Literature DB >> 2970894

Coexpression of opsin- and VIP-like-immunoreactivity in CSF-contacting neurons of the avian brain.

R Silver1, P Witkovsky, P Horvath, V Alones, C J Barnstable, M N Lehman.   

Abstract

Cerebrospinal fluid-contacting (CSF) cells in both the septal and the tuberal areas in the brain of the ring dove are labeled by RET-P1, a monoclonal antibody to opsin that reacts with inner and outer segment membranes of rod photoreceptors in a variety of vertebrates. Immunoblot analysis of proteins from diverse brain regions, however, revealed bands of anti-RET-P1 immunoreactivity that did not correspond to opsin. Binding of RET-P1 to opsin-containing membranes, was not inhibited by membranes rich in muscarinic and beta-adrenergic receptor proteins (red blood cells, heart, lung) taken from doves. RET-P1-immunoreactive CSF-contacting cells emit a dendritic process that penetrates the ependyma and ends in a knob-like terminal suspended in the ventricle. These cells also possess other processes that penetrate more or less deeply into the neuropil. Additionally, a band of labeled fibers occurs in the external layer of the median eminence. A double-label technique demonstrated that RET-P1-positive cells coexpress VIP-like immunoreactivity. VIP-positive cells in other brain areas are not RET-P1-positive.

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Year:  1988        PMID: 2970894     DOI: 10.1007/bf00221754

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  33 in total

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Authors:  R A Dixon; B K Kobilka; D J Strader; J L Benovic; H G Dohlman; T Frielle; M A Bolanowski; C D Bennett; E Rands; R E Diehl; R A Mumford; E E Slater; I S Sigal; M G Caron; R J Lefkowitz; C D Strader
Journal:  Nature       Date:  1986 May 1-7       Impact factor: 49.962

Review 2.  Comparative ultrastructure of the cerebrospinal fluid-contacting neurons.

Authors:  B Vigh; I Vigh-Teichmann
Journal:  Int Rev Cytol       Date:  1973

3.  Monoclonal antibodies to rhodopsin: characterization, cross-reactivity, and application as structural probes.

Authors:  R S Molday; D MacKenzie
Journal:  Biochemistry       Date:  1983-02-01       Impact factor: 3.162

4.  The pineal organ of Raja clavata: opsin immunoreactivity and ultrastructure.

Authors:  I Vigh-Teichmann; B Vigh; M J Manzano e Silva; B Aros
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

5.  Antibodies against filamentous components in discrete cell types of the mouse retina.

Authors:  U C Dräger; D L Edwards; C J Barnstable
Journal:  J Neurosci       Date:  1984-08       Impact factor: 6.167

6.  The comparative physiology of extraocular photoreception.

Authors:  G Groos
Journal:  Experientia       Date:  1982-09-15

7.  Prolactin release by vasoactive intestinal polypeptide in rats.

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8.  Immunoreactive vasoactive intestinal polypeptide in rat hypophysial portal blood.

Authors:  A Shimatsu; Y Kato; N Matsushita; H Katakami; N Yanaihara; H Imura
Journal:  Endocrinology       Date:  1981-02       Impact factor: 4.736

9.  Cerebrospinal fluid-contacting neurons, sensory pinealocytes and Landolt's clubs of the retina as revealed by means of an electron-microscopic immunoreaction against opsin.

Authors:  B Vigh; I Vigh-Teichmann; P Röhlich; A Oksche
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

10.  Rhodopsin-like sensitivity of extra-retinal photoreceptors mediating the photoperiodic response in quail.

Authors:  R G Foster; B K Follett; J N Lythgoe
Journal:  Nature       Date:  1985 Jan 3-9       Impact factor: 49.962

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  39 in total

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8.  The Role of VIP in Social Behavior: Neural Hotspots for the Modulation of Affiliation, Aggression, and Parental Care.

Authors:  Marcy A Kingsbury; Leah C Wilson
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9.  Development of visual cells in the Pacific bluefin tuna Thunnus orientalis.

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Review 10.  The evolution of irradiance detection: melanopsin and the non-visual opsins.

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Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2009-10-12       Impact factor: 6.237

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