Abstract
This chapter describes the development of the medaka diencephalon, optic tectum, and cerebellum. The diencephalon of teleosts is divided into two main parts, the medial and lateral parts. The medial diencephalon is further divided into five regions, and these subdivisions become visible in the larvae at stage 39. The lateral diencephalon contains migrated cell groups, such as the corpus glomerulosum system and preglomerular nuclear complex (PG). Developmental studies by in situ hybridization using a pax6b2 gene probe suggest that the PG is migrated alar nuclei and a teleost homologue of the mammalian thalamus. According to recent studies, however, neurons of different origins may also contribute to the PG. The optic tectum has cell proliferation zones in the marginal edges, named the marginal proliferating zone. The generated cells are added tangentially at the tectum’s edge as a column of cells spanning the whole thickness of the tectum to form a laminated tectum. The cerebellar primordium is formed from the alar plates of the isthmic and the first rhombomeres. At stage 26, the isthmic rhombomere protrudes into the mesencephalic ventricle to form the valvula cerebelli, a cerebellar structure specific in ray-finned fishes except for polypteriforms. The cerebellar primordium is connected to the mesencephalon proper by the mesencephalic sheet, a thin neuroepithelium. The left/right halves of the primordium start to fuse at stage 34, and several cell proliferation zones are formed in the cerebellum at stage 36.
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References
Ahrens K, Wullimann MF (2002) Hypothalamic inferior lobe and lateral torus connections in a percomorph teleost, the red cichlid (Hemichromis lifalili). J Comp Neurol 449:43–64
Altman J, Bayer SA (1997) Development of the cerebellar system: in relation to its evolution, structure, and functions. CRC Press, Boca Raton
Bae Y-K, Kani S, Shimizu T, Tanabe K, Nojima H, Kimura Y, Higashijima S-I, Hibi M (2009) Anatomy of zebrafish cerebellum and screen for mutations affecting its development. Dev Biol 330:406–426
Bloch S, Thomas M, Colin I, Galant S, Machado E, Affaticati P, Jenett A, Yamamoto K (2019) Mesencephalic origin of the inferior lobe in zebrafish. BMC Biol 17:22
Bloch S, Hagio H, Thomas M, Heuzé A, Helmel J-M, Lasserre E, Colin I, Saka K, Affaticati P, Jenette A, Kawakami K, Yamamoto N, Yamamoto K (2020) Non-thalamic origin of zebrafish sensory nuclei implies convergent evolution of visual pathways in amniotes and teleosts. elife 9:e54945
Braford MR Jr, Northcutt RG (1983) Organization of the diencephalon and pretectum of the ray-finned fishes. In: Davis RE, Northcutt RG (eds) Fish neurobiology, vol 2. The University of Michigan Press, Ann Arbor, pp 117–163
Butts T, Modrell MS, Baker CVH, Wingate RJT (2014) The evolution of the vertebrate cerebellum: absence of a proliferative external granule layer in a non-teleost ray-finned fish. Evol Dev 16:92–100
Ishikawa Y (2018) Medaka de saguru nou no hasseigaku (Developmental understanding of the vertebrate brain, using the medaka). Kouseisha Kouseikaku Co., Tokyo
Ishikawa Y, Yamamoto N, Yoshimoto M, Yasuda T, Maruyama K, Kage T, Takeda H, Ito H (2007) Developmental origin of diencephalic sensory relay nuclei in teleosts. Brain Behav Evol 69:87–95
Ishikawa Y, Yasuda T, Kage T, Takashima S, Yoshimoto M, Yamamoto N, Maruyama K, Takeda H, Ito H (2008) Early development of the cerebellum in teleost fishes: a study based on gene expression patterns and histology in the medaka embryo. Zool Sci 25:407–418
Ishikawa Y, Yamamoto N, Yasuda T, Yoshimoto M, Ito H (2010) Morphogenesis of the medaka cerebellum, with special reference to the mesencephalic sheet, a structure homologous to the rostrolateral part of mammalian anterior medullary velum. Brain Behav Evol 75:88–103
Ito M (1993) Nou to kokoro wo kangaeru (Thinking about the brain and mind). Kinokuniya Shoten, Tokyo
Ito M (2006) Cerebellar circuitry as a neuronal machine. Prog Neurobiol 78:272–303
Ito M (2008) Control of mental activities by internal models in the cerebellum. Nat Rev Neurosci 9:304–313
Ito H, Yoshimoto M (1991) Shinkeikei (Nervous system). In: Itazawa Y, Hanyu I (eds) Gyorui seirigaku (Fish physiology). Kouseisha Kouseikaku Co., Tokyo, pp 363–402
Johnston JB (1909) The morphology of the forebrain vesicle in vertebrates. J Comp Neurol 19:457–539
Kamoi Y (1953) Koukotsugyorui Shishou no hikakukaibougakuteki kenkyu (Comparative studies of the thalamus in bony fishes). In: Collection of papers from the first Department of Anatomy, School of Medicine, Kyoto University, Kyoto, pp 1–43 with five figures
Kani S, Bae Y-K, Shimizu T, Tanabe K, Satou C, Parsons MJ, Scott E, Higashijima S-I, Hibi M (2010) Proneural gene-linked neurogenesiss in zebrafish cerebellum. Dev Biol 343:1–17
Meek J, Nieuwenhuys R (1998) Holosteans and teleosts. In: Nieuwenhuys R, Donkelaar HJT, Nicholson C (eds) The central nervous system of vertebrates, vol 2. Springer-Verlag, Berlin, pp 759–937
Moens CB, Prince VE (2002) Constructing the hindbrain: insights from the zebrafish. Dev Dyn 224:1–17
Nakane Y, Ikegami K, Ono H, Yamamoto N, Yoshida S, Hirunagi K, Ebihara S, Kubo Y, Yoshimura T (2010) A mammalian neural tissue opsin (opsin 5) is a deep brain photoreceptor in birds. Proc Natl Acad Sci U S A 107:15264–15268
Nakane Y, Ikegami K, Iigo M, Ono H, Takeda K, Takahashi D, Uesaka M, Kimijima M, Hashimoto R, Arai N, Suga T, Kosuge K, Abe T, Maeda R, Senga T, Amiya N, Azuma T, Amano M, Abe H, Yamamoto N, Yoshimura T (2013) The saccus vasculosus of fish is a sensor of seasonal changes in day length. Nat Commun 4:2108
Nguyen V, Deschet K, Henrich T, Godet E, Joly JS, Wittbrodt J, Chourrout D, Bourrat F (1999) Morphogenesis of the optic tectum in the medaka (Oryzias latipes): a morphological and molecular study, with special emphasis on cell proliferation. J Comp Neurol 413:385–404
Nieuwenhuys R, Ten Donkelaar HJ, Nicholson C (1998) The central nervous system of vertebrates, vol 1-3. Springer-Verlag, Berlin
Palmgren A (1921) Embryological and morphological studies on the mid-brain and cerebellum of vertebrates. Acta Zool 2:1–94
Shimizu M, Yamamoto N, Yoshimoto M, Ito H (1999) Fiber connections of the inferior lobe in a percomorph teleost, Thamnaconus (Navodon) medestus. Brain Behav Evol 54:127–146
Swanson LW (2012) Brain architecture, 2nd edn. Oxford University Press, New York
Vaage S (1973) The histogenesis of the isthmic nuclei in chick embryos (Gallus domesticus). Z Anat Entwicklungsgesch 142:283–314
Wullimann MF, Umeasalugo KE (2020) Sonic hedgehog expression in zebrafish forebrain identifies the teleostean pallidal signaling center and shows preglomerular complex and posterior tubercular dopamine cells to arise from shh cells. J Comp Neurol 528:1321–1348
Yamamoto N, Hagio H (2021) Cerebellum-like systems in actinopterygian fishes with a special focus on the diversity of cerebellum-like system in the mesencephalon. In: Mizusawa H, Kakei S (eds) Cerebellum as a CNS hub. Springer Nature, Cham, pp 25–60
Yamamoto N, Ito H (2002) Koukotsugyorui no shikyutaizenkaku (Preglomerular nucleus in bony fishes). Comp Physiol Biochem 19:198–202
Yamamoto N, Ito H (2008) Visual, lateral line, and auditory ascending pathways to the dorsal telencephalic area thorough the rostral region of lateral preglomerular nucleus in cyprinids. J Comp Neurol 508:615–647
Yang CY, Yoshimoto M, Xue HG, Yamamoto N, Imura K, Sawai N, Ishikawa Y, Ito H (2004) Fiber connections of the lateral valvular nucleus in a percomorph teleost, tilapia (Oreochromis niloticus). J Comp Neurol 474:209–226
Yang C-Y, Xue H-G, Yoshimoto M, Ito H, Yamamoto N, Ozawa H (2007) Fiber connections of the corpus glomerulosum pars rotunda, with special reference to efferent projection pattern to the inferior lobe in a percomorph teleost, tilapia (Oreochromis niloticus). J Comp Neurol 501:582–607
Yasuda T, Aoki K, Matsumoto A, Maruyama K, Hyodo-Taguchi Y, Fushiki S, Ishikawa Y (2006) Radiation-induced brain cell death can be observed in living medaka embryos. J Radiat Res 47:295–303
Yasuda T, Yoshimoto M, Maeda K, Matsumoto A, Maruyama K, Ishikawa Y (2008) Rapid and simple method for quantitative evaluation of neurocytotoxic effects of radiation on develo** medaka brain. J Radiat Res 49:533–540
Yasuda T, Oda S, Ishikawa Y, Watanabe-Asaka T, Hidaka M, Yasuda H, Anzai K, Mitani H (2009) Live imaging of radiation-induced apoptosis by yolk injection of acridine orange in the develo** optic tectum of medaka. J Radiat Res 50:487–494
Zervas M, Millet S, Ahn S, Joyner AL (2004) Cell behaviors and genetic lineages of the mesencephalon and rhombomere 1. Neuron 43:345–357
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Ishikawa, Y., Yamamoto, N., Hagio, H. (2022). Development of Diencephalon, Optic Tectum, and Cerebellum. In: Brain Development of Medaka Fish. Springer, Singapore. https://doi.org/10.1007/978-981-19-4324-9_11
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