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Neuroscience
Immagini di corteccia cerebrale primario celle utilizzando un sistema 2D cultura dal vivo
Immagini di corteccia cerebrale primario celle utilizzando un sistema 2D cultura dal vivo
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
Live Imaging of Primary Cerebral Cortex Cells Using a 2D Culture System

Immagini di corteccia cerebrale primario celle utilizzando un sistema 2D cultura dal vivo

Full Text
8,740 Views
10:12 min
August 9, 2017

DOI: 10.3791/56063-v

Bruna Soares Landeira1, Jéssica Alves de Medeiros Araújo1, Timm Schroeder2, Ulrich Müller3, Marcos R. Costa1

1Brain Institute,Federal University of Rio Grande do Norte, 2Department of Biosystems Science and Engineering,ETH Zurich, 3The Solomon H. Snyder Department of Neuroscience,Johns Hopkins University

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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 article outlines a detailed protocol for time-lapse video-microscopy aimed at observing cellular behaviors in primary cerebral cortex cells. The method enables researchers to investigate the lineage progression from neural stem cells to differentiated neurons and glial cells, providing insights into neurodevelopmental processes.

Key Study Components

Area of Science

  • Neurodevelopment
  • Cellular Behavior
  • Imaging Techniques

Background

  • Live imaging is an effective method to examine cellular dynamics.
  • The study focuses on neural stem cells transitioning into various cell types.
  • The method allows for long-term observation of cell lineage.
  • It helps in understanding key questions about cell division and growth rates.

Purpose of Study

  • To observe cell behaviors during lineage progression from neural stem cells to neurons or glial cells.
  • To investigate the implications of symmetric and asymmetric cell divisions.
  • To enable detailed tracking of neurogenesis and glial genesis.

Methods Used

  • The platform used is time-lapse video-microscopy of primary cerebral cortex cells.
  • Primary neural stem cells are isolated from e14 embryos following detailed dissection protocols.
  • The cells are cultured and observed under controlled temperature and CO2 conditions during imaging.
  • Images are captured at specified intervals to minimize phototoxicity, and software aids in tracking cell lineages.

Main Results

  • Cell lineage tracking reveals shifts from neurogenesis to glial genesis over time.
  • Quantitative data on cell viability and tracking outcomes are presented.
  • The increase in GFP expressing cells indicates successful tracking and differentiation observations.
  • Mechanistic insights into division, death, and lineage tracing are captured throughout the experiment.

Conclusions

  • This study demonstrates a robust method for live imaging to investigate neural lineage development.
  • The protocol enables researchers to answer critical questions in neurodevelopment, potentially aiding in the understanding of related diseases.
  • Findings from the study can inform future research on cell differentiation processes in the nervous system.

Frequently Asked Questions

What are the advantages of using live imaging?
Live imaging allows for real-time observation of cellular behaviors, enabling detailed analysis of lineage progression over extended periods.
How is the primary neural stem cell model implemented?
Neural stem cells are isolated from the embryonic telencephalon and cultured in a controlled environment to study their development.
What types of data are obtained from this method?
The method produces time-lapse images that track cell lineage, viability, and differentiation status, providing quantitative and qualitative insights.
Can this method be adapted for different cell types?
Yes, while this study focuses on cortical cells, the protocol can be modified to study other types of stem cells or progenitors by adjusting dissection and culture parameters.
What are some limitations of this approach?
Limitations may include the complexity of the dissection process and the potential for variabilities in cell culture conditions that can affect results.

La formazione immagine dal vivo è un potente strumento per studiare i comportamenti cellulari in tempo reale. Qui, descriviamo un protocollo per time-lapse video-microscopia delle cellule della corteccia cerebrale primario che consente un esame dettagliato delle fasi promulgata durante la progressione di lignaggio da cellule staminali neurali primarie a differenziato neuroni e cellule gliali.

L'obiettivo generale di questo esperimento è osservare i comportamenti cellulari durante la progressione del lignaggio dalle cellule staminali neurali ai neuroni o alle cellule gliali. Questo metodo può aiutare a rispondere a domande nel campo dello sviluppo neurologico come il ruolo delle divisioni cellulari simmetriche e asimmetriche, l'allungamento del ciclo cellulare e i tassi di crescita cellulare. Il vantaggio principale di questa tecnica è che consente l'osservazione della linea cellulare per lunghi periodi.

Ciò consente l'osservazione del passaggio dalla neurogenesi alla genesi gliale all'interno di un singolo lignaggio e una comporazione diretta di progenitori neurali e gliali sublineari. Inizia rimuovendo i cervelli da 5 a 10 embrioni e14 in una capsula di Petri con mezzo di dissezione freddo. Usa il forcipe per estrarre con cura la pelle e il cranio e isolare il cervello.

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