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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of pineal research 8 (1990), S. 0 
    ISSN: 1600-079X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Pineal synaptic ribbon (SR) populations of the early posthatch white leghorn chick were counted to determine if they demonstrate a rhythm that is in accordance with the light/dark cycle. SRs were counted between day 7 and day 10 and on day 14 of posthatch development, with samples at midlight, middark (14L:10D), and constant darkness. SR populations did not exhibit significant changes on days 7 and 8 under cycled lighting conditions nor on days 9 and 10 under constant darkness. A second experiment demonstrated that the dark:light ratio of SR populations of day 14 chicks, under cycled lighting, was 3.4:1.0, indicating SR rhythmicity by that stage of development. In that a preliminary experiment had demonstrated a 4.2:1.0 darklight ratio in SR populations in a predominantly day-10 population of chicks, we believe that SR rhythmicity begins on, or near, day 10 of posthatch development. To determine if the invasion of sympathetic fibers from the superior cervical ganglion (SCG) correlates with the initiation of SR light/dark population differences, we employed tyrosine hydroxylase immunofluorescence to reveal the distribution of catecholaminergic fibers in chick pineal follicles Follicular innervation doubled over the day 7 to day 14 period, during which time light/dark differences in SR populations were established. There is a correlation, in time, between the invasion of the pineal by the sympathetic fibers and the initiation of SR light/dark differences. The circadian rhythm of pineal N-acetyltransferase (NAT) activity, the rate-limiting enzyme in the melatonin pathway, is established earlier (day 2) than the light/dark differences in SR populations (day 10). It is possible that SR rhythmicity is influenced by the ingrowth of the pineal sympathetic innervation, and that SRs respond to an extrapineal oscillator rather than the independent oscillators of the chick pineal responsible for the rhythm of NAT activity and melatonin synthesis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of pineal research 4 (1987), S. 0 
    ISSN: 1600-079X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The objective of this study was to evaluate the effect of lighting (day-night) changes on pinealocyte synaptic ribbon shape (conformation) and numbers. Three-dimensional reconstruction analysis of pinealocyte basal processes revealed that 30% (6/20) of all ribbons from dark-adapted animals were either curved or split. Synaptic ribbons from light-adapted animals did not show this variant morphology; all were linear structures. An analysis of each section from each series, containing curved or split ribbons, revealed that 44% (16/36) of all ribbon profiles would yield inflated counts if used in random morphometric sampling protocols. Therefore, split and curved (variant) ribbon morphologies could result in an overestimation of synaptic ribbon populations of approximately 13% (0.44 × 30%) of dark-adapted samples. In spite of this potential sampling error, the fourfold increase in the number of synaptic ribbons observed during the dark phase of a light-dark cycle remains highly significant (P 〈 0.0001).
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 268 (1992), S. 531-538 
    ISSN: 1432-0878
    Keywords: Retinal pigment epithelium ; Myeloid bodies ; Regeneration ; Notophthalmus viridescens (Urodela)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Myeloid bodies are believed to be differentiated areas of smooth endoplasmic reticulum membranes, and they are found within the retinal pigment epithelium in a number of lower vertebrates. Previous studies demonstrated a correlation between phagocytosis of outer segment disc membranes and myeloid body numbers in the retinal pigment epithelium of the newt. To test the hypothesis that myeloid bodies are directly involved in outer segment lipid metabolism and to further characterize the origin and functional significance of these organelles, we examined the effects on myeloid bodies of eliminating the source of outer segment membrane lipids (neural retina removal) and of the subsequent return of outer segments (retinal regeneration) in the newt Notophthalmus viridescens. Light- and electron-microscopic analysis demonstrated that myeloid bodies disappeared from the pigment epithelium within six days of neural retina removal. By week 6 of regeneration, rudimentary photoreceptor outer segments were present but myeloid bodies were still absent. However, at this time, the smooth endoplasmic reticulum in some areas of the retinal pigment epithelial cells had become flattened, giving rise to small (0.5 μm long), two-to-four layer-thick lamellar units, which are myeloid body precursors. Small myeloid bodies were first observed one week later at week 7 of retinal regeneration. This study revealed that newt myeloid bodies are specialized areas of smooth endoplasmic reticulum. It also showed that a contact between functional photoreceptors and the retinal pigment epithelium is essential to the presence of myeloid bodies in the epithelial cells.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0878
    Keywords: Retinal pigment epithelium ; Myeloid bodies ; Morphometry ; Ultrastructure ; Endoplasmic reticulum ; Lighting effects ; Temperature effects ; Urodeles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Myeloid bodies (MBs) are specialized regions of endoplasmic reticulum which occur in the retinal pigment epithelium of a number of vertebrate species. In the newt, Notophthalmus viridescens, the effects of temperature and brief exposure to bright flashed-light on myeloid bodies have been studied. Morphometric analysis has shown that in animals sampled at 06.30 h, myeloid body sectional area remained unchanged in animals maintained in the cold (1°C), compared with control animals at 15°C, whereas phagosome area was significantly increased. At higher temperatures (30° C), myeloid body area was observed to decline from control values, while phagosome area was substantially increased. During the first 2 h of the light phase of a normal (15° C) 12:12 LD lighting cycle, myeloid-body sectional area dropped significantly from values recorded in the latter part of the dark phase. This reduction of MB area at the normal time of “lights-on” was greatly reduced when animals experienced an extended period of darkness. When animals experiencd a bright flashed-light at the normal time of “lights-on”, followed by a period of extended darkness, reduction in MB area was less pronounced when compared to cycled control animals. These results are discussed in the context of the hypothesis (Yorke and Dickson 1984) that MBs represent a temporary storage site for lipids entering the pigment epithelium after phagocytosis of shed outer segment tips, prior to their permanent storage in lipid droplets. These results are consistent with the proposal that myeloid bodies are removed from the cytoplasm of the newt pigment epithelium by metabolic processes which are active over time, but accelerated by increased temperatures or the presence of light.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 240 (1985), S. 641-648 
    ISSN: 1432-0878
    Keywords: Retinal pigment epithelium ; Myeloid bodies ; Ultrastructure ; Lipid metabolism ; Endoplasmic reticulum ; Cytochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary It has been suggested (Yorke and Dickson 1984) that myeloid bodies (MBs) in the retinal pigment epithelium (RPE) of the newt, Notophthalmus viridescens, may represent areas of endoplasmic reticulum where lipids, such as 11-cis retinal derived from phagocytized outer segment tips, accumulate prior to esterification. Experiments in which an artificial ester substrate was added during in-vitro incubations have shown that esterase activity is represented in all areas of the newt RPE endoplasmic reticulum, including sites adjacent to all MBs. In related tests in which the localization of enzyme activity was restricted to areas of the cell where there had been accumulations of naturally-occurring (endogenous) esters, the products of ester hydrolysis were restricted to profiles of endoplasmic reticulum associated with lipid droplets, and with the interior of about 20% of those MBs that appeared completely circular in sections. This enzyme activity was not associated with other MB configurations. Results from endogenous-ester hydrolysis were identical to those obtained after staining with ZIO. This ZIO-reactivity was not affected by pre-incubation with agents that blocked or protected sulphydryl groups, and ZIO-reactive sites associated with MBs did not form complexes with digitonin. These observations suggest that MBs are a site of lipid-ester formation, but that they do not represent unique intracellular areas for this activity.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 235 (1984), S. 177-186 
    ISSN: 1432-0878
    Keywords: Retinal pigment epithelium ; Myeloid bodies ; Diurnal variation ; Morphometrics ; Ultrastructure ; Lipid metabolism ; Endoplasmic reticulum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Myeloid bodies (MBs) occur in the newt (Notophthalmus viridescens) retinal pigment epithelium (RPE) and are similar to areas of specialized endoplasmic reticulum found in a variety of other cell types. The function of these structures is unknown, although a role in lipid metabolism has been strongly suggested. Random samples from conventionally-fixed and sectioned newt RPE, obtained over a 24-hr cycle (LD 12∶12), were examined by electron microscopy. Myeloid bodies appear as stacks of flattened endoplasmic reticulum-associated saccules which increase in length and number as the RPE accumulates shed outer segment material, prior to increase in the amount of stored lipid. Associations of MBs with the nuclear envelope can be related to this increased length. Myeloid bodies decrease numerically in the cell as phagosomes are removed from the cytoplasm, but a decrease in mean sectional MB area, seen in the light phase, is counteracted in darkness where individual MBs are larger than those found in the light. The total sectional area of MBs within a cell and their mean length varied depending on the lighting condition; differences were also found between eyes after extended periods of continuous light and dark. Ribosomes were found in association with the surfaces of both flattened and circular MBs, but they were consistently more densely associated with the shorter concave surfaces of curved regions. A new hypothesis for MB function is presented, which is concerned with their role in isolating toxic lipids such as retinoids, which are accumulated during phagocytosis of shed outer segment tips, and which are capable of disrupting membrane-bound systems necessary for their eventual metabolism and safe storage.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-0878
    Keywords: Retinal pigment epithelium ; Ultrastructure ; Endoplasmic reticulum ; Lipid phase transitions ; Metamorphic mosaic model ; Myeloid bodies ; Urodeles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The retinal pigment epithelium (RPE) of the newt (Notophthalmus viridescens) was examined ultrastructurally under both in-vivo and in-vitro conditions. Five distinct conformations of smooth endoplasmic reticulum (SER), two lamellar and three tubular, were observed. The two lamellar conformations included myeloid bodies, which have previously been described (Yorke and Dickson 1984), and fenestrated SER. The latter appeared as layers of flattened or curved cisternae which were penetrated by fenestrations. Fenestrated SER became indistinguishable from the highly branched and convoluted random-tubular SER through the formation of an intermediate configuration (“tubular sheets”). The remaining tubular SER conformations appeared to arise from random-tubular SER through a progressive reduction in branching and a straightening of individual tubules. Fascicular SER was represented by the hexagonal organization of straight, unbranched tubules into bundles (fascicles). Spiral SER consisted of a similar hexagonal arrangement, but the unbranched tubules spiralled about one another. Neighbouring tubules in areas of spiral SER were also joined together by pairs of electrondense bars. Although lamellar (especially myeloid bodies) and random-tubular configurations of the SER were common features in vivo, fascicular and spiral SER were primarily conformations encountered in vitro. Conditions favouring bilayer lipid phases also appear to facilitate the formation of both myeloid bodies and fascicular SER. These conditions included increased duration of incubation, low (〈20° C) incubation temperatures, and Ca2+-free incubations with EGTA. Random-tubular SER was most prevalent in media supplemented with fetal calf serum and also after warmer (30° C) incubation temperatures. We speculate that the different conformations of SER observed in the newt RPE may be due, in part, to lipid phase transitions within the membranes of this organelle. However, the specific formation of fascicular and spiral SER may also involve some additional factor, possibly a protein.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 176 (1986), S. 1-17 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: In order to test whether the alterations in photoreceptor synaptic terminal size and shape reported in lower vertebrates occur in a mammalian visual system, adult and fetal guinea pig retinas were exposed to an LD 12:12 lighting cycle, as well as to long-term light (LL) and long-term dark (DD) regimes. Representative random samples from all retinal quadrants, obtained at various times during these lighting regimes, were processed for electron microscopy. The synaptic terminals of all three photoreceptor cell types in this retina (alpha and paranuclear rods, and cones) were analyzed with computer-assisted morphometrics for changes in their area, perimeter, synaptic vesicle density, and the degree of plasmalemmal infolding. The data showed all three types of adult receptor terminals to have increased area and vesicle density, as well as decreased membrane infolding, during the light period, while both types of rods showed increased perimeter measurements in the dark. Results from adults maintained under extended lighting conditions (LL and DD) showed no difference when compared with sample times during a typical LD 12:12 lighting regimen where clear statistical differences existed. Data from fetal retinas showed no significant sustainable pattern in any of the measured variables. These quantitative findings have led to the conclusion that while alterations in perimeter measurements may be explained by using the vesicle recycling hypothesis, observed changes in terminal size and shape may be controlled by a light-initiated or light-enhanced mechanism and effected through an annular configuration of cross-striated fibrils found within these photoreceptor synaptic terminals.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 154 (1979), S. 321-336 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Development of the retina of the ammocoete begins early in embryogenesis, with the formation of the optic vesicle, but development of the rudimentary eye is suspended and remains arrested during larval life. Prior to the onset of metamorphosis, the retina of the ammocoete is completely undifferentiated, with the exception of a small area (Zone II) surrounding the optic nerve head, where all of the adult retinal layers are found. The photoreceptors in this area have developed to include synaptic contacts as well as inner and outer segments. The pigment epithelium in this area, too, has differentiated to include well-formed melanin granules, myeloid bodies and endoplasmic reticulum and is closely associated with the receptor cell outer segments. With the approach of metamorphosis, differentiation of the remainder of the retina (Zone I) begins, taking place in a radial fashion from the optic nerve head. Differentiating pigment epithelial cells adjacent to the differentiated retinal zone begin to accumulate melanin granules. In the neural retina, junctional complexes are established in the form of an external limiting membrane, and connecting cilia project into the optic ventricle. Photoreceptor differentiation begins with the formation of a mitochondria-filled ellipsoid within the inner segment.Development and differentiation of the ammocoete retina is unique to vertebrates in that only a small area of differentiated retina is present during the larval stage. The remainder of the retina differentiates and becomes functional during metamorphosis.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 165 (1982), S. 83-98 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The cornea of the adult lamprey has both dermal (spectacle) and scleral components. These are separated by a thin mucoid layer that allows free movement of the globe.This study has shown that during the larval (ammocoete) stage, the lamprey cornea develops in a manner similar to that of other lower vertebrates. Just prior to the period of transformation to the adult parasite, the outer dermal portion of the ammocoete cornea (spectacle) consists of an anterior stratified columnar epithelium with goblet cells at the surface. The stroma of the dermal cornea consists of a thick outer layer of orthogonally oriented collagen with branching fibroblasts and a thin, loosely organized inner layer with slender elongated fibroblasts. The scleral cornea is lined internally by a flattened monolayer of mesodermal cells, the corneal endothelium. Its narrow stroma is composed entirely of thin, orthogonally aranged, collagen-fiber lamellae, and is bounded externally by a thin continuous mesothelial layer of cells that abuts directly onto the loose stromal component of the dermal cornea.During the early stages of transformation, the anterior epithelium of the dermal cornea becomes stratified squamous in type. Later, the inner loose stroma of the dermal cornea (spectacle) begins to separate from the scleral cornea components, and a third complete mesothelial layer forms a distinct inner border for the dermal cornea. A mucoid layer is formed between the dermal (spectacle) and scleral corneas and remains throughout the adult life.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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