A. Oksche

Cell Biology of the Subcommissural Organ

Publisher Summary This chapter highlights the cell biology of the subcommissural organ (SCO) and discusses its structure–function relationships to provide a basis for further experimental work. SCO is a complex of nonneuronal secretory cells covering and penetrating the posterior commissure. This complex protrudes toward the third ventricle, occupies the posterior portion of the diencephalic roof caudal to the pineal organ, and marks the entrance to the Sylvian aqueduct. SCO is formed by two populations of secretory cells, which, in many species, are arranged into two distinct layers: the ependyma and the hypendyma. The bulk of the secretory products of the SCO, apparently a complex containing different glycoproteins, are released into the ventricular cerebrospinal fluid (CSF). In the ventricle, the secretion is condensed into a thread-like structure, Reissners fiber (RF) that terminates in the ampulla caudalis of the central canal. The blood vessels of the SCO represent a highly specialized vascular structure within the CNS. The SCO is sequestered within a double-barrier system of unknown functional significance, thereby indicating the unique character of this circumventricular organ.

Identification and partial characterization of the secretory glycoproteins of the bovine subcommissural organ-Reissner's fiber complex. Evidence for the existence of two precursor forms

The subcommissural organ (SCO) is a brain gland whose secretory material is released into the cerebrospinal fluid where it condenses into a thread-like structure known as Reissners fiber (RF). This fiber extends along the aqueduct, fourth ventricle and central canal of the spinal cord. The present investigation was designed to identify and partially characterize the secretory products of the bovine SCO in their intracellular location and after they have been released and packed into RF form. 5,000 SCOs were dissected out under a microscope, whereas RF of 30,000 cows were collected by perfusing the central canal of the spinal cord with artificial cerebrospinal fluid. Extracts of SCO and RF were used for (i) raising polyclonal antibodies; (ii) immunoblotting; (iii) lectin binding on electrotransfers: concanavalin A (affinity = mannose, glucose) and Limax flavus agglutinin (affinity = sialic acid); (iv) immunoaffinity chromatography; (v) preparative SDS-PAGE and raising of polyclonal antibodies against each of the secretory glycoproteins identified in the immunoblots. All antibodies and the two lectins were also applied to tissue sections of the SCO and RF of several species. The immunocytochemical study of the bovine SCO using an anti-RF serum showed that the secretory material present in the rough endoplasmic reticulum (RER), secretory granules and in RF is strongly immunoreactive. Con A binding sites were only found in the endoplasmic reticulum, whereas Limax flavus agglutinin revealed secretory granules and RF, only. In the blots the immunostaining was used to identify secretory polypeptides. The glycosylated nature of the latter was established by their affinity for Con A and/or Limax flavus agglutinin. Furthermore, this latter lectin allowed us to distinguish whether the intracellular source of a secretory glycoprotein is from a pre-Golgi (RER) or a post-Golgi (secretory granules) compartment. Four glycoproteins were identified in the SCO with apparent molecular weights of 540, 450, 320 and 190 kDa. The three former were also purified by immunoaffinity chromatography. The 540 and 320 kDa forms are present in the SCO but missing in RF, have affinity for Con A, but not for LFA. It is suggested that these two compounds correspond to two precursor forms. The 450 and 190 kDa glycoproteins are present in both, the SCO and RF, and have affinity for Con A and Limax flavus agglutinin. These most likely correspond to processed forms. The presence of more than one precursor was further substantiated by immunocytochemical findings using antisera against the 540, 450 and 320 kDa forms.(ABSTRACT TRUNCATED AT 400 WORDS)

Immunocytochemical investigation of the hypothalamo-neurohypophysial system in birds

SummaryThe results of an immunohistochemical investigation of the hypothalamo-neurohypophysial system in several species of birds have shown that: (1) mesotocin and vasotocin are synthesized in separate neurons; (2) in all species investigated the distribution of mesotocinergic and vasotocinergic perikarya follows a common pattern; (3) the external zone of the avian anterior median eminence contains exclusively vasotocinergic nerve fibers, originating in supraoptic and ventral paraventricular regions; (4) the distribution of immunoreactive elements in the neural lobe shows a definite species-dependent pattern.

Acetylcholinesterase-containing nerve cells in the pineal complex and subcommissural area of the frogs, Rana ridibunda and Rana esculenta.

SummaryIn Rana esculenta and Rana ridibunda the frontal organ and the pineal organ (epiphysis cerebri) form a pineal complex. Approximately 60 nerve cells of the frontal organ and 220–320 nerve cells of the pineal organ display a positive acetylcholinesterase reaction (Karnovsky and Roots, 1964). The dorsal wall of the pineal organ is considerably richer in acetylcholinesterase-positive neurons than the ventral wall (ratio 3∶1); a group of unusually large-sized nerve cells occurs in the rostral portion of the frog pineal. Two different types of nerve cells were observed in the pineal complex: multipolar and pseudounipolar elements. The former are embedded in the pineal parenchyma and their processes penetrate radially into the plexiform layer, whereas the latter are distributed along the roots of the pineal tract near the basal lamina. The ratio of the multipolar to pseudounipolar neurons is 1∶4 for the frontal organ and 3∶5 for the pineal organ. The multipolar elements may be interneurons; the pseudouni-polar cells send one of their processes into the pineal tract. At the caudal end of the pineal organ 30–50 unipolar nerve cells are clustered in juxtaposition with the pineal tract, and other 30–50 unipolar neurons are scattered along the basis of the subcommissural organ. Some of these nerve cells emit their processes toward the mesencephalon and others toward the pineal organ via the pineal tract. The results are discussed with respect to previous physiological and morphological findings on the pineal complex of Anura.

Opsin-immunoreactive outer segments in the pineal and parapineal organs of the lamprey (Lampetra fluviatilis), the eel (Anguilla anguilla), and the rainbow trout (Salmo gairdneri)

SummaryThe pineal complex of Lampetra fluviatilis, Anguilla anguilla and Salmo gairdneri was studied by means of the indirect immunohistochemical antiopsin reaction.Opsin-immunoreactive material was demonstrated in the outer segments of the photoreceptor cells in the pineal organ of all three species investigated. In the lamprey, the opsin-positive outer segments were located in the lumen of the pineal vesicle and atrium. In the two teleost species, the immunoreactive outer segments were observed in abundance in the pineal end-vesicle and stalk. These structures were found to accumulate in the prominent initial portion of the pineal stalk of the eel. In the rainbow trout, immunoreactive outer segments occurred in the wide orifice of the pineal recess at the roof of the third ventricle.In addition, outer segments of photoreceptor cells of the parapineal organ (“parapinealocytes”) displayed opsin immunoreactivity. In the lamprey, opsin immunoreactivity was restricted to the central portion of the ventral parapineal retina, while the parapinealocytes in the lateral portions did not bind the antibody. In the two teleosts, immunoreactive outer segments displayed a scattered pattern.These immunocytochemical results provide direct evidence that the photosensitivity of the pineal demonstrated electrophysiologically in lampreys and teleosts (cf. Dodt 1973) is based on an opsin-containing photopigment. The presence of opsin in cells of the parapineal organ strengthens the view that also this organ may be capable of direct light perception. In the lamprey, the exclusive opsin immunoreactivity of a circumscribed group of parapineal cells suggests the existence of two types of parapinealocytes. The significance of opsin-containing photoreceptor outer segments occurring in the most proximal portion of the teleost pineal stalk is discussed, especially with regard to the interpretation of results obtained from pinealectomy experiments.

Opsin-immunoreactive outer segments and acetylcholinesterase-positive neurons in the pineal complex of Phoxinus phoxinus (Teleostei, Cyprinidae).

SummaryThe pineal complex of the teleost, Phoxinus phoxinus L., was studied light-microscopically by the use of the indirect immunocytochemical antiopsin reaction and the histochemical acetylcholinersterase (AChE) method.Opsin-immunoreactive outer segments of photoreceptor cells were demonstrated in large numbers in all divisions of the pineal end-vesicle and in the pineal stalk. Moreover, they were found in the roof of the third ventricle, adjacent to the orifice of the pineal recess as well as scattered in the parapineal organ. These immunocytochemical observations provide direct evidence of the presence of an opsin associated with a photopigment in the photosensory cells of the pineal and parapineal organs of Phoxinus. By means of the AChE reaction (Karnovsky and Roots 1964) inner segments of pineal photoreceptors, intrinsic nerve cells, several intrapineal bundles of nerve fibers, and a prominent pineal tract were specifically marked. The pineal neurons can be divided into two types: one is located near the pineal lumen, the other near the basal lamina. The latter perikarya bear stained processes directed toward the photoreceptor layer. A rostral aggregation of two types of AChE-positive nerve cells occurs in the ventral wall of the pineal end-vesicle. The main portion of the AChE-positive pineal tract, which lies within the dorsal wall of the pineal stalk, can be followed to the posterior commissure where some of the nerve fibers course laterally. A few AChE-positive pineal nerve fibers run toward the lateral habenular nucleus via the habenular commissure. In the region of the subcommissural organ single AChE-positive neurons accompany the pineal tract. The nerve cells of the parapineal organ exhibit a moderate AChE activity.These findings extend the structural basis for the remarkable light-dependent activity of the pineal organ of Phoxinus phoxinus.

Neurone und zentralnervöse Verbindungen des Pinealorgans der Anuren

SummaryThe problem of interneurons appears to be very important for the functional interpretation of the chromatic and achromatic responses of pineal sense organs. Previous results seemed to indicate a bineuronal chain in the pineal organ (epiphysis cerebri) ofRana temporaria andRana esculenta. Precise images of pineal receptors, neurons and their connexions were obtained in the present studies using methylene-blue and Golgi methods. A limited number of interneurons probably exist in theepiphysis ofR. temporaria andR. esculenta: the images of these scattered neurons were observed to differ from the classical bipolar, horizontal and amacrine cells of the amphibian retina. The pineal tract of R. temporaria andR. esculenta is formed by the axons of large multipolar and smaller scarcely ramified nerve cells. The central projection of this pinealo-fugal (afferent) pathway is of great functional interest. After complete surgical interruption of the pineal tract degenerating nerve fibers were traced in Nauta (Fink-Heimer) preparations. Degenerating fibers were observed within and beneath the posterior commissure, in the pretectal region and in the nuclear areas of the “periventricular gray”. The subependymal layer and the basal aminergic nuclei of the frog mesencephalon were always free of degenerating fibers. The anatomical connexion of the pineal tract described in this paper could serve as a basis for some light-dependent (phototactic) reflexes. Further investigations concerned with the central projections of the pineal tract are in progress.ZusammenfassungDas Problem der Zwischenneurone nimmt bei der Deutung der chromatischen und achromatischen Antworten der pinealen Sinnesorgane eine Schlüsselstellung ein. Frühere Ergebnisse schienen darauf hinzuweisen, daß der nervöse Apparat des Pinealorgans (Epiphysis cerebri) vonRana temporaria undRana esculenta bineuronal organisiert ist. Mit modifizierten Methylenblau- und Golgi-Methoden gelang es jetzt, die nervösen Strukturen der pinealen Rezeptoren und Nervenzellen präziser darzustellen. Das neurohistologische Bild der Epiphysis cerebri enthält auch Nervenzellen, die an Zwischenneurone denken lassen. Diese diffus verstreuten kleinen Elemente unterscheiden sich von den klassischen Typen der retinalen Bipolar-, Horizontal- und Amakrinzellen. Der Tractus pinealis vonR. temporaria undR. esculenta wird von Axonen großer multipolarer und kleiner, wenig verzweigter Ganglienzellen gebildet. Die zentrale Projektion dieser pinealofugalen (afferenten) Bahn ist von großem funktionellem Interesse. Nach vollständiger Unterbrechung des Tr. pinealis finden sich degenerierende Faserelemente innerhalb und am unteren Rand der Comm. posterior, in der Area praetectalis und in den Kernarealen des sog. „Zentralen Graus“. Keine degenerierenden Tractusfasern sind in der subependymalen Schicht und in den aminergen Kerngebieten des Mesencephalon zu beobachten. Die beschriebenen Verbindungen des Tr. pinealis könnten die anatomische Basis einiger lichtabhängiger (phototaktischer) Reflexe darstellen. Weitere Untersuchungen über die zentralnervöse Projektion des Tr. pinealis sind im Gang.

Electron microscopic and experimental studies of the pineal organ in the white-crowned sparrow, Zonotrichia leucophrys gambelii.

SummaryThe structure of the pineal organ of Zonotrichia leucophrys gambelii, as revealed by light- and electron-microscopy, resembles that of Passer domesticus (Oksche and Kirschstein, 1969; Ueck, 1970). The typical cellular element is the pinealocyte with certain basic structural features of the pineal photoreceptors of lower vertebrates (see Oksche, 1971). However, instead of the characteristic, cone-like outer segments, there are, as in other species of birds, only bulbous cilia with ectopic whorls of lamellae. This structure of the outer segment is, in a sense, contrary to the demonstration of synaptoid contacts, numerous unmyelinated, and occasional myelinated nerve fibers by electron microscopy. In Nissl preparations it was possible to demonstrate typical nerve cells. The pinealocytes of Z. l. gambelii are secretory; their Golgi complex forms granulated vesicles (800–1,400 Å in diameter) that belong to the group of granular inclusions characteristic of monoamines. Autonomie nerve fibers course within the connective tissue capsule of the pineal organ. In many pinealocytes of Z. l. gambelii, the granular endoplasmic reticulum contains extensively expanded cisternae that are filled with a flocculent material and closely associated with bundles of filaments. In a number of cases such loop-like structures are selectively stainable with aldehyde fuchsin. It was not possible to demonstrate specific secretory activity in the supporting cells. Extirpation of the pineal organ in Z. l. gambelii had no definitely detectable influence on the photoperiodic control of testicular growth.

Intrinsic neurons and neural connections of the pineal organ of the house sparrow, Passer domesticus, as revealed by anterograde and retrograde transport of horseradish peroxidase

SummaryIn Passer domesticus, intrapineal nerve cells were labeled by uptake of microiontophoretically administered horseradish peroxidase (HRP). Unipolar nerve cells with a dichotomously branching stem process are the main source of the dominant pinelaofugal component of the pineal tract, whereas multipolar and bipolar neurons appear to represent interneurons.HRP-labeled nerve fibers are observed in the distal division (end-piece) of the pineal organ; they can be regarded either as processes of intrapineal neurons or projections of pinealopetal axons originating from central neurons.Furthermore, scattered labeled nerve fibers occur in different portions of the pineal stalk. Nerve fibers containing HRP were also demonstrated in the medial and lateral divisions of the habenular complex and in the periventricular layer of the hypothalamus; these axons apparently represent anterogradely labeled pinealofugal elements. On the other hand, retrogradely labeled neurons were found in the medial habenular complex and in the periventricular hypothalamic gray near the paraventricular nucleus, indicating that the pineal organ receives a pinealopetal innervation arising from the central nervous system.Ultrastructurally, the neuropil of the pineal organ of P. domesticus displays single basal processes of pinealocytes containing synaptic ribbons in association with clear synaptic vesicles. Occasionally, conventional synapses were observed the presynaptic terminals of which exhibit granular inclusions.The pineal tract consisting of four to six spatially separated fiber bundles comprises mainly unmyelinated elements accompanied by only few myelinated axons.The functional role of the neural apparatus revealed in the present study is discussed in context with the humoral (hormonal) control of circadian functions; the latter type of activity has been shown to exist in the pineal organ of P. domesticus (Zimmerman 1976).

Human subcommissural organ, with particular emphasis on its secretory activity during the fetal life.

The subcommissural organ (SCO) is a conserved brain gland present throughout the vertebrate phylum. During ontogeny, it is the first secretory structure of the brain to differentiate. In the human, the SCO can be morphologically distinguished in 7‐ to 8‐week‐old embryos. The SCO of 3‐ to 5‐month‐old fetuses is an active, secretory structure of the brain. However, already in 9‐month‐old fetuses, the regressive development of the SCO‐parenchyma is evident. In 1‐year‐old infants, the height of the secretory ependymal cells is distinctly reduced and they are grouped in the form of islets that alternate with cuboid non‐secretory ependyma. The regression of the SCO continues during childhood, so that at the ninth year of life the specific secretory parenchyma is confined to a few islets of secretory ependymal cells. The human fetal SCO shares the distinct ultrastructural features characterizing the SCO of all other species, namely, a well‐developed rough endoplasmic reticulum, with many of its cisternae being dilated and filled with a filamentous material, several Golgi complexes, and secretory granules of variable size, shape, and electron density. The human fetal SCO does not immunoreact with any of the numerous polyclonal and monoclonal antibodies raised against RF‐glycoproteins of animal origin. This and the absence of RF in the human led to the conclusion that the human SCO does not secrete RF‐glycoproteins. Taking into account the ultrastructural, lectin‐histochemical, and immunocytochemical findings, it can be concluded that the human SCO, and most likely the SCO of the anthropoid apes, secrete glyco‐ protein(s) with a protein backbone of unknown nature, and with a carbohydrate chain similar or identical to that of RF‐glycoproteins secreted by the SCO of all other species. These, as yet unidentified, glycoprotein(s) do not aggregate but become soluble in the CSF. Evidence is presented that these CSF‐soluble proteins secreted by the human SCO correspond to (1) a 45‐kDa compound similar or identical to transthyretin and, (2) a protein of about 500 kDa. Microsc. Res. Tech. 52:573–590, 2001.