随跟踪攻击作用．     

异色瓢虫若虫的限域搜索行为

在Ｎａｋａｍｕｔａ装置中,通过对两种我照照条件下（强光照３６８０－４６２０ｌｘ,弱光照１３０－２２０ｌｘ）异色标虫若虫搜索麦蚜行为轨迹的研究,得出摄食麦蚜前后０－１５ｓ搜索行为轨这弯曲角度总和之间差异均显著,摄食后大于摄前;摄食麦蚜前后０－１５ｓ、１５－３０ｓ、３０－４５ｓ、４５－６０ｓ内的各对应停点间距离差异均显著,摄食前大于摄食后;其搜索速度,摄食前显著大于摄食后。     

泥河湾盆地三棵树遗址ESR年代学

泥河湾盆地因发育良好的晚新生代湖相地层、丰富的旧石器遗址和哺乳动物化石而广受关注.盆地内已发现旧石器遗址100余处,被学术界称为"东方奥杜韦(Olduvai)峡谷".由于缺乏合适的年代测定方法,许多重要的遗址,尤其是中更新世时间段的遗址缺乏年龄数据,如三棵树遗址,使得旧石器遗址研究少了时间轴合理的年代学框架.电子自旋共...     

天敌对麦长管蚜和麦二叉蚜种群数量影响程度的分析

通过对１９９３～１９９６年两种麦蚜种群数量及其天敌数量的系统调查,并采用灰色关联分析法,研究各种天敌对两种麦蚜种群数量的影响程度,得出对麦长管蚜种群数量影响最大的是龟纹瓢虫、蚜茧蜂和食蚜蝇;对麦二叉蚜种群数量影响最大的是草间小黑蛛,其次是龟纹瓢虫．     

GoFigure: automated Gene Ontology annotation

SUMMARY: We have developed a web tool to predict Gene Ontology (GO) terms. The tool accepts an input DNA or protein sequence, and uses BLAST to identify homologous sequences in GO annotated databases. A graph is returned to the user via email. AVAILABILITY: The tool is freely available at: http://udgenome.ags.udel.edu/frm_go.html/     

药用植物栀子的组织培养

栀子(Gardenia jasminoides)为药用木本植物。以栀子果皮、种子团和种子为外植体,研究不同激素配比及不同培养方式对愈伤组织诱导和芽分化的影响。研究结果表明,培养基成分为MS+0.5 mg·L–12,4-D+0.25 mg·L–16-BA较适宜果皮和种子愈伤组织的诱导,诱导率分别为83.3%和88.5%;培养基成分为MS+1.0 mg·L–12,4-D+1.0 mg·L–16-BA较适宜种子团愈伤组织的诱导,诱导率为78.1%。3种外植体诱导的愈伤组织中,只有种子愈伤组织能通过液体培养分化出芽;TDZ对芽分化有明显的促进作用;最佳的芽分化培养基为MS+0.05 mg·L–1NAA+0.10 mg·L–1TDZ,其愈伤组织分化率为8.75%。该研究以栀子种子为外植体,并获得了再生植株,为药用植物栀子转基因体系的建立奠定了基础。     

Design,synthesis and biological evaluation of artemisinin derivatives containing fluorine atoms as anticancer agents

Ten novel artemisinin derivatives containing fluorine atoms were synthesized and their structures were confirmed by ¹H NMR, ¹³C NMR and HRMS technologies in this study. The in vitro cytotoxicity against U87MG, SH-SY5Y, MCF-7, MDA-MB-231, A549 and A375 cancer cell lines was evaluated by MTT assay. Compound 9j was the most potent anti-proliferative agent against the human breast cancer MCF-7 cells (IC₅₀?=?2.1?μM). The mechanism of action of compound 9j was further investigated by analysis of cell apoptosis and cell cycle. Compound 9j induced cell apoptosis and arrested cell cycle at G1 phase in MCF-7 cells. Our promising findings indicated that the compound 9j could stand as potential lead compound for further investigation.