麝香腺分泌周期中组织学及组织化学的初步研究

麝是重要的经济动物,它所分泌的麝香是贵重的药材和香料,研究麝香腺在泌香周期中的组织学结构以及有关组织化学成分,将有助于阐明麝香的化学组成和它的分泌机理,为提高麝香产量提供形态学依据。     

喜树的分泌结构及其与喜树碱积累的关系(英文)

为了揭示喜树碱(camptothecin,CPT)在喜树(Camptotheca acuminata Decne.)中的积累部位及积累规律,运用组织化学技术和高效液相色谱技术对喜树茎、叶中喜树碱的积累部位和含量进行了相关性分析。结果发现两类分泌结构与喜树碱积累密切相关:一类是分布于幼茎和幼叶表面的单细胞腺毛;另一类是分布于喜树幼茎和幼叶中的由1～2层细胞包围而成的分泌道。由此推断,喜树中的分泌结构为喜树碱的主要积累部位。     

北柴胡分泌道的发育及组织化学研究

利用植物解剖学和组织化学的方法对北柴胡根、茎和叶中分泌道的分布、发生发育过程以及组织化学进行了研究.研究结果表明,分泌道分布在根中柱鞘组织和次生韧皮部、茎韧皮部和髓,以及叶脉韧皮部内和木质部上方.根中柱鞘中的分泌道来源于中柱鞘细胞,次生韧皮部中的分泌道来源于维管形成层切向分裂向外形成的衍生细胞;茎和叶脉韧皮部内的分泌道起源于原形成层束原生韧皮部外侧的2～3层细胞;茎髓中和叶脉木质部上方的分泌道来源于基本分生组织.这些分泌道腔隙的形成都属于裂生型.组织化学结果表明分泌道是挥发油积累的重要场所.     

喜树的分泌结构及其与喜树碱积累的关系

为了揭示喜树碱(camptothecin,CPT)在喜树(Camptotheca acuminata Decne.)中的积累部位及积累规律,运用组织化学技术和高效液相色谱技术对喜树茎、叶中喜树碱的积累部位和含量进行了相关性分析.结果发现两类分泌结构与喜树碱积累密切相关:一类是分布于幼茎和幼叶表面的单细胞腺毛;另一类是分布于喜树幼茎和幼叶中的由1～2层细胞包围而成的分泌道.由此推断,喜树中的分泌结构为喜树碱的主要积累部位.     

臭椿茎中分泌道的发育及其组织化学研究

利用植物解剖学方法研究臭椿茎和叶柄中分泌道的结构、分布和发育过程.结果表明:臭椿茎和叶柄中的分泌道分布于髓的周缘,次生木质部中无分泌道.分泌道是由一层分泌细胞围绕分泌腔而构成,分泌细胞外有1～2层鞘细胞.分泌道以裂生方式形成,其发育过程可分为3个阶段:原始细胞阶段、形成阶段和成熟阶段.在原始细胞阶段,一群原始细胞具浓厚细胞质,细胞核清晰可见;形成阶段,原始细胞的中央细胞间细胞壁中层降解,细胞壁分离,形成腔隙,随着分泌细胞数量的增加,分泌腔体积扩大;成熟阶段的分泌道具有12～16个分泌细胞,1～2层鞘细胞,分泌腔直径为30～50μm.组织化学研究表明,分泌细胞及分泌道内含物中含大量的萜类、多糖和脂类物质.机械创伤能够诱导次生木质部中产生创伤分泌道.臭椿茎中的分泌道和创伤性分泌道在抵御生物和非生物胁迫中起重要作用.     

神经肽Y免疫反应神经和细胞在大鼠颌下腺的分布

本研究应用免疫组织化学ＡＢＣ技术,观察了含神经肽Ｙ神经和细胞在大鼠颌下腺内的分布特点。结果显示：含神经肽Ｙ神经纤维主要走行于腺泡、导管及血管周围。颌下腺内神经节细胞和颗粒曲管细胞亦呈神经肽Ｙ免疫反应阳性。提示：大鼠颌下腺的腺体分泌和血液供应可能受神经肽Ｙ能神经调控。     

贯叶连翘的分泌结构及其与金丝桃素积累的关系

贯叶连翘（ＨｙｐｅｒｉｃｕｍｐｅｒｆｏｒａｔｕｍＬ．）地上器官分布着分泌细胞球（黑色腺点）、分泌囊（半透明腺点）和分泌道（半透明腺条）３类内部分泌结构。分泌细胞球在茎、叶和花器官中均有分布,由２层鞘细胞包围多个分泌细胞构成实心的分泌细胞团。分泌囊主要分布于叶片中,分泌道则分布于花器官中,它们都是由１～２层切向扁平细胞围绕圆形或长形腔道构成,腔道的贮存物为精油。利用组织化学方法,结合荧光显微镜观察,证实金丝桃素类物质是由分泌细胞球（黑色腺点）所合成和积累的。通过用戊二醛和锇酸固定样品的显微和超微结构观察,发现金丝桃素类物质积累在成熟腺体分泌细胞的中央大液泡中,细胞周围浓厚的细胞质中分布着大量小液泡和高尔基体、内质网等细胞器。在此基础上对金丝桃素类物质的积累过程进行了初步探讨     

蕤核叶片解剖结构和组织化学定位研究

采用解剖学和组织化学方法,研究了蕤核(Prinsepia uniflora Batal.)叶片的解剖结构,并对叶片中的黄酮类、生物碱类及多糖的组织化学定位进行了研究。结果表明:蕤核叶片上表皮有角质层,下表皮有气孔分布,气孔密度为278个·mm-2,近轴面栅栏组织细胞2～3层,排列紧密而整齐,含有许多晶体;叶片主脉木质部发达,由多列导管组成。上述特征说明蕤核叶片的解剖结构与环境之间的适应性。组织化学定位显示黄酮多分布于栅栏组织和厚角组织,生物碱含量少,多糖均匀分布于叶肉中。     

潘氏细胞在昆明小鼠弓形虫病发病过程中的变化

每只昆明小鼠灌胃1×104个弓形虫卵囊,分别在灌胃后1,3,5,6 DAI(days after inoculation),采用HE方法和免疫组织化学方法对小鼠回肠潘氏细胞的变化以及弓形虫在回肠的分布和数量进行研究,探讨潘氏细胞(paneth cells,PCs)在小鼠弓形虫病感染期间的变化。结果发现,回肠隐窝总数、含PCs的隐窝数、PCs总数及颗粒总数呈先增加后迅速减少至消失的趋势,回肠后段表现明显,6 DAI各参数与对照组比较差异显著(P0.05)。弓形虫在回肠中的分布面积呈增大趋势,6 DAI与1 DAI、3 DAI相比差异显著(P0.05)。该研究结果表明,弓形虫卵囊感染昆明小鼠可减少回肠潘氏细胞及其分泌颗粒的数量,为以小肠潘氏细胞为基础的弓形虫病的防治提供了实验依据。     

夹竹桃科2种引种植物分泌结构的解剖学研究

为了解夹竹桃科(Apocynaceae)植物乳汁管的发生发育,对爱之蔓(Ceropegia woodii)和百万心(Dischidia ruscifolia)营养器官中的分泌结构进行了显微观察。结果表明,爱之蔓和百万心营养器官中均有无节分枝乳汁管的分布,茎皮层中的乳汁管大部分具有明显的分枝,叶中乳汁管具明显分枝,分布与走向多与叶脉维管组织平行。另外,爱之蔓营养器官中的分泌结构除乳汁管外,还有分泌腔。这为夹竹桃科植物的系统分类研究提供了解剖学依据。     

Structures, Components and Functions of Secretory Tissues in Houttuynia cordata

Houttuynia cordata Thunb., traditionally used as a therapeutic plant in folk medicine, has shown antioxidant and anticancer activities. The species, as a core component of paleoherbs, is normally characterized based on the presence of different types of secretory tissue： oil cells, three types of secretory cells and glandular hairs. The aim of this work was to study the structural, componential, and the functional characteristics of the secretory tissues in both the floral and vegetative parts. The results indicate that oil cells and secretory cells are distributed in all organs of the plant, while glandular hairs are situated on the aerial stems and leaves. Both oil cells and glandular hairs initiate from the protoderm, but their developmental processes are different. Although three types of secretory cells initiate from different primary meristems, the developmental patterns of different secretory cells are the same. Also, although the origins of secretory cells are different from oil cells, their early developmental processes are the same. Histochemical results show that oil cells, secretory cells and glandular hairs produce flavonoids, phenolic compounds, tannins, lipids, aldehyde and ketone-compounds. In addition, there are terpenoids and pectic-like substances in oil cells, alkaloids in secretory cells of aerial stems, and terpenoids and alkaloids in glandular hairs. These compounds play very important roles in protecting plants from being eaten by herbivores （herbivory） and infected by microbial pathogens. The oil cell and secretory cell, as unicellular secretory tissues, are intermediates between the primitive surface glandular and secretory cavity and canal during the evolution of secretory structures.     

A unique spacer domain of synaptotagmin IV is essential for Golgi localization

Synaptotagmin (Syt) family members consist of six separate domains: a short amino terminus, a single transmembrane domain, a spacer domain, a C2A domain, a C2B domain and a short carboxyl (C) terminus. Despite sharing the same domain structures, several synaptotagmin isoforms show distinct subcellular localization. Syt IV is mainly localized at the Golgi, while Syt I, a possible Ca(2+)-sensor for secretory vesicles, is localized at dense-core vesicles and synaptic-like microvesicles in PC12 cells. In this study, we sought to identify the region responsible for the Golgi localization of Syt IV by immunocytochemical and biochemical analyses as a means of defining the distinct subcellular localization of the synaptotagmin family. We found that the unique C-terminus of the spacer domain (amino acid residues 73-144) between the transmembrane domain and the C2A domain is essential for the Golgi localization of Syt IV. In addition, the short C-terminus is probably involved in proper folding of the protein, especially the C2B domain. Without the C-terminus, Syt IVdeltaC proteins are not targeted to the Golgi and seem to colocalize with an endoplasmic reticulum (ER) marker (i.e. induce crystalloid ER-like structures). On the basis of these results, we propose that the divergent spacer domain among synaptotagmin isoforms may contain certain signals that determine the final destination of each isoform.     

Translucent Glands and Secretory Canals in Hypericum perforatum L. (Hypericaceae): Morphological, Anatomical and Histochemical Studies During the Course of Ontogenesis

Hypericum perforatum L., traditionally used in folk medicineas a therapeutic plant, is today being evaluated for its antidepressantand antiretroviral activities. The species is characterizedby the presence of different types of secretory structure: translucentglands or cavities, black nodules and secretory canals. Theaim of this work was to characterize the translucent glandsand secretory canals in both the floral and vegetative parts,from morphological, anatomical and histochemical points of view.Translucent glands consist of a sub-epidermal cavity delimitedby two layers of cells. There are three types of secretory canal:type A, with a narrow lumen, and types B and C, both with awide lumen, but with different patterns of development. Histochemicaltests showed that all these structures contain alkaloids andlipids but not pectic-like substances and proteins. Tests forresins, essential oils and tannins gave different responsesin different parts of the plant. Copyright 2001 Annals of BotanyCompany Hypericum perforatum, St. John's wort, secretory structures, morphology, anatomy, histochemistry     

Survey of leaf anatomy,especially secretory structures,of tribeCaesalpinieae (Leguminosae,Caesalpinioideae)

We studied leaflet anatomy, emphasizing secretory structures, from herbarium specimens of 128 species of 44 genera of tribeCaesalpinieae, using clearings, resin sections, and scanning electron microscopy. These observations, combined with those from our three earlier papers, provide a survey of 210 species representing all genera. Seventy-three species had secretory structures: 21 had glands or gland-like trichomes, 40 had living mesophyll idioblasts, and nine had cavities (three species each had two different types). Five additional species, all inCercidium (Caesalpinia group), had paired or clustered large spheroidal, thick-walled, empty cells (veinlet idioblasts) interconnected by perforation plate-like gaps. Secretory structures have systematic significance at various taxonomic levels.     

Comparative anatomy of secretory structures of leaves in Hypericum L.

The structure, type, morphology and location of secretory structures in leaves of 43 species, 1 subspecies and 1 variety of 9 sections in Hypericum L. were comparatively studied using tissue clearing, paraffin sectioning and thin sectioning. The results have shown that the presence of secretory structures is a common feature of leaves in this genus. According to their anatomical characteristics, the secretory structures can be divided into nodules, secretory cavities (canals) and tiny secretory tubes. In their distribution in leaves the nodules fall into two types: the leaf edge type and the scattered type. According to the location of cavities in the cross sections of leaves, the cavities can be divided into 4 types: the median type which is situated between the palisade tissue and spongy tissue, the palisade tissue type, the spongy tissue type and the across-mesophyll type. Based on the location of cavities and nodules in leaves, the species in Hypericum can be divided into 3 groups: group Ⅰ , in which only cavities are present; group Ⅱ, in which only nodules are present; group Ⅲ, in which both cavities and nodules are present. The type, location, distribution density and morphology of secretory structures are of some taxonomic value at the level of species and of section in Hypericum L. From these observations, the evolutionary trends concerning the morphology and anatomy of secretory structures and the affinity among sections in the genus Hypericum ate dis-cussed.     

MAP30蛋白结构功能的生物信息学研究

使用protparam、PHDhtm、PredictProtein等生物信息学在线服务器,对MAP30蛋白进行全面分析预测,研究MAP30蛋白具有的抗HIV活性,为临床应用提供抗科学依据和理论基础。结果表明:MAP30蛋白为稳定的碱性疏水蛋白,序列上存在三段跨膜螺旋结构和一段无序化位区域,肽链上的二硫键可使分子间形成聚集体,是一种分泌蛋白。MAP30蛋白序列包含信号肽、低复杂度区域和RIP样活性区域3个区域,具有细胞外被膜、异构酶、免疫应答三种功能。序列上分布着N-糖基化位点、N-豆蔻酰化位点、Shiga/ricin核糖体失活蛋白活性位点和多段蛋白激酶磷酸化位点。     

An antibody against secretogranin I (chromogranin B) is packaged into secretory granules

We have investigated the sorting and packaging of secretory proteins into secretory granules by an immunological approach. An mAb against secretogranin I (chromogranin B), a secretory protein costored with various peptide hormones and neuropeptides in secretory granules of many endocrine cells and neurons, was expressed by microinjection of its mRNA into the secretogranin I-producing cell line PC12. An mAb against the G protein of vesicular stomatitis virus--i.e., against an antigen not present in PC12 cells--was expressed as a control. The intracellular localization and the secretion of the antibodies was studied by double-labeling immunofluorescence using the conventional and the confocal microscope, as well as by pulse-chase experiments. The secretogranin I antibody, like the control antibody, was transported along the secretory pathway to the Golgi complex. However, in contrast to the control antibody, which was secreted via the constitutive pathway, the secretogranin I antibody formed an immunocomplex with secretogranin I, was packaged into secretory granules, and was released by regulated exocytosis. Our results show that a constitutive secretory protein, unaltered by genetic engineering, can be diverted to the regulated pathway of secretion by its protein-protein interaction with a regulated secretory protein. The data also provide the basis for immunologically studying the role of luminally exposed protein domains in the biogenesis and function of regulated secretory vesicles.     

Lymphoid cells in the Harderian gland of birds

Summary Numerous secretory parvocellular perikarya were found in the preoptic region of the domestic fowl (Gallus gallus). The dense-core secretory vesicles belong to two categories: vesicles with a diameter of (i)80–90 nm and (ii) 110–140nm. Scattered magnocellular elements display larger dense-core granules. The parvocellular neurons form unit-like clusters, showing also zones of direct apposition of neuronal membranes. The surrounding neuropil is rich in synaptic structures, formed by at least three types of axon terminals, distinguishable on the basis of vesicular morphology. These observations confirm the findings in other avian species. The hypothetical function of this system of peptidergic neurons in the rostral hypothalamus of birds is discussed.     

Exocrine pancreas under experimental conditions

Summary After the application of parachlorophenylalanine (pCPA), an amino acid analogue, paracrystalline inclusions are observed in the exocrine pancreas of the rat. The formation of the paracrystalline structures varies according to the dose and the time of examination. Although the first alterations can be seen in the Golgi apparatus and the condensing vacuoles, the main localization of these structures is within the cisternae of the RER. At the same time as degenerative changes occur in the cells, involving autophagic and heterophagic processes, regneration also takes place. With the freeze-fracturing method, the paracrystalline inclusions are interpreted as lamellae or plates of probably altered secretory proteins in extremely extended RER-cisternae. The fracture surfaces of the paracrystals show a periodicity of about 80 Å running diagonally to the main axis of the paracrystalline structures, which are mainly oriented from the basal parts of the exocrine pancreatic cells to the cell apices.The mechanism of paracrystalline formation is discussed on the basis of the morphologic results. It could be shown that after pCPA administration the amylase content is decreased concomittantly with degranulation. pCPA seems not to be incorporated into secretory proteins; high intracellular concentrations, however, are required to induce the formation of the paracrystalline structures. This morphological study is the basis for other studies dealing with secretion and intracellular transport in the pancreatic acinar cell under experimental conditions.We are very grateful to Mrs. B. Brühl, Mrs. I. Stenull and cand. med. P. Zahn for technical assistence. We also gratefully acknowledge Prof. Dr. R. Taugner for the help with freeze-fracturing     

An excursion through the ultrastructural world of quick-frozen pancreatic islets

In this article we have presented a philosophical and historical perspective on quick freezing, freeze-drying, freeze-substitution, and immunocytochemical localization of pancreatic islet hormones. A compilation of our findings indicates that quick-freezing does not produce any gross distortion of islet tissue; the amount of usable islet tissue for ultrastructural analysis is approximately 13 micron deep from the frozen edge; three different cell types can be identified in quick-frozen tissue based on general morphological characteristics; freeze-substitution with tetrahydrofuran produces a unique ultrastructural appearance in which ribosomes are particularly striking; with the use of protein A-gold, insulin and glucagon can be localized immunocytochemically on silver-gray (50-nm-thick) sections treated with 1% ovalbumin at room temperature overnight; secretory granules of quick-frozen alpha and beta cells may exist in either a swollen or condensed state; swollen beta cell secretory granules contain a filamentous material that demonstrates immunogold labeling for insulin; insulin and glucagon can be localized within the cisternae of endoplasmic reticulum; our methods provide not only discrete immunocytochemical localization of hormone, but also well-preserved cellular compartments; energy electron loss spectroscopy (EELS) has shown that quantifiable nitrogen maps can be used as an index of hormone packaging in secretory granules; and the sectioning properties of secretory granules at the ultramicrotome change when islet tissue is unosmicated and sectioned on glycerol.