75 research outputs found
Cyan fluorescent protein expression in ganglion and amacrine cells in a thy1-CFP transgenic mouse retina
PURPOSE: To characterize cyan fluorescent protein (CFP) expression in the retina of the thy1-CFP (B6.Cg-Tg(Thy1-CFP)23Jrs/J) transgenic mouse line.
METHODS: CFP expression was characterized using morphometric methods and immunohistochemistry with antibodies to neurofilament light (NF-L), neuronal nuclei (NeuN), POU-domain protein (Brn3a) and calretinin, which immunolabel ganglion cells, and syntaxin 1 (HPC-1), glutamate decarboxylase 67 (GAD(67)), GABA plasma membrane transporter-1 (GAT-1), and choline acetyltransferase (ChAT), which immunolabel amacrine cells.
RESULTS: CFP was extensively expressed in the inner retina, primarily in the inner plexiform layer (IPL), ganglion cell layer (GCL), nerve fiber layer, and optic nerve. CFP fluorescent cell bodies were in all retinal regions and their processes ramified in all laminae of the IPL. Some small, weakly CFP fluorescent somata were in the inner nuclear layer (INL). CFP-containing somata in the GCL ranged from 6 to 20 microm in diameter, and they had a density of 2636+/-347 cells/mm2 at 1.5 mm from the optic nerve head. Immunohistochemical studies demonstrated colocalization of CFP with the ganglion cell markers NF-L, NeuN, Brn3a, and calretinin. Immunohistochemistry with antibodies to HPC-1, GAD(67), GAT-1, and ChAT indicated that the small, weakly fluorescent CFP cells in the INL and GCL were cholinergic amacrine cells.
CONCLUSIONS: The total number and density of CFP-fluorescent cells in the GCL were within the range of previous estimates of the total number of ganglion cells in the C57BL/6J line. Together these findings suggest that most ganglion cells in the thy1-CFP mouse line 23 express CFP. In conclusion, the thy1-CFP mouse line is highly useful for studies requiring the identification of ganglion cells
Localization of substance P-like and enkephalin-like immunoreactivity within preganglionic terminals of the avian ciliary ganglion: light and electron microscopy
The avian ciliary ganglion receives its only recognized input from the nucleus of Edinger-Westphal. This is known to be a cholinergic input. In the present study, using fluorescein isothiocyanate and peroxidase- antiperoxidase immunohistochemical methods, substance P-like and enkephalin-like immunoreactivity has been found within preganglionic terminals of the avian ciliary ganglion. The ciliary ganglion is known to consist of two distinct cell populations: small choroid cells that project to the smooth muscle coat of the choroid and large ciliary neurons that send axons to both the iris and the ciliary body. Preganglionic terminals on choroid cells consist of small boutonal endings, whereas ciliary neurons receive a calyx-like cap ending around the hilus of the cell. Substance P-like and enkephalin-like immunoreactivity was localized to preganglionic axons and to both boutonal and calyx-like terminations upon cells of the ciliary ganglion. Electron microscopic studies of both substance P-like and enkephalin-like immunoreactive terminals revealed small clear core vesicles (approximately 58 nm in diameter) and two sizes of dense core vesicles (approximately 85 and approximately 119 nm in diameter). Immunoreactive staining was observed only in the smaller dense core vesicles. The unlabeled clear core vesicles were clustered at synaptic release sites, while the immunoreactive and larger unlabeled dense core vesicles usually were not near these synaptic specializations. These observations strongly imply that neuropeptides co-occur with acetylcholine in preganglionic axons of the ciliary ganglion
Two-Level Atom in an Optical Parametric Oscillator: Spectra of Transmitted and Fluorescent Fields in the Weak Driving Field Limit
We consider the interaction of a two-level atom inside an optical parametric
oscillator. In the weak driving field limit, we essentially have an atom-cavity
system driven by the occasional pair of correlated photons, or weakly squeezed
light. We find that we may have holes, or dips, in the spectrum of the
fluorescent and transmitted light. This occurs even in the strong-coupling
limit when we find holes in the vacuum-Rabi doublet. Also, spectra with a
sub-natural linewidth may occur. These effects disappear for larger driving
fields, unlike the spectral narrowing obtained in resonance fluorescence in a
squeezed vacuum; here it is important that the squeezing parameter tends to
zero so that the system interacts with only one correlated pair of photons at a
time. We show that a previous explanation for spectral narrowing and spectral
holes for incoherent scattering is not applicable in the present case, and
propose a new explanation. We attribute these anomalous effects to quantum
interference in the two-photon scattering of the system.Comment: 10 pages, 17 figures, submitted to Phys Rev
A model of direction selectivity in the starburst amacrine cell network
Displaced starburst amacrine cells (SACs) are retinal interneurons that exhibit GABAA receptor-mediated and Cl− cotransporter-mediated, directionally selective (DS) light responses in the rabbit retina. They depolarize to stimuli that move centrifugally through the receptive field surround and hyperpolarize to stimuli that move centripetally through the surround (Gavrikov et al, PNAS 100(26):16047–16052, 2003, PNAS 103(49):18793–18798, 2006). They also play a key role in the activity of DS ganglion cells (DS GC; Amthor et al, Vis Neurosci 19:495–509 2002; Euler et al, Nature 418:845–852, 2002; Fried et al, Nature 420:411– 414, 2002; Gavrikov et al, PNAS 100(26):16047–16052, 2003, PNAS 103(49):18793–18798, 2006; Lee and Zhou, Neuron 51:787–799 2006; Yoshida et al, Neuron 30:771–780, 2001). In this paper we present a model of strong DS behavior of SACs which relies on the GABA-mediated communication within a tightly interconnected network of these cells and on the glutamate signal that the SACs receive from bipolar cells (a presynaptic cell that receives input from cones). We describe how a moving light stimulus can produce a large, sustained depolarization of the SAC dendritic tips that point in the direction that the stimulus moves (i.e., centrifugal motion), but produce a minimal depolarization of the dendritic tips that point in the opposite direction (i.e., centripetal motion). This DS behavior, which is quantified based on the relative size and duration of the depolarizations evoked by stimulus motion at dendritic tips pointing in opposite directions, is robust to changes of many different parameter values and consistent with experimental data. In addition, the DS behavior is strengthened under the assumptions that the Cl− cotransporters Na + -K + -Cl − and K + -Cl − are located in different regions of the SAC dendritic tree (Gavrikov et al, PNAS 103(49):18793–18798, 2006) and that GABA evokes a long-lasting response (Gavrikov et al, PNAS 100(26):16047–16052, 2003, PNAS 103(49):18793–18798, 2006; Lee and Zhou, Neuron 51:787–799, 2006). A possible mechanism is discussed based on the generation of waves of local glutamate and GABA secretion, and their postsynaptic interplay as the waves travel between cell compartments
Direction-Selective Circuitry in Rat Retina Develops Independently of GABAergic, Cholinergic and Action Potential Activity
The ON-OFF direction selective ganglion cells (DSGCs) in the mammalian retina code image motion by responding much more strongly to movement in one direction. They do so by receiving inhibitory inputs selectively from a particular sector of processes of the overlapping starburst amacrine cells, a type of retinal interneuron. The mechanisms of establishment and regulation of this selective connection are unknown. Here, we report that in the rat retina, the morphology, physiology of the ON-OFF DSGCs and the circuitry for coding motion directions develop normally with pharmacological blockade of GABAergic, cholinergic activity and/or action potentials for over two weeks from birth. With recent results demonstrating light independent formation of the retinal DS circuitry, our results strongly suggest the formation of the circuitry, i.e., the connections between the second and third order neurons in the visual system, can be genetically programmed, although emergence of direction selectivity in the visual cortex appears to require visual experience
Coexpression of vesicular glutamate transporters 1 and 2, glutamic acid decarboxylase and calretinin in rat entorhinal cortex
We studied the distribution and coexpression of vesicular glutamate transporters (VGluT1, VGluT2), glutamic acid decarboxylase
(GAD) and calretinin (CR, calcium-binding protein) in rat entorhinal cortex, using immunofluorescence staining and multichannel
confocal laser scanning microscopy. Images were computer processed and subjected to automated 3D object recognition, colocalization
analysis and 3D reconstruction. Since the VGluTs (in contrast to CR and GAD) occurred in fibers and axon terminals only, we
focused our attention on these neuronal processes. An intense, punctate VGluT1-staining occurred everywhere in the entorhinal
cortex. Our computer program resolved these punctae as small 3D objects. Also VGluT2 showed a punctate immunostaining pattern,
yet with half the number of 3D objects per tissue volume compared with VGluT1, and with statistically significantly larger
3D objects. Both VGluTs were distributed homogeneously across cortical layers, with in MEA VGluT1 slightly more densely distributed
than in LEA. The distribution pattern and the size distribution of GAD 3D objects resembled that of VGluT2. CR-immunopositive
fibers were abundant in all cortical layers. In double-stained sections we noted ample colocalization of CR and VGluT2, whereas
coexpression of CR and VGluT1 was nearly absent. Also in triple-staining experiments (VGluT2, GAD and CR combined) we noted
coexpression of VGluT2 and CR and, in addition, frequent coexpression of GAD and CR. Modest colocalization occurred of VGluT2
and GAD, and incidental colocalization of all three markers. We conclude that the CR-containing axon terminals in the entorhinal
cortex belong to at least two subpopulations of CR-neurons: a glutamatergic excitatory and a GABAergic inhibitory
Cellular localization and laminar distribution of AMPA glutamate receptor subunits mRNAs and proteins in the rat cerebral cortex.
Enkephalin-containing amacrine cells in the avian retina: immunohistochemical localization.
Neurokinin 1 receptor expression in the rat retina
Tachykinin (TK) peptides influence neuronal activity in the inner retina of mammals. The
aim of this investigation was to determine the cellular localization of the neurokinin 1
receptor (NK1), whose preferred ligand is the TK peptide substance P (SP), in the rat retina.
These studies used a polyclonal antiserum directed to the C-terminus of rat NK1. The
majority of NK1-immunoreactive (IR) cells were located in the proximal inner nuclear layer
(INL), and very rarely they were found in the distal INL. Some small and large NK1-IR
somata were present in the ganglion cell layer. NK1-IR processes were densely distributed
across the inner plexiform layer (IPL) with a maximum density over lamina 2 of the IPL.
Immunoreactive processes also crossed the INL and ramified in the outer plexiform layer
where they formed a sparse meshwork. NK1-IR processes were rarely observed in the optic
nerve fiber layer. Double-label immunofluorescence studies with different histochemical
markers for bipolar cells indicated that NK1 immunoreactivity was not present in bipolar
cells. Together, these observations indicate that NK1 immunoreactivity is predominantly
expressed by amacrine, displaced amacrine, interplexiform, and some ganglion cells. Doublelabel
immunofluorescence experiments were also performed to characterize NK1-containing
amacrine cells. Sixty-one percent of the g-aminobutyric acid (GABA)-IR cells, 71% of the large
tyrosine hydroxylase (TH)-IR cells, and 100% of the small TH-IR cells contained NK1
immunoreactivity. In addition, most (91%) of the NK1-IR cells had GABA immunoreactivity.
In contrast, vasoactive intestinal polypeptide-, TK-, choline acetyltransferase-, and parvalbumin-
IR amacrine cells did not express NK1 immunoreactivity. Overall, the present findings
suggest that SP acts directly upon several cell populations, including GABA-containing
amacrine cells and ganglion cells, to influence visual information processing in the inner
retina
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