The parapineal and pineal organs of the elver (glass eel), Anguilla anguilla L.

Summary The parapineal organ of the glass eel (elver) consists of approximately 400 cells and is situated to the left of the connection of the pineal stalk to the third ventricle. A conspicuous nerve tract containing approximately 350 fibers arises from the parapineal organ and runs in spatial relationship to the habenular commissure toward the left habenular nucleus. The dominating cell type of the parapineal organ of the elver is a neuron (sensory neuron) of small diameter provided with atypical cilia (9×2+0, or rarely 8×2+0 types). Well-developed photoreceptor outer segments are lacking, and no interstitial cells of ependymal type have been observed with certainty in the parapineal organ. The axonal processes from the nerve cells form the tract leaving the parapineal organ.The pineal organ proper of the elver consists of photoreceptor cells with well-developed outer segments, interstitial cells of ependymal type, and ganglion cells. Axons from the latter form the pineal tract, which leaves the pineal organ and runs in close contact with the subcommissural organ toward the posterior commissure. The proximal part of the pineal stalk contains only a few photoreceptor cells the outer segments of which are less developed than those of the pineal body and the distal part of the pineal stalk.     

The structure and function of the cephalic organ of a nemertine Lineus ruber

The structure of the organ has been studied by light- and electron-microscopy. The organ is composed of both glandular and neural cells. The glandular cells pour their secretions into a ciliated tube which connects the organ with the external medium. Within the organ lobule, the tube forms three right-angled bends and is divided longitudinally into ingoing and outgoing channels by the adhesion of two groups of dilated cilia arising from opposite sides of the canal epithelium. Neural elements, backing the ciliated cells, constitute a possible neural chain to the central nervous system. The function of the organ is discussed.     

Ultrastructure of the nuchal organ and cerebral organ in Onchnesoma squamatum (Sipuncula, Phascolionidae)

 The ultrastructure of the nuchal organ and cerebral organ is described for the first time in a species of the Sipuncula, Onchnesoma squamatum. The nuchal organ is an unpaired structure lying outside and dorsal to the tentacular crown; furrows give the organ a paired appearance. The cerebral organ is an unciliated pad anterior to the nuchal organ. The nuchal organ consists of ciliated supporting cells, non-ciliated supporting cells and bipolar primary sensory cells. The cerebral organ is composed of unciliated supporting cells and numerous bipolar sensory cells. This clearly favours the hypothesis that this structure has a sensory function in adults rather than being a vestige of a larval organ. The sensory cells are similar in both organs and exhibit features indicative of chemoreception. Since the density of the sensory cells is low in the nuchal organ, an exclusively sensory function is questioned. There is some evidence that the two organs represent a functional unit. The present findings do not support the view that the nuchal organs of Sipuncula and ”Polychaeta” are homologous, but instead suggest that they are convergent structures. Accepted: 18 September 1996     

The secretory ependymal cells of the subcommissural organ: Which role in hydrocephalus?

Ependyma in the central nervous system gives rise to several specialized cell types, including the secretory ependymal cells located in the subcommissural organ. These elongated cells show large cisternae in their cytoplasm, which are filled with material secreted into the cerebrospinal fluid and toward the leptomeningeal spaces. A specific secretion of the subcommissural organ was named SCO-spondin, regarding its marked homology with developmental proteins of the thrombospondin superfamily (presence of thrombospondin type 1 repeats). The ependymal cells of the subcommissural organ and SCO-spondin secretion are suspected to play a crucial role in cerebrospinal fluid flow and/or homeostasis. There is a close correlation between absence of the subcommissural organ and hydrocephalus in rat and mouse strains exhibiting congenital hydrocephalus, and in a number of mice transgenic for developmental genes. The ependymal cells of the subcommissural organ are under research as a key factor in several developmental processes of the central nervous system.     

Benign and Malignant Renal Cells Are Differentially Inhibited during Prolonged Organ Preservation

The worry of potential residual renal cancer cells in donor kidney after resection of small renal cancer impedes the extensive use of such controversial donor source. To explore the impacts of organ preservation process on the survival of renal cancer cells, we detected cell proliferation and viability of benign and malignant renal cell lines and clinical renal samples after treated with simulated organ preservation process. It was found that the viability and proliferation of malignant renal cells are inhibited much more than that of benign renal cells during prolonged organ preservation. The inhibition of proliferation in benign renal cells is fully reversible, while in malignant renal cancer cells is not fully reversible after a certain time. So potential residual renal cancer cells could be partly inhibited and eliminated by organ preservation process.     

La formation et l'evolution de l'organe dorsal chez les embryons de cinq collemboles (Insecta : Apterygota)

The appearance and development of the dorsal organ of collembolan embryos were analyzed by electron microscopy, to get a better insight into the cytodifferentiation and properties of the cells that constitute the organ.When the blastular epithelium surrounds the yolk as a thick cellular covering, the veryfirst rudiment of the dorsal organ can be detected as a somewhat thicker calotte of cells, particularly rich in lipid globules. Rapid morphogenetic processes result in the concentration of this first rudiment into a lens-shaped primordium, whose median cells sink into the yolk at their basal poles. All the cells of the dorsal organ contribute by their apical surfaces to the secretion of the first blastodermic membrane, a very atypical equivalent of an external epicuticle, then to the deposition of the outer layers of the second blastodermic cuticle.The dorsal organ takes the form of a plug and its central cells become columnar. Their considerable growth is marked by the internal presence of numerous regularly grouped microtubules, that will later contribute to the mechanical support of their apical processes. The blastoderm and the dorsal organ then secrete the procuticular portion of the second blastodermic cuticle (folded membrane of other authors). This inner part shows a very regular alternation of dense and less dense layers, eventual clues for a rapid, non-circadian, rhythm of activity in the cells.When the embryonic band becomes molded, the central cells of the dorsal organ send out very long apical processes, whose terminal contacts with the second cuticle, now swollen apart from the surface of the egg, in our opinion might play a role in the control of cuticle permeability. When the embryo grows older, the dorsal organ gets into its presumed functional phase; meanwhile, its constituent cells become diversified into several lines, according to a concentric pattern. The central cells are then surrounded by two cellular rings whose components show different amplifications, leaflets and microvilli, of their apical membranes. These cells are eventually supposed to play a role in exchanges with the external fluid.The involution of the dorsal organ begins at a relatively young stage of the embryonic band and continues during embryonic organogenesis.     

Association of reticular cells with CD34+/Sca-1+ apoptotic cells in the hemopoietic organ of grasshopper, Euprepocnemis shirakii

Hemopoiesis in orthopteran insects occurs in a hemopoietic organ that is located bilaterally along the aorta. This organ is also known as a reticulo-hemopoietic organ because of the rich presence of reticular cells. This study was performed to further elucidate hemopoiesis in the reticulo-hemopoietic organ of an orthopteran, Euprepocnemis shirakii. We focused on the question why reticular cells are so abundant (35% of cells in hemopoietic organ). Interestingly, 21% of these reticular cells surrounded hemocytes with their reticular cytoplasm. The surrounded hemocytes were distinguished by their different size and darkly stained nucleus. These cells were characterized by immunostaining using antibodies against several types of hemocytes: 45% of the surrounded hemocytes were CD34+, and these positive cells were double stained (over 85%) when immunostained by another hemopoietic pluripotent cell marker, Sca-1. Transmission electron microscopic analysis showed that reticular cells surrounded hemocytes containing large nuclei and poorly developed cytoplasmic organelles. This strongly suggests that the reticular cells surround hemopoietic stem cells. Additionally, surrounded hemopoietic progenitor cells are undergoing apoptosis as indicated by the TUNEL assay. The enclosed apoptotic cells are engulfed and then phagocytosed by reticular cells. Our results suggest that reticular cells are related to the differentiation and apoptosis of hemopoietic stem cells.     

Characterization of different microenvironments at the surface of the frog's taste organ

We used a panel of histochemical techniques to identify and characterize the cell-associated extracellular material at the surface of the frog's taste organ. We employed morphological and histochemical techniques using both the light microscope and the electron microscope. Results show that the apical, external aspect of cells reaching the surface of the taste organ is in close contact with a layer of amorphous material. The histochemical characteristics of this material vary according to the cell type with which it is in contact. Three different microenvironments can be identified at the surface of the frog's taste organ: type 1 microenvironment is associated with the superficial layer of mucus (secretory) cells; type 2 microenvironment characterizes the surface of the so-called wing cells, which reach the surface of the taste organ as thin laminae running among mucus cells; and type 3 microenvironment shrouds the free endings of putative taste cells and is rich in calcium and lipids. Type 2 and type 3 microenvironments fix peroxidase (a sapid macromolecule) with increasing affinity. We conclude that highly differentiated microenvironments exist at the surface of the frog's taste organ, and these could play a role in the chain of biological events leading to the taste sensation. Furthermore, characterization of the cell-associated, specific microenvironments can help clarify the role of the different cell types in the frog's taste organ.     

Two microvillar organs, new to Crustacea, in the Mystacocarida

The mystacocarid crustacean Derocheilocaris typica has two microvillar organs, one new, the other previously unappreciated in crustacean literature. The first is situated on the head-shield and consists of three pairs of cells: one with microvilli and a ballooned nucleus; one smaller and without special features; the third large and investing the other two and extending down to the foregut. We call this new organ the "cephalic microvillar organ" and discuss the value of the concept "dorsal organ", to which it might have been included. The second organ consists of about 21 cells that cover the proximal part of the dorsal surface of the labrum. The cells are alike, being characterized by an apical field of microvilli and a large residual body. This organ is here called the "labral microvillar organ". Both organs are neither sensory nor secretory and do not qualify for membership in any of the other recognized organ systems. We are unable to deduce their Dero-cheilocaris functions.     

The adoral sense organ in protobranch bivalves (Mollusca): comparative fine structure with special reference to Nucula nucleus

Abstract. The adoral sense organ in bivalve molluscs is a paired ridge of specialized epithelium positioned laterally at the base of the labial palps near the mouth opening, clearly distinguishable from the surrounding epithelia. Six species of the protobranch order Nuculoida, and one species of Solemyoida, were investigated by light microscopy concerning presence, gross anatomy, and innervation of the adoral sense organ. The organ was described in detail for Nucula nucleus and N. nitidosa by transmission electron microscopy; in these two species, the organ was characterized as a pseudostratified epithelial thickening with specialized cells bearing a specialized microvillar border and a basal matrix with a lamellar layer. Three types of bipolar primary receptor cells were recognized and these were reconstructed for N. nucleus. Most of the receptor cells had 2 cilia orientated parallel to the cell surface; in addition, there were 2 types of supporting cells and 1 type of basal cell. The surrounding epithelial cells were narrow with short microvilli and lacked cilia. The homology of the organ within protobranch bivalves was suggested by a character-complex of (1) position, (2) dimension of the epithelium, (3) innervation, (4) pseudostratified construction, (5) dimension of the specialized microvillar border, (6) thickening of the basal matrix, and (7) presence of specialized cell types such as receptor cells. Despite the estimated high number of protobranch species there is only scant information available on the adoral sense organ from 24 species of 8 genera. Structures and receptor types that are similar to those found in the adoral sense organ are widespread in molluscs and other invertebrate groups; this may indicate a plesiomorphy of these characters rather than an apomorphy for the protobranch clade. Therefore, the adoral sense organ may be of minor phylogenetic value above the level of protobranch orders.     

Green fluorescent protein-transgenic rat: a tool for organ transplantation research

The purpose of this study is to evaluate green fluorescent protein (GFP) transgenic rats for use as a tool for organ transplantation research. The GFP gene construct was designed to express ubiquitously. By flow cytometry, the cells obtained from the bone marrow, spleen, and peripheral blood of the GFP transgenic rats consisted of 77, 91, and 75% GFP-positive cells, respectively. To examine cell migration of GFP-positive cells after organ transplantation, pancreas graft with or without spleen transplantation, heart graft with or without lung transplantation, auxiliary liver and small bowel transplantation were also performed from GFP transgenic rat to LEW (RT1(1)) rats under a 2-week course of 0.64 mg/kg tacrolimus administration. GFP-positive donor cells were detected in the fully allogenic LEW rats after organ transplantation. These results showed that GFP transgenic rat is a useful tool for organ transplantation research such as cell migration study after organ transplantation without donor cell staining.     

The frontal organ of a triclad flatworm,Dugesia lugubris

Summary In an examination of the ultrastructure of the anteromedian portion of the head of Dugesia lugubris we demonstrated a frontal glandulo-muscular organ which consists of a voluminous glandular complex with three types of secretory cells and a well-developed musculature derived from the sub-epidermal fibers. The presence of neurosecretory cells, free nerve endings and single axons with sensitive cilia at the apex is characteristic. The last of these ultrastructural observations, together with functional tests, lead us to believe that the frontal organ possesses a marked chemosensitivity. The nature and structure of this organ are compared with the glandulo-muscular organ described in other Tricladida paludicola, thus contributing toward their much-debated classification.     

Transcriptional regulation of atonal required for Drosophila larval eye development by concerted action of eyes absent, sine oculis and hedgehog signaling independent of fused kinase and cubitus interruptus

Bolwig's organ is the larval light-sensing system consisting of 12 photoreceptors and its development requires atonal activity. Here, we showed that Bolwig's organ formation and atonal expression are controlled by the concerted function of hedgehog, eyes absent and sine oculis. Bolwig's organ primordium was first detected as a cluster of about 14 Atonal-positive cells at the posterior edge of the ocular segment in embryos and hence, atonal expression may define the region from which a few Atonal-positive founder cells (future primary photoreceptor cells) are generated by lateral specification. In Bolwig's organ development, neural differentiation precedes photoreceptor specification, since Elav, a neuron-specific antigen, whose expression is under the control of atonal, is expressed in virtually all early-Atonal-positive cells prior to the establishment of founder cells. Neither Atonal expression nor Bolwig's organ formation occurred in the absence of hedgehog, eyes absent or sine oculis activity. Genetic and histochemical analyses indicated that (1) responsible Hedgehog signals derive from the ocular segment, (2) Eyes absent and Sine oculis act downstream of or in parallel with Hedgehog signaling and (3) the Hedgehog signaling pathway required for Bolwig's organ development is a new type and lacks Fused kinase and Cubitus interruptus as downstream components.     

Comparative study of the femoral organ in Zodarion spiders (Araneae: Zodariidae)

The femoral organ of Zodarion spiders has not been investigated in detail yet. In this study we describe the external and internal structure of this organ. The organ is situated at the distal tip of the femora of all the legs during all developmental stages. The size of the organ (expressed as the number of hairs) increased with the ontogenetic development of Zodarion species. The organ was confirmed to occur in both sexes of all 47 Zodarion species examined. It is possibly present in all species of this genus. The size of the organ increased with the size of the species. A comparative anatomical study was performed in juveniles and adults of both sexes of Zodarion rubidum, and females of both Z. cyrenaicum and Z. jozefienae. The femoral organ represents an exocrine gland composed of a group of secretory cells located below the epidermis. Each gland cell is connected with the leg surface by a single duct. The ducts run in intercellular spaces and specialised canal cells are lacking. The structure of the secretory cells, namely the abundance of smooth endoplasmic reticulum, suggests that the gland produces a volatile compound(s). The composition and the role of the secretion, however, remains unknown.     

Fine structural studies of the nervous system and the apical organ in the planula larva of the sea anemone Anthopleura elegantissima

The nervous system of the planula larva of Anthopleura elegantissima consists of an apical organ, one type of endodermal receptor cell, two types of ectodermal receptor cells, central neurons and nerve plexus. Both interneural and neuromuscular synapses are found in the nerve plexus. The apical organ is a collection of about 100 long, columnar cells each bearing a long cilium and a collar of about 10 microvilli. The cilia of the apical organ are twisted together to form an apical tuft. The ciliary rootlets of the apical organ cells are extremely long, reaching to the basal processes of the cells adjacent to the mesoglea. All three types of sensory cells are tall and slender in profile and are identified by the presence of one or more of the following features: microtubules, small vesicles, membrane-bound granules and synapses. The interneurons are bipolar cells with somas restricted to the aboral end, adjacent to the apical organ. All synapses observed are polarized or asymmetrical. A diagram including all the elements of the nervous system is presented and the possible functions of the nervous system are discussed in relation to larval behavior.     

Histological,histochemical and electron microscopical studies on the nervous apparatus of the pineal organ in the tiger salamander,Ambystoma tigrinum

Summary 150–190 photoreceptor cells form a basic structural component of the pineal organ of Ambystoma tigrinum. Most of the outer and inner segments of these cells project into the lumen horizontally. Only 10 percent of the total number of photoreceptor cells are located within the pineal roof which is composed of a single cell layer. The photoreceptor cells are connected with nerve cells by synapses displaying characteristic ribbons. Different types of synaptic contacts, i.e. simple, tangential, dyad, triad and invaginated, are found. They are embedded in extended neuropil zones. A particular type of synapse indicates the presence of interneurons. The basal processes of some photoreceptor cells leave the pineal organ and make synaptic contacts with nervous elements located within the area of the subcommissural organ. Employing the method of Karnovsky and Roots (1964) for histochemical demonstration of acetylcholinesterase (AChE) approximately 70 neurons (intrapineal neurons) can be discerned in the pineal organ of Ambystoma tigrinum. In analogy to the distribution of photoreceptor cells only few nerve cells are observed in the roof portion of the pineal organ. Evidently, two different types of AChE-positive intrapineal neurons are present. About 40–50 AChE-positive neurons (extrapineal neurons) are scattered in the area of the subcommissural organ. In this area two types of nerve cells can be distinguished: 1) neurons which send pinealofugal (afferent) axons toward the posterior commissure and 2) neurons which emit pinealopetal (efferent) axons into or toward the pineal organ.The nervous pathways connecting the pineal organ with the diencephalomesencephalic border area are represented by a distinct pineal pedicle and several accessory pineal tracts.Granular nerve fibers run within the posterior commissure and establish synaptic contacts in the commissural region adjacent to the pineal organ. Some of these granular elements enter the pineal organ.The morphology of the nervous apparatus of the pineal organ of Ambystoma tigrinum is discussed in context with evidence from physiological experiments.In partial fulfillment of the requirements for the degree of Dr. med., Faculty of Medicine, Justus Liebig University, GiessenThe author is indebted to Professors A. Oksche and M. Ueck for their interest in this study. Thanks are due to Professor Ch. Baumann, Giessen, and Professor H. Langer, Bochum, for stimulating discussions. The technical assistance of Miss R. Liesner is gratefully acknowledgedDedicated to Professor Berta Scharrer on the occasion of her 70th birthday. Supported by grants from the Deutsche Forschungsgemeinschaft to A.O. and M.U.     

Tonotopic organization of auditory receptors of the bushcricket Pholidoptera griseoaptera (Tettigoniidae, Decticinae)

The peripheral and central tonotopy of auditory receptors of the bushcricket Pholidoptera griseoaptera is described. Out of 24 auditory receptor cells of the crista acustica 18 were identified by single-cell recordings in the prothoracic ganglion and complete staining with neurobiotin. Proximal receptor cells of the crista acustica were most sensitive to 6 kHz, with medial cells being sensitive to 20–30 kHz, whereas distal cells were most sensitive to frequencies higher than 50 kHz. Projection areas within the auditory neuropile in the prothoracic ganglion were to- notopically arranged. Proximal cells projected anteriorly, medial cells ventrally and posteriorly, and distal cells to more dorsal regions. Identified receptor cells revealed an interindividual variability of tuning and central projections. Receptor cells from the intermediate organ of a bushcricket were identified for the first time. Receptors of the distal intermediate organ were broadly tuned and less sensitive than those of the crista acustica. Receptor cells of the proximal intermediate organ were most sensitive to frequencies below 10 kHz. They projected in anterior portions of the auditory neuropile, whereas cells of the distal intermediate organ had terminations spread over almost the whole auditory neuropile.     

Hepatic progenitor cells

Liver diseases are associated with a marked reduction in the viable mass of hepatocytes. The most severe cases of liver disease (liver failure) are treated by orthotopic liver transplantation. One alternative to whole organ transplantation for patients with hepatic failure (and hereditary liver disease) is hepatocyte transplantation. However, there is a serious limitation to the treatment of liver diseases either by whole organ or hepatocyte transplantation, and that is the shortage of organ donors. Therefore, to overcome the problem of organ shortage, additional sources of hepatocytes must be found. Alternative sources of cells for transplantation have been proposed including embryonic stem cells, immortalised liver cells and differentiated cells. One other source of cells for transplantation found in the adult liver is the progeny of stem cells. These cells are termed hepatic progenitor cells (HPCs). The therapeutic potential of HPCs lies in their ability to proliferate and differentiate into hepatocytes and cholangiocytes. However, using HPCs as a cell therapy cannot be exploited fully until the mechanisms governing hepatocyte differentiation are elucidated. Here, we discuss the fundamental cellular and molecular elements required for HPC differentiation to hepatocytes.     

Cholinergic and GABAergic neuronal elements in the pineal organ of lampreys, and tract-tracing observations of differential connections of pinealofugal neurons

The putative cholinergic and GABAergic elements of the pineal organ of lampreys were investigated with immunocytochemistry to choline acetyltransferase (ChAT) and γ-aminobutyric acid (GABA), and by acetylcholinesterase (AChE) histochemistry. For comparison we also carried out immunocytochemistry to serotonin (5-HT) and a tract-tracing investigation of the two types of projecting cells, i.e., ganglion cells and long-axon photoreceptors. Most photoreceptors were ChAT-immunoreactive (ChAT-ir) and AChE-positive, while ganglion cells and the pineal tract were ChAT-negative and AChE-negative or only faintly positive. These results strongly suggest the presence of a cholinergic system of photoreceptors in the lamprey pineal organ. GABA-ir fibers that appear to originate from faintly to moderately stained ganglion cells were observed in the pineal stalk. Immunocytochemistry to 5-HT indicated the presence of two types of 5-HT-ir cells, bipolar cells and ganglion-like cells. The connections of the ganglion cells and long-axon photoreceptors were also studied by application of DiI to the pineal stalk in fixed brains or of biotinylated dextran amine (BDA) to one of the main targets of pinealofugal fibers (optic tectum or mesencephalic tegmentum) in isolated brains in vitro. Some long-axon photoreceptors and ganglion cells were labeled from the optic tectum. However, BDA application to the tegmentum exclusively labeled ganglion cells in the pineal organ. These results indicate that the two morphological types of afferent pineal neuron have different projections. No labeled cells were observed in the parapineal organ in BDA experiments, indicating that this organ and the pineal organ are involved in different neural circuits.