腹毛目纤毛虫拟翁口虫细胞微管类胞器及射出胞器的研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
腹毛目纤毛虫是纤毛虫中最高等的一个类群,其最典型的特征即具有纤毛聚集成的复杂的纤毛器结构。这些纤毛器结构主要包括纤毛器微管及基部附属微管,即口围带及其附属微管(小膜托架、小膜附属微管)、波动膜及其附属微管(波动膜托架)、额腹横棘毛及其附属微管(前纵微管束、后纵微管、横微管)、左右缘棘毛及其附属微管(前纵管束、后纵微管束和横微管)、尾棘毛和背触毛。且纤毛器结构的主要成分是微管蛋白,因此腹毛目纤毛虫是用以研究纤毛虫皮层微管胞器和微管蛋白的常用材料。
     根据纤毛形态结构及发生等特征的不同,可将腹毛目纤毛虫划分为不同的种类。腹毛目侧毛虫科纤毛虫在分类地位上属于尾柱虫科和尖毛虫科之间的过渡类群。该类群纤毛虫种类及数量较少,且相关研究报道不多见,导致其科内分类较为混乱。本文以一种侧毛虫科(Pleurotrichidae)纤毛虫拟翁口虫(Onychodromopsissp)为研究材料,应用荧光紫杉醇(FLUTAX)直接荧光标记法、透射电镜术、扫描电镜术、SDS-PAGE电泳和生化抽提等方法,就本种纤毛虫的皮层微管胞器的形态及其形态发生、射出胞器的形态结构及发生、微管蛋白等方面展开研究,初步得到了相应的研究结果,从显微和亚显微水平上为侧毛虫科纤毛虫的种间分类提供材料和证据。所得结果如下:
     1拟翁口虫纤毛器微管的形态及形态发生
     应用荧光紫杉醇直接荧光标记方法显示本种纤毛虫的腹皮层纤毛器微管胞器及形态发生。其中,口围带含30~35片小膜;波动膜一片;额腹横棘毛为典型的8-5-5模式,左缘棘毛2列,右缘棘毛3列;背面含6列背触毛;额、腹棘毛基部的前纵微管束与后纵微管束均较发达,但未见横微管束;横棘毛前纵微管束发达,前4根横棘毛基部前纵微管束向前伸展并汇聚成一个三角结构;左缘棘毛横微管束极不发达。形态发生过程中,细胞缘棘毛起始于最外侧右缘棘毛,且每列老缘棘毛的前、后部棘毛都瓦解,并在相应位置产生的新棘毛不断延伸代替老棘毛。据该纤毛虫的皮层纤毛模式和纤毛器基部微管的形态,将其归为侧毛虫科(Pleurotrichidae)拟翁口虫属(O.sp);并据后仔虫口原基的发生、左右缘棘毛原基的发生不同于已报道的柔软拟翁口虫(Onychodromopsis flexilis)的情况,认为该纤毛虫可能为另一种拟翁口虫。
     2拟翁口虫细胞及微管类细胞骨架的超微结构
     应用透射电镜术显示本种纤毛虫皮层细胞骨架的超微结构。结果显示拟翁口虫的表膜具高度发达的实质状表膜泡;纤毛杆轴纤丝排列成“9+2”模式,相邻两根纤毛基体之间具有连接结构;在同一虫体中每个口围带小膜单元的组成模式有两种:2列长度相当的纤毛组成和3列长度相当的纤毛;围棘纤维篮围着一层纤维,且向周围发出许多微管束,其中前纵微管束及其发达;表膜下一般具3-5层微管层,口区附近具由数十上百根微管紧密叠加在一起成为的加厚的微管层;大核复制带为透明均一状,未出现染色质状态不一的前部区、后部区。结果表明拟翁口虫表膜及表膜下纤维结构、大核复制带均具不同于其他腹毛目纤毛虫的特征,且其特征是符合腹毛目纤毛虫由尾柱虫类(Urostylidae)—侧毛虫类(Pleurotrichidae)—尖毛虫类(Oxytrichidae)—游仆虫类(Euplotidae)的进化规律的,从亚显微水平上为侧毛虫科内纤毛虫种群划分提供资料。
     3拟翁口虫射出胞器的超微结构
     应用扫描电镜和透射电镜术对腹毛目纤毛虫拟翁口虫细胞中射出胞器的超微结构进行了研究。结果显示该射出胞器扫描电镜下为颗粒状突起,口区分布较少:透射电镜下散布在整个细胞中,成熟后定位于表膜下,且顶部中间(靠近表膜的一端)的纤维物质密度较少,有的几乎出现空洞;射出胞器的发生过程中形成可高低电子密度相间的同心圆结构,且囊泡结构中间出现缢痕,随后一分为二,形成两个具电子密度相间的同心圆结构的囊泡。射出胞器体外及成熟定位后的形态特征表明该射出胞器可能为一种类粘液泡;囊泡随缢痕一分为二的现象可能为射出胞器的一种新型起源方式;该射出胞器可能行使一种防御或应激功能,对捕食行为无直接作用。
     4拟翁口虫全蛋白和γ-微管蛋白基因初步分析
     应用SDS-PAGE电泳技术对拟翁口虫全蛋白组分进行了分析,并对其γ-微管蛋白基因片段进行了扩增。电泳结果显示:116KD与66.2KD之间、45KD与35KD之间的蛋白条带密集度高,在约30KD、20KD、16KD附近的条带蛋白表达量高达7.0%-7.9%;特异性地扩增出一条约为1200bp的γ-微管蛋白条带。结果表明本种纤毛虫具有不同于其他纤毛虫的全蛋白和γ-微管蛋白基因含量。
Hypotrichous ciliate are highest group in ciliates, it's most typical groups with characteristics namely complicated ciliature apparatus. These ciliature apparatus consist of microtubular organelles and the base associated microtubules of these ciliatures:adoral zone of membranelles (AZM) and its base associated microtubules (membranelle brackets, membranelle associated microtubules), undulating membranes (UM) and its base associated microtubules, frontal-ventral-transverse cirri (FVTC) and its base associated microtubules(anterior longitudinal microtubules (ALM), posterior longitudinal microtubules (PLM), transverse microtubules (TM)), marginal cirri (MC) and its base associated microtubules(ALM, PLM, TM), caudal cirri (CC), dorsal kineties (DK). The main ingredients of ciliature are microtubulins, therefore ciliated protozoa are common materials for research of microtubular organelles and microtubulins of ciliates.
     According to different characteristics on morphology and morphogenetic, ciliated protozoa can be classified into different groups. In taxonomy, Pleurotrichidae is a transition gronp between Urostylidae and Oxytrichidae. For Pleurotrichidae have low category and quantity, and few related researches, its classification are out of order. In this study, by using direct-fluorescent labeling、TEM、SEM、SDS-PAGE、biochemical extraction, the strucutures and functional components of microtubular organelles, morphological structure of extrosomes, and microtubulin were discussed. Expect to provide materials and evidence for taxonomic research of Pleurotrichidae. Results are as follows:
     1 The morphology and morphogenetic of the ciliature microtubular organelles in Onychodromopsis Sp
     The morphology and morphogenetic of the ciliature microtubular organelles in the ventral cortex of Onychodromopsis Sp were visualized using FLUTAX direct fluorescent labeling. In the front of cell, the AZM possesses 30~50 adoral membranelles; UM possesses 2 rows of cilia; FVTC distribute into 8 frontal,5 ventral and 5 transverse cirri; 2 left marginal cirri (LMC) and 3 right marginal cirri (RMC),6 DK rows; Developed ALM and PLM of FVC, and developed ALM of TC, the first four ALM of TC extend forward together into a triangle structure. TM of LMC are extreme underdevelopment. During morphogenesis, the new MC primordium first originate from the outest RMC, and then MC primordium presents in the front and the middle part of th degenerated site if the old marginal cirri. On the features of its ciliature and the base-associated microtubules, this species qualifies to be the genus Onychodromopsis. However, the morphogenetic study shows the originating position of oral primordium of the opisthe and differentiation of the marginal rows were different from other related species Onychodromopsis flexilis, this species was probably another species in the genus Onychodromopsis.
     2 The ultrastructure of cytoskeleton in Onychodromopsis Sp
     The results of TEM showed that ultrastructure of microtubular cytoskeleton of Onychodromopsis Sp. It showed that a layer of alveolar membrane beneath the pellicle; ciliary shafts possess "9+2" doublet microtubules; and basal bodies of the cirri are also linked by different kinds of connections. Each membranelle of AZM has two types of compositional model:2 rows of cilia and 3 rows of cilia; A layer fiber is cover around FCB, and lots of microtubules send forth from FCB, developed ALM. There has 3-5 microtubules layers beneath the pellicle. The pellicle closed to AZM has thicken microtubules layers, which was consisted of hundreds of layers. During morphogenesis, Macronucleus appeared replication band, it's a homogeneous structure. Reasults shows compared with others ciliates, Onychodromopsis Sp have different microtubules layers beneath the pellicle and republication band of Macronucleus. These characters are correpond with evolutionary discipline from Urostylidae, Pleurotrichidae, Oxytrichidae to Euplotidae. To provide the mateials for taxonomic research of Pleurotrichidae at sub-microscopy level.
     3 The ultrastructure of the extrusomes in Onychodromopsis Sp
     By using SEM and TEM, the ultrastructure of extrusomes in Onychodromopsis Sp to be observed. SEM shows there has granulate structure on surface of the body, and less in vicinity of AZM; TEM shows that extrusomes distributed in the cortical cytoplasm of Onychodromopsis Sp Mature organelles are located beneath pellicle,the top part of extrusome have low density fibrous matter, even appear cavity; In the process of morphogenesis of extrusomes, it appear concentric circles structure with high-low electron-dense matter. And vesicle extended to be divided in two parts, which also has concentric circles structure. The morphology and morphogenetic of extrusomes indicated this extrusome was probably a kind of mucocyst, the divide of its probably a new way of origin. And this extrusome might be a protective or defensive response to the environment changes, irrelevant with predatory behavior.
     4 The protein composition of Onychodromopsis Sp and cloning analysis of gramma-tubuliln gene fragment from Onychodromopsis Sp
     By using the methods of SDS-PAGE analyse the protein composition of Onychodromopsis Sp, meanwhile cloning of gamma-tubulin gene fragment from Onychodromopsis Sp. The result of SDS-PAGE shows that the molecular weight of protein range from 66.2-116kD and 35-45KD was rather higher, the protein composition of 30kD,20kD, and 16kD bands come to 7.0-7.9%; The result of clonging showed that the molecular weight of gamma-tubulin is 1000bp approximately. It demonstrated that Onychodromopsis Sp has different characters in the protein composition and gamma-tubulin gene fragment.
引文
[1]Berger H. Monograph of the Oxytrichidae (Ciliophora, Hypotrichia). London: Kluwer Academic Publishers,1999,102-766.
    [2]施心路.下毛目纤毛虫的系统修订Ⅲ.散毛亚目:游仆亚目(纤毛动物门).动物分类学报,2000,25:9-25.
    [3]王梅,朱明壮,宋微波,等.侧毛虫科系统关系的讨论与属级定义的重厘订(纤毛门,腹毛目).青岛海洋大学学报,2002,32(3):375-379.
    [4]Petz W, Foissner W. Morphology and morphogenesis of Lamtostyla edaphoni Berger and Foissner and Onychodromopsis flexilis Stokes, two hypotrichs (Protozoa:Ciliophora) from Antarctic soils. ACTA Protozool,1996,35(4): 257-280.
    [5]Song W. Morphology and morphogenesis of the marine ciliate Ponturostyla enigmatica (Dragesco & Dragesco-Kerneis,1986) Jankowski,1989 (Ciliophora, Hypotrichida, Oxytrichidae). Eur J Protistol,2001,37:181-197.
    [6]Gupta R, Arora S, Sapra G R, et al. Pleurotricha curdsi (Shi, Warrenand Song 2002) nov.comb. (Ciliophora:Hypotrichida):morphology and ontogenesis of an Indian population; redefinition of the genus. Eur J Protistol,2003,39:275-285.
    [7]高巍,史磊,顾福康.异毛虫(Allotricha curdsi)皮层纤毛器基部微管的荧光标记.复旦学报:自然科学版,2007,46(6):976-980.
    [8]何兰,曾红,顾福康,等FLUTAX法显示纤毛虫微管胞器的改良.动物学杂志,2006,41:59-61.
    [9]曾红,倪兵,顾福康.原生动物贻贝棘尾虫微管胞器的荧光标记与显示.动物学杂志,2006,41(4):71-76.
    [10]张作人,庞延宾,顾福康.急纤虫(Tachysoma pellionella)无性生殖周中核器和纤毛器的演化.动物学研究,1984,5(2):189-200.
    [11]鲍小娟,倪兵,顾福康,等.异毛虫(Allotricha curdsi)的形态及形态发生的扫描电镜观察.复旦学报:自然科学版,2007,46(6):981-991.
    [1]顾福康,季玲妹.包囊游仆虫皮层和营养核的超微结构研究.动物学研究,1996,17(1):16-22.
    [2]张丽萍,倪兵,季玲妹,等.阔口尖毛虫纤毛器皮层和细胞核的超微结构观察.上海市动物学会论文集,1997.
    [3]朱慧.腹毛目纤毛虫的皮层细胞骨架及其结构分化的研究,华东师范大学博士学位论文,2005.
    [4]倪兵.不同类群腹毛目纤毛虫的细胞超微结构的比较研究.华东师范大学博士学位论文,2006.
    [5]汤蕾.贻贝棘尾虫皮层微管骨架的超微结构及微管蛋白的免疫电镜定位.华东师范大学硕士学位论文,2007.
    [6]赵柳.纤毛虫华美游仆虫微管胞器和核器的细胞与分子生物学研究.华东师范大学博士学位论文,2008.
    [7]尹飞.腹毛目纤毛虫鬃棘尾虫细胞纤毛器微管胞器及微管蛋白的研究.华东师范大学博士学位论文,2009.
    [8]周瑶.腹毛目纤毛虫新伪尾柱虫微管胞器和射出胞器的研究.华东师范大学博士学位论文,2010..
    [9]Petz W, Foissner W. Morphology and morphogenesis of Lamtostyla edaphoni Berger and Foissner and Onychodromopsis flexilis Stokes, two hypotrichs (Protozoa:Ciliophora) from Antarctic soils. ACTA Protozool,1996,35(4): 257-280.
    [10]Song W. Morphology and morphogenesis of the marine ciliate Ponturostyla enigmatica (Dragesco & Dragesco-Kerneis,1986) Jankowski,1989 (Ciliophora, Hypotrichida, Oxytrichidae). Eur J Protistol,2001,37:181-197.
    [11]Gupta R, Arora S, Sapra G R, et al. Pleurotricha curdsi (Shi, Warrenand Song 2002) nov.comb. (Ciliophora:Hypotrichida):morphology and ontogenesis of an Indian population; redefinition of the genus. Eur J Protistol,2003,39:275-285.
    [12]高巍,史磊,顾福康.异毛虫(Allotricha curdsi)皮层纤毛器基部微管的荧光标记.复旦学报:自然科学版,2007,46(6):976-980.
    [13]鲍小娟,倪兵,顾福康,等.异毛虫(Allotricha curdsi)的形态及形态发生的扫描电镜观察.复旦学报:自然科学版,2007,46(6):981-991.
    [14]鲍小娟.异毛虫的形态发生及微管蛋白的免疫电镜定位.华东师范大学硕士学位论文,2008.
    [15]顾福康,倪兵.包囊游仆虫休眠包囊的超微结构研究.实验生物学报,1995,28(2):163-171.
    [16]Grim J N, Halcrow K R, Harshbager R D. Micro tubules beneath the petticles of two ciliate protozoa as seen with the SEM. J Protozool,1980,27(3):308-310.
    [17]Bussers J C, Hoesdorff M, Bolome M, et al. L'enkystement du cilie hypotriche Euplote muscicola. Protistologica,1986,22(4):457-460.
    [18]Arikawa M, Watanabe A. High-resolution scanning electron microscopy of chromatin bodies and replication bands of isolated macronuclei in the hypotrichous ciliate Euplotes aediculalus. Eur J Protistol,2000,36:40-45.
    [19]张莹,倪兵,季玲妹,等.红色伪角毛虫无性生殖中大核DNA合成的形态学.华东师范大学学报(自然科学版),2005,8(3):109-112.
    [20]Shi X,Warren A, Song W. Studies on the Morphology and Morphogenesis of Allotricha curdsi Spn.(Ciliophora:Hypotrichida). Acta Protozool,2002, 41:397-405.
    [21]张作人,庞延斌,顾福康.棘尾虫Stylonychia mytilus包囊形成和解脱过程的研究.华东师范大学学报(自然科学学报),1981,2:113-119.
    [1]顾福康编.原生动物学概论.北京:高等教育出版社,1991.
    [2]Anderer R, Hausmann K. Properties and structures of isolated extrusive organelles. J Ultrastruct Res,1977,60:21-26.
    [3]Krugen P, Lee R E, Corliss J O. Ultrastructure, biogenesis and functions of extrusive organelles in selected non-ciliate protists. Protoplasma,1994,181: 164-190.
    [4]Steers E J, Beisson J, Marchesi V T. A structural protein extracted from the trichocysts of Paramecium aurelia. Exp Cell Res,1969,57:392-396.
    [5]Wagtendonk W J V. Paramecium-A Current Survey. Amsterdam:New York: Elsevier Scientific Pub Co,1974,273-275.
    [6]Allen R D, Ueno M S, Fok A K. A survey of lectin binding in Paramecium. J Protozool,1988,35:400-407.
    [7]Plattner H, Kissmehl R. Dense-core secretory vesicle docking and exocytotic membrane fusion in Paramecium cells. Bio Bio Act,2003,1641:183-193.
    [8]Jerka-Dziadosz M. Urostyla cristata Spn.(Urostylidae, Hypotrichida), the morphology morphgenesis. Acta protozool,1964,2:123-129.
    [9]Suganuma Y. Electron microscopy of the trichocysts in Urostyla cristata, a hypotrichous ciliate. J Electron Microsc,1973,22:347-352.
    [10]Weinke K A. Unique organization of microtubules in a protozoan trichocyst(Abstr.). Anat Eec,1972,172:432.
    [11]Grim J N, Manganaro C A. Form of the extrusomes and secreted material of the ciliated protozoon Pseudourostyla cristata with some phylogenetic. Microsc Soc, 1985,104(4):350-359.
    [12]Zhang J, Sheng C, Tang L, et al. The ultrastructure of the extrusomes in Pseudourostyla cristata, a hypotrichous ciliated protozoan. Protoplasma,2010.
    [13]Zhou Y, Wang Z J, Zhang J. Ultrastructure of extru some in hypotrichous ciliate Pseudourostyla nova. J Oceanol Limnol,2011,29(1):103-108.
    [14]章骏,倪兵,盛春,大尾柱虫粘液泡的超微结构观察.复旦学报(自然科学版),2007,46(6):972-975.
    [15]柳伟君,栾菊敏,俞丽丽,等.伪红色双轴虫皮层色素颗粒和粘液泡的显微、亚显微结构观察.复旦学报(自然科学版),2009,48(3):381-385.
    [16]宋微波等编.原生生物学.中国海洋大学出版社,2007.
    [17]Kovacs P, Muller W EG, Csaba G. A lectin-like molecule is discharged from mucocysts of Tetrahymena pyriformis in the presence of insulin. J Eukaryot Microbiol,1997,44:487-491.
    [18]Del Monte Corrado M U, Chessa M G,等Ultrastructural survey of mucocysts throughout the life cycle of Colpoda cucullus (Ciliophora, Colpodea). Acta Protozool,1996,35:125-129.
    [1]谭明,谷福,梁爱华.γ-微管蛋白:微管蛋白超家族的新成员.山西大学学报()自然科学学报),1998,21(3):297-302.
    [2]Shang Y, Li B, Gorovsky M A. Tetrahymena thermophila contains a conventional y-tubulin that is differentially required for maintenance of different MTOCs. J Cell Biol,2002,158(7):1195-1206.
    [3]Mckean P G, Braines A,Vaughan S, et al. Gamma-tubulin functions in the nucleation of a discrete subset of microtubules in the eukaryotic flagellum. Curr Biol,2003,13(7):598-602.
    [4]谭明,梁爱华.八肋游仆虫γ-微管蛋白cDNA序列及其在大肠杆菌中的表达.高技术通讯,2000(4):1-8.
    [5]柴宝峰,王景涛,梁爱华.八肋游仆虫一个新B-微管蛋白基因的克隆与序列分析.山西大学学报(自然科学学报),2007,30(2):261-264.
    [6]Marziale F, Pucciarelli S, Ballarini P, et al. Different roles of two y-tubulin isotypes in the cytoskeleton of Antarctic ciliate Euplotes focardii. FEBS Journal, 2008,275:5367-5382.
    [7]Weich H, Geier B M, Paschke T, et al. Characterization of green alga, yeast, and human centrins-Specific subdomain features determine functional diversity. J Biol Chem,1996,271(37):22453-22461.
    [1]Wichterman R. The Biology of Paramecium.1st ed.1953, Blakiston, New Youk. Hashimoto,K. Stomatogenesis and formation of cirri in fragments of Oxytricha fallas stein. J Protozool.1961,8(4):433-422.
    [2]Diller W F. Corelation of ciliary and nuclear development in the life cycle of Euplotes. J Protozool,1966,13(1):43-54.
    [3]Borror A C. Nigrosin-HgCl2-Formalim:a stain-fixative for ciliates (Protozoa,Ciliophora). Stain Tech,1968,43:293-295.
    [4]史新柏.黑色素染色法在纤毛虫和鞭毛虫研究中的使用与改进.生物学通报,2003,38(8):52-55.
    [5]Klein B M. Ergebnisse mit einer silbermethode bie ciliaten. Arch.Protist,1926, 56:243.
    [6]Gelei J V, Horvath P. Eine nasse Silber-bzw Goldmethode fur die Herstellung der reizlcitenden Elementebeiden Ciliten. Ztschr wiss Mikr,1931,48:9.
    [7]Chatton E, Lwoff A. Impregnation,par diffusion argentique,de I'infraciliature des cilies marins et d'eau douce aqres fixation cytologique et sans dessication. Compt Rend Soc Biol,1930,104:834-836.
    [8]史新柏.银浸法在纤毛虫研究中的应用.哈尔滨师范大学学报,1963,78-83.
    [9]宋微波,王梅,应用于纤毛虫银线系染色~的干银法新改良.动物学杂志,1995,30(1):38-39.
    [10]Schwartz v. Die Sicherung der arttypischen Zellform bei Ciliaren. Naturwissenschaften,1963,50:631-641.
    [11]史新柏.草履虫口器的形态和形态发生及其系统发生的意义.口器的形态学.动物学报,1980,26(3):205-212.
    [12]史新柏.草履虫口器的形态和形态发生及其系统发生的意义Ⅱ.口器发生.动物学报,1980,26(4):289-300.
    [13]Jerka-Dziadosz M, Frankel J. An analysis of the formation of ciliary promordia in the hypotrich ciliate Urostyla weissei. J Protozool,1969,16:612-637.
    [14]Ng S F, Nelsen E M. The protargol staining technique:an improved version for Tetrahumena pyriformis. Trans Amer Micros Soc,96:369-376.
    [15]Tuffrau M. Pefectionnements et pratique de la technique d'impregnation au protargol des infusories cilies.Protistologica,1967,3:91-98.
    [16]庞延斌,顾福康,邹士法.应用于腹毛类纤毛虫的一种改进的蛋白银染色方法.1983,4:87-92.
    [17]张作人,庞延斌,顾福康.急纤虫Tachysoma pellionella无性生殖周期中核器和纤毛器的演化.动物学研究,1984,5(2):189-198.
    [18]张作人,庞延斌,邹士法.尾柱虫(Urostyla cristata)的形态发生研究.动物学研究,1982,3(1):1-9.
    [19]张作人,庞延斌,顾福康.红色角毛虫的形态学和形态发生过程的研究.动物学报,1985,31(1):1-6.
    [20]庞延斌,顾福康,张作人.红色角毛虫生理改组过程的研究.动物学研究,1986,7(3):263-271.
    [21]施心路.改进的蛋白银法在伪尾枝虫类群上的应用.生物学通报,2006,41(11):52-55.
    [22]宋微波.九脊游仆虫(Euplotes novemcarinata Wang,1930)的纤毛下器与银线系.青岛海洋大学学报,1991,21(1):76-84.
    [23]刘小意,金立培.念珠伪角毛虫的形态及形态发生的研究.中山大学学报()自然科学版),2000,39(2):82-86.
    [24]Fernandez-Galiano D. Silver Impregnation of ciliated Protozoa:procedure yielding good result with the pyridinated silver carbonated method. Trans Amer Micros Soc,1976,95:557-560.
    [25]Augustin H, Foissner W, Adam H. An improved pyridinated silver carbonate method which needs few specimens and yields permanent sileds of impregnated ciliates(Protozoa,Ciliophora). Mikroskope,1984,41:134-137.
    [26]Wilbert N. Eine verbesserte Technik der Protargol impragnation fur Ciliaten Mikrokosmos,1975,6:171-179. Wilbert N. Eine neue Impragnation der Basalkorper bei Wimpertieren. Mikrokosmos,1983,7:193-197.
    [27]宋微波.氨银法的新改良—一种应用于海洋纤毛虫永久制片的新方法.海洋科学,1992,9(5):4-5.
    [28]Arnal I, Wade R H. How does taxol stabilize microtubules. Curr Biol,1995,5(8): 900-908.
    [29]Amos L A, Lwe J. How Taxol(R) stabilizes microtubule structure. Chen Biol (London),1999,6(3):R65-R69.
    [30]Arregui L, Munoz-Fontela C, Serrano S, et al. Direct visualization of the microtubular cytoskeleton of ciliate protozoa with a fluorescent taxoid. J Euk Microbiol,2002,49:312-318.
    [31]Arregui L, Munoz-Fontela C, Guinea A, et al. FLUTAX facilitates visualization of the ciliature of oxytrichid hypotrichs. Europ J Protostol,2003,39:169-172.
    [32]何兰,曾红,沈洁,等FLUTAX法显示纤毛虫微管胞器的改良.动物学杂志,2006,41(3):59-61.
    [33]曾红,倪兵,顾福康,原生动物贻贝棘尾虫微管胞器的荧光标记与显示.动物学杂志,2006,41(4):71-76.
    [34]娄慧玲,高巍,倪兵,等.魏氏拟尾柱虫福皮层纤毛器微管胞器的形态及形态发生.动物学报,2007,5(4):742-749.
    [35]沈洁,何兰,顾福康.红色伪角毛虫微管胞器的免疫荧光观察.华东师范大学(自然科学版),2007,3(2):126-128.
    [36]赵柳,运迷霞,柳伟君,等.华美游仆虫细胞微管胞器的直接荧光和免疫荧光标记.动物学杂志,2008,43(3):1-6.
    [37]周素娟,尹飞,生欣,等.冠突伪尾柱虫的腹皮层纤毛器微管胞器及其形态发生.动物学报,2008,54(2):299-308.
    [38]高巍,史磊,顾福康.异毛虫Allotricha curdsi皮层纤毛器基部微管的荧光标记,复旦学报(自然科学版),2007,46(2):976-980.
    [39]史磊,运迷霞,顾福康.草丛土毛虫皮层纤毛器的微管胞器研究.分子细胞生物学报,2009,42(2):109-116.
    [40]尹飞,生欣,顾福康.腹毛目纤毛虫鬃棘尾虫纤毛器基部微管的荧光标记.四川动物,2009,28(3):350-353.
    [41]周瑶,余齐耀,俞丽丽,等.新伪尾柱虫腹皮层纤毛器微管胞器的形态和形态发生.动物学杂志,2009,44(3):74-80.
    [42]刘兰侠,余齐耀,俞丽丽.腹毛目纤毛虫大尾柱虫腹皮层纤毛器基部微管的荧光标记.四川动物,2010,29(4):576-579.
    [43]陈晶,邱子健,王瑞清,等.运用激光共聚焦显微技术研究大草履虫口胞器与消化胞器.动物学报,2005,51(4):718-722.
    [44]Small E B, Marszalek D S. Scanning Electron Microscopy of Fixed, Frozen, and Dried Protozoa. Science,1969,163(3871):1064-1065.
    [44]Ruffolo J J Jr. Critical point drying of protozoan cells and other biological specimens for scanning electron microscopy:apparatus and methods of specimen preparation. Trans Amer Micros Soc,1974,93(1):124-134.
    [46]顾福康,庞延斌,张作人.一种游仆虫无性分裂生殖的研究Ⅰ形态学和核器的演化.动物学报,1987,33(3):244-247.
    [47]顾福康,庞延斌,张作人.一种游仆虫无性分裂生殖的研究Ⅱ无性分裂过程中皮层结构的形态发生,1987,33(4):362-366.
    [48]顾福康,张作人.包囊游仆虫的皮层及其纤毛结构的形态学研究.华东师范大学学报(自然科学学版),1990,(4):102-109.
    [49]顾福康,张作人,包囊游仆虫包囊形成和解脱过程中纤毛器的分化.动物学报,1991,37(3):287-292.
    [50]顾福康,张作人,阔口尖毛虫无性生殖和生理改组过程的比较.动物学研究,1992,(4):375-380.
    [51]顾福康,倪兵.原生动物扫描电镜样品制备方法的探讨.电子显微学报,1993,6:525-529.
    [52]顾福康,周庆新.伍氏游仆虫无性生殖中前仔虫口围带的起源.华东师范大学(自然科学版),1993,(1):111-112.
    [53]邹士法,张作人.苔藓织毛虫的形态和形态发生.动物学报,1992,38(4):345-351.
    [54]戴美玲,顾福康,周庆新.尾草履虫分裂及非分裂期间皮层表面的形态学研究.宁波大学学报(理工版),1994,7(1):38-45.
    [55]顾福康,倪兵.似旋毛草履虫的光镜和扫描电镜观察.华东师范大学学报(自然科学版),1995,(3):38-45.
    [56]金立培,张志宇.伪尾柱虫有性周期中纤毛器原基的发生与决定.中山大学学报(自然科学版),1997,36(1):60-63.
    [57]鲍小娟,冯玲玲,倪兵.异毛虫Allotricha curdsi的形态及形态发生的扫描电镜观察.复旦学报(自然科学版),2007,46(6):981-991
    [58]汤蕾,倪兵,顾福康.贻贝棘尾虫腹皮层纤毛器形态发生的扫描电镜观察.华东师范大学学报(自然科学版),2008,(2):100-106.
    [59]冯玲玲,郭键,鲍小娟,等.草丛土毛虫的超微结构观察.复旦学报(自然科学版),2009,48(3):367-374.
    [60]王正君.纤毛虫三缘双轴虫的皮层纤毛器及细胞质胞器的超微结构.华东师范大学硕士毕业论文,2010.
    [61]Grim J N, Halcrow K R, Harshbager R D. Microtubules beneath the pellicles of two ciliate protozoa as seen with the SEM. J Protozool,1980,27(3):308-310. Bussers J C, Hoesdorff M, Bolome M, Greco N, Goffinet G, et al. L'enkystement du cilie hypotriche Euplotes muscicola. Protistologica,1986,22(4):457-460.
    [62]邹士法,张作人.近亲游仆虫Euplotes affinis Dujardin的毛基体水平的扫描电镜研究.动物学报,1989,(4):360-363.
    [63]顾福康,张作人.一种游仆虫棘毛基部纤维的形态及其在形态发生过程中 的演化.动物学研究,1989,10(2):89-96.
    [64]顾福康,邹士法,李艺松,等.镰游仆虫腹面皮层细胞骨架的扫描电镜观察.动物学报,2003,49(4):514-521.
    [65]朱慧,邹士法,李艺松,等.用非离子去垢剂抽提获得的小游仆虫皮层细胞骨架的构形.动物学研究,2004,25(5):422-428.
    [66]Arikawa M, Watanabe A. SEM Observation on the Ultrastructure of Isolated Macronucleus in Euplotes aediculatus, Jap J Protozool,1998,31(1):39.
    [67]顾福康,季玲妹.包囊游仆虫皮层和营养核的超微结构研究.动物学研究,1996,17(1):16-22.
    [68]赵柳.纤毛虫华美游仆虫微管胞器和核器的细胞与分子生物学研究.华东师范大学硕士毕业论文,2008.
    [69]Grim J N. Ultrastructure pellicular and ciliary structures of Euplotes eurystomus. J Protozool,1967,14(4):625-634.
    [70]尹飞.腹毛目纤毛虫鬃棘尾虫细胞纤毛器微管胞器及微管蛋白的研究.华东师范大学博士毕业论文,2009.
    [71]周瑶.腹毛目纤毛虫新伪尾柱虫微管胞器和射出胞器的研究.华东师范大学博士毕业论文,2010.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700