Browse > Article
http://dx.doi.org/10.14405/kjvr.2020.60.4.203

Dopaminergic neuronal development in the embryonic mesencephalon of mouse  

Kim, Mun-Ki (Institute of Animal Medicine and Department of Veterinary Medicine, Gyeongsang National University)
Lee, Si-Joon (Institute of Animal Medicine and Department of Veterinary Medicine, Gyeongsang National University)
Won, Chung-Kil (Institute of Animal Medicine and Department of Veterinary Medicine, Gyeongsang National University)
Publication Information
Korean Journal of Veterinary Research / v.60, no.4, 2020 , pp. 203-207 More about this Journal
Abstract
This study presents neuronal migration pattern of dopamine (DA) neurons generated in separate regions occupying the ventral mesencephalic territory. A single pulse 5-bromodeoxyuridine (BrdU) was administered at embryonic day (E)10-E15. Distribution of tyrosine hydroxylase (TH) positive cells was determined at E13-postnatal day 0 (P0) by immunohistochemistry. BrdU positive cells labeled at E10 were spread out uniformly in the mesencephalon from E13 to E15, migrating through dorsal and ventral routes at E17 and P0. TH expression labeled at E10 was observed at E13 in the ventromedial region and clearly formed in the ventral tegmental area (VTA) at E15. At E17, TH expression in the substantia nigra (SN) was observed in the ventrolateral region, spreading more outward of the mesencephalon at P0. Generation of TH-positive cells labeled at E13 was also observed in VTA and SN of the mesencephalon at E17 and P0. The expression of these cells labeled after E15 was markedly decreased. These results demonstrated that an almost complete primary structure of DA neuron was formed at the early embryonic stage in the ventral mesencephalon, showing the most active neuronal migration was occurred at E13-E17.
Keywords
development; dopaminergic neuron; mesencephalon; neuronal migration;
Citations & Related Records
Times Cited By KSCI : 4  (Citation Analysis)
연도 인용수 순위
1 Corbin JG, Nery S, Fishell G. Telencephalic cells take a tangent: non-radial migration in the mammalian forebrain. Nat Neurosci 2001;4 Suppl:1177-1182.   DOI
2 Hatten ME. New directions in neuronal migration. Science 2002;297:1660-1663.   DOI
3 Marin O, Rubenstein JL. A long, remarkable journey: tangential migration in the telencephalon. Nat Rev Neurosci 2001;2: 780-790.   DOI
4 Nadarajah B, Parnavelas JG. Modes of neuronal migration in the developing cerebral cortex. Nat Rev Neurosci 2002;3: 423-432.   DOI
5 Parnavelas JG. The origin and migration of cortical neurones: new vistas. Trends Neurosci 2000;23:126-131.   DOI
6 Altman J, Bayer SA. Development of the brain stem in the rat. V. Thymidine-radiographic study of the time of origin of neurons in the midbrain tegmentum. J Comp Neurol 1981; 198:677-716.   DOI
7 Smits SM, Burbach JP, Smidt MP. Developmental origin and fate of meso-diencephalic dopamine neurons. Prog Neurobiol 2006;78:1-16.   DOI
8 Nair-Roberts RG, Chatelain-Badie SD, Benson E, WhiteCooper H, Bolam JP, Ungless MA. Stereological estimates of dopaminergic, GABAergic and glutamatergic neurons in the ventral tegmental area, substantia nigra and retrorubral field in the rat. Neuroscience 2008;152:1024-1031.   DOI
9 German DC, Manaye KF. Midbrain dopaminergic neurons (nuclei A8, A9, and A10): three-dimensional reconstruction in the rat. J Comp Neurol 1993;331:297-309.   DOI
10 Prakash N, Wurst W. Development of dopaminergic neurons in the mammalian brain. Cell Mol Life Sci 2006;63:187-206.   DOI
11 Bodea GO, Blaess S. Establishing diversity in the dopaminergic system. FEBS Lett 2015;589 24 Pt A:3773-3785.   DOI
12 Damier P, Hirsch EC, Agid Y, Graybiel AM. The substantia nigra of the human brain. II. Patterns of loss of dopamine-containing neurons in Parkinson's disease. Brain 1999;122: 1437-1448.   DOI
13 Kawano H, Ohyama K, Kawamura K, Nagatsu I. Migration of dopaminergic neurons in the embryonic mesencephalon of mice. Brain Res Dev Brain Res 1995;86:101-113.   DOI
14 Soriano E, Del Rio JA. Simultaneous immunocytochemical visualization of bromodeoxyuridine and neural tissue antigens. J Histochem Cytochem 1991;39:255-263.   DOI
15 Ohyama K, Kawano H, Asou H, Fukuda T, Oohira A, Uyemura K, Kawamura K. Coordinate expression of L1 and 6B4 proteoglycan/phosphacan is correlated with the migration of mesencephalic dopaminergic neurons in mice. Brain Res Dev Brain Res 1998;107:219-226.   DOI
16 López-Bendito G, Sánchez-Alcañiz JA, Pla R, Borrell V, Pic E, Valdeolmillos M, Marin O. Chemokine signaling controls intracortical migration and final distribution of GABAergic interneurons. J Neurosci 2008;28:1613-1624.   DOI
17 Korotkova TM, Ponomarenko AA, Brown RE, Haas HL. Functional diversity of ventral midbrain dopamine and GABAergic neurons. Mol Neurobiol 2004;29:243-259.   DOI
18 Vasudevan A, Won C, Li S, Erdelyi F, Szab G, Kim KS. Dopaminergic neurons modulate GABA neuron migration in the embryonic midbrain. Development 2012;139:3136-3141.   DOI
19 Kim MK, Lee SJ, Vasudevan A, Won C. Neurogenesis and neuronal migration of dopaminergic neurons during mesencephalon development in mice. J Biomed Transl Res 2018; 19:125-129.   DOI
20 Castelo-Branco G, Wagner J, Rodriguez FJ, Kele J, Sousa K, Rawal N, Pasolli HA, Fuchs E, Kitajewski J, Arenas E. Differential regulation of midbrain dopaminergic neuron development by Wnt-1, Wnt-3a, and Wnt-5a. Proc Natl Acad Sci U S A 2003;100:12747-12752.   DOI
21 Shults CW, Hashimoto R, Brady RM, Gage FH. Dopaminergic cells align along radial glia in the developing mesencephalon of the rat. Neuroscience 1990;38:427-436.   DOI
22 Kim MK, Lee SJ, Vasudevan A, Won CK. GABAergic neuronal development in the embryonic mesencephalon of mice. Korean J Vet Res 2019;59:201-205.   DOI