黑翅痂蝗血细胞形态学的研究

【目的】蝗虫血细胞的研究以及不同血细胞类型间的演化关系,是蝗虫细胞免疫学的依据,也是防蝗治蝗的重要依据。【方法】本研究通过Wright-Giemsa对黑翅痂蝗Bryodema nigroptera Zheng血细胞进行了混合染色,并使用光学显微镜进行了观察。【结果】发现黑翅痂蝗血细胞包括原血胞、浆血胞、粒血胞、类绛色血细胞、囊血胞、脂血胞、蠕形细胞和巨核血细胞8种类型。【结论】在成虫体内,原血胞占细胞总数的1%,浆血胞占32.2%,粒血胞占57.3%,类绛色血细胞占1%,囊血胞占6%,脂血胞占1%,蠕形细胞占1%,巨核细胞占细胞总数的0.5%,粒血胞数量最多,巨核细胞最少。     

幼虫密度对草地螟血细胞数量和组成的影响

为了阐明幼虫密度对草地螟Loxostege sticticalis L.（鳞翅目： 螟蛾科）细胞免疫能力的影响, 本研究调查了在活体灰菜植株上1,5,10和20头/瓶（900 mL）4种密度条件下的其5龄幼虫血细胞种类、数量和组成。结果表明： 草地螟幼虫血淋巴中有原血细胞、浆血细胞、 颗粒血细胞、珠血细胞和类绛色血细胞等5种（类）血细胞。血细胞总数、 浆血细胞、颗粒血细胞数量随幼虫密度的增加而显著递增, 但原血细胞、珠血细胞和类绛色血细胞数量在幼虫密度间的差异不明显;各种血细胞所占血细胞总数的比例在4个密度中的排序相同, 但10和20头/瓶密度下的浆血细胞比例显著高于1头/瓶的,其余4种血细胞的比例在不同密度之间无显著差异。可见, 幼虫密度主要是通过影响草地螟幼虫浆血细胞和颗粒血细胞的数量及血细胞总数, 从而影响草地螟的细胞免疫能力。     

斜纹夜蛾幼虫造血器官的形态、组织及超微结构

斜纹夜蛾Spodoptera litura Fabricius幼虫的造血器官位于翅芽部位,由发育层次不同的许多细胞岛和一些单个或成串的梭形细胞组成.各细胞岛或细胞均裹有一层非细胞性膜鞘.环绕同一翅芽的众多细胞岛和细胞相互间由其膜鞘连结成簇.膜鞘紧裹着的单个或成串梭形细胞具未分化细胞特征.发育初期的单个细胞岛体积较小,直径约20—45μm以下,岛内均为排列紧密的分化中未成形原血细胞.较发育的细胞岛体积较大,细胞间排列较松,岛内除原血细胞外,还出现少量浆血细胞、颗粒细胞和小球细胞的分化.此外,还发现一个具颗粒细胞和小球细胞特征的混合细胞类型.发育初期的细胞岛膜鞘表面结构完好.随着岛内细胞的增殖分化,膜鞘出现破裂,且破裂逐渐增大,以致完全破裂而裸露岛内细胞团,以此释放血细胞.大量血细胞释放出现于幼虫预备脱皮至下一龄幼虫初期的造血器官.各龄幼虫的各发育阶段血淋巴血细胞总数(THC)的变动与造血器官释放血细胞密切相关.     

菜粉蝶蛹血细胞体外细胞免疫反应及蝶蛹金小蜂毒液的影响

为探明蝶蛹金小蜂Pteromalus puparum毒液对其寄主菜粉蝶Pieris rapae蛹颗粒血细胞和浆血细胞的包囊与吞噬能力的影响, 本研究分别采用Na₂-EDTA处理和尼龙毛法对菜粉蝶蛹颗粒血细胞与浆血细胞进行分离纯化; 再采用离体细胞培养方法, 研究了菜粉蝶蛹颗粒血细胞、 浆血细胞各自在包囊和吞噬反应中的作用, 以及蝶蛹金小蜂毒液对其所产生的影响。结果表明： 颗粒血细胞和浆血细胞均参与了包囊反应, 其中前者包囊作用明显, 后者作用微弱, 但两者同时存在时包囊作用最为明显; 血淋巴浆质对颗粒血细胞和浆血细胞包囊反应均无显著影响。毒液对颗粒血细胞和浆血细胞的包囊能力均存在显著的抑制作用, 且抑制作用具有明显的剂量效应特征。此外, 菜粉蝶蛹颗粒血细胞和浆血细胞均具吞噬能力, 其中前者吞噬能力显著强于后者; 毒液对颗粒血细胞与浆血细胞的吞噬能力亦均存在显著的抑制作用, 且该抑制作用亦具有显著的剂量效应特征。结果说明, 菜粉蝶蛹颗粒血细胞及浆血细胞均参与寄主的细胞免疫反应, 蝶蛹金小蜂毒液对其寄主颗粒血细胞和浆血细胞的包囊与吞噬能力均存在显著的抑制作用。     

罗氏沼虾与克氏原螯虾血细胞的比较研究

对罗氏沼虾与克氏原螫虾血细胞的分类与组成进行了染色观察比较研究。根据染色后光镜下血细胞的核质比、颗粒的大小和数量等来对血细胞进行分类,罗氏沼虾与克氏原螯虾的血细胞均可分为透明细胞、半颗粒细胞和颗粒细胞三类;其血细胞浓度分别为1.02±0.21×10⁷ Ind·ml^-1和0.85±0.15×10⁷Ind·ml^-1。2种虾血细胞的颗粒形态存在显著差异;透明细胞、半颗粒细胞和颗粒细胞占血细胞总量的百分比在罗氏沼虾为21.3±6.3%,45.7±2.5%,33.0±6.8%:在克氏原螯虾为12.0±5.8%、49.5±5.1%和38.5±9.5%。     

栉孔扇贝血液细胞的免疫功能

利用光镜、扫描电镜和透射电镜技术对栉孔扇贝(Chlamysferreri)血细胞与细胞免疫功能相关的几个因素进行了初步研究。对血细胞的数量和不同功能细胞的比例研究结果表明,健康血淋巴中血细胞的平均密度为3.03±0.11×107cell/ml,其中颗粒细胞占42.6%,透明细胞占57.4%;病贝血淋巴中血细胞的平均密度为2.78±0.34×107cell/ml,其中颗粒细胞占40.2%,透明细胞占59.8%。扫描电镜观察表明,血细胞的表面结构主要有表面光滑型,表面松果型和表面褶皱阿米巴型3类。透射电镜观察表明,颗粒细胞吞噬外源性颗粒(Ⅰ型颗粒)通过溶酶体(Ⅱ型颗粒)进行降解。并观察到同心片层结构出现在吞噬泡的降解过程中。利用APIZYM试剂盒对栉孔扇贝血细胞及血清中的19种酶进行检测,结果在血清中检测到了13种酶,在血细胞中检测到10种酶,健康血淋巴中酶的含量高于病贝。对血细胞吞噬活性的研究结果表明,血细胞对大肠杆菌和对类立克次体(RLO)的吞噬率分别为25.4%和21.7%。颗粒细胞的吞噬活性(30%-40%)远远大于透明细胞(4.8%-14%)。环境胁迫对血细胞吞噬活性的影响的研究结果表明,病原菌感染和温度、盐度等环境胁迫因素对血细胞的吞噬活性均有不同程度的影响,其中高温因素影响较大,但未发现贝龄有显著影响     

胚后发育期臭腹腺蝗中的血细胞种类

应用血球计数器统计了胚后发育期臭腹腺蝗Zonocerus variegatus中存在的血细胞类型和数目。从1龄幼虫至成虫的发育阶段中共观察到6种血细胞类型,即原血细胞 （PRS）、 浆血细胞 （PLS）、粒细胞 （GRS）、珠血细胞 （SPS）、绛色细胞（OES） 和adipohaemocytes （ADS）。不过,在1龄幼虫期未发现OES。在这6种血细胞中,PLS的总平均数最高,OES的总平均数最低。成虫期的血细胞数目显著高于其他发育阶段（P<0.05）,而1龄幼虫和2龄幼虫期的血细胞数目不存在显著差异（P>0.05）。     

草履蚧血细胞的显微形态与超微结构观察

为研究蚧虫血淋巴中血细胞的种类及其结构特征,采用相差显微镜、荧光显微镜和扫描电镜与透射电镜技术,观察了草履蚧雌成虫血细胞的显微形态与超微结构特征.结果显示,在荧光显微镜和扫描电镜下观察识别出草履蚧血淋巴中的5种血细胞,即：原血胞、浆血胞、粒血胞、囊血胞和类绛色血细胞.在透射电镜下可见,原血胞的细胞核明显,表现出高的细胞质密度;浆血胞最典型的特征是细胞质中有大量的囊泡;粒血胞的细胞质中有发达的粗面内质网和许多玫瑰形的细颗粒.类绛色血细胞最典型的特征是有许多结晶,并在细胞质的空泡区内分布的更多.囊血胞透明性强,具有围核空间,膨大成潴泡状.     

贝类血细胞及其免疫功能研究进展

贝类由于是开放性系统,不存在特异性体液免疫,贝类的宿主免疫防御包括以血细胞为基础的细胞和体液系统。血细胞能够在体内或体外吞噬各种有机和无机颗粒,清除病原生物和自身损伤或死亡细胞,而且血细胞能够产生各种非特异性体液因子来参与宿主的免疫防御过程。所以贝类的血细胞在宿主免疫防御机制中起着重要作用。近年来,随着贝类养殖规模的扩大,贝类病害日益严重,给中国的贝类养殖业造成了重大经济损失[1,2]。所以研究贝类免疫学,特别是贝类血细胞的免疫防御功能和机制,以解决贝类养殖中发生的病害问题已成为研究的热点。本文依据国内外有关文献,就贝类血细胞的分类、结构及免疫功能方面的研究作一综述,为国内外研究提供理论基础及资料。1贝类血细胞结构、分类贝类血细胞的分类一直分歧很大,有人将其分为三类:无颗粒细胞、小颗粒细胞、大颗粒细胞,也有人将其分为四类:大颗粒细胞、小颗粒细胞、透明细胞、浆细胞,还有人将其分为八类,甚至几十类,至今无统一命名[3]。关于血细胞的分类,Moore等[4]根据血细胞超微结构和对染色反应的不同,将紫贻贝(Mytilus galloprovincialis)血细胞分为两大类,无颗粒的嗜碱性细胞和有颗粒的嗜酸性颗粒细胞...     

重金属Cd2+对棕尾别麻蝇血细胞数量、包囊作用和形态结构的影响

为了揭示重金属对昆虫细胞免疫的影响及其机理,本文采用血细胞计数、台盼蓝染色、延展与包囊率测定, 以及显微与超微结构观察等方法,以经重金属Cd²⁺（浓度为150 μg/g）处理的棕尾别麻蝇Boettcherisca peregrina及其对照为研究对象,分别测定了处理组与对照组血细胞的数量与存活率、延展与包囊率,观察其形态结构,并比较了两组间的差异。结果表明： 棕尾别麻蝇初产幼虫经连续喂饲含Cd²⁺的饲料24,48,72和96 h后,与对照相比其血细胞总数和存活率显著下降,而血细胞的延展率和包囊作用的显著下降则分别出现于取食72和48 h之内,此后则下降不显著;由Cd²⁺处理幼虫发育形成蛹的血细胞包囊作用也显著低于对照。形态结构观察结果表明,Cd²⁺处理对幼虫的原血细胞、浆血细胞、颗粒血细胞和类绛色血细胞的显微形态影响不大,但可导致部分浆血细胞不能产生伪足;但均能导致各类血细胞的超微结构发生不同程度的变化,其中主要变化包括：细胞膜受损或破裂,染色质呈现凝聚, 线粒体和内质网等细胞器明显减少,以及胞质内出现空囊泡。结果说明重金属Cd²⁺对棕尾别麻蝇的血细胞可具有毒害作用。     

Classification of larval circulating hemocytes of the silkworm,<Emphasis Type="Italic"> Bombyx mori</Emphasis>, by acridine orange and propidium iodide staining

Circulating hemocytes of the silkworm can be classified by fluorescence microscopy following staining with acridine orange and propidium iodide. Based on their fluorescence characteristics, three groups of circulating hemocytes can be distinguished. The first group, granulocytes and spherulocytes, is positive for acridine orange and contain bright green fluorescent granules when observed by fluorescence microscopy. In granulocytes, these green granules are heterogeneous and relatively small. In contrast, in spherulocytes, the green granules appear more homogenous and larger. The second group of hemocytes consists of prohemocytes and plasmatocytes. These cells appear faint green following staining with acridine orange and do not contain any green fluorescent granules in the cytoplasm. Prohemocytes are round, and their nuclei are dark and clear within a background of faint green fluorescence. Inside the nucleus there are one or two small bright green fluorescent bodies. Plasmatocytes are irregularly shaped and their nuclei are invisible. Oenocytoids belong to the third group, and their nuclei are positive for propidium iodide. Therefore, all five types of circulating hemocytes of the silkworm, including many peculiar ones that are difficult to identify by light microscopy, can now be easily classified by fluorescence microscopy following staining with acridine orange and propidium iodide. In addition, we show that hemocytes positive for acridine orange and propidium iodide are in fact living cells based on assays for hemocyte composition, phagocytosis, and mitochondrial enzyme activity.     

Hemocyte differentiation in the hematopoietic organs of the silkworm, <Emphasis Type="Italic">Bombyx mori</Emphasis>: prohemocytes have the function of phagocytosis

Hemocytes isolated from the larval hematopoietic organs of the silkworm were classified following staining with acridine orange and propidium iodide. Among the hemocytes isolated from the hematopoietic organs of whole fifth larval and wandering stages, most were prohemocytes (60%–70%) and oenocytoids (30%–40%). Granulocytes comprised only about 0.5%–1% at the wandering stage and were even rarer at other stages; no spherulocytes or plasmatocytes were found. Therefore, hemocyte differentiation inside larval hematopoietic organs is not as extensive as previously thought. Following 10–30 min in vitro culture of hemocytes isolated from larval hematopoietic organs, many young granulocytes and plasmatocytes appeared. Furthermore, during phagocytosis assays, prohemocytes were seen to adopt the morphology of plasmatocytes, containing fragments of phagocytosed cells. Our results underline the similarities between Drosophila and Bombyx hematopoiesis.     

Reexamination of phenoloxidase in larval circulating hemocytes of the silkworm, Bombyx mori

We have developed a modified method to detect phenoloxidase activity on hemocytes by using freshly prepared l-DOPA (1 mg/ml in 35% ethanol) to fix and incubate larval hemocytes. This method is more sensitive than the common method, in which hemocytes were fixed in 4% formaldehyde and then incubated with 2 mg/ml l-DOPA in water separately. Phenoloxidase assayed using this modified method can be inhibited by phenyltiourea (phenoloxidase inhibitor). After incubation with l-DOPA solution in ethanol, most prohemocytes, all plasmatocytes and young granulocytes are stained brown due to oxidation of l-DOPA into pigments, indicating that they have phenoloxidase. Oenocytoids are dimly stained because many of their cell inclusions have been released during the treatment. Large propidium-iodide-negative prohemocytes have strong phenoloxidase activity and are easily misunderstood as propidium-iodide-positive oenocytoids if the fluorescent method is not used for identification. Thus, in addition to oenocytoids and plasmatocytes, some prohemocytes and granulocytes in the silkworm also have phenoloxidase.     

Immunocytochemical localization of β-1,3-glucan recognition protein in the silkworm,Bombyx mori

Summary A monospecific antibody against -1,3-glucan recognition protein (a 62 kDa protein) of the larval silkworm prophenoloxidase activating system was used to study the localization of the protein. Among tissues from 5th instar larvae, only hemocytes and plasma were shown to contain a 62 kDa polypeptide immunoreactive with the antibody. Ultra-thin sections of the hemocytes were stained by an indirect immunogold staining method. Labelling occurred in the granules and cytoplasm of granulocytes and in the spherules and cytoplasm of spherulocytes. It was most conspicuous in granules of granulocytes and uniformly labelled spherules of spherulocyte, whereas no labelling was evident in prohemocytes, plasmatocytes and oenocytoids. The results are discussed in relation to the mode of recognition of fungi as non-self in insect hemocoel.     

Ultrastructure of the hemocytes of Cetonischema aeruginosa larvae (Coleoptera,Scarabaeidae): involvement of both granulocytes and oenocytoids in in vivo phagocytosis

In the context of comparative studies on immunity defence mechanisms of adults and larvae of the coleopteran Cetonischema aeruginosa (Drury, 1770) the ultrastructure of the circulating hemocytes of the third instar larval stage has been investigated by means of light and transmission electron microscopy (TEM). Six types of hemocytes were found in the hemolymph of C. aeruginosa and they were identified as prohemocytes, granulocytes, plasmatocytes, coagulocytes, oenocytoids and spherule cells. In order to identify the "professional" phagocyte cell, phagocytosis assays were performed in vivo by injection of 0.9 microm carboxylate-modified polystyrene latex beads. It was demonstrated that the granulocytes and the oenocytoids of C. aeruginosa were the only hemocyte types involved in this cellular response.     

Données sur la localisation ultrastructurale d'une activité phénoloxydasique dans les hémocytes circulants d'Antheraea pernyi au dernier âge larvaire

Phenoloxidase activity has been demonstrated (with Dopa as a substrate) only in oenocytoids and in intermediate forms between plasmatocytes and oenocytoids (pro-oenocytoids) among five haemocyte types identified in the last larval stage of silkworm Antheraea pernyi. This activity is localized within the cytosol and also in the dense granules. No phenoloxidase reaction product has been observed within premelanosome-like granules of granulocytes and pro-oenocytoids. Control and experiment incubations suggest that the localization of reaction product correspond to two forms of phenoloxidase: one bound to cytoplasmic bodies an the other soluble in the cytosol.     

东亚飞蝗血细胞形态学研究

通过Wright's染色和光学显微镜对不同地区东亚飞蝗的血细胞进行了观察,发现东亚飞蝗Locusta migratoria manilensis(Meyen)的血细胞包括原血胞、浆血胞、粒血胞和类绛血胞4种类型.原血胞的细胞核为红色,而其它3种血细胞的细胞核均被Wright's染液染成红色和蓝色2种类型.故认为浆血胞是...     

Ultrastructural and functional characterization of circulating hemocytes from Plutella xylostella larva: Cell types and their role in phagocytosis

The hemocytes of different types encountered in the diamondback moth Plutella xylostella larvae of each instar and the development of the differential hemocytes counts were herein presented. Hemocytes classes/populations characterized based on their affinity with fluorescent dye (acridine orange) and ultrastructural differences comprised the prohemcoytes (<10–16%), plasmatocytes (22–65%), granulocytes (25–72%), oenocytoids (<1–9%), and spherulocytes (<1%). Prohemcoytes were the smallest cells with a comparatively tremendous nucleus. Plasmatocytes and granulocytes occupied the main proportion of total cell numbers. Oenocytoids were in a most stable presence, i.e. rotund in a diameter of 10 μm and with a nucleus deviated from the central location; however, sometimes with two nuclei which were adjoining with each other. Spherulocytes were rare and only could be observed occasionally. Ultrastructural investigation revealed that hemocytes in the diamondback moth larvae were of the typical model as in the Lepidoptera insect larvae. It is interesting to find that the cell which could phagocytize bacteria in vitro was granulocyte, not the other types of hemocytes, although plasmatocyte was usually declared to participate in this reaction in various previous studies.     

Immunolocalization of prophenoloxidase among hemocytes of the silkworm, Bombyx mori

Silkworm (Bombyx mori) hemocytes were fixed immediately after collection. Thin sections of the hemocytes were stained by an indirect immunogold staining method using rabbit anti-prophenoloxidase/IgG as a primary antibody and colloidal gold coated with goat anti-rabbit/IgG as a secondary antibody. Electron micrographs of the sections revealed that only plasmatocytes and oenocytoids have prophenoloxidase both in cytoplasm and nucleus whereas granulocytes, spherulocytes and prohemocytes do not have appreciable amounts of the proenzyme. Cytoplasmic inclusions of oenocytoids also contain the proenzyme. A wide variety of concentrations of prophenoloxidase was observed among oenocytoids. Plasmatocytes appeared to have less prophenoloxidase than any oenocytoids. Once materials in the granules of granulocyte were discharged into the plasma and formed coagula, they cross-reacted with antiprophenoloxidase/IgG, suggesting that prophenoloxidase was trapped in the coagula by unknown mechanisms. This observation is discussed in relation to the dispute concerning the presence of prophenoloxidase or phenoloxidase in the granulocyte.