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Mesencephalic origin of the rostral Substantia nigra pars reticulata

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dc.contributor.author Pilar-Madrigal, M
dc.contributor.author Moreno-Bravo, Juan-A
dc.contributor.author Martínez-López, Jesus-E
dc.contributor.author Puelles, Eduardo
dc.contributor.author Martínez, Salvador
dc.date.accessioned 2026-10-20T11:46:10Z
dc.date.available 2026-10-20T11:46:10Z
dc.date.issued 2016-04
dc.identifier.citation Madrigal MP, Moreno-Bravo JA, Martínez-López JE, Martínez S, Puelles E. Mesencephalic origin of the rostral Substantia nigra pars reticulata. Brain Struct Funct. abril de 2016;221(3):1403-12. doi:10.1007/s00429-014-0980-9
dc.identifier.issn 1863-2653
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/28530
dc.description.abstract In embryonic development, the neurons that will constitute a heterogeneous nucleus may have distinct origins. The different components of these populations reach their final location by radial and tangential migrations. The Substantia nigra pars reticulata (SNR) presents a high level of neuronal heterogeneity. It is composed by GABAergic neurons located in the mes-diencephalic basal plate. These inhibitory neurons usually display tangential migrations and it has been already described that the caudal SNR is colonized tangentially from rhombomere 1. Our aim is to unveil the origin of the rostral SNR. We have localized a Nkx6.2 positive ventricular domain located in the alar midbrain. Nkx6.2 derivatives' fate map analysis showed mainly a rostral colonization of this GABAergic neuronal population. We confirmed the mesencephalic origin by the expression of Six3. Both transcription factors are sequentially expressed along the differentiation of these neurons. We demonstrated the origin of the rostral SNR; our data allowed us to postulate that this nucleus is composed by two neuronal populations distributed in opposite gradients with different origins, one from rhombomere 1, caudal to rostral, and the other from the midbrain, rostral to caudal. We can conclude that the SNR has multiple origins and follows complex mechanisms of specification and migration. Our results support vital information for the study of genetic modifications in these extremely complex processes that result in devastating behavioral alterations and predisposition to psychiatric diseases. Understanding the development, molecular identity and functional characteristics of these diverse neuronal populations might lead to better diagnosis and treatment of several forms of neurological and psychiatric disease.
dc.language.iso eng
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/deed.es *
dc.subject.mesh Animals
dc.subject.mesh Cell Movement
dc.subject.mesh Eye Proteins/metabolism
dc.subject.mesh Female
dc.subject.mesh GABAergic Neurons/metabolism/physiology
dc.subject.mesh Homeodomain Proteins/metabolism
dc.subject.mesh Male
dc.subject.mesh Mice
dc.subject.mesh Mice, Transgenic
dc.subject.mesh Nerve Tissue Proteins/metabolism
dc.subject.mesh Pars Reticulata/embryology/metabolism
dc.subject.mesh Transcription Factors/metabolism
dc.subject.mesh Homeobox Protein SIX3
dc.title Mesencephalic origin of the rostral Substantia nigra pars reticulata
dc.type info:eu-repo/semantics/article 
dc.identifier.pmid 25579066
dc.relation.publisherversion http://link.springer.com/10.1007/s00429-014-0980-9
dc.identifier.doi 10.1007/s00429-014-0980-9
dc.journal.title Brain Structure & Function
dc.identifier.essn 1863-2661


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