Literature DB >> 28256705

The centrifugal visual system of a palaeognathous bird, the Chilean Tinamou (Nothoprocta perdicaria).

Quirin Krabichler1, Tomas Vega-Zuniga1, Denisse Carrasco2, Maximo Fernandez2, Cristián Gutiérrez-Ibáñez1, Gonzalo Marín2,3, Harald Luksch1.   

Abstract

The avian centrifugal visual system, which projects from the brain to the retina, has been intensively studied in several Neognathous birds that have a distinct isthmo-optic nucleus (ION). However, birds of the order Palaeognathae seem to lack a proper ION in histologically stained brain sections. We had previously reported in the palaeognathous Chilean Tinamou (Nothoprocta perdicaria) that intraocular injections of Cholera Toxin B subunit retrogradely label a considerable number of neurons, which form a diffuse isthmo-optic complex (IOC). In order to better understand how this IOC-based centrifugal visual system is organized, we have studied its major components by means of in vivo and in vitro tracing experiments. Our results show that the IOC, though structurally less organized than an ION, possesses a dense core region consisting of multipolar neurons. It receives afferents from neurons in L10a of the optic tectum, which are distributed with a wider interneuronal spacing than in Neognathae. The tecto-IOC terminals are delicate and divergent, unlike the prominent convergent tecto-ION terminals in Neognathae. The centrifugal IOC terminals in the retina are exclusively divergent, resembling the terminals from "ectopic" centrifugal neurons in Neognathae. We conclude that the Tinamou's IOC participates in a comparable general IOC-retina-TeO-IOC circuitry as the neognathous ION. However, the connections between the components are structurally different and their divergent character suggests a lower spatial resolution. Our findings call for further comparative studies in a broad range of species for advancing our understanding of the evolution, plasticity and functional roles of the avian centrifugal visual system.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  RRID:AB_10013220; RRID:AB_2315144; RRID:AB_2336126; RRID:AB_2534088; RRID:AB_477329; association amacrine cells; divergent terminals; ectopic centrifugal neurons; isthmo-optic nucleus; optic tectum; retinopetal; tecto-isthmal; tyramide signal amplification

Mesh:

Year:  2017        PMID: 28256705     DOI: 10.1002/cne.24195

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  5 in total

1.  Anatomy and Physiology of Neurons in Layer 9 of the Chicken Optic Tectum.

Authors:  Marinus Kloos; Stefan Weigel; Harald Luksch
Journal:  Front Neural Circuits       Date:  2019-10-14       Impact factor: 3.492

2.  In situ proximity labeling identifies Lewy pathology molecular interactions in the human brain.

Authors:  Bryan A Killinger; Lee L Marshall; Diptaman Chatterjee; Yaping Chu; Jose Bras; Rita Guerreiro; Jeffrey H Kordower
Journal:  Proc Natl Acad Sci U S A       Date:  2022-02-01       Impact factor: 12.779

3.  The Medial Ventrothalamic Circuitry: Cells Implicated in a Bimodal Network.

Authors:  Tomas Vega-Zuniga; Dominik Trost; Katrin Schicker; Eva M Bogner; Harald Luksch
Journal:  Front Neural Circuits       Date:  2018-02-09       Impact factor: 3.492

4.  Did you choose appropriate tracer for retrograde tracing of retinal ganglion cells? The differences between cholera toxin subunit B and Fluorogold.

Authors:  Fei Yao; Endong Zhang; Zhaolin Gao; Hongpei Ji; Mahmoud Marmouri; Xiaobo Xia
Journal:  PLoS One       Date:  2018-10-05       Impact factor: 3.240

5.  A specialized reciprocal connectivity suggests a link between the mechanisms by which the superior colliculus and parabigeminal nucleus produce defensive behaviors in rodents.

Authors:  Alfonso Deichler; Denisse Carrasco; Luciana Lopez-Jury; Tomas Vega-Zuniga; Natalia Márquez; Jorge Mpodozis; Gonzalo J Marín
Journal:  Sci Rep       Date:  2020-10-01       Impact factor: 4.379

  5 in total

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