The organization of the zebrafish pallium from a hodological perspective
- PMID: 34697803
- DOI: 10.1002/cne.25268
The organization of the zebrafish pallium from a hodological perspective
Abstract
We studied the connections (connectome) of the adult zebrafish pallium using carbocyanine dye tracing and ancillary anatomical methods. The everted zebrafish pallium (dorsal telencephalic area, D) is composed of several major zones (medial, lateral, dorsal, central, anterior, and posterior) distinguishable by their topography, cytoarchitecture, immunohistochemistry, and genoarchitecture. Our comprehensive study reveals poor interconnectivity between these pallial areas, especially between medial (Dm), lateral/dorsal (Dl, Dd), and posterior (Dp) regions. This suggests that the zebrafish pallium has dedicated modules for different neural processes. Pallial connections with extrapallial regions also show compartmental organization. Major extratelencephalic afferents come from preglomerular nuclei (to Dl, Dd, and Dm), posterior tuberal nucleus (to Dm), and lateral recess nucleus (to Dl). The subpallial (ventral, V) zones dorsal Vv, Vd, and Vs, considered homologues of the striatum, amygdala, and pallidum, are mainly afferent to Dl/Dd and Dp. Regarding the efferent pathways, they also appear characteristic of each pallial region. Rostral Dm projects to the dorsal entopeduncular nucleus. Dp is interconnected with the olfactory bulbs. The central region (Dc) defined here receives mainly projections from Dl-Dd and projects toward the pretectum and optic tectum, connections, which help to delimiting Dc. The connectome of the adult pallium revealed here complements extant studies on the neuroanatomical organization of the brain, and may be useful for neurogenetic studies performed during early stages of development. The connectome of the zebrafish pallium was also compared with the pallial connections reported in other teleosts, a large group showing high pallial diversity.
Keywords: Danio rerio; DiI; connectome; neural tracing; telencephalon.
© 2021 The Authors. The Journal of Comparative Neurology published by Wiley Periodicals LLC.
References
REFERENCES
-
- Abellán, A., Desfilis, E., & Medina, L. (2014). Combinatorial expression of Lef1, Lhx2, Lhx5, Lhx9, Lmo3, Lmo4, and Prox1 helps to identify comparable subdivisions in the developing hippocampal formation of mouse and chicken. Frontiers in Neuroanatomy, 8, 59.
-
- Aleström, P., D'Angelo, L., Midtlyng, P. J., Schorderet, D. F., Schulte-Merker, S., Sohm, F., & Warner, S. (2019). Zebrafish: Housing and husbandry recommendations. Laboratory Animals, 54, 213-224.
-
- Amo, R., Fredes, F., Kinoshita, M., Aoki, R., Aizawa, H., Agetsuma, M., Aoki, T., Shiraki, T., Kakinuma, H., Matsuda, M., Yamazaki, M., Takahoko, M., Tsuboi, T., Higashijima, S.-i, Miyasaka, N., Koide, T., Yabuki, Y., Yoshihara, Y., Fukai, T., & Okamot, H. (2014). The habenulo-raphe serotonergic circuit encodes an aversive expectation value essential for adaptive active avoidance of danger. Neuron, 84, 1034-1048. https://doi.org/10.1016/j.neuron.2014.10.035.
-
- Aoki, T., Kinoshita, M., Aoki, R., Agetsuma, M., Aizawa, H., Yamazaki, M., Takahoko, M., Amo, R., Arata, A., Higashijima, S.-i. Tsuboi, T., & Okamoto, H. (2013). Imaging of neural ensemble for the retrieval of a learned behavioral program. Neuron, 78, 881-894. https://doi.org/10.1016/j.neuron.2013.04.009.
-
- Batten, T. F. C., Cambre, M. I., Moons, L., & Vandesande, F. (1990). Comparative distribution of neuropeptide-immunoreactive systems in the brain of the green molly, Poecilia latipinna. Journal of Comparative Neurology, 302, 893-919.
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