Natural apoptosis in developing mice dopamine midbrain neurons and vermal Purkinje cells

Natural cell death by apoptosis was studied in two neuronal populations of BALB/c, C57BL/6 and B6CBA-A/A hybrid stock mice: (I) dopaminergic (DA) neurons in choosing coronal levels throughout the anteroposterior extent of the substantia nigra pars compacta (SNc), and (II) Purkinje cells (PCs) in eac...

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Detalles Bibliográficos
Autor: Martí-Clúa, Joaquín|||0000-0002-6774-0092
Tipo de recurso: artículo
Fecha de publicación:2016
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:215104
Acceso en línea:https://ddd.uab.cat/record/215104
https://dx.doi.org/urn:doi:10.5114/fn.2016.60385
Access Level:acceso abierto
Palabra clave:Postnatal
Dopamine
Substantia nigra pars compacta
Cerebellar cortex
Purkinje cells
Neurogenetic timetables
Apoptosis
Descripción
Sumario:Natural cell death by apoptosis was studied in two neuronal populations of BALB/c, C57BL/6 and B6CBA-A/A hybrid stock mice: (I) dopaminergic (DA) neurons in choosing coronal levels throughout the anteroposterior extent of the substantia nigra pars compacta (SNc), and (II) Purkinje cells (PCs) in each vermal lobe of the cerebellar cortex. Mice were collected at postnatal day (P) 2 and P14 for the midbrain study, and at P4 and P7 for the analysis of the cerebellum. No DA cells with morphologic criteria for apoptosis were found. Moreover, when the combination of tyrosine hydroxylase and TUNEL or tyrosine hydroxylase and active caspase-3 immunohistochemistry were performed in the same tissue section, no DA cells TUNEL positives or active caspase-3-stained DA neurons were seen. On the other hand, when PCs were considered, data analysis revealed that more dying PCs were observed at P4 than at P7. Values of neuron death were highest in the central lobe; this was followed by the posterior and anterior lobes and then by the inferior lobe. To determine if apoptotic death of PCs is linked to their time-of-origin profiles, pregnant dams were administered with [H]TdR on embryonic days 11-12, 12-13, 13-14 and 14-15. When TUNEL and [H]TdR autoradiography or active caspase-3 immunohistochemistry and [H]TdR autoradiography were combined in the same tissue section, results reveal that the naturally occurring PC death is not related to its time of origin but, rather, is random across age.