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Neuroscience
Homochronic trasplante de precursores de interneurona en cerebros de ratón Postnatal temprana
Homochronic trasplante de precursores de interneurona en cerebros de ratón Postnatal temprana
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
Homochronic Transplantation of Interneuron Precursors into Early Postnatal Mouse Brains

Homochronic trasplante de precursores de interneurona en cerebros de ratón Postnatal temprana

Full Text
8,316 Views
10:08 min
June 8, 2018

DOI: 10.3791/57723-v

Giulia Quattrocolo1, Maria Isaac2, Yajun Zhang2, Timothy J. Petros2

1Kavli Institute for Systems Neuroscience and Centre for Neural Computation,Norwegian University of Science and Technology, 2Eunice Kennedy Shriver National Institute of Child Health and Human Development,National Institutes of Health

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This study investigates how environmental changes impact the fate and maturation of interneuron precursors in postnatal mouse pups. The protocol details the harvesting and transplantation of these precursors from distinct brain regions to assess neuronal development.

Key Study Components

Area of Science

  • Developmental neuroscience
  • Neuronal fate determination
  • Transplantation techniques

Background

  • Understanding the interaction of genetic programs and environmental signals is crucial for neuronal development.
  • The study focuses on interneurons, which play a key role in brain circuitry.
  • Protocols aim to elucidate how young neurons can adapt to new environments.
  • The procedure highlights the importance of technique precision in successful transplantation.

Purpose of Study

  • To provide a method for harvesting and transplanting interneuron precursors.
  • To assess how these precursors adapt and mature in different brain environments.
  • To explore fundamental questions about neuronal fate under varying environmental conditions.

Methods Used

  • The study employs a protocol for harvesting brain tissues from postnatal mouse pups.
  • Interneuron precursors are isolated from regions such as the striatum and hippocampus.
  • The harvested tissues are transplanted into age-matched recipients for examination.
  • Important steps include using razor blades for slicing tissue and fluorescence microscopy for tissue identification.
  • Cell dissociation and sorting methods are utilized prior to transplantation.

Main Results

  • The technique allows for the successful harvesting and transplantation of interneuron precursors.
  • Subsequent assessments reveal how these cells mature within their new environments.
  • Findings could deepen understanding of how environmental factors influence neuronal development and integration.
  • Key conclusions suggest the technique enables exploration of cellular behavior in different contexts.

Conclusions

  • This study demonstrates a significant method for investigating neuronal adaptability and maturation.
  • The findings contribute to understanding the interplay between genetic and environmental influences on neuronal fate.
  • The protocol enhances the capacity to explore developmental questions in neuroscience.

Frequently Asked Questions

What are the advantages of this transplantation technique?
The protocol allows for direct analysis of interneuron precursor fate in varying environments, providing insights into developmental mechanisms.
How are the brain tissues harvested for transplantation?
Tissues are harvested using razor blades for precision slicing, followed by careful identification under a dissecting microscope.
What types of data are obtained from this study?
The study assesses the fate and maturation of transplanted interneuron precursors, focusing on integration and environmental influences.
Can this method be adapted for other types of neuronal studies?
Yes, the harvesting and transplantation techniques can be modified for various neuronal types and research questions.
What limitations should researchers consider with this protocol?
Small errors in technique can lead to inefficient or unsuccessful transplantation, highlighting the need for precision in each step of the protocol.
How does this research advance the field of developmental neuroscience?
It provides a systematic approach to exploring how environmental factors shape neuronal development, which is critical for understanding related disorders.

Desafiando las neuronas jóvenes en nuevas regiones del cerebro puede revelar penetraciones importantes en cómo el entorno esculpe maduración y destino neuronal. Este protocolo describe un procedimiento para cosechar precursores interneurona de regiones específicas del cerebro y transplantarlas o homotopically o heterotopically en el cerebro de crías de postnatales.

El objetivo general de este procedimiento es recolectar precursores de interneuronas de distintas regiones del cerebro en cachorros de ratón postnatales y trasplantar estas células en receptores de la misma edad para evaluar cómo los cambios ambientales influyen en el destino y la maduración de las interneuronas. Este método puede ayudar a responder preguntas clave en el campo de la neurociencia del desarrollo sobre cómo interactúan los programas genéticos intrínsecos y las señales ambientales para esculpir el destino de las células neuronales. La principal ventaja de esta técnica es que las alteraciones en el destino y la maduración de los precursores de las interneuronas pueden analizarse después de su transferencia adoptiva a un nuevo entorno cerebral.

La demostración visual de los pasos de recolección e injerto de células es fundamental porque pequeños errores en la técnica pueden conducir a experimentos de trasplante ineficientes y fallidos. Para comenzar, coloque una hoja de afeitar a través del lóbulo frontal anterior del cerebro de un cachorro posnatal y hojas de afeitar adicionales en las ranuras justo después de la primera hoja de afeitar para generar dos cortes de 0,5 milímetros. Transfiera las rodajas estriadas a una placa de Petri con sacarosa burbujeante, líquido cefalorraquídeo artificial o sACSF, y coloque el tejido cerebral restante en una placa de Petri con sACSF en hielo.

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