杜仲次生木质部导管分子分化中的程序性死亡

运用原位末端标记法,证明了杜仲（ＥｕｃｏｍｍｉａｕｌｍｏｉｄｅｓＯｌｉｖ．）次生木质部的导管分子分化过程是程序性死亡（ｐｒｏｇｒａｍｍｅｄｃｅｌｄｅａｔｈ,ＰＣＤ）过程。它包括一系列的物质合成和细胞结构的解体和自溶：细胞核逐步变得极不规则,染色质高度凝集,有些细胞核的核周腔膨大,核周腔内存在着包裹有核物质的内膜凸起,最后,核膜消失,核解体。细胞核是ＰＣＤ中最后消失的细胞器之一。线粒体有两种解体方式,一种为线粒体内部结构紊乱,嵴极不清晰,线粒体皱缩变形;另一种为线粒体出现一些电子密度低的透明区,进而裂开。内质网囊泡化,相邻的内质网槽库之间互相连接,形成分隔。内质网和液泡共同行使溶酶体功能,吞噬各种细胞器残体。解体后的物质可能有两种去向,一是通过纹孔运输到邻近的细胞中,二是转化成构建自身次生壁的物质     

荔枝雄花性别决定过程中细胞超微结构的变化

荔枝雄花雌蕊原基在大孢子母细胞减数分裂后开始衰退.内质网历经增生扩展,穿壁相连,同心缠绕,多条平行弯曲,不规则堆叠.内质网和高尔基体产生许多囊泡,囊泡在细胞内含物的降解和运输过程中起着重要的作用.线粒体在雌蕊原基细胞衰败的前、中期数量增加,后期分批降解.过氧化物酶体在雌蕊原基细胞衰败的中期紧挨核短暂出现.细胞核的染色质凝集断裂;核周腔扩大,形成胀泡;染色质趋边,外泄.细胞原生质表现出有序的、在膜包裹下的降解,首先是核糖体,而后依次是:过氧化物酶体、内质网、高尔基体、线粒体、核.雌蕊原基的衰败历程可能是一种程序性细胞死亡的过程.     

Differentiation and Ultrastructure of the Protophloem Sieve Elements of Minor Veins in the Maize Leaves: Changes in the Protoplast

Protophloem sieve element differentiation in the minor veins of the maize ( Zea mays L. ) leaves was first evidenced as an increase of the wall thickness, which began in the comers of the cell and then extended to other parts of the wall, and the appearance of long rough endoplasmic reticulum cistemae distributed throughout the cytoplasm, and then the presence of characteristic crystalloid inclusions within the plastids. As differentiation progressed, long cisternae of rough endoplasmic reticulum appeared to transform into shorter forms and eventually aggregated into small stacks, losing their ribosomes during the process. The nuclei degenerated, although frequently persisted until very late in differentiation the stages of maturation, as darkly stained amorphous aggregates surrounded by double nuclear envelope or only inner membrane of nuclear envelope. Subsequently, the nuclear envelope collapsed and became discontinuous. At the beginning of nuclear degeneration the perinuclear spaces were partly dilated and sometimes the outer nuclear envelope in the dilated portions then ruptured, and was accompanied by the disappearance of the cytoplasmic portion near it. During the peried of nuclear degeneration, in addition to the endoplasmic reticulum, plastids and mitochondria underwent structural modification, while components such as ribosomes, cytoplasmic ground substances, vacuoles and dictyosomes disintegrated and disappeared. At maturity, the surviving protoplasmic components, including plasmalemma, mitochondria, small stacked smooth endoplasmic reticulum and P-type plastids with crystalloids, became parietal in position. As differentiation of adjacent metaphloem sieve elements proceeded, the protoplasmic components of the mature protophloem sieve elements progresively degenerated and finally obliterated.     

Nuclear Degeneration during Ballistospore Formation of Cronartium asclepiadeum (Uredinales)*

When basidia of Cronartium asclepiadeum (Uredinales) develop basidiospores, nuclei migrate from the basidial cells into the basidiospores. A mitotic nuclear division yields two nuclei in the basidiospore. One of these nuclei degenerates if the basidiospore develops a secondary ballistospore. Several stages in the degeneration of the nuclei can be recognized: (1) Condensation of chromatin, (2) separation of the nucleus into a portion containing the chromatin and a portion containing the nucleoplasm by an invagination of the nuclear envelope, (3) reduction of nuclear volume, (4) enveloping and (5) twisting of nuclear membranes around the degenerating nucleus, (6) homogenization of the chromatin with reduction of the nuclear envelope, and reduction of the enclosing membrane complex from a multilamellar structure to a single membrane layer, and (7) invagination or splitting off of the spiralled membranes. The nuclear behavior during early developmental stages of secondary spore formation is similar to that of budding basidiomycetous yeasts. Basidiomycetes producing ballistospores may possibly have arisen from those whose reproducing phase is yeast-like.     

杜仲次生木质部分化和脱分化过程中酸性磷酸酶的超微细胞化学定位

杜仲（EucommiaulmoidesOliv．）次生木质部分化过程中,在形成层刚衍生的木薄壁细胞中,酸性磷酸酶（APase）主要分布于核膜边缘和高尔基体;在分化程度较高的木薄壁细胞中,APase散布于整个核中,进而,在各种细胞器残体上聚集;在成熟的木薄壁细胞中,APase沿细胞壁内侧分布。在未成熟导管分子中,核、质膜及纹孔上明显存在APase聚集,进而,核解体;在即将分化成熟的导管分子中,APase主要集中于初生壁;在已分化成熟的导管分子中,APase集中于次生壁。脱分化过程中,只在细胞质中可见分散的APase活性,而细胞核和细胞壁上未见此酶的分布;更深层的即将分化成熟和已分化成熟的导管分子,未见有细胞分裂,其上APase的分布与剥皮前相同。通过比较分化和脱分化过程中APase的分布,推测不同的APase同工酶可能分别参与了次生木质部细胞程序性死亡过程中原生质体的解体和次生壁的建成。APase的聚集程度可能是决定细胞能否脱分化的一个重要特征。     

Nucellar degeneration inCortaderia (Gramineae)

Summary Vigorous degradation of nucellar tissue in the apomictic grassCortaderia jubata is associated with early degeneration of the megaspore mother cell and the subsequent enlargement of several cells to form somatic embryo sacs. Nucellar degeneration is recognised by the separation of the nuclear membranes, at first along only small sectors of the nucleus, and the appearance within the enlarging perinuclear space of vesicles formed by blebbing of both the inner and outer membranes of the nuclear envelope. Invaginations of the bounding membrane of the dilating RER are responsible for many single-membrane-bound vesicles lying in cisternae throughout the cytoplasm. Eventually the nucleus, enclosed mainly in the inner nuclear membrane, and the cytoplasm, are subject to extensive vesicularization. An electron opaque substance is present in the perinuclear space, in the ER, in vacuoles, and outside the plasmalemma adjacent to the degenerating cell wall, and is similar to a substance which appears on the inner and outer membrane surfaces of mitochondria during later stages of cell degeneration. It is suggested that the genesis and growth of embryo sacs inC. jubata are linked with a programmed nucellar cell autolysis.     

The formation of “accessory nuclei” in the developing oöcytes of the parasitoid hymenopterans Ophion luteus (L.) and Apanteles glomeratus (L.)

Summary The appearance and subsequent distribution of accessory nuclei in the developing oöcytes of the Ichneumonoid Ophion luteus and Braconid Apanteles glomeratus is described. They are produced by a folding of annulate lamellae produced from the nuclear envelope. The nucleus and accessory nuclei give rise to other annulate lamellae by two distinct modes of budding. These organelles are involved in membrane formation.     

Ultrastructural analysis of the effects of dominant cataract-Fr gene in mouse embryos]

An electron microscope study of lenses in 11--15 and 17 days old embryos of mice homozygous by dominant cataract-Fr (CatFr) gene has shown that ultrastructural changes in the nuclear envelope are the earliest expression of the mutant gene. The primary lens fibers of 12 days old embryos CatFr/CatFr, unlike those of the normal ones, are characterized by the decrease in the number of nuclear pores, evagination of the outer nuclear membrane, marked and unequal extension of perinuclear space which connects itself with the endoplasmic reticulum cisternae. In 14 days old embryos breaks in the outer nuclear membrane and evaginations in the inner one, fusion of nuclear membranes and breaks of the nuclear envelope are observed and resulted in the release of the nuclear contents with the nucleolus in the cytoplasm. Similar ultrastructural changes are characteristic also of the nuclei of secondary lens fibers at a comparable stage of differentiation. The destructive changes of nuclei are accompanied by the degeneration and autophagocytosis of cellular organelles and matrix.     

Kinetic and Morphological Observations on the Yeast Phase of Histoplasma capsulatum During Protoplast Formation

Protoplast formation by Histoplasma capsulatum yeasts using high concentrations of MgSO(4) occurs either by lysis of the bud or lysis of the entire cell wall. Both mechanisms may also occur simultaneously. Neither the protoplast emerging through a hole in the cell wall nor the freshly released protoplast has a recognizable cell wall or the remnant of such. The protoplast contains all the organelles of the normal cell except for mesosomes. During protoplast formation the nucleus increases in size and produces several nuclear masses by the invaginations of the internal layer of the nuclear membrane. All these nuclear masses are surrounded by the external layer of the nuclear membrane. Several nuclei with a normal nuclear membrane are formed later.     

淹水对玉米叶片细胞超微结构的影响

对淹水过程中玉米（Ｚｅａ ｍａｙｓ Ｌ．）叶片细胞超微结构的变化进行连续观察。淹水２ｈ后,液泡膜发生明显内陷。淹水６ｈ后,液泡膜内陷加剧,呈极度松弛状态;叶发体被膜局部向外突出一个由单层膜包裹的泡状结构。淹水１２ｈ后,液泡膜局部破裂;叶绿体被膜破坏加剧,成为一松弛的单膜结构,同时,基质类囊体出现空泡化。淹水１８ｈ后,叶绿体的破坏进一步加剧：被膜完全消失,基质类囊体开始消化;同时,线粒体膜和核膜也开     

Spermiogenesis in the Marine Shrimp, Sicyonia ingentis

Spermiogenesis in the marine prawn Sicyonia ingentis was examined using transmission electron microscopy. The acrosomal vesicle, derived from the fusion of pro-acrosomal vesicles blebbed from the nuclear envelope, contains the membrane pouches, anterior granule and a spike. The anterior granule is formed from the coalescence of granular aggregates within the proacrosomal vesicles. Primordia underlying the apical acrosomal vesicle membrane polymerize to form a spike approximately 6 μm long. The convoluted pouch membranes arise from the posterior acrosomal vesicle membrane. Lateral and apical portions of the acrosomal vesicle are surrounded by a pentalaminar membrane comprised of the spermatid plasma membrane and the acrosomal vesicle membrane. Subacrosomal structures include the dense saucer plate, granular core and crystalline lattice. These components condense just posterior to the acrosomal vesicle and are separated from the chromatin by a nuclear plate.
The spermatid nucleus becomes surrounded by rough endoplasmic reticulum (RER) and membranous lamellar bodies. RER gives rise to smooth endoplasmic reticulum. These membrane systems degenerate, forming a band of reticular elements around the lateral and posterior portions of the nucleus. The nucleus undergoes condensation followed by decondensation with concomitant breakdown of the nuclear envelope. The resultant chromatin is fibrillar in appearance.     

小麦与叶锈菌互作过程中细胞程序性死亡的细胞学观察

小麦(Triticum aesetivum)品种洛夫林10和叶锈菌(Puccinia recondita f.sp tritici)小种162、165分别组成不亲和组合与亲和组合。透射电镜观察表明,在小麦与叶锈菌的不亲和组合中,接种后12h,侵染点周围叶肉细胞核变形;接种后24h,核内染色质开始凝聚,并趋于细胞核边缘,同时叶绿体膨胀;接种后48h,核内染色质凝聚加剧,叶绿体开始解体;最终在接种后72h,细胞核、叶绿体完全解体,线粒体开始退化。此外,内质网和液泡共同行使溶酶体功能,吞噬各种细胞器残体及原生质降解组分。以上结果表明：在小麦与叶锈菌不亲和组合的互作过程中,寄主细胞呈现细胞程序性死亡的典型特征。而在亲和组合中,叶肉细胞间隙中可见有大量菌丝蔓延,菌丝与寄主细胞壁接触后分化产生吸器母细胞。菌丝的存在对寄主细胞的超微结构产生一定影响。从接种后24h开始,与菌接触的细胞出现质膜下陷,叶绿体稍显膨胀;在接种后48h、72h,大部分叶绿体膨胀,而其它细胞器无明显变化。     

非洲狼尾草未受精无孢子生殖胚囊退化研究

为理解植物无孢子生殖胚囊未受精条件下的退化,对无孢子生殖植物非洲狼尾草未受精成熟胚囊中央细胞退化做了细胞形态学研究。没有受精的中央细胞退化时最显著的特点是细胞核产生核膜囊泡。核膜囊泡有两种类型:单层膜的囊泡和双层膜的囊泡,单层膜囊泡在细胞质中,双层膜囊泡在细胞核内。核膜囊泡有两种发生方式:1)核膜的外膜向细胞质一侧膨胀产生囊泡,囊泡进入细胞质;2)核膜向核内凹陷形成囊泡,囊泡进入细胞核。核膜囊泡类型与产生方式密切关联。核膜囊泡吞噬并消化包括线粒体在内的细胞质和核质。     

Study on Degeneration of Unfertilized Aposporous Embryo Sac in Pennisetum squamulatium (Gramineae)

To understand the degeneration of unfertilized aposporous embryo sac in an aposporous species Pennisetum squamulatum, the central cell in the unfertilized embryo sac was characterized ultrastructurally . The most prominent sign of degeneration is that the central cell nucleus produced nuclear vacuoles . These nuclear vacuoles can be classified into singleanddouble- layered types . Single- layered nuclear vacuoles are found in the cytoplasm, while the double-layered are inside the nucleus . There are two ways to produce nuclear vacuoles . One is that the outer membrane of the nuclear envelope distends towards the cytoplasm to form nuclear vacuoles ; and the other is the double-layered nuclear envelope derives vacuoles by depressing inwards . Nuclear envelope types are in relation to the ways they are produced . All nuclear vacuoles absorb cytoplasm or nuclear matrix , and trap organelles such as mitochondria .     

Cell age-related differences in the interaction of a potential-sensitive fluorescent dye with nuclear envelopes of Acetabularia mediterranea

Abstract. To study whether an electrical potential difference exists across the nuclear envelope or inner nuclear membrane of plant cells, the authors have used an optical probe of membrane potential, the cationic fluorescent dye, DiOC₆(3) (MW = 572.5). This dye was microinjected into the nucleoplasm of isolated Acetabularia nuclei (which are still surrounded by a thin layer of cytoplasm) and its subnuclear localization visualized by fluorescence microscopy. Striking differences, which seemed to be correlated with the developmental stage of the isolated nucleus, were observed. In nuclei isolated from cells at the stage of early cap stage formation, the dye was restricted to the nuclear envelope. In nuclei isolated from cells with intermediate or fully developed caps, there was increased nucleoplasmic staining, and the staining of the envelope was frequently diminished or abolished. In all nuclei, the dye remained within the nucleus after injection. Cytoplasmic staining was only observed when nuclei isolated from cells at the stage of early cap formation were incubated in a hyper- or hypo-tonic medium. Various ionophores, injected before the dye into the nucleoplasm, had no effect on the subsequent nuclear localization of DiOC₆(3), although they did rapidly induce nucleolar condensation in nuclei isolated from cells at the stage of early cap formation. The results suggested that the electrical properties of Acetabularia nuclear envelopes or inner nuclear membranes change during cell maturation. Furthermore, the retention of the dye in the nucleoplasm under isotonic conditions indicated that the nuclear pores were not open channels for molecules of this size.     

Occurrence of Mitochondria in the Nuclei of Tobacco Sperm Cells

Tobacco sperm cells contain intact mitochondria within their nuclei with a frequency of 0.35 [plusmn] 0.13 per cell. These inclusions appear to originate from mitochondria found among chromatids in the highly elongated metaphase plate of the dividing generative cell. These organelles are apparently captured during the reconstitution of the nuclear envelope. Only sperm cells were observed to contain these nuclear mitochondria; generative cells, vegetative pollen cells, transmitting tissue cells, unfertilized egg cells, and central cells lacked them. Nuclear mitochondria were also seen in the nuclei of the egg and central cell after fusion with sperm nuclei, suggesting that nuclear mitochondria are transmitted into the zygote and primary endosperm cells during double fertilization. Organellar inclusions in the sperm nucleus provide a potential mechanism for transmitting organellar DNA into the next generation and could potentially facilitate the transfer of genetic material between the nucleus and other organelles.     

一种特殊的长寿细胞:毛竹茎秆纤维细胞

利用显微和细胞化学方法,对毛竹(Phyllostachys edulis)茎秆纤维次生壁形成过程中超微结构变化以及ATP酶、Ca2 -ATPase和酸性磷酸酶的超微细胞化学定位进行了研究.研究发现,次生壁形成早期,细胞核具有双层核膜,染色质凝聚,可见大量的线粒体、粗面内质网和高尔基体等细胞器存在于纤维细胞中;随后,双层核膜消失,细胞器将逐渐解体,多泡体开始出现在纤维细胞的细胞质;随着年龄的增加,纤维细胞壁逐渐增厚,并出现多层结构现象,而运输小泡、细胞膜、胞间连丝和凝聚的染色质将持续存在.在次生壁形成的整个过程中,ATP酶、Ca2 -ATPase和酸性磷酸酶在运输小泡、细胞膜、质膜内陷、胞间连丝和凝聚的染色质中将持续存在.结果表明,毛竹茎秆纤维细胞是一种不同于木本双子叶植物的长寿细胞,纤维原生质体中ATP酶和酸性磷酸酶的持续存在与次生壁的持续增厚密切相关.     

Morphofunctional study of the organization of the peripheral parenchyma of Acoela Oxyposthia praedator

The ultrastructure of undifferentiated cells in the peripheral parenchyma of Oxyposthia praedator was studied, along with the ways of their differentiation. The type I cells (3.5-4.0 microns in diameter) undergo mitotic division, while the type II cells (9 microns in diameter) produce specialized cells of the parenchyma. At the beginning of secretory cell differentiation one cistern of the rough endoplasmic reticulum (RER) is formed by the outer membrane of the nuclear envelope, the formation of other cisternae follows. The Golgi complex is formed simultaneously. The differentiated secretory cells are characterized by the abundance of RER cisternae and Golgi complexes. In the course of differentiation of other cell types RER cisternae are formed by several portions of the nuclear envelope. The Golgi complex appears in cells 12-14 microns long. The differentiation of digestive cells is characterized by autophagy. Autophagosomes are formed by RER cisternae. The consecutive stages of autophagosome formation are described. Using a cytochemical reaction revealing acid phosphatase the process of digestion of the autophagosome content was followed.     

Electron microscopy of human skin fibroblasts in situ during growth in culture

We have studied the electron microscopic (EM) appearance of cultured diploid human skin fibroblasts during logarithmic and confluent stages of growth using a simple technique which permits in situ visualization of individual cells in monolayer. By comparison, cells disrupted from a monolayer and pelleted showed drastic distortion of the cell surface and appearance of organelles: mechanical scraping produced massive dilatation of the rough endoplasmic reticulum (RER); and trypsin-produced multiple blebs of the plasma membrane and cytoplasmic vacuoles. In situ, these changes in trypsinized cells disappeared within 1 h after plating. Six hours later, microtubules and microfilaments had surrounded the nucleus and were oriented in longitudinal bundles beneath the plasma membrane during rapid growth. At confluence these cytoskeletal elements seemed to extend beyond the plasma membrane at intercellular junctions. Pinocytotic vesicles were abundant at those surfaces devoid of filaments. Mitochondria, aligned with the long axis of the cell, were extremely long and narrow. During logarithmic growth there were many free ribosomes, polysomes, and some flat cisternae of RER. At confluence most ribosomes were found in spirals on dilated saccules of RER which contained electron-dense material. Lysosomes of several types were present during all phases of growth and varied in number from cell to cell. Late in culture the lysosomes tended to be larger, often occupying whole areas of cytoplasm or even extruding from the cell, and resembled those seen in lysosomal storage diseases. Understanding the in situ ultrastructure of normal human fibroblasts during growth in culture will permit systematic examination of such cells in a variety of pathological states.