苹果试管苗不定根起源及其发育状况的研究

利用光学和扫描电子显微镜观察结果表明,经琼脂生根培养基诱导产生的长富—2苹果 (Malus pumila Mill.) 试管苗的不定根起源于维管形成层。这种不定根发育不良,根表面缺乏根毛,内部解剖构造为典型的初生结构。为避免因不定根吸收、运输能力差而影响试管苗移栽成活,宜采用通透性良好的基质进行瓶内或瓶外生根,可诱导出优质不定根。     

柚木(Tectona grandis)无性系繁育及造林技术

柚木为马鞭草科柚木属植物,是世界上最珍贵的用材树种之一。文章介绍了柚木的生物学特性、无性繁殖即组培技术要点以及造林技术,论述了柚木在我省的推广前景。     

月季组织培养过程中的影响因素

综述了月季组织培养过程中的影响因素，重点介绍了植物生长调节剂、外植体、培养基和培养条件等对月季试管苗生长的影响。同时分析了月季组培影响因素研究中存在的不足，提出对多因素、复杂因子共同影响行为的研究和探讨是今后月季组培影响因素研究中的重点内容。     

苹果组培芽露地嫁接技术研究

提高苹果组培芽露地嫁接成活率的关键技术措施,主要有三个方面:培育壮芽,嫁接前对组培芽进行3至5天通风锻炼,增强其对外部环境条件的适应性;正确选择砧木及嫁接部位和方法,尽可能缩小砧穗间形态结构及木质化程度的差异,人为创造适宜的环境条件,搭棚遮荫避免阳光直射,适时灌水增加土壤及空气湿度,滴注激素促进接口愈合.本试验组培芽露地嫁接成活率达到93.3%,枝条最大月生长量为38厘米.     

Expression and modulation of connective tissue growth factor in renal interstitial fibrosis

CTGF, a member of the CCN family of immediate early genes, is a recently discovered profibrotic growth factor, which is involved in many pathophysiologic procedures. CTGF acts as a downstream effector of TGF-β acting on interstitial cells to enhance the progression of fibrotic renal diseases. It has been shown that CTGF gene expression can be induced or blocked by some kinds of cytokine and drugs. It is an interesting candidate target for future intervention strategies of renal interstitial fibrosis.     

贮藏中福桔果皮细胞结构的显微观察及果实理化成分测定

贮藏期间福桔果皮细胞始终具有分裂增殖能力,细胞生长的养分主要通过维管束向果肉吸取,因而促进果肉衰老,形成枯水.枯水果实在贮藏早期就发现果皮细胞层和油腔分泌细胞无丝分裂旺盛,双核细胞多,果皮增厚多.严重枯水时,果皮细胞还具细胞核、线粒体、有色体等超微结构,未枯水果实细胞分裂少见.经预贮后贮藏的果实,由于中断了果皮组织与维管束的联系,果皮细胞生长受抑制,果肉水分、养分消耗少,枯水率最低,     

In vitro expression and inhibition of procoagulant activity produced by bovine alveolar macrophages and peripheral blood cells

Local and systemic activation of coagulation is frequently associated with bacterial sepsis. The coagulopathy is due, at least in part, to expression of tissue factor (TF) by monocytes and macrophages. The purpose of this study was to evaluate the expression of procoagulant activity by bovine alveolar macrophages, leukocytes and platelets, and to determine the relative potency of three chemical inhibitors of TF expression (pentoxifylline, retinoic acid, and cyclosporin A). Bovine alveolar macrophages were stimulated with lipopolysaccharide (LPS) derived from Pasteurella haemolytica or recombinant bovine tumour nervous factor (TNF) and dose- and time-dependent effects on TF expression were studied. LPS and TNF induced TF expression in alveolar macrophages and LPS treatment of whole blood induced TF expression in mononuclear cells. Neutrophils and platelets also expressed procoagulant activity, but this activity was not inhibited by anti-bovine TF monoclonal antibody. Pentoxifylline (40 mol/L), retinoic acid (0.01 mmol/L) and cyclosporin A (0.08 mol/L) inhibited TF expression when added concurrently with LPS or TNF, but not when added 4 h after stimulation. TF mRNA was not detected in unstimulated alveolar macrophages by Northern blot analysis. In contrast, exposure to LPS or TNF for 6 h induced marked expression of TF mRNA, which was inhibited by treatment with pentoxifylline, retinoic acid and cyclosporin A. Expression of TNF by alveolar macrophages stimulated with LPS was also inhibited by these compounds. Our results indicate that procoagulant activity expressed by alveolar macrophages and monocytes is associated with expression of TF, whereas procoagulant activity expressed by neutrophils and platelets is not. The concentrations of pentoxifylline and retinoic acid necessary for inhibition of TF expression in vitro may not be achievable in vivo owing to their toxic effects. However, the in vitro concentration of cyclosporin A that inhibited TF expression did not exceed the plasma concentration observed in humans, and therefore may be useful for inhibition of TF expression in vivo.Abbreviations BAL bronchoalveolar lavage - LPS lipopolysaccharide - cDNA cloned deoxyribonucleic acid - cAMP cyclic adenosine monophosphate - GAPDH glyceraldehyde phosphate dehydrogenase - mRNA messenger ribonucleic acid - TF tissue factor - TNF tumour necrosis factor - DPBS Dulbecco's phosphate-buffered saline     

猕猴桃实生苗组织培养体系建立的研究

以饱满成熟的猕猴桃种子为起始材料,用 2. 5g·L-1赤霉素处理 5小时,再用次氯酸钠灭菌消毒后,将萌芽的种子接种到MS+蔗糖 20g·L-1 +肌醇 100mg·L-1和 0. 75%琼脂的培养基上,根、茎、叶生长表现良好,初步建立了猕猴桃实生苗组织培养体系。猕猴桃实生苗组织培养同利用茎段、茎尖组织培养一样,培养基中无须附加任何激素。     

红千层的离体培养及快速繁殖

 研究了红千层离体快繁的若干影响因素。结果表明: 叶片在MS + 6-BA 115 mg·L ^{- 1}+NAA015 mg·L ^{- 1}中的愈伤组织诱导率43% , 并可直接从愈伤组织表面分化出不定芽, 分化率为69.2%; 腋芽启动培养基为MS + 6-BA 1～1.5 mg·L ^{- 1} + NAA 0.5 mg·L ^{- 1} , 萌动率为77%; 继代和增殖培养基为MS + 6-BA 1 mg·L ^{- 1} +NAA 0.25 mg·L ^{- 1} , 平均增殖系数为16.7; 生根壮苗培养基为1 /2MS +NAA 0.25 mg·L ^{- 1} , 生根率96.1%; 试管苗生根培养30～35 d移栽, 成活率最高可达90%以上。