细叶黄芪叶肉原生质体发育早期几种细胞器的变化

在细叶黄芪叶肉原生质体发育早期,细胞器的变化较大。离体培养４ｈ后,线粒体的嵴和基质物质开始增加。培养３－５天后,线粒体的数量增加５倍以上,此时可见大部分线粒体围绕细胞核分布。,在培养２４ｈ后,高尔基体开始发育,它们主要分布在细胞质周边区域。多糖细胞化学染色表明,高尔基体内沉积着大量嗜银物质。培养１天后,粗面内质网开始发育。培养３天时,部分叶绿体边缘出现一些空隙结构。随着叶绿体内膜结构的消失,淀粉粒     

大豆种子萌发过程中线粒体的发生和发育

从萌发一天的大豆种子中用蔗糖密度梯度离心,不能分离出线粒体,种子萌发两天后,线粒体才开始出现,然后迅速增长。电镜和线粒体标记酶(细胞色素C氧化酶)分析,也证明萌发一天的种子细胞中既不能见到线粒体的结构,也检测不出线粒体酶的活性。种子萌发第2天到第6天线粒体量成百倍地增加,但很少见到线粒体的分裂相,似乎说明线粒体主要不是依靠分裂增殖的。线粒体本身也有一个发育过程,萌发第2天的种子中线粒体结构简单,只有网状膜系统和较大的基质区,萌发第3～4天就开始出现嵴膜,基质区缩小,至第5～6天嵴膜密集,基质区更小,线粒体的出现似乎和氧供应有关,因为线粒体是在种皮破裂的同时出现的。高等植物线粒体在个体发育中似乎并非连续存在,主要也不是以自我分裂方式繁殖,因此推测原质体作为未分化的细胞器既是叶绿体的前体,也是线粒体的前体。     

向日葵幼叶及其培养的愈伤组织细胞的超微结构研究

通过超微结构的观察,向日葵幼叶及其经培养后10天的愈伤组织细胞之间有明显区别。叶肉细胞的细胞质、细胞器及核的结构和发育都比较完整。当外植体组织发生变化和愈伤组织形成时,观察到线粒体相互连接成链状围绕在叶绿体周围,而叶绿体有的围绕在核的周围;线粒体的嵴和基质,叶绿体的基粒和片层结构常发生退化或解体,细胞质稀薄,核糖体和胞质凝成线状或网状,微体和高尔基体消失,液泡化程度高并含有较多的次生物质;而细胞核在后期才发生明显变化,轮廓不够清晰。     

NaCl对小麦幼苗叶肉细胞超微结构的影响

在含NaCl的培养液中培养小麦幼苗,3天后取样观察叶肉细胞,其超微结构基本正常,细胞核和细胞壁没有明显变化。但线粒体结构普遍受到损害,表现在外膜、内膜和嵴膨胀,结构模糊。叶绿体被膜和片层结构仍保持完整,仅有部分叶绿体的片层排列方向发生改变,由原来平行排列扭转为近于垂直排列。     

Na+和Cl- 在小麦叶肉细胞超微结构中的分布

小麦经200mmol NaCl溶液培养3天后,采用改进的焦锑酸钾方法对叶肉细胞中Na~+及Cl~-进行超微结构定位。电镜观察及电子探针X-射线显微分析表明,Cl~-主要分布在细胞间隙、细胞壁及细胞质膜中。用电子探针X~-射线能谱仪在这些部位中未探测出Na~+,提示Cl~-比Na~+更多地进入小麦的叶肉细胞。此外,在叶肉细胞的细胞核、线粒体及叶绿体中也可见到离子沉淀颗粒。经氯化钠溶液培养的小麦幼苗,其叶肉细胞的叶绿体、线粒体的超微结构受损,植株生长受到抑制。     

Na+和Cl-在小麦叶肉细胞超微结构中的分布

小麦经200mmol NaCl溶液培养3天后,采用改进的焦锑酸钾方法对叶肉细胞中Na⁺及Cl^-进行超微结构定位。电镜观察及电子探针X-射线显微分析表明,Cl^-主要分布在细胞间隙、细胞壁及细胞质膜中。用电子探针X~-射线能谱仪在这些部位中未探测出Na⁺,提示Cl^-比Na⁺更多地进入小麦的叶肉细胞。此外,在叶肉细胞的细胞核、线粒体及叶绿体中也可见到离子沉淀颗粒。经氯化钠溶液培养的小麦幼苗,其叶肉细胞的叶绿体、线粒体的超微结构受损,植株生长受到抑制。     

干旱胁迫对红松幼苗针叶超微结构的影响

在土壤逐渐失水和PEG溶液模拟的两种不同形式的干旱胁迫下,红松幼苗针叶细胞中叶绿体和线粒体超微结构的变化呈现出显著的差异。在土壤干旱胁迫下,叶绿体的片层结构发生严重的扭曲并在中央部分形成电子密度较高的黑色团块物质。PEG模拟的干旱胁迫下,叶绿体肿胀,空泡化明显,但在叶绿体的中央没有黑色团块物质的形成。在土壤干旱胁迫后,线粒体的膜结构仍然完整清晰,基质比胁迫前更为浓厚,而PEG溶液的干旱胁迫下,线粒体的数量增多,嵴明显减少,基质变得十分稀薄。可见两种不同方式的干旱胁迫处理下,细胞结构的损伤机制及损伤后产生的生理意义并不完全相同。     

缺铁对黄瓜叶肉细胞超微结构及某些形态的影响

利用透射电镜,对缺铁黄瓜幼叶肉细胞的超微结构及植株的某些形态学进行了观测,发现缺铁后的幼叶细胞内首先受到影响的细胞器是叶绿体,其次是线粒体,细胞核、内质网结构完好。幼苗缺铁20天后, 大部分叶绿体的基粒片层和间质片层受到了严重的破坏。少量线粒体出现空泡化倾向,植株在形态学上表现为幼苗长势衰弱,叶色发黄、叶绿素含量下降。     

低温对桂花‘状元红’叶肉细胞超微结构的影响

为探讨北引桂花(Osmanthus fragrans)在低温胁迫下叶肉细胞超微结构的变化,揭示桂花于低温胁迫下细胞结构变化规律,该研究以3年生桂花品种‘状元红’(O.fragrans‘Zhuangyuan Hong’)为试材,分别于一系列低温下处理,经制样切片后,用透射电子显微镜观察叶肉细胞超微结构的变化。结果表明:常温(20~25°C)处理时,各细胞器超微结构正常;5°C低温处理时,叶绿体有轻微膨大现象,线粒体结构正常;0°C处理时叶绿体内嗜锇体增多,叶绿体肿胀加剧,线粒体数量增加,淀粉粒出现亮暗相间的轮纹;–10°C处理时,细胞器降解。在同一低温胁迫下不同细胞的叶绿体敏感程度不同,这为遭受低温后植株的恢复生长提供了细胞学基础。叶肉细胞中叶绿体、线粒体、细胞核的稳定性可作为桂花对低温响应的重要参考指标。     

La3+对墨兰根状茎某些细胞器发育的影响

以１／２ＭＳ＋ＢＡ（１ｍｇＬ－１）＋ＮＡＡ（１ｍｇＬ－１）＋Ｌａ３＋（１０ｍｇＬ－１）培养墨兰根状茎３０ｄ后,取样观察根状茎细胞叶绿体、线粒体和细胞核的发育特点并与对照进行比较,发现：①处理组叶绿体发育较快,有较丰富的片层结构和嗜锇颗粒,而对照组的发育慢,含大型的淀粉粒,无明显的片层结构．②处理组线粒体体积较大,内含物较丰富,而对照组的较小,内含物较少。③处理组细胞核内的染色质较对照组丰富．上述结果表明,ｔａ３＋对墨兰根状茎细胞器的发育有一定的调节作用。     

THE EFFECTS OF ENUCLEATION ON THE CYTOPLASMIC MEMBRANES OF AMOEBA PROTEUS

The dependence of cytoplasmic membranes upon the nucleus was studied by examining enucleated amebae with the electron microscope at intervals up to 1 wk after enucleation. Amebae were cut into two approximately equal parts, and the fine structure of the enucleated portions was compared with that of the nucleated parts and starved whole cells which had been maintained under the same conditions. Golgi bodies were diminished in size 1 day after enucleation and were not detected in cells enucleated for more than 2 days. The endoplasmic reticulum of enucleated cells appeared to increase in amount and underwent changes in its morphology. The sparsely scattered short tubules of granular endoplasmic reticulum present in unmanipulated amebae from stock cultures were replaced in 1–3-day enucleates by long narrow cisternae. In 3–7-day enucleates, similar cisternae of granular endoplasmic reticulum encircled areas of cytoplasm partially or completely. It was estimated that in most cases hundreds of these areas encircled by two rough membranes were formed per enucleated cell. The number of ribosomes studding the surface of the endoplasmic reticulum decreased progressively with time after enucleation. In contrast, the membranes of nucleated parts and starved whole cells did not undergo these changes. The possible identification of membrane-encircled areas as cytolysomes and their mode of formation are considered. Implications of the observations regarding nuclear regulation of the form of the Golgi apparatus and the endoplasmic reticulum are discussed.     

LYSOSOMES AND GERL IN NORMAL AND CHROMATOLYTIC NEURONS OF THE RAT GANGLION NODOSUM

The rat ganglion nodosum was used to study chromatolysis following axon section. After fixation by aldehyde perfusion, frozen sections were incubated for enzyme activities used as markers for cytoplasmic organelles as follows: acid phosphatase for lysosomes and GERL (a Golgi-related region of smooth endoplasmic reticulum from which lysosomes appear to develop) (31–33); inosine diphosphatase for endoplasmic reticulum and Golgi apparatus; thiamine pyrophosphatase for Golgi apparatus; acetycholinesterase for Nissl substance (endoplasmic reticulum); NADH-tetra-Nitro BT reductase for mitochondria. All but the mitochondrial enzyme were studied by electron microscopy as well as light microscopy. In chromatolytic perikarya there occur disruption of the rough endoplasmic reticulum in the center of the cell and segregation of the remainder to the cell periphery. Golgi apparatus, GERL, mitochondria and lysosomes accumulate in the central region of the cell. GERL is prominent in both normal and operated perikarya. Electron microscopic images suggest that its smooth endoplasmic reticulum produces a variety of lysosomes in several ways: (a) coated vesicles that separate from the reticulum; (b) dense bodies that arise from focal areas dilated with granular or membranous material; (c) "multivesicular bodies" in which vesicles and other material are sequestered; (d) autophagic vacuoles containing endoplasmic reticulum and ribosomes, presumably derived from the Nissl material, and mitochondria. The number of autophagic vacuoles increases following operation.     

超声破碎拟南芥原生质体后的再生培养初报

拟南芥原生质体在超声破碎过滤后,对其叶绿体、细胞核等细胞器进行再生培养.观察到超声破碎对叶绿体有一定破坏作用导致叶绿体在蓝色荧光下不发荧光,在培养115 h后叶绿体有聚集现象;细胞核明显增多;出现内质网的明亮绿色荧光点.细胞核和内质网都是形成新原生质体的必要细胞器,通过对其再生培养可为细胞器重组乃至细胞重建提供启示.     

Spatial structure of mitochondria and ER denotes changes in cell physiology of cultured tobacco protoplasts

The structure of mitochondria and of the endoplasmic reticulum (ER) in mesophyll protoplasts and regenerated cells was studied in vivo using the dye DiOC₆(3) (3,3'-dihexyloxacarbocyanine iodide) and confocal laser scanning microscopy (CLSM). The relation to the cell's physiology was investigated using a hormone-based model system for elongation and division. The structure of the mitochondria and of their population depends on the status of the cell. In freshly isolated protoplasts small spherical mitochondria are clustered around the nucleus and the chloroplasts. During the first 4 days of culture they are transformed into long vermiform organelles which distribute evenly throughout the cytoplasm. In a medium containing only auxins, cells then enter a period of expansion. Their mitochondria retain the same structure but increase in quantity. In a medium with auxins and cytokinins cells start dividing. Their mitochondria typically become numerous and very small, and are distributed throughout the cytoplasm. Both types of organization were observed during weeks of ongoing expansion or division. The ER is always present as a network close to the cell membrane. In freshly isolated protoplasts a considerable part of the ER is clustered around the chloroplasts, the remaining part of the network has a reduced complexity and is partly broken. During subsequent protoplast culture the network grows into a complex web with fine meshes incorporating lots of plate-like structures. This is the case in elongating cells as well as in dividing cells. Finally, the ER looks similar to the structure found in epidermal cells of the intact plant.     

ULTRASTRUCTURE OF THE GREEN ALGA DICHOTOMOSIPHON TUBEROSUS WITH SPECIAL REFERENCE TO THE OCCURRENCE OF STRIATED TUBULES IN THE CHLOROPLAST1

The ultrastructure of the siphonous green alga Dichotomosiphon tuberosus (A. Br.) Ernst is compared with that of other siphonous plants. There is a characteristic association between the Golgi bodies and endoplasmic reticulum, but. the mitochondria are not involved in the association as they are in Vaucheria and the phycomycete Saprolegnia. An unusual structure and arrangement of the chloroplasts is described as well as a previously unreported type of “striated tubule” which occurs in most if not all chloroplasts, and amyloplasts. The structure of these tubules is compared with that of other tubules recently found in green algae and higher plants. In addition, cytoplasmic microtubules arranged in the longitudinal direction of the siphon suggest a function in cytoplasmic streaming.     

油菜花蜜腺发育过程的超微结构变化与泌蜜机理的研究

油菜花蜜腺由２枚侧蜜腺和２枝中蜜腺组成,其基本结构类似。在蜜腺发育过程中,产蜜组织细胞内的内质网、高尔基体、质体和线粒体以及液泡都发生有规律变化。泌蜜前,细胞器的数量增加。其中,质体内积累淀粉,此过程与蜜腺内初皮部的分化并和线粒体的增加相关。泌蜜时,内质网数量增多,并产生小泡．小泡向质膜移动。泌蜜后,细胞液泡化,细胞器数量减少,细胞萎缩。根据观察结果分析,其原蜜汁来源于韧皮部,转运至产蜜组织细胞的质体、内质网和高尔基体内加工成蜜汁,最后通过胞吐和渗透相结合的方式泌出。     

锦橙汁囊的超微结构

用常规电镜方法观察了锦橙［Ｃｉｔｒｕｓｓｉｎｅｎｓｉｓ （Ｌ．） Ｏｓｂ．］汁囊从原始细胞到发育为一个具柄的成熟汁囊的过程中,汁囊构成细胞超微结构的变化。锦橙汁囊原始细胞及发育为球状体时的构成细胞以及柱状结构顶端的细胞都是一种典型的分生组织细胞。在细胞质中有包括线粒体、质体、内质网、核糖体等丰富的细胞器,但没有观察到高尔基体。这些分生细胞分裂一段时期后就停止活动,逐渐分化为适应贮藏功能的液泡化薄壁细胞。分生细胞开始分化时,在细胞中出现许多小液泡和高尔基体。这些小液泡逐渐地融合,同时细胞质变少,最后形成一个有中央大液泡的薄壁细胞,在紧贴细胞膜的薄薄的一层细胞质中有线粒体、质体、高尔基体以及含有许多脂滴的杂色体。但成熟果实中汁囊的薄壁细胞中几乎没有任何细胞器。     

内质网及其标志酶在离体培养脊髓神经元中的发育变化

本文采用形态学与细胞化学相结合的方法,在超微结构水平观察了与突触酶、受体和结构蛋白的合成有关的内质网和高尔基复合体、GERL以及它们的标志酶的发育变化。结果表明神经元本身有一发育过程,发育早期的细胞器较少,成熟时逐渐增多,以内质网和高尔基复合体最为明显。用G一6一Pase、TPPase和CMPase可分别标记内质网及同源结构、高尔基复合体的成熟而膜囊和GERL。这些酶的出现及阳性水平与神经元的发育呈同步关系。可作为判断细胞分化程度和功能状态的指标。G-6-Pase还分布在突触后树突的内质网中,突触形成大都从含G-6-Pase阳性内质网的树突开始。本文对内质网及G-6-Pase在神经元中的发育变化及功能进行了讨论。     

CORRELATED MORPHOMETRIC AND BIOCHEMICAL STUDIES ON THE LIVER CELL : II. Effects of Phenobarbital on Rat Hepatocytes

The changes occurring in rat hepatocytes during a 5 day period of treatment with phenobarbital were determined by morphometric and biochemical methods, particular attention being paid to the endoplasmic reticulum. The hepatocytic cytoplasm played an overwhelming part in the liver hypertrophy, while the hepatocytic nuclei contributed to only a moderate extent. The endoplasmic reticulum accounted for more than half of the increase in cytoplasmic volume. The increase in the volume and number of hepatocytic nuclei in the course of phenobarbital treatment was associated with changes in the ploidy pattern. Until the 2nd day of treatment both the rough-surfaced endoplasmic reticulum (RER) and the smooth-surfaced endoplasmic reticulum (SER) participated in the increase in volume and surface of the whole endoplasmic reticulum (ER). Subsequently, the values for RER fell again to control levels, whereas those for SER continued to increase, with the result that by the 5th day of treatment the SER constituted the dominant cytoplasmic element. The specific volume of mitochondria and microbodies (peroxisomes) remained constant throughout the duration of the experiment, while that of the dense bodies increased. The specific number of mitochondria and microbodies displayed a significant increase, associated with a decrease in their mean volume. The phenobarbital-induced increase in the phospholipid and cytochrome P-450 content of the microsomes, as well as in the activities of microsomal reduced nicotinamide-adenine dinucleotide phosphate-cytochrome c reductase and N-demethylase, was correlated with the morphometric data on the endoplasmic reticulum.     

CHARACTERIZATION OF FORCED SUSPENSION CULTURE OF SPONTANEOUSLY TRANSFORMED MOUSE FIBROBLASTS (B-6)

Mouse fibroblasts (B-6) were cultured on agar-coated dishes. After cells grew for 2–3 generations relatively rapidly in suspension, they began to grow very slowly (stationary phase). Electron microscopic studies showed that cells in a stationary phase developed intracellular organella: membranous structures (endoplasmic reticulum and Golgi apparatus) became manifest and the number of mitochondria increased. The specific activities of succinic-cytochrome c reductase and 5′-nucleotidase were three and five times higher, respectively, than those of cells on the dish.