Effects of juvenile hormone and molting hormone on rectal pad development in Hyalophora cecropia (L.)

The histology of the rectal pads was examined in H. cecropia that had been injected as pupae with juvenile hormone or molting hormone. The appearance of the rectal tissues was related to the degree of imaginal differentiation which in turn depended on the dose of juvenile hormone applied. Juvenile hormone inhibits the division of the small hindgut cells that normally form the general rectal wall of the adult. High doses totally suppress the differentiation of the cortical cells. The medullary cells are very sensitive to juvenile hormone even in animals in which the external morphology is only slightly affected. Relatively high doses of molting hormone result in the formation of large, elongate complexes of cortex cells. These are more typical of primitive insects than of Lepidoptera.     

The distribution of (Na+ + K+)-ATPase along the villus crypt-axis in the rabbit small intestine

The migration of intestinal epithelial cells from the crypts to the tips of villi is associated with progressive cell differentiation. The changes in Na+-pump levels during migration have been measured in epithelial cells isolated from rabbit small intestine. A significant proportion of ouabain-sensitive (Na+ + K+)-ATPase in the cell homogenates was latent but could be unmasked by detergent treatment. Highest detergent activation was observed in villus cells. The distribution of pumping sites was also assessed by measuring ouabain binding to intact cells. The kinetics of specific binding was consistent with the interaction of the cardiac glycoside with a single population of binding sites with an apparent Kd of around 10(-7) M. Both enzyme assay and ouabain-binding measurements suggest that a 2-3-fold increase in the number of Na+-pumping sites accompanies cell differentiation in rabbit jejunal epithelium. This increase in pumping capacity might be an adaptation of the cells to their absorptive function.     

Cell renewal in the epidermis of the loach Misgurnus anguillicaudatus (Cypriniformes)

Cell kinetics of the epidermal cells of normal juvenile loach ( Misgurnus anguillicaudatus ) were studied with autoradiography. Fish were labelled with single tritiated thymidine injections and killed at regular time intervals. Three cell types are identified by light microscopy, namely the epithelial cells, the club cells and the mucous cells. Epithelial cells are the only cell type that is involved in cell proliferation and, like the epithelial cells in the epidermis of other teleosts, proliferation of these cells occurs at all epidermal layers. The club cells and the mucous cells seem to be differentiated from the epithelial cells. Based on the time-course study of the labelling index and the grain count halving method, the generation time of the epithelial cells is estimated to be 4 days. From the labelling index of double injections, the duration of the S phase is determined as 8.3 h. Significant cell loss from the outermost layer and cell translocation from the lower layer to the upper layer within 4 days are inferred from the fluctuations of the labelling index curve. The renewal of these cells in the tissue seems rapid in comparison to the epidermis of terrestrial vertebrates.     

Development and differentiation of the reproductive system of Tropidurus catalanensis (Squamata: Tropiduridae)

Development and differentiation of the reproductive system in lizards begin in the embryonic period, although the stage and time of their occurrence vary according to populations and species. In this study, the events of the development and differentiation of the reproductive system of males and females of Tropidurus catalanensis were characterized during the embryonic, neonatal, and juvenile periods. Embryos at Stages 27, 34, 37, 40, and 41, neonates and juveniles, from Corrientes, Argentina, were analyzed. At Stage 27, the genital ridge was not observed but primordial germ cells were recorded in the yolk sac as well as the mesenteric mesenchyme, indicating the beginning of germ cell migration. Gonadal differentiation commenced at Stage 34. In males from Stage 37, the testes possessed seminiferous cords with Sertoli cells and spermatogonia, while in hatchlings seminiferous tubules and interstitial tissue with mature Leydig cells were present. Spermatogenesis was observed in a specimen of 51.9 mm snout-vent length, corresponding to the minimum reproductive size. In females, from Stage 37 until hatching, the ovaries had a cavernous medulla and a cortex with somatic cells and abundant oogonia. The onset of meiosis and folliculogenesis occurred in the juvenile period.     

Epidermal club cells and the innate immune system of minnows

Thousands of fish species belonging to the Superorder Ostariophysi possess specialized club cells in their epidermis. Damage to the cells, as would occur during a predator attack, releases chemical substances that evoke antipredator responses in nearby shoalmates. These chemical substances have often been referred to as alarm substances and the cells that release them as alarm cells. Understanding the evolution of the cells in an alarm context has been difficult. The fish needs to be captured prior to the chemicals being released, hence the benefit to the receiver is unclear. Recent studies have suggested that the club cells are part of the immune system and are maintained by natural selection owing to the benefits that they confer against pathogens, parasites, and general injury to the epidermis. In the present study, we gave fathead minnows intraperitoneal injections of cortisol, a known immunosuppressant, or injections of a control substance (corn oil). We found that fish exposed to cortisol had suppressed immune systems (as measured by a respiratory burst assay) and that they also reduced their investment in club cells. This is the best evidence to date indicating that the club cells of Ostariophysan fishes are part of the innate immune system and that the alarm function of the cells evolved secondarily. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 98 , 891–897.     

Socializing makes thick-skinned individuals: on the density of epidermal alarm substance cells in cyprinid fish, the crucian carp (Carassius carassius)

In cyprinid fish, density of epidermal club cells (i.e. alarm substance cells) has been found to vary between lakes with different predator fauna. Because predators can be labelled with chemical cues from prey, we questioned if club cell density could be controlled indirectly by predators releasing prey cues. In particular, we suspected a possible feedback mechanism between chemical alarm signals and their cellular source. We raised crucian carp singly and in groups of four. For both rearing types, fish were exposed to skin extracts of either conspecifics or brown trout (without club cells), and provided either low or high food rations. Independent of rearing type, condition factor and club cell density increased with food ration size, but no change was found in club cell density following exposure to conspecific alarm signals. However, the density of club cells was found significantly higher for fish raised in groups than for fish raised alone. We conclude that an increased condition factor results in more club cells, but crucian carp may also possess an awareness of conspecific presence, given by higher club cell densities when raised in groups. This increase in club cell density may be induced by unknown chemical factors released by conspecifics.     

气候变暖对青藏高原牧草营养含量及其体外消化率影响模拟研究

全球气候变暖,气温上升的趋势逐步被众人接受,而青藏高原这一独特地理单元的生态系统对气候变暖十分敏感.为更好地了解气候变暖对青藏高原牧草品质的影响,利用大板山北坡3 200～3 800 m的海拔梯度,以温度为主要影响因子,用海拔高度不同造成的温差模拟全球变暖带来的升温效应,研究气候变暖对青藏高原牧草营养含量及其体外消化率的影响.针对羊茅(Festuca ovina)、早熟禾(Poa annua)、草(Koeleria cristata)、矮嵩草(Kobresia humilis)和黑褐苔草 (Carex alrofusca) 5种生长在不同海拔梯度的高原牧草中酸性洗涤纤维(ADF)、木质素(ADL)、粗蛋白(CP)、粗脂肪(EE)、无氮浸出物(NFE)、灰分等营养含量及其经绵羊瘤胃液培养后的体外消化率差异,经过1999和2000年两年的测定分析,结果表明:随着温度升高,牧草CP、EE和NFE的百分含量都呈现降低的趋势;牧草ADF和ADL百分含量与温度存在正相关关系,随着温度升高牧草ADF、ADL百分含量都呈增加的趋势;牧草体外消化率与牧草生长的环境温度存在负相关关联,随着温度升高牧草体外消化率呈降低趋势.模拟研究表明,就温度这一重要环境因素而言,未来气候变暖尤其是夜间温度的升高引起青藏高原牧草营养品质的变化,牧草CP、EE、NFE含量的降低,中性洗涤纤维(NDF)、ADL含量的增加,牧草消化率降低,从而不利于反刍动物对牧草的消化利用.     

The club‐shaped gland of amphioxus: export of secretion to the pharynx in pre‐metamorphic larvae and apoptosis during metamorphosis

In amphioxus larvae, the club‐shaped gland is a tube connecting the pharyngeal lumen with the external environment. The functions of the gland and its fate during the larva‐to‐juvenile metamorphosis have long been controversial. Here we use a fixative including ruthenium red to preserve extracellular secretions (presumably glycoproteins) in late pre‐metamorphic larvae. This procedure reveals reddish, fibrogranular material in the lumen of the club‐shaped gland and in the pharynx adjacent to the gland's inner opening. This finding strengthens the idea that secretions of the club‐shaped gland are exported to the pharyngeal lumen to help form a mucous trap for capturing food particles entering the mouth. We also use the terminal desoxynucleotidyl transferase‐mediated dUTP nick end labelling (TUNEL) assay to study apoptosis in the tissues of metamorphosing larvae. One of the earliest events of metamorphosis is the massive apoptotic destruction of the club‐shaped gland. Therefore, despite some previous opinions to the contrary, the cells of the gland do not survive to participate in the genesis of the definitive endostyle or any other post‐larval structures.     

Quantitative studies on cell differentiation during morphogenesis of the cellular slime mold Dictyostelium discoideum

Taking advantage of the fact that differentiation of the prespore cell of Dictyostelium discoideum is characterized by synthesis of a prespore specific antigen, the process of its differentiation during the course of morphogenesis was quantitatively studied by determining the proportion of prespore cells and their cellular contents of the antigen, using the method of microfluorometry in combination with immunocytochemistry with antispore serum. The cells synthesizing the antigen became first detectable in the early aggregation center which was about to form a papilla. As the papilla elongated, the number of prespore cells rapidly increased up to the stationary level (70–80% of total cells) before completion of slug formation. During the process antigenic contents of prespore cells were gradually increased and leveled off in the early migration stage. When culmination was induced, antigenic contents were markedly increased to the maximum, which was followed by a sudden decrease immediately before spore formation. On the other hand, the proportions of prespore to total cells were kept constant at the stationary level all through the migration and culmination stages, in spite of a persistent decrease during culmination in the total number of cells due to continuous differentiation of the prestalk into the mature stalk cells. These results were discussed in relation to possible mechanisms of differentiation in this organism.     

Development of Chemoreceptor Cells in Oral Epithelium of Adult Jelly-Fish Beroë cucumis

In oral epithelium of adult jelly-fish Beroë cucumis, the main stages of differentiation of chemoreceptor cells replacing damaged degenerating chemoreceptors are described. The initial stages are connected with transformation of the so-called precursor cells that on transformation into juvenile cells, are inserted from mesoglea into basal epithelial areas. In the juvenile chemoreceptor cells, there continue ultrastructural transformations connected with differentiation of the apical sensory apparatus, central process, and innervation. Consecutive spatial translocations of these cells in epithelium are traced, up to their insertion into the superficial layer and replacement of degenerated chemoreceptors. The literature and the authors' own data about possible sources of origin and ways of utilization of damaged jelly-fish chemoreceptor cells are discussed.     

Analysis of cell surface glycoprotein changes related to hematopoietic differentiation

A high-resolution technique has been used to study differentiation-related and leukemia-associated glycoproteins. Cells are labeled with the membrane-impermeable probe sulfo-N-hydroxysuccinimidyl-biotin. Nonionic detergent extracts are subjected to affinity chromatography on a number of immobilized lectins and after polyacrylamide gel electrophoresis in sodium dodecyl sulfate (SDS-PAGE) and western transfer, the biotin-labeled glycoproteins are visualized by using avidin-horseradish peroxidase and 4-chloronaphthol. With the aid of the lectins concanavalin A, Dolichos biflouros agglutinin, Lens culinaris hemagglutinin, peanut agglutinin, pokeweed mitogen, Ricinus communus agglutinin I, soybean agglutinin, Ulex europeus agglutinin I (UEA), and wheat germ agglutinin, each purifies different glycoprotein subsets from the same cell type. Mature cells of distinct hematopoietic lineages differ considerably in their cell surface glycoprotein patterns. This technique was used to analyze the glycoproteins of human leukemia cells before and after the induction of differentiation. K562 cells differentiated along different lineages after treatment with phorbol 12-myristate 13-acetate, sodium butyrate, dimethyl sulfoxide, or hemin. Limited specific alterations were observed with a number of lectins when K562 erythroleukemia cells were induced to differentiate. Among these, a number of bands were identified that were either lost or appeared after induction of differentiation with all four agents. In contrast, the glycoproteins bound by UEA were drastically diminished after induction of differentiation, and the remaining UEA-bound glycoproteins bore little resemblance to those of the cells before treatment. This high-resolution technique may be useful as a general method for the examination of cell surface glycoprotein differences. Once specific glycoprotein alterations are detected, lectin affinity chromatography and SDS-PAGE allow purification of antigens for the production of monoclonal antibodies.     

Spontaneous immortalization of neural crest‐derived corneal progenitor cells after chromosomal aberration

Objectives: In a previous study, we have reported the existence of neural crest‐derived stem cell‐like cells originating from the corneal limbus of juvenile mice (termed murine corneal cells, MCCs). To yield a sufficient number of MCCs, for example, for cell‐therapy approaches, here we have investigated MCCs’ ability for extensive proliferation, and we have evaluated their stem cell qualities and genetic stability after large‐scale culture. Materials and methods: MCCs were established from corneal limbal tissue of juvenile mice. To determine their cell proliferation and self‐renewing potential, MTT tests and an estimation of colony forming unit efficiency were carried out. Multipotency of cell differentiation was examined by applying adipogenic and osteogenic differentiation protocols. Moreover, karyotyping was performed and expression of stem cell markers and cell cycle‐associated genes was analysed. Results: MCCs, as primary cells, could be cultured for more than 60 passages. We observed increased cell proliferation and high number of colony forming units (CFUs) after extensive culture. Interestingly, there were no changes in expression of MCC markers. Furthermore, cell differentiation potentials remained comparable with MCCs at early passages. However, karyotyping revealed numeric chromosomal aberrations at higher passages. Moreover, tumour suppressor genes such as p16 and p21 were found to be down‐regulated after large‐scale cell culture. Conclusions: MCCs immortalize spontaneously after extensive cell culture, but still demonstrate stem cell‐like qualities.     

Morphological and structural study of Landolt's club in the chick retina

Light and electron microscopy were used to study Landolt's club of the bipolar cells in the newborn chick retina as well as in early embryonic stages. In the embryo, the bipolar cells were connected to the outer limiting membrane by Landolt's club. Some of the bipolar cells disconnect from this membrane, by complete retraction of Landolt's club, giving rise to bipolar cells without this process. The newly hatched chick, was used for analysis of the ultrastructure of Landolt's club. Zones of apposition between Muller cells and Landolt's club are associated with cytoplasmic vesicles in both cells. Muller cells appear to transmit vesicular material, possibly nutrients, to bipolar cells through Landolt's club. Thus, Landolt's club provides substrates to bipolar cells in the poorly vascularized region of the chick retina.     

Response of club cells in the skin of the carp Cyprinus carpio to exogenous stressors

The ultrastructure of club cells and neighbouring filament cells and leucocytes in the epidermis of carp, was studied under normal conditions and after exposure to several stressors: acid water, heavy metals, organic manure, brackish water and wounding. The effects of the stressors were remarkably similar. The club cells increased in size and contained more endoplasmic reticulum and Golgi areas. In both control and stressed fish, most mitotic figures of the filament cells were found adjacent to club cells, as was demonstrated after colchicine injection. Whereas in the controls apoptosis of filament cells was scarce and limited to the upper layer of the epithelium, in the stressed fish it was commonly seen in close proximity to the club cells but not in other mid-epidermal parts of the epithelium. This indicates that club cells influence the cellular kinetics of the filament cells. Under stress conditions leucocytes infiltrated the epidermis. Some were seen inside club cells. Apparently these leucocytes were taken up in phagosomes and subsequently they showed signs of necrotic degeneration. Leucocyte incorporation and degeneration in club cells were not observed in control fish. Control of the cellular turnover of filament cells and the elimination of leucocytes may represent new functions for club cells, which have mainly been associated with the production of pheromones.     

Mispatterning in the ommatidia of Apis mellifera pupae treated with a juvenile hormone analogue

To further understand the function of morphogenetic hormones in honeybee eye differentiation, the alterations in ommatidial patterning induced by pyriproxyfen, a juvenile hormone (JH) analogue, were studied by scanning and transmission electron microscopy. Prepupae of prospective honeybee workers were treated with pyriproxyfen and the effects on ommatidial differentiation were described at the end of the pupal development. The results show that the entire ommatidia, i.e., the dioptric as well as the receptor systems, were affected by the JH analogue. The wave of ommatidial differentiation, which progresses from the posterior to the anterior region of the pupal eyes, was arrested. In treated pupae, the rhabdomeres only differentiated at the apical axis of the retinula, the secondary and tertiary pigment cells did not develop their cytoplasm protrusions, and the cone cell quartet did not pattern correctly. Simultaneously, an intense vacuolization was observed in cells forming ommatidia. In a previous study we showed that pyriproxyfen exerts an inhibition on pupal ecdysteroid secretion. In this sense, the arrested ommatidial differentiation in pyriproxyfen-treated pupae could be due to a secondary effect resulting from an alteration in pupal ecdysteroid titers.     

Development and fate of the secretory granules of juxtaglomerular epithelioid cells

Summary The development and fate of the secretory granules in murine, rat and human juxtaglomerular epithelioid cells were examined using ultrastructural and immunocytochemical methods. The formation of mature renin granules occurs by fusion of rhomboid protogranules followed by coalescence of their paracrystalline contents, and by the fusion of roundish juvenile granules having an amorphous internum. Protogranules with paracrystalline contents are prominent in animals with stimulated renin synthesis, indicating an overcharge in processing and/or packaging of the secretory product, renin, under these conditions. Various similarities between lysosomes/multivesicular bodies (MVBs) and juvenile renin granules have been observed. With the exception of small MVBs, no renin-negative organelles that could be regarded as lysosomes were found in epithelioid cells of mice and rats. Therefore, we suggest that renin granules are modified lysosomes. Immunocytochemical findings indicate that juvenile secretory granules of epithelioid cells represent the converting and activating compartment for prorenin. Endocytosed foreign tracers such as HRP or cationized ferritin are preferentially internalized by juvenile renin granules, which hence appear to be outstanding by their fusogeneity. Consequently, juvenile granules are probably responsible for the secretion of prorenin, and mature granules for that of active renin.These studies were supported by the German Research Foundation within the Forschergruppe Niere/Heidelberg     

Solubilization and hydrophobic immobilization assay of a cAMP binding protein from Dictyostelium discoideum plasma membranes

A cAMP binding site present on isolated plasma membranes of aggregation-competent $\text{D.}\text{discoideum}$ cells has been solubilized with the nonionic detergent Emulphogene BC-720. An assay has been developed based on the principle of hydrophobic chromatography, in which the detergent solubilized cAMP binding protein is immobilized on alkyl-agarose beads at low detergent concentration. This allows the necessary rapid separation of bound and free [³H]-cAMP by filtration of the beads. The kinetics and nucleotide specificity of the detergent solubilized cAMP binding protein are comparable to those of the cAMP chemotactic receptor on intact cells and plasma membranes. The alkyl-agarose bead assay may have general utility for the assay of detergent solubilized membrane receptors.     

Development of epidermal and mucosal galectin containing cells in metamorphosing leptocephali of Japanese conger

The epidermis of premetamorphic leptocephali of Japanese conger Conger myriaster consisted of only a few cell layers including congerin- (a galectin) containing club cells. The epidermis increased in thickness after metamorphosis, mainly due to a preponderant development of club cells. This suggested that the biological significance of congerins increased at this stage, which may be related to a change in life style. Epidermal mucous cells showed only limited distribution. Immuno-positive cells in the mucosal epithelia of the buccal cavity wall and oesophagus were not found in the youngest individuals. Though these cells were observed at the commencement of metamorphosis, the development of the epithelia and club cells was apparently retarded compared to that of the epidermis. No immuno-staining was found in the gills at any stages.     

白花泡桐不定根发生过程中内源激素和RNA的变化

白花泡桐（Ｐａｕｌｏｗｎｉａｆｏｒｔｕｎｅｉ（Ｓｅｅｍ．）Ｈｅｍｓｌ．）成年型和幼年型茎切段体外培养时不定根发生过程中内源ＩＡＡ、ＣＴＫ和ＡＢＡ含量测定表明：幼年型材料中内源ＩＡＡ和ＣＴＫ的含量在诱导的第２天同时达到高峰,而成年型材料中ＩＡＡ和ＣＴＫ含量的高峰则在第４天出现．两种类型切段根原基出现的时间都与其内源ＩＡＡ和ＣＴＫ的高峰一致．幼年型材料的内源ＡＢＡ含量在第４天达到高峰,随后迅速下降．成年型材料中内源ＡＢＡ则逐步下降．成年型和幼年型材料中ＲＮＡ的变化相同,在诱导的第２天稍有下降,随后显著增加．结果显示,不定根的发生与其内源激素和ＲＮＡ的变化密切相关．     

Association of the cyclic AMP chemotaxis receptor with the detergent-insoluble cytoskeleton of Dictyostelium discoideum

Treatment of 6-h differentiated Dictyostelium discoideum cells with the nonionic detergent Triton X-100 dissolves away membranes and soluble components, as judged by marker enzyme distributions, leaving intact a cytoskeletal residue that contains approximately 10% of the cell protein and 50% of the actin. Nitrobenzooxadiazo-phallacidin staining for F-actin and electron microscopy of detergent-extracted whole-mounts indicate that the cytoskeletons retain the size and shape of intact cells and contain F-actin in cortical meshworks. The cytoskeletons contain little if any remaining membrane material by morphological criteria, and the plasma membrane enzymes cyclic nucleotide phosphodiesterase and alkaline phosphatase are absent from the insoluble residue, which retains only 15% of the membrane concanavalin A-binding glycoproteins. This detergent-insoluble residue retains a specific [3H]cAMP-binding site with the nucleotide specificity, rapid kinetics and approximate affinity of the cAMP receptor on intact cells. Upon detergent extraction of cells, the number of cAMP-binding sites increases 20-70%. The binding site is attached to the insoluble residue whether or not the cAMP receptor is occupied at the time of detergent addition. The pH dependence for recovery of the insoluble cAMP-binding site is much sharper than that on intact cells or membranes with an optimum at pH 6.1. Conditions of pH and ionic composition that lead to disruption of the cytoskeleton upon detergent treatment also result in the loss of cAMP binding. During differentiation, the detergent- insoluble cAMP binding increases in parallel with cell surface cAMP receptors and chemotaxis to cAMP.