B. Aros

Special dendritic and axonal endings formed by the cerebrospinal fluid contacting neurons of the spinal cord.

SummaryThe cerebrospinal fluid (CSF) contacting neurons have a dendritic process which protrudes into the central canal, and is provided with one long kinocilium and many shorter stereocilia (about 80 in the turtle) as revealed by scanning electron microscopy. The shape, number and arrangement of the cilia are similar to those of known receptor endings.The silver impregnated axons of these cells converge to a paired centrosuperficial tract forming terminal enlargements at the ventrolateral surface of the spinal cord. Lying among glial endfeet these terminals are ultrastructurally similar to those present in known neurosecretory areas. The nerve endings are attached to the basal lamina, and they comprise many synaptic vesicles (200 to 400 Å in diameter), as well as granular vesicles of different sizes (diameter 600 to 1800 Å). The axons may lie within finger-like protrusions on the surface of the spinal cord, or they may terminate around vessels.Morphological evidence suggests that these nerve terminals and the corresponding CSF contacting perikarya represent a spinal neurosecretory system possibly influenced by information taken up by its special dendrites protruding into the inner CSF space.

Cerebrospinal fluid-contacting neurons, ciliated perikarya and “peptidergic” synapses in the magnocellular preoptic Nucleus of teleostean fishes

SummaryThe magnocellular preoptic nucleus of fishes (Anguilla anguilla, Amiurus nebulosus, Cyprinus carpio, Carassius auratus, Ctenopharyngodon idella, Cichlasoma nigrofasciatum) has been studied by light and electron microscopy.Two kinds of neurons were found: a) large, electron-dense, Gomori-positive cells with moderate acetylcholinesterase (AChE) positivity which contain granulated vesicles of 1400 to 2200 Å (in average 1600 to 1800 Å), and b) small, strongly AChE-positive, electron-lucent neurons containing granulated vesicles of 900 to 1200 Å. The nerve cells are supplied with axo-somatic and axo-dendritic synapses. These are formed by axon terminals containing either 1. synaptic vesicles of 500 Å, or 2. synaptic vesicles of 500 Å and dense-core vesicles of 600 to 800 Å, or 3. synaptic vesicles of 600 Å and granulated vesicles of up to 1100 Å, or 4. synaptic vesicles of about 400 Å and granulated vesicles of up to 1800 Å. The presence of “peptidergic” and numerous other synapses shows the complexity of the organization and afferentation of the magnocellular preoptic nucleus.In the eel, both types of nerve cells form dendritic terminals within the cerebrospinal fluid (CSF). These CSF contacting dendrites are supplied with 9×2+0 cilia. In the other species investigated, only some large neurons build up intraventricular endings. The ependymofugal process of the CSF contacting neurons enters the preoptic-neurohypophysial tract.Perikarya of both the large and the small cells may give rise to single, paired or multiple 9×2+0 cilia extending into the intercellular space. The number of CSF contacting neurons is reciprocal to the number of perikarya with intercellular cilium. These latter cells may represent modified, more differentiated forms of the CSF contacting neurons. We think that atypical cilia protruding into the intercellular space may have the same significance for the intercellular fluid as the cilia of the intraventricular dendrites of the CSF contacting neurons for the CSF.

Elektronenmikroskopische Untersuchung der Neurosekretion im Cerebralganglion des Regenwurmes (Lumbricus terrestris)

ZusammenfassungDie Feinstruktur der neurosekretorischen Nervenzellen und der Gliazellen im Cerebralganglion des Regenwurmes (Lumbricus terrstris) wurde untersucht.Die Nervenzellen zeigen verschiedenartige Erscheinungsformen. Einzelne sind mit reifen Neurosekretgranula (Durchmesser von rund 280 mμ) gefüllt („Speicherzellen“). In anderen dominieren leere Vesikel, oder das Ergastoplasma nimmt die ganze Zelle ein. In einzelnen Fällen erweitern sich die Ergastoplasmacysternen sackartig, so daß die Zelle ein vakuolisiertes Aussehen gewinnt. Der für ein Sekret charakteristische Stoff wird zuerst in den flachen Cysternen des Golgi-Apparates und in den Golgi-Vesikeln der entleerten Zellen gefunden. Daraus kann geschlossen werden, daß der Golgi-Apparat in enger Beziehung zur Sekretbildung steht. In einigen Zellen werden reife Sekretgranula im Interzellularraum zwischen den Fortsätzen der Glia- und Nervenzellen beobachtet.Charakteristisch für die Gliazellen sind ein gut entwickelter Golgi-Apparat, Stützfilamente und einzelne Vesikelreihen. Letztere stehen vermutlich mit der Pinocytose und Phagocytose in Zusammenhang. Oft kommen in den Gliazellen — aber in geringer Menge auch in den Nervenzellen — große, dunkle Körper (Durchmesser 0,5–2,5 μ) mit feinkörnigem, homogenem oder lamellärem Inhalt vor. Anscheinend bestehen zwischen diesen Körpern und den Gliamitochondrien Übergangsformen.Erweiterungen des Interzellularraumes an isolierten Abschnitten stehen aller Wahrscheinlichkeit nach mit der Entleerung des Sekretes in Verbindung. In ihnen ist ein blasser, fein präzipitierter Stoff zu finden. Die Wand der Kapillaren wkd von einer feinen Basalmembran und einer Myoendothelzellschicht gebildet. Oft sind zwischen benachbarten Endothelzellen und zwischen ihnen und der Basalmembran kleine homogene, dunkle Gebilde mit verwaschenem Umriß zu beobachten, die vielleicht mit der Entleerung der Sekretgranula in die Kapillaren in Zusammenhang stehen.

Ciliated neurons and different types of synapses in anterior hypothalamic nuclei of reptiles.

SummaryThe magnocellular paraventricular and supraoptic nuclei and the parvocellular preoptic and periventricular nuclei have been studied by light and electron microscopy in Emys orbicularis, Lacerta agilis and Elaphe longissima. The ultrastructure of cerebrospinal fluid (CSF)-contacting neurons was described in the preoptic and periventricular nuclei of Emys and Lacerta species. Single 9×2+0 cilia similar to those of the CSF-contacting dendritic terminals were found on perikarya of non CSF-contacting nerve cells, in all four investigated nuclei. The cilia project from funnel-like invaginations of the perikarya into the intercellular space. In the neurons of the nuclei studied, granular vesicles were found, their size being mainly 1,600 Å in the paraventricular nucleus, about 1,800 Å in the supraoptic nucleus, 1,100 Å in the periventricular nucleus and 800 Å, or up to 1,250 Å in the preoptic nucleus. In general, the neurons possess synapses of the axo-somatic, axo-somatic spine, axo-dendritic and axo-dendritic spine types. In the supraoptic nucleus, multiple interdigitated synapses were observed. Presynaptically, either synaptic vesicles only, or synaptic vesicles and dense core vesicles of different sizes (600 to 800 Å, about 1,100 Å, 1250 Å, and up to 2,000 Å) were found. It is discussed whether the above described 9×2+0 cilia may represent some kind of hypothalamic sensory structure that earlier physiological studies postulated to exist. The ciliated hypothalamic perikarya are considered by the authors to be a more differentiated form of the CSF-contacting neurons. The different types of synapses indicate multilateral connections of the nerve cells of the nuclei studied.

Comparative ultrastructure of cerebrospinal fluid-contacting neurons and pinealocytes.

SummaryThe pinealocytes of fishes, amphibians, reptiles, birds and mammals have been compared with cerebrospinal fluid (CSF) contacting neurons. We found that the intraventricular dendrite terminal of the latter resembles the pinealocytic inner segment and that the atypical cilium (9x2+0 tubules) of the CSF contacting neurons is analogous with the outer segment of the pinealocytes, even though the outer segment bears photoreceptor lamellae in lower vertebrates. Regular, but small-sized photoreceptor outer segments were also found on pinealocytes of the chicken. In mammals, too, primitive outer segments are present in the form of 9x2+0 cilia similar to those of CSF contacting dendritic terminals.In the Golgi areas of the perikarya of both cell types there are granulated vesicles which may contain transmitter substances and/or neurohormones.The synaptic junctions of the pinealocytes differ from those of the CSF contacting neurons. Many synapses occur on the latter, but they appear only rarely on pinealocytes. The axons of the CSF contacting neurons form synaptic connections with other cells, or terminate as neurohormonal synaptic hemidesmosomes on the basal lamina of the brain surface. The pinealocyte axons give rise to terminals containing synaptic ribbons. Such ribbons do not occur in CSF contacting neurons. In Lacertilians, we found pinealocytic terminals without ribbons on dendrite-like profiles.On the basis of the ultrastructural comparisons, we consider the CSF contacting neurons and pinealocytes to be very similar, but not to represent precisely the same cell type.

CSF contacting axons and synapses in the lumen of the pineal organ

SummaryFree-running, naked axons (diameter 2000 to 7000 Å) can be found in the lumen of the pineal organ. Their axoplasm contains microtubules, mitochondria as well as synaptic (diameter 350 to 450 Å) and granulated vesicles (diameter 500 to 1500 Å). In Pleurodeles waltlii, the axons in the pineal lumen form synapses on the free, apical surface of the pineal ependyma which is supplied with microvilli. In addition to usual cytoplasmic elements the innervated ependymal cells contain myeloid bodies and accumulations of glycogen granules. Without forming synapses these axons pass by and occasionally contact the inner and/or outer segments of the pinealocytes. The synapses found on the pineal ependymal cells furnish evidence of a neuronal control of these glial elements.The nerve fibers of the pineal lumen are being compared with known CSF contacting axons; they resemble one another in their ultrastructure and synaptic connections. Therefore and since in amphibians the pineal lumen communicates with the 3rd ventricle, the axons of the pineal lumen are considered to represent CSF contacting axons and to belong to the so-called CSF contacting axon system of the brain.In addition, the pineal CSF contacting axons are being compared with the following nerve fibers and terminals found in the pineal tissue: 1) axons containing large, granulated vesicles (diameter 1300 to 1500 Å) and terminating on the dendrites of nerve cells situated among the basal processes of the pinealocytes; 2) the synaptic ribbons-containing pinealocyte processes forming likewise synapses on the nerve cells; 3) the neurohormonal, synaptic semidesmosomes of pinealocytic processes on the lamina basalis separating the connective tissue spaces of the pia mater from the proper nervous tissue of the pineal organ; 4) the perivasal, autonomic nerve fibers of the pial septa. Though granulated vesicles of various diameters are present in all these terminals the greatest morphological similarity is found between the pineal CSF contacting axons and those nerve fibers containing large, granulated vesicles and forming axo-dendritic synapses on the pineal nerve cells. A similar nature and origin of both axons are suggested.ZusammenfassungIm Lumen des Pinealorgans können frei verlaufende, nackte Axone (Durchmesser 2000–7000 Å) beobachtet werden. Ihr Axoplasma enthält Mikrotubuli, Mitochondrien, synaptische (Durchmesser 350–450 Å) und granulierte Vesikel (Durchmesser 500–1500 Å). Bei Pleurodeles waltlii bilden die im Lumen des Pinealorgans verlaufenden Axone Synapsen auf der freien, apikalen Oberfläche der pinealen Ependymzellen. In den innervierten Ependymzellen kommen neben sonstigen Zytoplasmabestandteilen Myeloidkörper und Anhäufungen von Glykogengranula vor. Die Axone verlaufen am Innen- und Außenglied der Pinealozyten vorbei, können diese berühren, bilden aber dort keine Synapsen. Die auf den pinealen Ependymzellen nachgewiesenen Synapsen beweisen eine neuronale Kontrolle dieser Gliaelemente.Die Nervenfasern des pinealen Lumens wurden mit bekannten Liquorkontaktaxonen verglichen. Sie ähneln einander in ihrer Ultrastruktur und ihren synaptischen Verbindungen. Aus diesem Grunde und da bei den Amphibien das pineale Lumen mit dem 3. Ventrikel kommuniziert, werden die Axone des pinealen Lumens als Liquorkontaktaxone und als Glied des sogenannten Liquorkontakt-Axonsystems des Gehirns angesehen.Ferner wurden die pinealen Liquorkontaktaxone mit folgenden Nervenfasern und Endigungen verglichen, die im pinealen Gewebe vorkommen: 1) Axone, die große, granulierte Vesikel (Durchmesser 1300–1500 Å) enthalten und an den Dendriten von Nervenzellen endigen, welche zwischen den basalen Fortsätzen der Pinealozyten liegen; 2) Pinealozytenfortsätze, die synaptische Bänder enthalten und ebenfalls an diesen Neuronen Synapsen bilden; 3) die neurohormonalen, synaptischen Semidesmosomen von Pinealozytenfortsätzen an der Lamina basalis, die die bindegewebigen Räume der Pia mater vom eigentlichen Nervengewebe des Pinealorgans begrenzt: 4) die perivasalen, autonomen Nervenfasern der pialen Septen. Obwohl granulierte Vesikel verschiedener Durchmesser in allen diesen Terminalen vorhanden sind, stellten wir die größte, morphologische Ähnlichkeit zwischen den pinealen Liquorkontaktaxonen und denjenigen Nervenfasern fest, die große, granulierte Vesikel aufweisen und an den pinealen Neuronen axo-dendritische Synapsen bilden. Eine ähnliche Natur und Herkunft beider Axone werden angenommen.

Liquorkontaktneurone im Nucleus infundibularis

SummaryThe infundibular nucleus of various reptiles was studied light and electron microscopically. Cells of this nucleus send processes through a stratified ependyma into the 3rd ventricle where they form free, intraventricular nerve terminals (“liquor contacting nerve endings”, LCNE). In the nucleus, two kinds of neurons could be distinguished light microscopically: a) small, AChE-negative, toluidine blue neurons, and b) large, AChE-positive cells staining light with toluidine blue.The club shaped LCNE contain elements of the endoplasmic reticulum, free ribosomes, a various amount of mitochondria, and single lysosomes. The terminals bear asymmetrical cilia (type 9+0) supplied with accessory basal bodies and rootlet fibres. Two kinds of LCNE are demonstrable: a) LCNE containing dense-core vesicles with a diameter of about 800–1100 Å, and b) LCNE with large, electron-dense granules (diameter about 1,200–1,600 Å). In the lumen of the 3rd ventricle, there occur small axons that contain small granulated vesicles (diameter about 700–900 Å), and that form intraventricular synapses with the LCNE of the infundibular nucleus.The perikarya of the infundibular nucleus contain an abundant endoplasmic reticulum, numerous polyribosomes, neurotubules and mitochondria. Similarly to the LCNE, two kinds of perikarya can be distinguished: a) perikarya containing granulated vesicles (diameter about 800–1100 Å), and b) perikarya with electron-dense granules (diameter about 1200–1700 Å). Furthermore, different types of axosomatic and axodendritic synapses occur.The function of the intraventricular nerve terminals and the different types of synapses in the nucleus is discussed with regard to an exchange of informations between the cerebrospinal fluid and the infundibular nucleus.ZusammenfassungDer Nucleus infundibularis verschiedener Reptilien wurde licht- und elektronenmikroskopisch untersucht. Zellen dieses Kernes entsenden Fortsätze durch ein mehrreihiges Ependym in den 3. Ventrikel und bilden dort freie, intraventrikuläre Nervenendigungen („Liquorkontakt-Nervenendigungen“, Lkne). Lichtmikroskopisch konnten in der Kerngruppe a) kleine, AChE-negative, toluidinblaue und b) große, AChE-positive, mit Toluidinblau hell erscheinende Nervenzellen unterschieden werden.Die knöpfchenförmigen LKNE weisen Elemente des endoplasmatischen Retikulums, freie Ribosomen, eine wechselnde Anzahl Mitochondrien, einzelne Lysosomen, asymmetrische Zilien (Typ 9+0) mit akzessorischem Basalkörper und Zilienwurzeln auf. Zwei LKNE-Typen sind unterscheidbar: a) LKNE mit granulierten Vesikeln mit einem Durchmesser von 800–1100 Å und b) LKNE mit großen, elektronendichten Granula (Durchmesser 1200–1600 Å).Im Lumen des 3. Ventrikels treten kleinkalibrige Axone auf, die kleine, granulierte Bläschen (Durchmesser 700–900 Å) enthalten und mit den LKNE des Nucleus infundibularis intraventrikuläre Synapsen bilden.Die Perikaryen des Nucleus infundibularis weisen ein reichliches endoplasmatisches Retikulum, zahlreiche Polyribosomen, Neurotubuli und Mitochondrien auf. Ähnlich wie bei den LKNE sind zwei Perikaryenarten zu unterscheiden: a) Perikaryen mit granulierten Vesikeln (Durchmesser 800–1100 Å) und b) solche mit elektronendichten Granula (1200–1700 Å). Außerdem kommen verschiedene Arten axosomatischer und axodendritischer Synapsen vor.Die Funktion der intraventrikulären Nervenendigungen und verschiedenen Synapsenarten in der Kerngruppe wird im Hinblick auf einen Informationsaustausch zwischen dem Liquor cerebrospinalis und dem Nucleus infundibularis diskutiert.

Licht- und elektronenmikroskopische Untersuchungen des Saccus vasculosus und des Nervus und Tractus sacci vasculosi

SummaryThe vascular sac of Anguilla anguilla, Cyprinus carpio and Amiurus nebulosus has been studied by light microscopy using AChE reaction and the fluorescence histochemical method for the demonstration of monoamines, and by electron microscopy.As demonstrated light microscopically, the cerebrospinal fluid (CSF) contacting neurons and their processes exert a strong AChE activity, while the coronet cells are inactive. The AChE-positive processes of the neurons form bundles that enter the nervus sacci vasculosi and pass on in the tractus sacci vasculosi. After crossing to the opposite side, this AChE-positive bundle can be traced into the neuropil of the ventral thalamus. Neither the CSF contacting neurons of the vascular sac, nor the nervus, tractus and nucleus sacci vasculosi show any monoamine fluorescence.As demonstrated electron microscopically, there are synapses on the perikarya of the coronet cells, their presynaptic cytoplasm being characterized by mitochondria, synaptic and granulated vesicles (diameter about 800 to 1000 Å). The perikarya of the CSF contacting neurons contain dense-core vesicles (diameter about 700 to 900 Å) besides of the usual cytoplasmic components. Axons displaying granulated vesicles with a diameter of 800 Å or 1300 Å, form synapses on these perikarya. In the basal part of the saccus epithelium, there are nerve fibres of different calibres containing dense-core vesicles (diameter about 800 Å or 1400 Å) and forming synapses. The nervus sacci vasculosi is characterized by thin and thick, unmyelinated nerve fibres, and rare synapses, while the tractus sacci vasculosi is composed of mainly small, unmyelinated fibres.ZusammenfassungDer Saccus vasculosus von Anguilla anguilla, Cyprinus carpio und Amiurus nebulosus wurde lichtmikroskopisch mit der AChE-Reaktion und dem fluoreszenzhistochemischen Monoaminnachweis, sowie elektronenmikroskopisch untersucht.Lichtmikroskopisch weisen die Liquorkontaktneurone und ihre Fortsätze eine starke AChE-Aktivität auf, während die Krönchenzellen inaktiv sind. Die AChE-positiven Fortsätze der Nervenzellen bilden Bündel, die in den Nervus sacci vasculosi eintreten und im Tractus sacci vasculosi weiterziehen. Diese AChE-positive Bahn kann nach Kreuzung zur Gegenseite bis in das Neuropil des Thalamus ventralis verfolgt werden. Die Liquorkontaktneurone des Saccus vasculosus, der Nervus und Tractus sacci vasculosi, sowie der Nucleus sacci vasculosi weisen keine Monoaminfluoreszenz auf.Auf den Perikaryen der Krönchenzellen kommen Synapsen vor, deren praesynaptisches Cytoplasma außer synaptischen Bläschen und Mitochondrien 800–1000 Å große granulierte Vesikel aufweist. Die Perikaryen der Liquorkontaktneurone enthalten neben den üblichen Cytoplasmabestandteilen dense core Vesikel, deren Durchmesser 700–900 Å beträgt. Axone, in denen granulierte Vesikel (Durchmesser 800 oder 1300 Å) vorkommen, bilden mit diesen Perikaryen Synapsen. Im basalen Teil des Saccusepithels findet man granulierte Bläschen (Durchmesser 800 oder 1400 Å) enthaltende Nervenfasern unterschiedlichen Durchmessers, ferner Synapsen. Der Nervus sacci vasculosi enthält klein- und großkalibrige, marklose Nervenfasern und vereinzelte Synapsen, während der Tractus sacci vasculosi aus vorwiegend kleinkalibrigen, marklosen Fasern besteht.

Intraependymal cerebrospinal fluid contacting neurons and axon terminals on the external surface in the filum terminale of the carp (Cyprinus carpio)

SummarySmall nerve cells are scattered among the ependymal cells of the central canal of the filum terminale in Cyprinus carpio. The dendrites of these neurons form bulb-like endings in the cerebrospinal fluid (CSF). These endings are similar to the CSF contacting dendritic terminals of the medulla oblongata and spinal cord. Therefore, we consider these nerve cells to belong to the CSF contacting neuronal system.The axons of these neurons enter the hypendymal fibrous zone where nerve processes of various calibres and axon terminals on dendrite-like profiles and sometimes on ependymal processes were found. In addition to cytoplasmic elements ordinarily present in nerve cells there are granulated vesicles of about 800 to 900 Å in diameter in the perikarya of the CSF contacting neurons. Axons containing synaptic and dense-core vesicles (diameter about 400 Å and 800 Å, respectively) build up synapses on the basal part of these neurons. The CSF contacting neurons described are dissimilar to the Dahlgren cells present in the urophysis and in the rostral part of the filum.In addition, we found axon terminals forming synaptic semidesmosomes on the basal lamina of the external surface of the filum. At some places these terminals are numerous, building up primitive median eminence-like areas on the surface of the filum. In addition to synaptic vesicles these terminals contain numerous granulated vesicles of 800 Å. The axons forming these terminals are supposed to originate from the CSF contacting neurons. The presence of special nerve terminals on the external surface furnishes morphological evidence for the passage of substances from the nervous tissue into the external CSF space at the level of the filum terminale.

Liquorkontaktneurone im Nucleus infundibularis des Kükens

SummaryThe neurons of the infundibular nucleus of the chicken are multipolar, partly bipolar. Part of the ventricular processes of the nerve cells passes by between the ependymal cells into the cerebrospinal fluid where they form globular, intraventricular nerve endings (diameter about 3,5 to 5,5 μ).The liquor contacting nerve endings (LCNE) contain numerous mitochondria, endoplasmic reticulum, polyribosomes, granulated vesicles (diameter about 1300 Å) and scattered microtubules. The intraventricular terminal bears a cilium (type 9+0), its basal body gives rise to slim rootlet fibres. Sometimes, free liquor cells occur on the LCNE. The ventricular nerve processes that build up the LCNE are dendrites. In the hypendymal synaptic zone, axons containing granulated vesicles (1000 Å, 1300 Å) form synapses with the ventricular dendrites.The perikarya of the nerve cells are characterized by an abundant endoplasmic reticulum, polyribosomes, Golgi areas, mitochondria, granulated vesicles (diameter about 1300 Å) and numerous axo-somatic synapses.In the region of the infundibular nucleus, two types of ependymal cells can be distinguished: light and dark cells. The apical part of the latter forms several smaller and larger cytoplasmic processes. The light cells bear numerous cilia (type 9+2).On the basis of the new morphological data, the possible function of the liquor contacting neurons of the infundibular nucleus is discussed.ZusammenfassungDie Neurone des Nucleus infundibularis des Kükens sind multipolar, teilweise bipolar. Ein Teil der ventrikulären Fortsätze der Nervenzellen dringt zwischen den Ependymzellen hindurch in den Liquor cerebrospinalis ein und bildet dort kugelförmige, intraventrikuläre Nervenendigungen (Durchmesser 3,5–5,5 μ).Die Liquorkontakt-Nervenendigungen (LKNE) enthalten zahlreiche Mitochondrien, endoplasmatisches Retikulum, Polyribosomen, etwa 1300 Å große granulierte Vesikel sowie locker verteilte Mikrotubuli. Die intraventrikuläre Endigung trägt ein Cilium von Typ 9+0, von dessen Basalkörper dünne Zilienwurzeln ihren Ursprung nehmen. Manchmal kommen freie Liquorzellen auf den LKNE vor. Der die intraventrikuläre Endigung bildende ventrikuläre Fortsatz hat Dendritennatur. In der hypendymalen synaptischen Zone bilden Axone, die dense-core Vesikel (1000 Å, 1300 Å) enthalten, mit den ventrikulären Dendriten Synapsen.Die Perikaryen der Nervenzellen sind durch ein reichliches endoplasmatisches Retikulum, Polyribosomen, Golgi-Areale, Mitochondrien, granulierte Vesikel (Durchmesser 1300 Å) und zahlreiche axo-somatische Synapsen charakterisiert.Im Gebiet des Nucleus infundibularis können helle und dunkle Ependymzellen unterschieden werden. Der apikale Abschnitt der letzteren bildet kleinere und größere Plasmafortsätze. Die hellen Zellen tragen zahlreiche Zilien (Typ 9+2).Aufgrund der neuen morphologischen Daten wird die mögliche Funktion der Liquorkontaktneurone des Nucleus infundibularis diskutiert.