Biomedical subjects

B Burnside

Publications and source records attributed to B Burnside.

At least 37 records · Page 2Linked to original sources

PubMed1994

Myosin I localizes to the midbody region during mammalian cytokinesis.

During cytokinesis, daughter cells are cleaved in two by the constriction of an actin-rich contractile ring which encircles the equator of the dividing cell. Filamentous myosin II is present in the contractile ring and necessary for constriction of the furrow, as shown in several cell types [Satterwhite and Pollard, 1992: Curr. Opin. Cell Biol. 4:43-52]. However, no functional role nor distinctive localization has been previously identified for non-filamentous "unconventional" myosins, such as myosin I, during cytokinesis. Using antibodies to adrenal medullary myosin I, we report that myosin I is localized in 3T3 fibroblasts to the mid-equatorial plane during late-cytokinesis, as well as to the polar edges as previously described in ameboid cells [Fukui et al., 1989: Nature 341:328-331]. Confocal microscopy revealed that myosin I is concentrated at the midbody region in a nearly continuous transverse disk, extending from the cortical region of the furrow through the midbody itself. These findings suggest that, in addition to the accepted role of filamentous myosin II in constriction of the contractile ring, nonfilamentous myosin I might contribute to motile events occurring late in cytokinesis.

3T3 Cells↗

PubMed1994

Myosin-I in retinal pigment epithelial cells.

PURPOSE: Myosin-I is a nonfilamentous motor protein associated with the actin cytoskeleton and cellular membranes in several cell types. The occurrence and subcellular distribution of myosin-I in mammalian and fish RPE were investigated to examine the possible role of myosin-I in retinal pigment epithelium (RPE) motility processes. METHODS: Antibodies directed against myosin-I proteins from bovine adrenal medulla or chicken intestinal brush border were used to examine cultured fetal human RPE cells and freshly isolated bovine or green sunfish RPE by Western immunoblots and immunocytochemistry, using both conventional and confocal fluorescence microscopy. RESULTS: The monoclonal antibody directed against bovine adrenal myosin-I identified a single strong immunoreactive band at 116 kD in Western blots of homogenates of cultured human RPE cells and 114 kD in bovine RPE sheets. An immunoreactive band of similar molecular weight was also observed in bovine and rabbit retina. Cell fractionation studies of bovine RPE cells revealed that myosin-I was present in all fractions that included cell membranes. The polyclonal antibody directed against chicken brush border myosin-I identified doublet immunoreactive bands at 115/110 kD in Western blots of homogenates of fish retina but identified a strong predominant immunoreactive band at 140 kD in fish RPE and brain homogenates; minor bands at 115/110 kD were identified in fish RPE homogenates. Immunocytochemistry of cultured human RPE cells using the bovine adrenal myosin-I antibody revealed a broad distribution of myosin-I that appeared to be most concentrated along the length of the lateral membranes; no colocalization was seen with actin-rich stress fibers. CONCLUSIONS: Proteins immunoreactive with myosin-I antibodies are present in both RPE and retina of mammals and green sunfish. In confluent cultures of human RPE cells, myosin-I is concentrated along the lateral cell membranes of the cuboidal cells.

Animals↗

PubMed1994

Suppression of cAMP-induced pigment granule aggregation in RPE by organic anion transport inhibitors.

PURPOSE: To investigate the mechanism(s) by which intracellular cAMP levels are elevated to induce pigment granule aggregation in teleost retinal pigment epithelium (RPE). METHODS: Pigment granule migration was studied in vitro using RPE sheets isolated from dark-adapted green sunfish, Lepomis cyanellus. After preculture to allow pigment granule dispersion, RPE sheets were incubated with various agents to test their ability to induce pigment granule aggregation. RPE sheets were then fixed, and pigment granule position was assessed microscopically. RESULTS: Pigment granule aggregation was induced by nonderivatized cAMP. At maximally effective concentration (1 mM), cAMP was as effective as its more membrane-permeant analogs dbcAMP and 8-Br-cAMP. Forskolin (1 or 10 microM), a stimulator of adenylyl cyclase, was also effective at inducing pigment aggregation. Two inhibitors of organic anion transport, probenecid and sulfinpyrazone, inhibited cAMP-induced aggregation by approximately 80% but had no effect on forskolin-induced aggregation. Several agents shown to stimulate RPE adenylyl cyclase in other species failed to induce pigment aggregation in isolated RPE sheets. CONCLUSIONS: Our observations strongly suggest that exogenously applied, nonderivatized cAMP can gain access to the cytoplasm of isolated RPE cells via organic anion transporters. Thus, if cAMP were secreted by retinal cells into the subretinal space, it could be taken up by RPE cells and subsequently act as an intracellular messenger to activate dark-adaptive physiological processes such as pigment granule aggregation.

Animals↗

PubMed1993

Light-activation of teleost rod photoreceptor elongation.

Rod photoreceptors in the retinas of teleost fish undergo changes in cell length in response to changing ambient light intensities. In the dark rods shorten and in the light rods elongate. These movements are mediated by actin-dependent processes which occur in the ellipsoid and myoid of the inner segment. As an approach to examining the underlying intracellular signaling pathways that link light absorption to actin-dependent motility in the inner segment, we have investigated the quantitative aspects of the light stimulus required to activate elongation in isolated rod inner/outer segments (RIS-ROS) of the green sunfish (Lepomis cyanellus). The intensity thresholds and strength-duration characteristics of the light stimulus required to activate teleost rod elongation were found to differ from those reported to activate vertebrate rod membrane hyperpolarization. In response to brief pulses of light, RIS-ROS elongated in a graded manner, both as a function of increasing light pulse intensity and light pulse duration. Half maximal activation of light-induced RIS-ROS elongation was produced by a stimulus of roughly 6 x 10(15) photons cm-2, which is calculated to bleach approximately 20% of the photopigment molecules in green sunfish rod outer segments. This degree of photopigment bleach is approximately 6-7 orders of magnitude greater than that required to elicit half maximal changes in membrane potential in other vertebrate rod preparations. Furthermore, the reciprocal relationship between light pulse intensity and duration in eliciting an equal elongation response held for relatively long light pulse durations.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1993

Identification of cyclic nucleotide-regulated phosphoproteins, including phosducin, in motile rod inner-outer segments of teleosts.

In teleost retinas, rods elongate in the light and shorten in the dark. Rod motility is mediated by the actin cytoskeleton of the inner segment and is regulated by cyclic AMP- or cyclic GMP-stimulated phosphorylation of target proteins. In this study, we have identified the target proteins of cyclic nucleotide-dependent kinases in rods, using preparations of isolated, motile rod inner-outer segments (RIS-ROS). Five proteins found in Percoll-purified RIS-ROS were phosphorylated in the presence of cAMP (> 10 nM), cGMP (> or = 10 microM) and exogenous catalytic subunit of cAMP-dependent protein kinase (PKA). The PKA inhibitor, PKI, blocked stimulation of phosphorylation by both cAMP and cGMP. Three cAMP-stimulated phosphoproteins were detected in cytoskeletal fractions of light- and dark-adapted RIS-ROS. One of these, PP33, appears to be a fish homologue of mammalian phosducin, based on immunolabeling by two different antibodies against mammalian phosducin and on electrophoretic characteristics in 2-D gels. Two additional phosducin immunoreactive bands were detected in Western blots. One, at 35 kDa, comigrated with a second cAMP-stimulated RIS-ROS phosphoprotein, PP35, which was also detected in the cytoskeleton. The other, at 37 kDa, was present in whole teleost retinas but not in purified RIS-ROS. Our results suggest that the effects of both cAMP and cGMP on teleost rod motility are mediated through PKA modulation of target phosphoproteins. These phosphoproteins include a cytoskeleton-associated phosducin homologue.

Animals↗

PubMed1993

Retinomotor movements in isolated teleost retinal cone inner-outer segment preparations (CIS-COS): effects of light, dark and dopamine.

Teleost cone inner segments elongate and contract in response to light and circadian signals. Previous studies have shown that teleost cone contraction is triggered by light or dopamine, while cone elongation is triggered by darkness or experimental elevation of cAMP. We have developed procedures for isolating and purifying motile cone fragments consisting of inner and outer segments (CIS-COS) to permit more detailed analysis of light and dopamine regulation of cone retinomotor movements. When retinas are dissected from long-term dark-adapted fish, CIS-COS break off at the base of the ellipsoid and remain attached to the RPE. CIS-COS can be detached from the RPE by brief protease treatment, thereby generating a highly enriched CIS-COS suspension. CIS-COS retain normal morphology and extend new myoids when cultured in darkness or in light plus forskolin, an activator of adenylate cyclase. The microtubule and actin cytoskeletons of the new myoids resemble those of intact cone myoids in vivo. Light inhibits CIS-COS myoid elongation, suggesting that light reception by the outer segment can directly influence cone motility. In dark-cultured CIS-COS, myoid elongation is inhibited half-maximally by nanomolar concentrations of dopamine, suggesting that dopamine effects on motility are mediated by D2-family receptors present on the cone inner and/or outer segment. After dark-induced elongation in culture, CIS-COS myoids can be induced to contract by subsequent culture in the light or with dopamine. Thus isolated cone inner and outer segments possess sufficient cytoskeletal and regulatory machinery to exhibit light- and dopamine-regulation retinomotor movement similar to that observed in intact cones in situ.

Animals↗

PubMed1993

Cyclic nucleotide regulation of teleost rod photoreceptor inner segment length.

Retinal rod photoreceptors of teleost fish elongate in the light and shorten in the dark. Rod cell elongation and shortening are both mediated by actin-dependent mechanisms that occur in the inner segment myoid and ellipsoid. The intracellular signaling pathways by which light and dark regulate the actin cytoskeleton in the inner segment are unknown. To investigate the intracellular signals that regulate teleost rod motility, we have been using mechanically isolated rod inner/outer segments (RIS-ROS) obtained from the retinas of green sunfish, Lepomis cyanellus. In culture, RIS-ROS retain the ability to elongate in response to light; myoids elongate 15-20 microns in length during 45 min of light culture. A pharmacological approach was taken to investigate the role of cyclic nucleotides, cyclic nucleotide-dependent kinases, and protein phosphatases in the regulation of RIS-ROS motility. Millimolar concentrations of cAMP and cGMP analogues were both found to inhibit light-induced myoid elongation and two cyclic nucleotide analogues, SpCAMPS and 8BrcGMP, promoted myoid shortening after RIS-ROS had elongated in response to light. The cyclic nucleotide-dependent kinase inhibitor, H8, mimicked light by promoting myoid elongation in the dark. The effects of H8 were dose dependent, with maximal elongation occurring at concentrations of approximately 100 microM. Similar to the effects of cyclic nucleotide analogues, the phosphatase inhibitor, okadaic acid (0.1-10 microM), inhibited light-induced elongation and promoted shortening. The results presented here suggest that RIS-ROS motility is regulated by protein phosphorylation: phosphorylation in the dark by cyclic nucleotide-dependent protein kinases promotes rod shortening, while dephosphorylation in the light promotes rod elongation.

1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine↗

PubMed1993

Light and circadian modulation of teleost retinal tyrosine hydroxylase activity.

PURPOSE: The authors examined the effects of both light and circadian phase on the synthetic activity of the dopamine producing enzyme, tyrosine hydroxylase (TH), in the retina of the Midas cichlid (Cichlasoma citrinellum). METHODS: TH activity was assayed in the retina-retinal pigment epithelium (RPE) complex of fish entrained to cyclic light regimens. The animals were killed throughout cyclic light and continuous dark cycles and after light exposure following short-term dark adaptation to assess the effects of both diurnal and circadian phase and light exposure on TH activity. Variations in retina-RPE TH activity were compared with cone retinomotor position. RESULTS: The authors report that TH activity was influenced both by light and by circadian phase. In both cyclic light and continuous darkness, TH activity fluctuated in cyclic fashion, increasing to peak values at night, declining through dawn, and reaching minimal values at midday. In continuous dark-adapted retinae, the peak activity at night was approximately sixfold greater than the minimum activity during the day. In cyclic light-adapted retinae at midday, the TH activity was 2.4-fold higher than that determined at the same time point in continuous dark-adapted retinae. Light onset enhanced the TH activity in previously dark-adapted animals by 2.2-fold at midday and 1.7-fold at dusk. Thus, retinal TH activity exhibits fluctuations of approximately sixfold in response to circadian signals and is stimulated approximately twofold by light. CONCLUSIONS: These observations indicate that dopamine production in the retina is regulated both by light and by circadian phase and that there are cyclic changes in dopamine production during the 24-hr cycle both in normal light and dark cycles and under conditions of constant darkness.

Animals↗

PubMed1992

Actin-dependent myoid elongation in teleost rod inner/outer segments occurs in the absence of net actin polymerization.

In the retinas of teleost fish, rod photoreceptors elongate in response to light. Light-activated elongation is mediated by the myoid of the rod inner segment and is actin-dependent. Inner segment F-actin filaments form bundles running parallel to the cell's long axis. We examined the mechanism of rod elongation using mechanically-detached rod fragments, consisting of the motile inner segment and sensory outer segment (RIS-ROS). When RIS-ROS are isolated from dark-adapted green sunfish and cultured in the light, they elongate 15 microns at 0.3-0.6 microns/min. Elongation was inhibited 65% by 0.1 microM Cytochalasin D, suggesting a requirement for actin assembly. To determine the extent of assembly during elongation, we used three approaches to measure the F-actin content in RIS-ROS: detection of pelletable actin by SDS-PAGE after detergent-extraction of RIS-ROS; quantification of fluorescein-phalloidin binding by fluorimetry, fluorescence-activated cell sorting and image analysis; estimation of total F-actin filament length by electron microscopy. All three assays indicated that no net assembly of RIS-ROS F-actin accompanied myoid elongation. An increase in F-actin content within the elongated myoid was counterbalanced by a decrease in F-actin content within the 13 microvillus-like calycal processes located at the end of the inner segment opposite to the growing myoid. O'Connor and Burnside (Journal of Cell Biology 89:517-524, 1981) showed that minus-ends of rod F-actin filaments are oriented towards the elongating myoid while plus-ends are oriented towards the shortening calycal processes. Our observations suggest that RIS-ROS elongation entails actin polymerization at the minus-ends of filaments coupled with depolymerization at the filament plus-ends.

Actin Cytoskeleton↗

PubMed1992

A role for endogenous dopamine in circadian regulation of retinal cone movement.

Cone movements in the retina of the Midas cichlid (Cichlasoma citrinellum) take place in response both to light and endogenous circadian signals. In the normal light/dark cycle (LD) cone myoids are long at night (50-55 microns), begin to contract before expected dawn, and with light onset contract to their fully contracted positions (5 microns) which are retained throughout the day. In continuous darkness (DD) cone myoids are fully elongate at night, but undergo pre-dawn contractions to partially contracted positions which they retain throughout expected day (20-25 microns). To investigate the mechanisms by which circadian signals modulate cone myoid movements in teleost retinas, we have tested the effects on circadian cone movements of optic nerve section, intraocular injection of dopamine agonists or antagonists, and intraocular injection of melatonin. We report here that both light-induced and circadian-driven cone myoid movements can occur in the absence of efferent input from higher centres: both are retained with full amplitude after optic nerve section in vivo. Intraocular injection studies suggest that circadian regulation of cone myoid movement is mediated locally within the eye by dopamine acting via a dopaminergic D2-receptor. Cone myoid contraction can be induced at midnight in LD or DD animals by intraocular injection of dopamine or the D2-receptor agonist LY171555. The partially contracted cones of DD animals at expected mid-day can be induced to fully contract by intraocular injection of dopamine or the D2-receptor agonist, or to elongate by intraocular injection of the dopamine D2-antagonist sulpiride. Furthermore, the pre-dawn cone myoid contraction observed in both LD and DD animals in response to circadian signals can be completely blocked in DD animals by intraocular injection of the D2-antagonist sulpiride shortly before the time of expected light onset. In contrast, circadian cone myoid movements were unaffected by intraocular injection of the D1-receptor agonist SCH23390, or the D1-receptor antagonist SKF38393. In addition, we report that intraocularly injected melatonin had no effect on cone position when injected in the light at mid-day, in darkness at midnight or in darkness just before expected light onset at dawn. However, both melatonin and iodomelatonin induced cone myoid contraction (the light-adaptive movement) when injected in darkness at expected mid-day in DD animals. This paradoxical result is not consistent with observations from other species in which melatonin induces dark-adaptive photoreceptor responses.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

PubMed1992

Shortening of the calycal process actin cytoskeleton is correlated with myoid elongation in teleost rods.

Light activates the elongation of rods within teleost retinas. Rod cell elongation is mediated by actin-dependent length changes of the myoid portion of the inner segment. The actin cytoskeleton of the inner segment consists of filament bundles, which run parallel to the long axis of the rod, from the calycal processes, through the ellipsoid and into the myoid. In isolated rod inner/outer segments (RIS-ROS), myoid elongation was found to occur in the absence of net polymerization of actin into filaments. Outgrowth of actin filaments within the myoid was counterbalanced by a shortening of actin filaments within the calycal processes. In this study, we have further examined light-activated modifications of the rod cytoskeleton using rhodamine-phalloidin to stain actin filaments within retinal cryosections as well as in isolated RIS-ROS. In RIS-ROS isolated from dark-adapted green sunfish, the phalloidin-stained calycal processes appeared as long, brush-like structures, averaging 4.2 microns in length. In light-cultured RIS-ROS populations, the calycal process actin cytoskeleton shortened from 4.2 microns to 1.7 microns. In control, dark-cultured populations, RIS-ROS that did not elongate maintained long calycal process actin cytoskeletons. However, in cases where dark-cultured RIS-ROS did elongate, despite the absence of a light stimulus, myoid elongation was accompanied by a shortening of the calycal process actin cytoskeleton, suggesting that the two events are correlated with one another. In light-adapted green sunfish and in light-cultured retinas from green sunfish and the Midas cichlid, the calycal process cytoskeleton of intact rods shortened by 40-60%. Within the two-tiered retina of green sunfish, shortening of the calycal process cytoskeleton, from 5.1 microns to 2.1-3.1 microns, was only evident in the shorter, inner tier of rods. The calycal process actin cytoskeleton did not appear to shorten within the longer, outer tier of rods; here, stained processes were short, averaging 2.3 microns in length, within dark-adapted retinas. Using scanning and transmission electron microscopy, we present evidence to suggest that the plasmalemmal surface of the calycal processes shortens along with the cytoskeletal actin core. We conclude that calycal processes of teleost rods are dynamic structures which shorten during light-activated myoid elongation.

Animals↗

PubMed1991

Posttranslational modifications of tubulin in teleost photoreceptor cytoskeletons.

1. Posttranslational modifications of tubulin by acetylation and detyrosination have been correlated previously with microtubule stability in numerous cell types. 2. In this study, posttranslational modifications of tubulin and their regional distribution within teleost photoreceptor cones and rods are demonstrated immunohistochemically using antibodies specific for acetylated, detyrosinated, or tyrosinated tubulin. 3. Immunolocalization was carried out on isolated whole cones and mechanically detached rod and cone inner/outer segments. 4. Acetylated tubulin within rods and cones is found only in microtubules of the ciliary axoneme of the outer segment. Detyrosinated tubulin is also enriched in axonemes of both rod and cone outer segments. 5. Distributions of tyrosinated and detyrosinated cytoplasmic microtubules differ within cones and rods. In cones, detyrosinated and tyrosinated tubulins are both abundant throughout the cell body. In rods, the ellipsoid and myoid contain much more tyrosinated tubulin than detyrosinated tubulin. Comparisons between whole cones and cone fragments suggest that detyrosinated microtubules are more stable than tyrosinated microtubules in teleost photoreceptors. 6. Our findings provide further evidence that microtubules of teleost cones differ from rod microtubules in their stabilities and rapidity of turnover within the photoreceptor inner segment.

Acetylation↗

PubMed1991

Effects of circadian phase on cone retinomotor movements in the Midas cichlid.

In retinas of the Midas cichlid (Cichlasoma citrinellum), cone myoid lengths change in response to both light and circadian signals. Cone myoids are short in day (or in the light), and long at night (or in darkness). During the normal light/dark cycle, cone myoids elongate to 58 microns after light offset at dusk, and remain long until just before dawn, at which time they begin to contract before the time of expected light onset and eventually (after light onset) assume daytime lengths of 5 microns. In continuous light, cone myoids remain fully contracted regardless of the time in the cycle. In continuous darkness, cone myoids undergo circadian movements; they elongate fully at night and contract partly during expected day to 23 microns (65% of the contraction seen at dawn in a normal light/dark cycle). To clarify further the regulation of these retinomotor movements, we have investigated the effects of circadian phase on cone movements induced by light or dark onset. Circadian phase had no significant effect on either the initial rate or the final extent of light-induced cone myoid contraction: at mid-dark cones began to contract immediately after light onset and contracted fully at 3.0 +/- 0.5 microns min-1; at mid-night cones contracted immediately and fully at 4.0 +/- 0.2 microns min-1. At all of the relatively high intensities of light tested (30-5000 lx) cones contracted at similar rates and to similar final extents.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1990

Microtubule nucleation and organization in teleost photoreceptors: microtubule recovery after elimination by cold.

Retinal photoreceptors have two separate populations of microtubules: axonemal microtubules of the modified cilium of the outer segment and cytoplasmic microtubules of the cell body. The axonemal microtubules originate from a basal body located at the distal tip of the photoreceptor inner segment and extend in a 9 + 0 configuration into the outer segment of rods and accessory outer segment of cones. The cytoplasmic microtubules of the cell body are axially aligned from the distal tip of the inner segment to proximal synapse, and are oriented with uniform polarity, their minus ends distal toward the outer segment and plus ends proximal toward the synapse (Troutt & Burnside, 1988). To investigate how this regular cytoplasmic microtubule array is generated, we have attempted to identify microtubule nucleation sites in the cones of the tropical teleost fish, Tilapia (Sarotherodon mossambicus) by examining the regrowth of cytoplasmic microtubules after cold disruption in whole retinas or in isolated cone fragments consisting of inner and outer segments (CIS-COS). Incremental stages of microtubule reassembly were examined both by electron microscopy of thin sections and by immunofluorescent localization of microtubules with an antitubulin antibody. Cold treatment completely abolished all cytoplasmic microtubules but did not disrupt axonemal microtubules. Within 2 min after rewarming, cytoplasmic microtubules reappeared in the most distal portion of the inner segment in a small aster-like array associated with the basal body, and subsequently appeared in more proximal parts of the cone. These observations suggest that a favoured microtubule nucleation site is associated with the basal body region of the cone outer segment, and thus that the basal body region could function as a microtubule organizing centre for the photoreceptor. These results are consistent with the findings of our previous investigation of cone microtubule polarity, which showed that the minus ends of the cytoplasmic microtubules of the cone are associated with the basal body region.

Animals↗

PubMed1990

Dopamine induces light-adaptive retinomotor movements in bullfrog cones via D2 receptors and in retinal pigment epithelium via D1 receptors.

In the eyes of lower vertebrates, retinal photoreceptors and melanin pigment granules of the retinal pigment epithelium (RPE) exhibit characteristic retinomotor movements in response to changes in ambient illumination and to signals from an endogenous circadian clock. We previously reported that 3,4-dihydroxyphenylethylamine (dopamine) mimicked the effect of light on these movements in photo-receptors and RPE cells of green sunfish, Lepomis cyanellus, by interacting with D2 dopaminergic receptors. Here, we report that dopamine also mimics the effect of light on cone and RPE retinomotor movements in bullfrogs, Rana catesbeiana, i.e., dopamine induces cone contraction and RPE pigment dispersion. Dopamine induced cone contraction in isolated dark-adapted bullfrog retinas incubated in constant darkness in the presence of the phosphodiesterase inhibitor 3-isobutyl-1-methylxanthine (IBMX). This effect of dopamine was inhibited by a D2 but not a D1 antagonist and mimicked by a D2 but not a D1 agonist. These results suggest that induction of cone contraction by dopamine is mediated by D2 dopaminergic receptors and that cone adenylate cyclase activity is inhibited. Thus, dopamine acts via the same type of receptor in both bullfrog and green sunfish retinas to induce cone contraction. In contrast, dopamine influences RPE retinomotor movement via different receptors in fish and bullfrog. Dopamine induced light-adaptive pigment dispersion in isolated dark-adapted bullfrog RPE-eyecups incubated in constant darkness in normal Ringer's solution. Because the retina was not present, these experiments demonstrate a direct effect of dopamine on bullfrog RPE. This effect of dopamine on bullfrog RPE was inhibited by a D1 but not a D2 antagonist and mimicked by a D1 but not a D2 agonist. Furthermore, agents that increase the concentration of intracellular cyclic AMP also induced pigment dispersion in dark-adapted bullfrog RPE-eyecups incubated in the dark. These results suggest that dopamine induces pigment dispersion in bullfrog RPE via D1 dopaminergic receptors. Thus, dopamine acts via different receptors on bullfrog (D1) versus green sunfish (D2) RPE to induce pigment dispersion. In addition, inhibitor studies indicate that pigment dispersion is actin dependent in teleost but not in bullfrog RPE. Dopamine-induced pigment dispersion was inhibited by cytochalasin D in isolated RPE sheets of green sunfish but not in RPE-eyecups of bullfrogs. Together, these observations indicate that dopamine mimics the effect of light on cone and RPE retinomotor movements in both fish and bullfrogs. However, in the RPE, different receptors mediate the effect of dopamine, and different cytoskeletal mechanisms are used to affect pigment transport.(ABSTRACT TRUNCATED AT 400 WORDS)

Adaptation, Physiological↗

PubMed1989

Role of microtubules in pigment granule migration in teleost retinal pigment epithelial cells.

In cells of the teleost retinal pigment epithelium (RPE), melanin pigment granules migrate in response to changes in environmental light conditions. Melanin granules disperse into the RPE cell's long apical projections in response to the onset of light, and aggregate towards the base of the RPE cell in response to the onset of darkness. The RPE cells possess numerous microtubules and actin filaments, which in the apical projections are aligned longitudinally. Previous cytochalasin studies have shown that intact actin filaments are required for pigment granule dispersion and maintenance of the dispersed state (Burnside, Adler and O'Connor (1983). Invest. Ophthalmol. Vis. Sci. 24, 1). We report here that pigment granule aggregation is strongly inhibited when the highly stable microtubules of RPE apical projections are disrupted by a combination of cold and nocodazole treatments. Pigment dispersion and maintenance of the dispersed and aggregated states are unaffected by microtubule disruption. These results indicate that microtubules are required for RPE pigment aggregation but not for dispersion.

Animals↗

PubMed1989

Light-induced dopamine release from teleost retinas acts as a light-adaptive signal to the retinal pigment epithelium.

In the retinal pigment epithelium (RPE) of lower vertebrates, melanin pigment granules migrate in and out of the cells' long apical projections in response to changes in light condition. When the RPE is in its normal association with the retina, light onset induces pigment granules to disperse into the apical projections; dark onset induces pigment granules to aggregate into the cell bodies. However, when the RPE is separated from the retina, pigment granule movement in the isolated RPE is insensitive to light onset. It thus seems likely that a signal from the retina communicates light onset to the RPE to initiate pigment dispersion. We have examined the nature of this retina-to-RPE signal in green sunfish, Lepomis cyanellus. In isolated retinas with adherent RPE, light-induced pigment dispersion in the RPE is blocked by treatments known to block Ca2+-dependent transmitter release in the retina. In addition, the medium obtained from incubating previously dark-adapted retinas in the light induces light-adaptive pigment dispersion when added to isolated RPE. In contrast, the medium obtained from incubating dark-adapted retinas in constant darkness does not affect pigment distribution when added to isolated RPE. These results are consistent with the idea that RPE pigment dispersion is triggered by a substance that diffuses from the retina at light onset. The capacity of the conditioned medium from light-incubated retinas to induce pigment dispersion in isolated RPE is inhibited by a D2 dopamine antagonist, but not by D1 or alpha-adrenergic antagonists. Light-induced pigment dispersion in whole RPE-retinas is also blocked by a D2 dopamine antagonist.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1989

Actin filament polarity at the site of rod outer segment disk morphogenesis.

The rod outer segment (ROS) is attached to the visual cell body by a connecting cilium. Axonemal components of this cilium extend into the ROS, an organelle which undergoes continuous renewal throughout life. New membranous disks are added at the ROS base, while older ones are shed from the tip. The formation of new disks is believed to result from plasma membrane evaginations at the distal end of the connecting cilium, but the mechanism responsible for disk morphogenesis is not yet understood. Within the ciliary axoneme, at the base of the ROS, an actin-rich domain has been localized with immunoelectron microscopy, and filamentous actin has been detected with fluorescent phallotoxin. However, actin filaments have not previously been observed in electron micrographs of this region. We now report that a meshwork of decorated actin filaments was observed within the center of the ciliary axoneme, at the base of the ROS, after visual cells were permeabilized with saponin and incubated with myosin subfragment-1 (S-1). Furthermore, individual filaments were seen to extend from the center of the axoneme into the base of the ROS disk stack by passing between pairs of ciliary microtubule doublets. Arrowheads on these filaments uniformly pointed toward the cilium, while the barbed (or fast-growing) ends were oriented in the direction of disk expansion and were often associated with the ROS plasma membrane. In control retinas, undecorated filaments were observed. Thus, S-1 binding did not induce filament formation. These results suggest that an actin filament network may provide cytoskeletal support and guidance for the growing ROS disks.

Actins↗