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1.
荇菜花蜜腺的发育研究   总被引:1,自引:0,他引:1  
荇菜花蜜腺的发育过程可分为:起源期、生长期、分泌期以及泌蜜停止期等4个时期。荇菜的5枚花蜜腺均起源于子房基部的表皮及表皮内的2-4层细胞。这些细胞经反分化后分别成为蜜腺的原分泌表皮及原泌蜜组织,两部分细胞径不断地分裂分化,最冬成为成熟蜜腺。在蜜腺发育过程中,蜜腺的分泌表皮及蜜腺组织内的内质网、质体、线粒体、液泡等细胞器结构均发生了有规律的变化,内质网在蜜腺分泌期最为发达,且产生大量的分泌小泡。质体  相似文献   

2.
油菜花蜜腺发育过程的超微结构变化与泌蜜机理的研究   总被引:4,自引:0,他引:4  
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。  相似文献   

3.
肝细胞与肝癌细胞内β-葡萄糖醛酸酶免疫电镜比较研究   总被引:3,自引:0,他引:3  
β-葡萄糖醛酸酶(β-Glucuronidase,简称β-G)在正常人体组织匀浆和体液中含量很低,在人体细胞中β-G超微结构定位尚未见报道。采用低温包埋,胶体金标记、免疫电镜技术,进行了人体肝细胞和肝癌细胞内β-G的定位。实验结果表明,β-G定位于内质网,同时观察到肝癌细胞中标记β-G的金颗粒数目明显多于肝细胞中金颗粒数目。这一结果可能对肝癌的期发现,早期诊断提供一种新方法  相似文献   

4.
迎红杜鹃(RhododendronmucronulatunTurca.)的成熟花粉为二细胞型,精细胞在花粉管中形成。花粉管中的两个精细胞及与营养核之间相联结,形成在雄性殖单位。两个精细胞的细胞质中均含有丰富的细胞器,包括质体,线粒体,小泡及微管,内质网和高尔基体稀少。  相似文献   

5.
幽门螺杆菌感染与血清抗体及滴度的相关性研究   总被引:1,自引:1,他引:0  
为了解幽门螺杆菌(HelicobacterPylori,HP)感染时机体的免疫状况,我们对134例上消化道疾病患者的血清免疫球蛋白进行了检测。结果表明,细菌培养阳性患者的三种血清抗体滴度显著高于细菌培养阴性患者。血清IgG、IgA、IgM阳性与细菌培养阳性的符合率分别为79.1%,74.6%和43.2%。活动性胃炎和非活动性胃炎的细菌培养阳性率分别为66%和42%。证实HP菌感染与活动性胃炎的发生密切相关,而与胃炎的严重程度无显著性差异。并证实了抗HP菌IgG、IgA检测具有较高的诊断HP菌感染的敏感性和特异性。  相似文献   

6.
β-葡萄糖醛酸酶(β-Glucuronidase,简称β-G)在正常人体组织匀浆和体液中含量很低,本实验采用胶体金标记,免疫电镜技术,进行了人体正常移行细胞与移行细胞癌细胞内β-G定位研究,实验结果表明,β-G存在于移行细胞和移行细胞癌细胞中的内质网、溶酶体内,同时观察到癌细胞中标记β-G的金颗粒数量多于正常移行细胞中金颗粒的数量,本实验结果可能对于移行细胞癌的早期发现、早期诊断提供了新的依据。  相似文献   

7.
荇菜腺毛的发育及其分泌过程的超微结构研究   总被引:8,自引:0,他引:8  
荇菜 (Nymphoides peltatum (Gmel.) O.Kuntz)腺毛由具分泌功能的单列圆筒状细胞组成。它们起源于苗端倒数第二叶原基近轴面 ,由原表皮细胞发育而来。处于分泌期的腺毛细胞其胞质浓厚 ,液泡化程度小。细胞内具丰富的线粒体、高尔基体和内质网等细胞器 ,还具发达的胞间连丝。粘液物质由高尔基体分泌小泡、内质网分泌小泡及多膜体共同携带至细胞边缘 ,经胞吐和渗透相结合的方式分泌至细胞外。腺毛细胞侧壁因积有大量分泌物而呈膨胀状态。经检测 ,粘液由多糖和蛋白质组成 ,对营养芽的生长发育起保护作用。  相似文献   

8.
油菜花蜜腺发育过程的超微结构变化与泌密机理的研究   总被引:1,自引:1,他引:0  
油菜花蜜腺由2枚侧蜜腺和2枚中蜜腺组成,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孢都发生有规律变化。泌蜜前,细胞器的数量增加。其中,质体内积累淀粉,此过程与蜜腺内韧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  相似文献   

9.
王岩  邢苗 《遗传学报》2000,27(10):896-901,T003
采用机械破碎和蔗糖梯度离心方法从洋葱根端分生组织中分离出细胞核并制备出核骨架。细胞核SDS-PAGE谱带中135kD处有一多肽,免疫印迹实验结果表明,该多肽可被抗鸡ScⅡ抗体标记,核骨架中没有此多肽。经抗ScⅡ抗体和FITC偶联的二抗标记后,细胞核发出代表ScⅡ的特异性荧光,而核骨架中无荧光发出。经抗ScⅡ抗体和蛋白A胶体金处理后,金颗粒特异性地结合在核内染色质区域。说明ScⅡ类似蛋白是洋葱根端细  相似文献   

10.
本文报道银耳(Tremellafuciformis)原基分化前期.在双核菌丝的幼细胞、成熟细胞和分生孢子中,与质膜相关联的两类膜结构──边缘体和质膜体的形成与功能。根据相似结构的存在.支持小泡或多泡体排出质膜之外附在细胞壁上成为边缘体和参于细胞壁合成的假定。银耳原基分化前期.双核菌丝迅速分裂的幼细胞.其质膜内陷产生泡状质膜体,内含数个小泡,或产生膜状质膜体;在成熟细胞中.质膜内陷通常形成回旋的膜结构──膜状质膜体.内含1—2个电子致密小泡.当这两类质膜体脱离质膜进入细胞质后,有的膜层和小泡局部被消化.因此,推断质膜体具有内吞和输送养料的作用。另外.在桶孔隔膜闭塞一侧电子致密度高的细胞质中.还观察到一种罕见的只有单个膜层的质膜体.其内充满3个电子致密小泡.估计它的形成与功能同膜状质膜体相似。作者认为.桶孔闭塞和质膜体的出现是与银耳原基细胞分化有关联的两个重要特征。最后,在成熟细胞中,尚可以观察到质膜体的膜层能够散开形成内质网.因此.内质网也可以来源于质膜体。  相似文献   

11.
Cotyledons of germinating papaya (Carica papaya L. ) seeds and exocarp of young fruits were used as materials for study. The ultrastructural changes occurring during differentiation of laticifer and the ultrastructural environment of papain synthesis were studied by means of TEM and immunocytochemistry. Electron microscopic observations showed that the differentiating laticiferous cells were rich in ribosomes and mitochondria. Endoplasmic reticulum (ER) was well developed and apparently active, forming secretory vesicles of various sizes. With further development, organelles were gradually degenerated and autophagy of cytoplasm within vacuole was evident. ER was dilated and split into fragments. Cell wall perforations occurred at several sites of adjacent laticifer elements. Towards maturity, laticifer was fully filled with vesicles containing electron-dense materials. Organelles disappeared thoroughly but plasmalemma remained. Sections were incubated with anti-chymopapain antibodies followed by goat-anti-rabbit IgG-gold. Labeled gold was found predominantly in ER and the associated vesicles of differentiating laticifer. Several controls were used to establish the specificity of the immunolaheling pattern. Investigations led to the conclusions that ER and polyribosomes were involved in papain synthesis. Papain was stored in the vesicles of ER origin temporally before reorganized into laticiferous vesicles with other components of latex.  相似文献   

12.
Many plants contain latex that exudes when leaves are damaged, and a number of proteins and enzymes have been found in it. The roles of those latex proteins and enzymes are as yet poorly understood. We found that papain, a cysteine protease in latex of the Papaya tree (Carica papaya, Caricaceae), is a crucial factor in the defense of the papaya tree against lepidopteran larvae such as oligophagous Samia ricini (Saturniidae) and two notorious polyphagous pests, Mamestra brassicae (Noctuidae) and Spodoptera litura (Noctuidae). Leaves of a number of laticiferous plants, including papaya and a wild fig, Ficus virgata (Moraceae), showed strong toxicity and growth inhibition against lepidopteran larvae, though no apparent toxic factors from these species have been reported. When the latex was washed off, the leaves of these lactiferous plants lost toxicity. Latexes of both papaya and the wild fig were rich in cysteine-protease activity. E-64, a cysteine protease-specific inhibitor, completely deprived the leaves of toxicity when painted on the surface of papaya and fig leaves. Cysteine proteases, such as papain, ficin, and bromelain, all showed toxicity. The results suggest that plant latex and the proteins in it, cysteine proteases in particular, provide plants with a general defense mechanism against herbivorous insects.  相似文献   

13.
Systematic investigations, mainly based on electron microscopy, have been conducted on constitutional changes in the laticifer and its adjoining parenchyma during the development of laticiferous system in garlic scape. The laticiferous system of the scape consists of several layers of articulated unbranched latieifers. About half of them are situated 2–3 cell layers below the epidermis, and the rest scattered throughout the cortex (Fig. 23). Latieifer differentiation starts with a thinning out and vacuolation of the dense protoplasm in the latieifer initials (Fig.2), which is followed by gradual degeneration of nuclei, plastids, endoplasmic reticulum, and dictyosomes; and by a sharp diminution of free ribosomes (Figs.3, 4). Remanent and defective forms of some organelles can still be found in the laticifer at the later stage. In spite of these drawbacks, the differentiating laticifer appears to function actively. Its protoplasm is delimited by a distinct plasmalemma (Figs. 3, 4). Its wall is interspersed with pits inclose spacings, to which most plasmodesmata are confined (Figs. 8, 24). The cell interior is packed with vesicles and mitoehondria (Figs. 4, 11, 15). Structurally, the laticifer seems well adapted to material exchange with the adjoining parenchyma. During the sprouting stage of the scape, the laticifer initials enlarge itself or fuse with each other by lateral wall dissolution to extend the diameter; at the same time, the laticifer elongates at an increasingly rapid rate. As a final result, the laticifer can attain 30–50 times the length and 2–3 times. the diameter of the adjoining parenchyma. The electron-dense material which protrudes into the laticifer initial from the parenchyma may be of lysosomal nature and probably concerned with wall dissolution and intracellular lytic processes in latieifer formation (Figs. 5, 7, 10). An excised garlic scape is employed in the observation of mature laticifers, which is always full of sap and is quite turgid. Once the scape is cut open, sap exudes almost exclusively from the cut end of the laticifers at the periphery, which lasts only some seconds. However, if the scape is left aside for a few days, exudation will again take place at the fresh cut end. Unlike the milky juice of many latex plants, the sap exuded from the garlic scape is watery and slightly turbid. The organic solute content is mainly made up of simple sugar and amino acids. It also contains a small amount of proteins and even protoplasmic fragments. Besides, it is worthy to note that decrease in organic solutes in the exudation is closely connected with the degree of exhaustion of cell contents from the withering scape, which is, as has already been shownm the sole agent of supplying materials required for the formation of apical cloves. All the above facts seem to indicate that there exists a loading and unloading process in the latieifer. Our electron micrographs (Figs. 16, 22) give evidence that vesicular transport through plasmodesmata in the pit field is capable of performing such a process: from the parenchyma to the laticifer in loading and from the latter to the former in unloading. The possible role of the laticifers in garlie scape could be a temporary storage of cell contents released successively from the deteriorating parenchyma. The sap content in the laticifer is in full turgidity as a result of loading, and can be readily drawn by unloading if so required. Transcellular cytosis is a term tentatively given by us to designate intercellular transport of sap, solutes, and macromolecular particles in small vesicles, which are formed and packed in one celt, traverse through plasmodesmata and merge into the other; whereas endo and exoeytosis refer to vesicular transport in a single cell only and to its moving in and out of the cell primarily through the plasma membrane, which also takes active part in the formation and dissolution of the vesicle and in the enclosure and release of its content. Transcellular cytosis was first observed by us in the withering parenchyma of an excised garlic scape; and, in the present case, between the latieifer and parenehyma, both being active functionally. As compared with the early notion that intercellular material transport is primarily carried out by secretion and reabsorption of highly degraded products through plasmalemma, transcellular eytosis appears to be a far more efficient means of translocating prefabricated assortment and well packed cargo from one cell into the other.  相似文献   

14.
The branched anastomosed laticifer system in the primary body of Cichorium intybus L. originates in embryos from files of laticiferous members at the boundary between phloic procambium and ground meristem. Upon seed germination, laticiferous members develop perforations in the end walls which become entirely resorbed. Perforations also develop in the longitudinal walls of contiguous laticiferous members and from lateral connections between developing laticifer branches. Additional laticiferous members originate as procambium differentiation proceeds, and their differentiation follows a continuous acropetal sequence in leaf primordia of the plumule. In roots, laticifers closely associated with sieve tubes in the secondary phloem originate from derivatives of fusiform initials in the vascular cambium. These laticifers develop wall perforations and in a mature condition resemble laticifers in the primary body. As the girth of the root increases, laticifers toward the periphery, unlike associated sieve tubes, resist crushing and obliteration. Laticifers vary in width from about 4 to 22 μm; the widest ones occur in involucral bracts and the narrowest ones in florets. There was no evidence that intrusive growth occurs during development of the laticifer system, although such growth may occur during development of occasional branches which extend through ground tissue independent of phloem and terminate in contact with the epidermis. Presence of amorphous callose deposits is related to aging of laticifers and mechanical injury.  相似文献   

15.
Yamamoto  H.  Tabata  M. 《Plant cell reports》1989,8(4):251-254
A protease similar to papain was produced by somatic embryos ofCarica papaya in association with the development of laticifers containing characteristic vesicles which probably originated from the endoplasmic reticulum. In contrast to somatic embryos, a papain-like protease was not detected in either friable or compact callus cultures which failed to develop laticifers. These observations strongly suggest that the differentiation into laticifers is required for papain production in papaya.  相似文献   

16.
从巴西橡胶树Hevea brasiliensis差减cDNA文库中分离到微管相关蛋白(Microtubule-associated protein,MAPs)基因片段,根据该基因片段序列信息,设计特异引物,采用cDNA末端快速扩增技术RACE(Rapid Amplification ofcDNA Ends)进行差异片段的5'和3'端的扩增,获得了长度为788bp的全长cDNA,该基因在GenBank中的登录号为AY461412.序列分析表明该基因包含完整的开放阅读框,编码144个氨基酸,与微管相关蛋白基因家族具有很高的同源性,推测该基因是微管相关蛋白基因.半定量RT-PCR检测证实它在胶乳中的表达强于叶中,胁迫处理(伤害及乙烯处理)使其表达上调.  相似文献   

17.
This review describes the development of the laticifer concept, with emphasis upon the nonarticulated type, from early observations of plant exudates and “juices” to the presentation of laticifers by Esau (1953). Classical writers and herbalists described practical applications of these substances. With the advent of the microscope early investigators believed that these substances occurred in structures present in most, if not all, plants and, wrongly, equated these structures to the circulatory system in animals. Introduction of the term, latex, into botany derived from its early use as a term for a blood component by physicians, and not for analogy to milk. However, the origin of the terms, laticifer and laticiferous, remains uncertain. Initial studies of laticifers were marked by the controversy of whether they represented intercellular spaces or elongated cells. Confirmation of their cellular character led to the designation of nonarticulated and articulated laticifers. Nonarticulated laticifers were shown to arise during early embryogeny in some plants. The ontogenetic origin of the articulated laticifer was unclear to early workers, but new laticifers were detected to be formed by cambium activity. Nonarticulated laticifers were described to develop by intrusive growth whereby tips of the cell penetrated between adjacent cells. The coenocytic condition of the nonarticulated laticifer resulted from nuclear divisions along the cell positioned in the growth region of the shoot and the subsequent distribution of the daughter nuclei along the length of the cell.  相似文献   

18.
Secretory cells of laticiferous canals contain many plastids and endoplasmic reticulum (ER) in Rhus verniciflua. The electron microscopy suggests that osmiophiiic Lacquer component is mainly synthesized in the plastids and ER. They may be eliminated from the protoplasts to the space between the plasmalemma and the cell wall in three ways: (1) by ER elements, (2) by vesicles approaching the plasmalemma and fusing their membrances with the latter, and (3) by their becoming surrounded by plasmalemma invaginations, and then they traverse the wall through the channels of plasmodesmata which became disconnected during the schizogenous development of the canals and percolate through the wall that faded into an even looser mesh of fibrillar material toward the canal lumen. More or less, nucleus, mitochondria, Golgi bodies and ground cytoplasm also take part in the above-mentioned process.  相似文献   

19.
漆树(Rhus verniciflua)乳汁道分泌细胞含有丰富的质体、内质网和嗜锇物质。电子显微镜的现察结果表明,嗜锇的生漆成分合成的可能场所是质体和内质网,并且通过内质网分子和小泡群与质膜相互接触并融合以及质膜内褶包被等三种形式释放到质膜和细胞壁之间的间隙中;再经过细胞壁中乳汁道腔形成时断裂了的胞间连丝通道和扩散渗透两条途径,越过细胞壁分泌到乳汁道腔中。细胞核、线粒体、高尔基体以及细胞质基质或多或少也参与了上述过程。  相似文献   

20.
Development of alkaloidal vesicles in laticifers of opium poppy, Papaver somniferum L., was investigated at the ultrastructural level. Laticifer initials possessed abundant endoplasmic reticulum throughout their dense cytoplasm. During differentiation the endoplasmic reticulum organized into long, folded sheets that were parallel to the longitudinal walls along the periphery of the cell. Vesicles appeared to be derived from dilation of endoplasmic reticulum. This relationship was confirmed through cytochemical data obtained with zinc iodide-osmium tetroxide and osmium tetroxide impregnation. Alkaloidal vesicles had electron-dense regions or caps that occurred early in laticifer differentiation, but these caps became less conspicuous in mature cells. Caps appeared to be derived from small particles which condensed along the inner surface of the vesicle membrane and subsequently accumulated at one or two positions along the membrane of the vesicle.  相似文献   

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