13种樟科植物叶油细胞和粘液细胞的分布和结构的比较研究

利用组织透明法、石蜡制片法和薄切片法比较研究了樟科５属１３种植物叶片中油细胞和粘液细胞的分布和结构．结果表明：５属１１种植物叶片中有油细胞分布,其形状多为圆形,体积较小且大小基本一致,ｄ３０～４５μｍ;４属８种植物叶片中有粘液细胞分布,其形状多为椭圆形,体积较大,ｄ６０～１００μｍ．根据透明叶片观察,不同植物油细胞的分布密度不同;从叶片横切面观察,有些种油细胞分布于整个叶肉中,有的分布于栅栏组织与海绵组织之间及海绵组织中,有的仅分布于栅栏组织内．粘液细胞有些种分布于整个叶肉,而有的仅分布于栅栏组织中．因此,叶片内油细胞的分布密度、油细胞和粘液细胞的分布位置及其大小在种与种之间存在明显的差异,此种结构特征具有分类学上的意义     

TS—303对未成熟油菜种子的子叶细胞中BL分布的影响

用胶体金免疫定位技术对未成熟油菜种子的子叶细胞中BL的定位研究结果表明，金颗粒除主要分布在细胞核外，细胞质中也有少量金颗粒标记，但液泡和细胞壁中没有观察到金颗粒存在外施TS-303可明显导致未成熟种子的子叶细胞核中金颗粒标记密度的大量增加，说明TS-303很可能只影响幼嫩组织的细胞核．     

Cu2+或表面活性剂AE对黄鳝肝损伤的超微结构观察

利用透射电镜研究了亚致死浓度的Cu^2 或表面活性剂AE(脂肪醇聚氧乙烯醚)对黄鳝肝细胞结构的损伤作用．观察发现，在ρ(Cu^2 )=4．5mg／L的污染环境中，黄鳝肝脏细胞核变形，染色质凝集，内质网囊泡化，细胞质中出现较多的溶酶体和过氧化物酶体；在ρ(AE)=4．0mg／L的表面活性剂污染下，黄鳝肝脏细胞核变形，内质网呈线状，溶酶体、过氧化物酶体体积大、数量多，部分细胞质解体，细胞中出现空腔甚至死亡．图版1参10     

植物耐受和解除重金属毒性研究进展

总结了植物细胞及分子水平对重金属耐性和解除其毒性的途径.植物通过避免增加细胞内敏感位点毒物浓度来解除重金属毒性.其途径主要有:一方面通过菌根化、细胞壁吸收及根系分泌物的螯合作用减少根系吸收重金属进入细胞质;另一方面通过体内调节机制解除重金属毒性和提高耐性,主要通过一系列膜蛋白对进入细胞质内的重金属排出细胞质外、隔离于液泡中,或将重金属转变为无毒性形态挥发入大气,或通过细胞质内的植物螯合素、金属硫蛋白、有机酸、氨基酸、多胺等对重金属螯合,解除重金属毒性;同时植物还可以在重金属胁迫下产生热休克蛋白修复胁迫伤害的蛋白质.本文提供了涉及植物重金属解毒和耐性广泛的观点和证据.     

Cd~(2+)对BY-2细胞的毒性机制及水杨酸的缓解作用

镉对生态环境的危害表现出对植物这种定生生物的毒害性。以绿色荧光蛋白(GFP)膜泡标记的烟草BY-2细胞为实验材料,分别在荧光显微镜和激光共聚焦显微镜下观察了Cd2+对植物细胞的毒害作用和机制,并研究了水杨酸(SA)处理对Cd2+植物细胞毒害的缓解作用。研究发现激光共聚焦显微镜可以观察到Cd2+处理3 h后细胞荧光亮度减弱,6 h时细胞皱缩和液泡缩小,9 h细胞大多死亡。在Cd2+胁迫同时加入SA,可显著提高细胞成活时间,荧光亮度增强、液泡化程度加大,同时能够观察到荧光标记的细胞膜包裹Cd2+的高荧光颗粒。SA处理的细胞还通过高度液泡化来缓解重金属Cd2+的毒性。结果表明具有生物活性的SA诱导细胞的液泡化,并通过膜成分对重金属的包裹和结合进一步降低了重金属对植物细胞的毒害。因此水杨酸缓解重金属对植物细胞的毒性,是通过诱导细胞的液泡化和膜对重金属离子的包裹束缚而实现的。     

姜黄素调控p53蛋白入核诱导骨髓瘤细胞凋亡

为探讨姜黄素对小鼠骨髓瘤细胞核内p53蛋白含量的影响及其凋亡作用,体外培养P3X63Ag8细胞,给予不同浓度姜黄素处理(0、10、20、30、40、50μmol/L)24 h,通过还原性辅酶Ⅰ氧化法测定乳酸脱氢酶(LDH)活性、Caspase3荧光分析试剂盒检测Caspase3活性的变化,采用2’,7’-二氯荧光黄双乙酸盐(DCFH-DA)法检测细胞活性氧(ROS)量的变化,利用Western-Blot技术检测细胞质与细胞核中p53蛋白的分布情况.结果显示,姜黄素浓度为20μmol/L时,P3X63Ag8细胞LDH活性极显著升高(P 0.01),并在40μmol/L组达到顶峰.30μmol/L姜黄素处理后,Caspase-3活性极显著提高(P 0.01),其余姜黄素处理组与未处理组相比未呈现显著变化.与阴性对照组相比,当姜黄素浓度为30μmol/L时细胞内活性氧水平显著上升(P 0.01),而随着姜黄素浓度提高到40和50μmol/L,细胞内活性氧水平均开始极显著下降(P 0.01),且高浓度组下降程度高于中浓度组.从细胞质和细胞核蛋白分离的试验结果可以看出,在细胞质蛋白中,p53蛋白含量随着姜黄素浓度的增加而降低,与此相反,细胞核蛋白中p53蛋白含量则呈现了上升趋势.因此,姜黄素通过调控LDH活性、Caspase-3活性以及活性氧水平来促进细胞损伤,从而抑制骨髓瘤细胞P3X63Ag8的增殖,促进其凋亡;在蛋白水平上促进p53蛋白入核,从而进一步刺激细胞凋亡程序的启动.(图4参25)     

Al~（3＋）对绿豆根生长和根类细胞核仁的影响

研究了不同浓度铝离子［ｃ（Ａｌ３＿）＝１０１，１０－２，１０－３，１０－４和平共处０－５ｍｏｌ／Ｌ）］对绿豆（ＰｈａｓｅｏｌｕｓｒａｄｉａｔｕｓＬ．）根生长及根尖细胞核仁的影响．结果表明：ｃ（Ａｌ３＋）在１０－３ｍｏｌ／Ｌ以上时对根生长和根尖细胞核仁都有着抑制作用．该仁受毒害后．核仁物质外溢细胞质内，严重时核仁物质几乎占据整个细胞质．该现象在分生组织细胞和根冠细胞中都可以观察到．     

适用于流式细胞术的三角褐指藻核DNA染色方法

为制备可用于配置有488 nm激发器的流式细胞仪检测核DNA含量的三角褐指藻细胞,取对数生长期的三角褐指藻细胞,分别采用70%乙醇、1%戊二醛、1%甲醛溶液进行细胞固定,经RNase A消化后的样品用碘化丙啶(PI)染色,用SYBR-green I对未经RNase A消化的细胞染色,在荧光显微镜下观察细胞染色情况,用流式细胞仪检测细胞核DNA含量.结果显示:在荧光显微镜下观察到,3种不同固定液固定的细胞均表现为SYBR-green I只对藻细胞核染色,PI对于藻的细胞核与细胞质均有着色.流式结果的DNA直方图显示,SYBR-green I染色的细胞的DNA直方图有明显的G1与G2/M峰,拟合度(RCS)在3左右,变异系数(CV)在8.6%左右.而PI染色细胞的DNA直方图表现为变异系数值偏大,拟合度较低,没有明显的G1与G2/M峰.本研究表明,SYBR-green I是一种无需对细胞进行RNase A处理,可应用于配置有488 nm激光器流式细胞仪的核酸染料,可为研究在整个细胞周期的调控机制奠定基础,同时也为其他浮游植物细胞核的染色提供参考.     

锌在长柔毛委陵菜细胞内的分布和化学形态研究

采用差速离心技术和化学试剂逐步提取法研究了Zn在长柔毛委陵菜(Potentilla grifithii Hook)叶片、叶柄和根系中的亚细胞分布和赋存形态。研究表明,细胞壁是Zn在长柔毛委陵菜细胞内的主要分布位点,其次是含核糖体的可溶部分和细胞核部分,而在叶绿体和线粒体的分布很少。叶片中,提高Zn处理水平,Zn向细胞壁和可溶部分的分配减少,而在细胞核部分的分配增加;叶柄中,提高Zn处理浓度增加了Zn在可溶部分的分配;根系中,Zn在各组分中的分配不受Zn浓度影响。在Zn赋存形态上,植物体内以氯化钠提取态和水提取态为主导形态;提高Zn处理水平,醋酸提取态的分配明显减少,水和乙醇两种提取态的分配增加;而其他形态Zn在植物体内的分配则很少。显示细胞壁和液泡是Zn在长柔毛委陵菜细胞内的重要结合位点,且可能主要与水溶性和酯溶性的有机配位体结合。     

镉在五节芒(Miscanthus floridulus)不同种群细胞中的分布及化学形态

通过营养液培养,以种子分别来自粤北大宝山矿区和惠州博罗非矿区的2个五节芒种群为试验材料,并采用差速离心技术和化学试剂逐步提取法,比较研究了Cd在2个种群根、茎和叶片中的亚细胞分布及化学形态.结果表明,五节芒2种群各部位的Cd主要富集在细胞壁和以液泡为主的可溶组分,在叶绿体、细胞核和线粒体中的分布较少;2种群根、茎、叶的亚细胞各组分Cd含量由高到低的次序均为:细胞壁组分(F1),可溶组分(F4),细胞核和叶绿体组分(F2),线粒体组分(F3).Cd在五节芒矿区种群根、茎、叶中的含量均显著高于非矿区种群.提高Cd处理质量浓度,对于非矿区种群,Cd在细胞壁(F1)和可溶组分(F4)的分配比例下降,在细胞核和叶绿体组分(F2)与线粒体组分(F3)的分配比例卜升;而对于矿区种群,Cd在细胞壁(F1)的分配比例上升,在可溶组分(F4)、细胞核和叶绿体组分(F2)与线粒体组分(F3)的分配比例下降,细胞壁对Cd的同持作用增强.五节芒2种群根中Cd的化学形态存在着明显差异:低Cd(5 mg·1-1)处理下,矿区种群根中的Cd以水提取态、氯化钠提取态和醋酸提取态为主,各占36.41%、28.15%和17.04%,其它形态所占比例较少;而非矿区种群根中的Cd以氯化钠提取态、水提取态和醋酸提取态所占比例较大,各占31.58%、23.15%和20.85%.提高Cd处理质量浓度,矿区种群根中的氯化钠提取态为优势形态,所占比例提高到41.29%,水提取态所占比例也提高到38.25%.其他提取态所占比例均有不同幅度下降;而非矿区种群根中氯化钠提取态Cd含量比例下降到21.45%,各化学形态的在分配比例上表现为平均化趋势.因此,细胞壁同持、可溶组分的液泡区隔化和向活性较弱的结合形态转移可能是五节芒矿区种群耐Cd的主要机制.     

Diatom Thalassiosira weissflogii in oligotrophic versus eutrophic culture: models and ultrastructure

Populations of marine diatom Thalassiosira weissflogii were grown in continuous cultures enriched with f/2 medium. One of the two contrasting cultures (‘eutrophic’) received 5.6 times more nutrients than the other (‘oligotrophic’). Two mathematical models are analyzed to estimate eutrophication differences. The second model based on the Michaelis–Menten uptake and Droop growth shows that cells in the eutrophic culture should have about 56% higher content of silica which is the limiting nutrient. Diatom samples were prepared for the transmission electron microscopy after cells have been kept in chemostats for 37 days. The structure of diatom cells was investigated and a comparison is made between cells grown in oligotrophic and eutrophic conditions. In eutrophic culture, dividing cells were encountered more frequently while cell concentration was approximately equal in both chemostats. The central vacuole of cells in eutrophic culture accumulated dispersed and compact material from amorphous to spherical shape. In some cells the large central vacuole had fibrilar and peppered dense materials in addition to translucent granules, vesicules and multivesicular bodies. In the cytoplasm we found increased number of multivesicular bodies, dense and lucent granules some of which enclose membrane particles and lucent vesicules. Dense material depositions observed in the vacuole are also seen in the cytoplasm associated with organelles, mitochondria and plasmalemma. Cells have well-developed, active and slightly increased number of dictyosomes (5–6). Some dictyosomes with dense secretory material in the cistern are apparently engaged in a granule formation process. Functional significance of dense material in the central vacuole, which has not been observed in cells grown in oligotrophic condition, is discussed.     

Ultrastructure of post-fertilization development in the red alga<Emphasis Type="Italic"> Callophyllis linearis</Emphasis> (Kallymeniaceae,Cryptonemiales, Rhodophyta)

The ultrastructure of post-fertilization development of the red alga Callophyllis linearis (Kyl.) Abb. & Norr. of the Kallymeniaceae showed that the Kallymeniaceae are more closely related to the Cryptomeniales than to the Gigartinales. The auxiliary cell produces multinucleate gonimoblast initials which divide to produce generative gonimoblast cells. These cells undergo repeated cleavages to form clusters of carpospore initials, which finally differentiate into carpospores. Carpospore differentiation is simple and occurs in three developmental stages. In the first stage, young carpospores are avacuolate, contain a large nucleus, have few undeveloped plastids and exhibit incipient dictyosome activity. During the intermediate stage, plastids develop their internal thylakoid system, starch granules are formed and dictyosomes continue to produce vesicles that contribute carpospore wall material. The formation of fibrous vacuoles originates from the fibrous vacuole associated organelles (FVAOs). In the final stage, mature carpospores form cored vesicles. They also contain well-developed plastids, fibrous vacuoles, numerous starch granules and are surrounded by a two-layered carpospore wall.Communicated by O. Kinne, Oldendorf/Luhe     

"川中岛"白桃雄性不育小孢子发育的细胞形态学

“川中岛”白桃是 2 0世纪 90年代初期从日本引进的优良晚熟品种 ,系日本长野县池田正元以“上海”ד白桃”杂交育种 .在生产中发现该品种花粉少、无发芽力 ,需配置授粉树 ,属于雄性败育品种[1～ 3 ] .关于“川中岛”白桃花粉败育的途径、机制尚未见报道 ;因此 ,对其小孢子发生发育细胞学特征进行观察研究 ,以揭示其雄性败育的途径 .1　材料与方法1.1　材料2年生盆栽”川中岛”白桃和对照品种庆丰 .1.2　方法为了避免早春低温等不适的环境因子对桃花器官发育造成不良的影响 ,试验在控制环境条件下进行 ,即在人工生长箱内对 2年生盆栽庆丰 …     

雨生红球藻不同形态细胞的超微结构研究

应用透射电镜观察比较雨生红球藻不同形态细胞的超微结构,结果表明,游动细胞除具有典型的绿藻门团藻目的特征性结构外,细胞壁与原生质体分离形成周质空间,细胞具有发达的可进一步发育的网状叶绿体,不动细胞除了无鞭毛,具厚壁外,它与游动细胞的主要不同是：细胞内的大部分区域被色素沉积物占据,叶绿体等细胞器被包裹,光合片层紧贴,早期的不动细胞还具有较大的线粒体,根据形态及超微结构上的差异,对红球藻游动细胞与不动细胞间的生理差异进行了解释。     

HaNPV多角体蛋白在宿主不同组织中的时相性表达

应用亲和凝胶过滤层析对多角体蛋白多克隆抗血清进行纯化,辣根过氧化物酶进行标记,用于ＥＬＩＳＡ法检测中肠、血淋巴、脂肪体中的多角体蛋白的含量变化．结果：中肠在感染２４ｈ含量最高,４８ｈ最低,７２ｈ较４８ｈ略有升高,９６ｈ和１２０ｈ与７２ｈ基本保持一致;血淋巴在感染４８ｈ含量最高,然后下降至９６ｈ,１２０ｈ又稍有升高;脂肪体在感染７２ｈ开始增加,直至１２０ｈ．三种组织中多角体蛋白含量变化并不同步．从表达的时相性看,与ＮＰＶ的感染过程基本一致,即从中肠至血腔再到脂肪体．免疫电镜观察表明,感染７２ｈ的中肠,在胞浆中合成的多角体蛋白此时已转运到细胞核中     

从绿色巴夫藻超微结构观察硒对锌毒性的保护效应

利用透射电镜研究绿色巴夫藻硒对锌毒性的保护效应 .从细胞超微结构特性比较对照和两个实验组 ,实验组 1培养基加入 15mgL-1Zn (ZnSO4·7H2 O) ,实验组 2培养基中加入 15mgL-1Se (Na2 SeO3 ·5H2 O)和 15mgL-1Zn .实验结果表明 ,在该浓度下单独加Zn ,藻细胞的叶绿体结构严重受损 ,而加入Se后可以阻止这种效应的产生 .藻细胞受Zn的影响 ,在细胞质和叶绿体基质中产生不同体积的电子致密的颗粒体 ,相反用Zn和Se处理的藻细胞则在液泡包含体中出现电子致密的颗粒体 .因此假设 :当单独加Zn时 ,藻细胞以形成电子致密的颗粒体的特殊分子形式分隔Zn ;而当形成锌硒化合物时 ,这一过程被阻止 ,此时Zn无活性 ,因而可保护细胞抵抗Zn的毒性 .图 3表 1参 2 8     

R-cells and the digestive cycle in Penaeus semisulcatus (Crustacea: Decapoda)

Shrimp, Penaeus semisulcatus, were collected from Kuwaiti waters in 1980, and the R-cells in the hepatopancreas were observed during the digestive cycle. During the first 12 h they absorb soluble material from the lumen of the gland and, subsequently, they take-up soluble and particulate material from the haemolymph. Within the cytoplasm, apical and basal systems of smooth endoplasmic reticulum are concerned with these processes. Pinocytosis only occurs at the basal cell membrane. The absorbed material is stored as lipid and glycogen, and copper, sulphur and other elements are accumulated in a large dense vacuole. These activities are integrated with those of the other cell types to effect the assimilation of food in the hepatopancreas. A scheme is proposed which accounts for the main processes of digestion. The hepatopancreas governs the duration of the digestive cycle, which takes at least 24 h. Observations on the nature of intracellular storage and waste products could be used to assess the dietary requirements of artificially reared shrimp.     

Oocyte development in the kuruma prawn Penaeus japonicus

Female kuruma prawns (Penaeus japonicus Bate) with undeveloped, early developing, developing, nearly ripe and ripe ovaries, were collected from Ise Bay, Japan, in 1984. Oocyte development of the kuruma prawn was classified into ten stages according to morphological characters, namely: (1) synapsis stage, (2) chromatin nucleolus stage, (3) early perinucleolus stage, (4) late perinucleolus stage, (5) oil globule Stage I, (6) oil globule Stage II, (7) yolkless stage, (8) yolk granule stage, (9) prematuration stage, and (10) maturation stage. The synapsis stage is a multiplication stage. The chromatin nucleolus stage, early and late perinucleolus stages are previtellogenesis and primary growth stages. Oil globule Stage I is an initial stage of primary vitellogenesis and secondary growth. Follicle cells on the oil globule Stage I oocytes expand rapidly and reach maximum size during oogenesis. Yolk granule stage oocytes are in the initial stages of secondary vitellogenesis. Strongly acidophilic yolk granules accumulate within basophilic vesicles of the cytoplasm. The yolk granules are first concentrated in the inner part of the cytoplasm, then gradually spread to the periphery. Cortical crypts, which are separated from the oocyte cytoplasm by the cytoplasmic membrane, are situated outside of oocyte cytoplasm. Germinal vesicle breakdown (GVBD) is initiated in the late phase of prematuration and continues until the late phase of maturation immediately prior to spawning. At the beginning of the maturation stage, the oocytes are ovulated, after which the nuclei further shrink and migrate out-wards. After ovulation, meiotic division of the ovarian oocyte progressed up to the metaphase of primary maturation division. Finally, the meiotic metaphase is visible just beneath the cytoplasmic membrane in the mature oocyte. Though ovulation is synchronous within the same ovary, GVBD is not completely synchronous. Ovulated mature oocytes have many club-shaped cortical crypts in the peripheral part of the cytoplasm and contain extensive accumulations of yolk granules dispersed throughout the cytoplasm. The apical end of the club-shaped cortical crypts and cytoplasmic membrane are coated by the vitellin envelope in the mature oocyte.     

Histochemical and ultrastructural characterisation of mantle storage cells in the hydrothermal-vent bivalve Bathymodiolus azoricus

This study reports on two types of storage cells that are present in the mantle connective tissue of the deep-sea mussel Bathymodiolus azoricus. One type corresponds to the adipogranular cells, a kind of storage cell previously described in other bivalves. In these cells extensive regions of the cytoplasm are filled with glycogen deposits and these zones became strongly stained after histochemical (PAS) or ultrastructural detection of polysaccharides. Several lipid droplets and membrane bound granules containing homogeneous electron-dense material are also present in adipogranular cells. A second type of cell contains large lysosomes in addition to numerous lipid droplets, but lacking cytoplasmic glycogen deposits. Due to these characteristics we named them adipolysosomal cells. They can be identified in semi-thin sections stained with PAS reaction because the lysosomes are the only positively stained structures. In the connective tissue of the mantle, some cells containing many lysosomes and a few lipid droplets were also observed. These cells differ from the adipolysosomal cells mainly because they have a reduced amount of lipid reserves, and could be an initial stage in the development of adipolysosomal cells. The vesicular connective tissue cells that in other Mytilidae are specialised in glycogen storage were not detected in B. azoricus. The reserves accumulated in the two types of storage cells described in B. azoricus may be important for the survival of these hydrothermal-vent bivalves if their nutrition is affected by a temporary loss or reduction of endosymbiotic bacteria due to sulphide and/or methane shortage caused by oscillations in vent activity.