The ultrastructural characterization of mitochondria‐rich cells as a response to variations in salinity in two types of teleostean pseudobranch: milkfish (Chanos chanos) and Mozambique tilapia (Oreochromis mossambicus)

The pseudobranchs of two euryhaline teleost species, the milkfish (Chanos chanos ) and the Mozambique tilapia (Oreochromis mossambicus ), were studied after acclimization to different salinities using optical and electron microscopy. The milkfish pseudobranch was the lamellae‐free type, with separate lamellae along the filaments containing two groups of mitochondria (Mt)‐rich cells: chloride cells (CCs) and pseudobranch type cells (PSCs). Conversely, the tilapia pseudobranch was the embedded type, covered with connective tissues and with only one group of Mt‐rich PSCs. Chloride cells were identified according to the apical openings and branched tubular networks around randomly distributed and diversely shaped Mt. Pseudobranchs type cells, however, were characterized according to the orderly arrangement of parallel tubules around closely packed Mt; both the tubules and the Mt were distributed in the vascular side of the cell, but were absent from the apical region. Compared with those of seawater (SW)‐acclimated milkfish, the pseudobranchial lamellae of freshwater (FW) specimens were longer on average, and the Mt of the CCs had fewer cristae, were less electron‐dense, and were often vacuolated. The Mt in the PSCs of FW‐acclimated milkfish and tilapia were larger and more electron‐dense than those of their SW‐acclimated counterparts; in addition, more tubules were found to aggregately surround the Mt and basolateral membranes in the PSCs of fish from the hypo‐osmotic environment. Conversely, the PSCs of tilapia were periodic acid‐Schiff (PAS)‐positive, and Mt in PSCs were concentrated with more parallel arrays of the tubule system than those of milkfish. Therefore, salinity‐dependent changes in the ultrastructures of PSCs suggest their potential role in energy metabolism of both lamellae‐free and embedded pseudobranchs, whereas the PAS‐positive staining characteristics suggest a role in releasing or storaging polysaccharides in the embedded pseudobranch. J. Morphol. 278:390–402, 2017. © 2017 Wiley Periodicals, Inc.     

Distribution and development of rodlet cells in the gills and pseudobranch of the bass, Dicentrachus labrax (L)

Rodlet cells in various stages of development were found in large numbers in the bass gill and pseudobranch. In the gill, rodlet cells were found in the epithelium at the base of the secondary lamellae and on the filament between adjacent lamellae, whilst in the pseudobranch they were found over the whole area of the secondary lamellae as well as in the filament epithelium.
During early development, rodlet cells are characterised by their amorphous cell inclusions, prominent supranuclear Golgi complex and network of granular endoplasmic reticulum. Later, with formation of a fibrous border the arrangement of the cell organelles undergoes reorganisation; the endoplasmic reticulum becomes distended, numerous vesicles appear and the mitochondria aggregate in the apical region of the cell. One of the most striking features is the development of club-shaped sacs containing electron dense cores, which are orientated towards the open apex of the cell.
Various staining properties of rodlet cells for light and electron microscopy were compared with those of mucous cells found in the same tissues. Possible functions of the cell are discussed.     

Fine structure of the pseudobranch of the flounder Paralichthys lethostigma

Summary The free or non-glandular pseudobranch of the flounder Paralichthys lethostigma was studied with the electron microscope. Cells typical of glandular type pseudobranchs are found. This indicates that, at least in the flounder, the free pseudobranch should be called glandular. In addition, the chloride-type cells, commonly found in the gill, buccal epithelium, and surface epithelium of other fish, have been found in the pseudobranch, where they have not been described previously. The fine structure of both the chloride-type and the pseudobranch-type cell has been characterized and contrasted. We have not been able to confirm previous reports that the specific cells in both pseudobranch and gill are identical in the flounder.Supported by grant-in-aid from the USPHS (General Medical Sciences Institute, GM-06836) and the National Science Foundation (GB-676).     

Comparison of 'Pseudobranch' type and 'Chloride' type cells in the pseudobranch of marine, freshwater and euryhaline teleosts

The degree of similarity between the 'pseudobranch type' and 'chloride type' cells in the pseudobranch of bass ( Dicentrachus labrax (L)), smelt ( Osmerus esperlangus ) and rainbow trout ( Salmo gairdneri ) was studied. The pseudobranch of bass and smelt contains two specialised cell types commonly known as 'chloride type' and 'pseudobranch type' cells, whereas rainbow trout only possess the latter type. 'Pseudobranch type' cells are characterised by the orderly arrangement of parallel tubules around their closely packed mitochondria. 'Chloride type' cells are identified by their highly branched tubular network, randomly distributed mitochondria, and the presence of an apical pit. Although ultra-structural changes were noted under osmotic stress, the 'chloride type' and 'pseudobranch type' cells remained distinguishable from each other and gave no reason to suggest that they were different forms of the same cell type. It was concluded that the two are distinct cell types, performing different, though possibly related, functions.     

Electron microscopic studies of the gill epithelium of the amphibian teleost Periophthalmus vulgaris]

The gill epithelium of the airdwelling fish Periophthalmus vulgaris has been studied with the electron microscope. The following celltypes can be distinguished: flat covering epithelial cells, chloride cells, mucous cells, basal cells, various leucocytes as well as a specific granule containing cell which is possibly an epithelial cell. The covering epithelial cells exhibit a relatively smooth apical surface and contain in their apical half densely packed microfilaments, pinocytotic vesicles are rare. These characteristics are not to be found in water dwelling fish and possibly represent adaptations to the air containing surroundings. In the chloride cells are numerous, especially in the basal halves of the secondary lamellae. The distal parts of the secondary lamellae the barrier for the respiratory gases measures about 0,9 micrometer. The basal cells are ribosome rich replacement cells. Two types of mucous cells occur. Individual intraepithelial nerve fibres have been observed.     

鲻和鲮鳃丝的扫描电镜比较观察

对鲻（Mugil cephalus）和鲮（Cirrhina molitorella）的鳃丝表面结构进行了扫描电镜比较观察,结果表明,鲻鳃丝杆状部比鲮粗．鲻鳃小片高度比鲮低;两者鳃丝表面分泌孔洞口径和密度不同;鲻和鲮细胞外被不同,鲻细胞外被稀疏,鲮的则致密复杂;鳃小片细胞和鳃丝表皮细胞的表面形态存在差异,文章还描述了鳃丝表皮形态特异的细胞。     

白鲢鳃部血管的研究

本文用甲基丙烯酸甲脂铸型技术,配合扫描电镜,研究白鲢鳃部血管的分布。鳃区具有双血液循环,动脉—动脉循环,主司血液与水体间气体交换;动脉—静脉循环主司鳃区营养交换。入鳃丝动脉上具有膨大的“血泡”结构,可能起“鳃心”作用,当鳃丝内收时将血液输送入入鳃动脉。伪鳃鳃小片彼此排列紧密,这种结构似不利于气体交换,可能没有什么呼吸功能。     

斑马鱼鳃的光镜和透射电镜观察

应用光学显微镜和透射电镜对斑马鱼(Danio rerio)鳃的组织结构及鳃丝、鳃小片超微结构进行了观察。结果表明,斑马鱼有4对全鳃,鳃耙呈长锥状,鳃丝呈梳状排列在鳃弓上,鳃小片均匀排列在鳃丝两侧。鳃小片由上皮细胞、柱细胞、内皮细胞和毛细血管网组成,鳃小片基部和血管周围分布有泌氯细胞,胞内有丰富的线粒体和排泄小泡,根据线粒体形态特征和细胞质电子密度可将其分为两个亚型。黏液细胞通常与泌氯细胞对生存在,并且有通外的开口。斑马鱼鳃组织结构与其他硬骨鱼鳃结构相似,其结构和功能有密切的关系。     

鲻鱼嗅囊组织形态结构观察及功能探讨

实验用鱼为全长35.5~40.0 cm的野生鲻(Mugil cephalus),采用石蜡切片以及透射电镜技术对鲻的嗅囊以及嗅板细胞进行观察。结果表明:鲻的嗅觉器官由左右两个呈扁平椭球形嗅囊构成,分别由前后两个鼻孔与外界相通。嗅囊长径与眼径之比为0.80,长径与短径之比为2.09。嗅囊的嗅轴左右两边分别有垂直于嗅轴并向上倾斜排列整齐的18~25个披针形嗅板,只有初级嗅板未见次级嗅板。嗅板由中央髓和两侧的嗅上皮两部分构成,中央髓由疏松的结缔组织和毛细血管组成。嗅上皮又分为感觉区和非感觉区,感觉区位于嗅板的内侧,具有发达纤毛,呈连续分布状态,非感觉区位于嗅板边缘,细胞纤毛较少。通过光镜和电镜的综合研究结果显示嗅上皮细胞大致可分为5类:基细胞、支持细胞、纤毛非感觉细胞、纤毛感觉细胞和柱状细胞。文章讨论了鲻的感官活动类型。     

Gross and fine structure of the pseudo branch of the climbing perch, Anabas testudineus (Bloch)

The structure of the glandular pseudobranch of the air-breathing fish Anabas testudineus is described on the basis of light and electron microscopy. It is shown that the pseudobranch has the same basic structure as a typical gill, although in this case it is not freely exposed to the water.
Individual secondary lamellae can be recognized in which well-defined, but narrow, blood channels are present between typical pillar cells. The epithelial layer is mainly represented by enlarged mitochondria-rich cells which constitute a large proportion of the whole organ. Mitochondria-rich cells contain an abundant endoplasmic reticulum which is in close contact with the mitochondria and becomes concentrated near the vascular borders of the cell and opens directly into the basement lamina.
The presence of numerous pinocytotic vesicles in the enlarged pillar cell flanges may transfer material to the blood channels. The precise nature and role of any materials released in this way remains to be investigated.     

LOCALIZATION OF Na+, K+-ATPASE AND OTHER ENZYMES IN TELEOST PSEUDOBRANCH : II. Morphological Characterization of Intact Pseudobranch, Subcellular Fractions, and Plasma Membrane Substructure

The pseudobranch of the pinfish Lagodon rhomboides is an unusually homogeneous and structurally simple tissue, well suited to cell fractionation studies. Its principal cell type, closely related to the chloride cells of teleost gill, is characterized by numerous mitochondria in close association with abundant tubular invaginations of the plasma membrane. Other cytoplasmic organelles are rarely encountered. In broken fresh pseudobranch cells negatively stained with ammonium molybdate, a 40 Å particulate layer was observed on the intracellular surface of the tubular plasma membrane fragments. Nuclear (N), mitochondrial-light mitochondrial (M+L), and microsomal (P) fractions, obtained by differential centrifugation, were characterized by examination of fixed, embedded pellets and unfixed preparations negatively stained with ammonium molybdate and potassium phosphotung-state. Mitochondria, in orthodox configuration and retaining their outer membranes, were observed in M+L and N. Significant amounts of tubular, sheetlike, or vesicular membrane fragments were observed in all three fractions. Many such fragments, when negatively stained, showed the 40 Å particulate surface layer characteristic of plasma membrane invaginations, and in some cases 20-Å projections could be resolved on the opposite (extracellular) surface. Since these morphological observations, together with previously presented biochemical data, suggest a plasma membrane localization of Na⁺, K⁺-ATPase, the possible association of the enzyme with membrane projections is discussed.     

Gill morphology in the zebrafish, Brachydanio rerio (Hamilton- Buchanan)

A light and electron microscopic study of the gills of the zebrafish, Brachydanio rerio , were made to serve as a morphological basis for future investigations. It was found that for fixation of B. rerio gills, a mixture of 1·5% gluturaldehyde and 1·5% paraformaldehyde gives a mucus-free surface. Morphometric measurements of structural components of the gill secondary lamellae were made. Observations at SEM were correlated with those made at TEM. The different cell types in the branchial epithelium were characterized. Chloride cells were mainly located in the interlamellar regions and on the afferent side of the primary lamellae. Two morphologically different chloride cells were seen. The first type communicates with the external environment through a reservoir-like lumen, which is normally absent in freshwater fishes. The second type of chloride cell has more direct contact with the ambient water, resembling chloride cells from other freshwater fishes. Another cell type with features similar to those of the rodlet cell was frequently observed. This cell is interposed between other types of cells in the epithelium, and sometimes junctional complexes were present between the rodlet cell and surrounding cells.     

Labyrinth cells,a new cell type in vertebrate olfactory organs

Summary Light microscopy and transverse electron microscopy has been employed to study the olfactory organs in 82 specimens of freshwater adapted young and homing adult Baltic sea trout Salmo trutta trutta L. In both sensory and indifferent epithelium the olfactory mucosa has scattered cells of a type that has not been described in any olfactory organ before. They are called labyrinth cells and are characterized by an extensive, turtuous, interconnected tubular system of smooth endoplasmatic reticulum intimately connected with numerous mitochondria. This cell type is similar to chloride and other cells which probably are involved in electrolyte transport in fish gills and pseudobranch, the rectal gland in elasmobranchs and the nasal gland in reptiles and birds. It is suggested that the olfactory organ in fish is serially homologous with the pseudobranch.Thanks are due to Prof. Dr. Gunnar Bloom, Section of Histology, University of Umeå for interesting discussions. The author also wish to acknowledge the technical facilities and assistance in the use of the electron microscope to Miss Karin Ekström and Miss Marianne Borg. The research was supported by grant 2389-11, 13 and 15 from the Swedish Natural Science Research Council.     

黄斑篮子鱼和金钱鱼鳃的扫描电镜观察

对两种鲈形目鱼类黄斑篮子鱼(Siganus oramin)和金钱鱼(Scatophagus argus)的鳃结构进行扫描电镜观察。结果表明,黄斑篮子鱼和金钱鱼鳃的表面结构及微细结构与其他硬骨鱼类基本相似,鳃丝表面都具有规则或不规则分布的环形微嵴、沟、坑、孔等结构。黄斑篮子鱼的鳃片中部鳃丝表皮有大量凸起,而端部鳃丝表皮的凹凸程度明显较低,黄斑篮子鱼的鳃小片高度较金钱鱼鳃小片高。黄斑篮子鱼和金钱鱼鳃上皮的扁平上皮细胞、氯细胞和黏液细胞的形态结构及数量分布存在细微的差异。黄斑篮子鱼鳃片鳃丝的端部和中部表面有黏液细胞,金钱鱼鳃丝表面的黏液细胞很难观察到,与大多数淡水鱼类相似。黄斑篮子鱼鳃丝表面分布的氯细胞数量多于金钱鱼,这可能与两种鱼生活环境、生活习性的长期演变相关。     

Scanning and transmission electron microscopy of the female reproductive system of Schistosoma margrebowiei Le Roux, 1933

Transmission electron microscopy shows that the uterus of female Schistosoma margrebowiei possesses the same ultrastructure as that of the tegument but lacks spines and sense organs. It does not possess secretory cells and opens at the gonopore which by scanning electron microscopy was seen to be composed of numerous leaf-like protrusions. The morphology of the ovary is comparable with that of other Digenea. Immature and mature ova possess cortically arranged granules and occur within the posterior zone of the ovary. Cilia and lamellae line the luminal surface of the oviduct and ootype, the lamellae running unidirectionally along the duct. Only a single type of secretory cell is seen within Mehlis' gland and this produces dense bodies which are associated with Goldi bodies. Narrow cytoplasmic channels supported by microtubules deliver these secretory bodies to the ootype. The vitelline duct is lined with cilia and lamellae and the vitelline gland contains four types of cells, S1, S2, S3 and S4. Calcareous corpuscles are found within mature S4 cells.     

20-羟基蜕皮甾酮处理后舞毒蛾外部形态和幼虫体壁超微结构的变化

为了探明20-羟基蜕皮甾酮对昆虫蜕皮过程中体壁的表皮层、 皮细胞及其细胞器的具体影响过程, 本研究利用透射电镜技术研究了20-羟基蜕皮甾酮对舞毒蛾Lymantria dispar （Linnaeus）5龄幼虫体壁超微结构的变化。结果表明, 用高浓度20-羟基蜕皮甾酮溶液浸过的白桦叶片饲喂幼虫, 处理6 h, 摄入约400 μg 20-羟基蜕皮甾酮后, 幼虫停止取食; 处理12 h时表皮细胞顶膜上的微绒毛减少, 在皮细胞与旧表皮之间形成蜕皮间隙, 旧头壳从幼虫头部脱离; 处理24 h时蜕皮间隙继续增大, 旧表皮与皮细胞进一步分离, 新表皮质层开始形成; 处理36 h时皮细胞顶膜形成较短的微绒毛, 胞质区域出现数量较多的电子疏松泡, 新表皮由上表皮、 外表皮及8层左右内表皮片层组成; 处理48 h时顶膜与内表皮界限模糊, 内表皮继续合成至16层左右; 72 h时细胞内出现大面积电子疏松泡, 内表皮合成至20层左右。 处理96 h时, 与对照组相比, 皮细胞细胞器较少, 核仁周围出现小部分空白区域, 胞质区域内含物减少; 虫体发黑缩小, 即将死亡; 内表皮层数仍旧保持20层左右。对照组幼虫6-96 h虫体活跃, 正常取食, 外部观察及透射电镜结果均未显现蜕皮现象; 表皮层由上表皮、 外表皮及内表皮组成; 皮细胞顶膜微绒毛密度高; 表皮细胞分泌活动旺盛, 胞质区域细胞界限明显, 内含物丰富; 细胞器典型而且活跃; 内表皮片层随时间不断增加至50层左右。结果提示, 外源20-羟基蜕皮甾酮能够导致舞毒蛾5龄幼虫的致死性蜕皮。     

Observations on the relationship between “chloride-type” and “pseudobranch-type” cells in the gills of a fish,Oligocottus maculosus

Summary Chloride cells in gill epithelium of Oligocottus maintained in sea water have a much branched system of agranular cytoplasmic tubules, numerous mitochondria, and a prominent apical crypt. The mitochondria are randomly dispersed and do not show preferential orientation with respect to the tubules.After brief exposure of fish to sea water diluted 1/100 with glass distilled water, the mitochondria and tubules become rearranged into parallel arrays and the apical crypts disappear. The appearance of these cells is similar to that of pseudobranch cells in Fundulus heteroclitus (Copeland and Dalton, 1959).These data suggest that chloride cells and pseudobranch cells represent different adaptive forms of a single cell type and that transformation from the chloride cell configuration to that of pseudobranch cells can be induced by osmotic stress.This work was performed in 1963 when the author was enrolled in the Fine Structure Training program of the Department of Biological Structure, University of Washington. Financial aid was provided by the United States Public Health Service (Grant No. 5T1 GM-136).     

Presence of chloride cells in gill filaments and lamellae of the skate Torpedo marmorata

The morphology of chloride cells in the gill of the skate Torpedo marmorata is described from a light and an electron microscopic study. Chloride cells have been regularly observed in both the gill filament (or primary epithelium) and the lamellae (or secondary epithelium). Chloride cells located in the filament usually display convex apical regions with microvilli protruding amongst microridges of neighbouring pavement cells, whereas chloride cells in the lamellae are located between the two epithelial layers, and contact with the external milieu is via a narrow apical opening. Present observations are discussed in relation to data on the presence of chloride cells in the lamellae of marine teleost fish, and it is suggested that the occurrence of chloride cells all along the lamellae might be in some way inversely related to fish activity.     

Propagation of the neuroid action potential of the carnivorous plantDrosera

Summary The neuroid action potentials ofDrosera rotundifolia recorded from single cells resemble those recorded from the surface of tentacle stalks. They have similar amplitudes and durations and they show the same variation of duration with interval that characterizes the extracellularly recorded action potentials. All living cells of the stalk appear to be excitable since cells from both layers were observed to produce action potentials when intracellular recording techniques were used.Propagation of electrically induced action potentials down the stalk occurred at a rate of 4.3 mm/s±0.6 S.E.M. while propagation up the stalk occurred at a rate of 9.9 mm/s±2.0 S.E.M. The fact that attenuated signals from electrical processes and stimulus artifacts in distant parts of the stalk were detected in recordings indicates that the cells of the stalk were closely coupled and that propagation from cell to cell is probably by an electrotonic mechanism. This hypothesis gains additional support from the observation of numerous cytoplasmic connections (plasmodesmata) through the cell walls separating the cells which are most likely to conduct the action potential.We wish to thank Dr. M.V. Parthasarathy for guidance in the use of the electron microscope. This work was supported in part by NSF Grant Number GB28124.     

Ultrastructural and histochemical study on gills and skin of the Senegal sole, Solea senegalensis

This study was undertaken to identify the normal ultrastructural features of gills and skin of the Senegal sole, Solea senegalensis, for a comparative measure to morphological alterations caused by environmental stressors such as reduced water quality and diseases. In the Senegal sole skin, four morphologically distinct layers were identified: cuticle, epidermis, dermis and hypodermis. The epidermis was composed of stratified epithelium containing three cellular layers: the outermost or mucosa layer, the middle or fusiform layer and the stratum germinativum or the basal layer. In the mucosa, two mucous cell types were differentiated: type A cells containing several round vesicles of different electron density and type B cells containing mucosomes of uniform electron density. Senegal sole have five pairs of gill arches, each containing two rows of well‐developed and compactly organized primary filaments and secondary lamellae. Fingerprint‐like microridges were observed on the surface of epithelial cells. The branchial lamellae epithelium consisted of different cell types: pavement, mucous and chloride. Between the chloride cells and the larger pavement cells, accessory cells were observed. Complexes of tight junctions and desmosomes were frequently observed between adjacent chloride and epithelial cells. Neutral mucosubstances and/or glycoconjugates were observed in the epidermis, dermis and hypodermis of S. senegalensis skin. Proteins rich in different amino acids, such as arginine and cysteine, reacted negatively or weakly positive in the epidermis, dermis and hypodermis. In gills, some mucous cells responded weakly positive to periodic acid‐Schiff (PAS) reaction but were strongly stained with Alcian Blue at pH 0.5, 1 and 2.5. When Alcian Blue pH 2.5–PAS reaction was performed, most mucous cells were stained blue (carboxylated mucins) and some mucocytes stained purple, indicating a combination of neutral and acid mucins. Proteins rich in cysteine‐bound sulphydryl (‐SH‐) and cystine disulphide (‐S‐S‐) groups were strongly detected in branchial and epidermal mucous cells, whereas lysine, tyrosine and arginine containing proteins showed very weak staining in both epidermal and branchial mucous cells. Protein reactions were strongly positive in the pillar cells, except for those rich in tryptophan, whereas the branchial cartilaginous tissue did not show an important reaction. The performed lipid reactions were negative in goblet and chloride cells. It is concluded from this study that ultrastructural and cytohistochemical features of the Senegal sole skin and gills may serve as control structures in both natural and aquaculture systems to monitor or detect environmental stress responses at the histological level.