Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark

Patrick Bovio; Deborah Roidl; Stefanie Heidrich; Tanja Vogel; Henriette Franz

doi:10.3791/56631

Isolement et culture des progéniteurs neurones suivie par immunoprécipitation de la chromatine de...

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JoVE Journal Neuroscience

Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark

Isolement et culture des progéniteurs neurones suivie par immunoprécipitation de la chromatine de marque d’Histone 3 Lysine 79 MBD

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10:09 min

January 26, 2018

DOI: 10.3791/56631-v

Patrick Bovio^1,2, Deborah Roidl¹, Stefanie Heidrich¹, Tanja Vogel¹, Henriette Franz¹

¹Institute for Anatomy and Cell Biology, Department of Molecular Embryology, Faculty of Medicine,University of Freiburg, ²Faculty of Biology,University of Freiburg

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Overview

This study presents a reproducible method for isolating and culturing neural progenitor cells from embryonic and postnatal brain tissue. The focus is on analyzing epigenetic modifications, specifically the histone mark H3K79me2, during brain development within the cerebral cortex and cerebellum.

Key Study Components

Area of Science

Neuroscience
Epigenetics
Cell Culture Techniques

Background

Neural progenitor cells are crucial for brain development.
Histone modifications play a significant role in gene expression.
The study investigates the specific impact of H3K79 methylation.
Understanding these mechanisms can provide insights into cortical and cerebellar layering.

Purpose of Study

To analyze epigenetic changes during brain development.
To explore the effects of histone modifications on neural differentiation.
To develop a reliable protocol for ChIP analyses of specific histone marks.

Methods Used

Cell culture techniques utilizing isolated neural progenitor cells.
Focus on embryonic and postnatal brain tissues, specifically cerebellar cells.
Instructions for tissue digestion, cell isolation, and histone extraction.
Detailed steps for Chromatin Immunoprecipitation (ChIP) to analyze histone modifications.

Main Results

The method successfully isolates and cultures cerebellar neural progenitor cells.
ChIP protocols can analyze H3K79me2 levels in various development stages.
Findings indicate a significant relationship between histone modifications and neuronal development.
Validations confirm the effectiveness and reproducibility of the technique.

Conclusions

This study demonstrates an effective methodology for exploring epigenetic regulation in neural development.
The approach enables detailed investigation into how histone modifications influence the neurodevelopmental process.
Insights gained can contribute to understanding neuronal mechanisms and potentially implicate disease models.

Frequently Asked Questions

What are the advantages of this cell culture method?

This method allows for the study of neural progenitor cells in a controlled environment, making it reproducible and efficient for epigenetic analysis.

How are the neural progenitor cells isolated?

The cells are isolated from cerebellar tissue by digestion, centrifugation, and trituration, ensuring a high yield of viable progenitor cells.

What type of data can be obtained from this method?

Researchers can obtain molecular readouts related to histone modifications and assess the impacts on cellular behavior and development.

How can this method be adapted for other brain regions?

The protocol can be modified for different brain regions by altering the source tissue and optimizing the digestion and culture conditions accordingly.

Are there any limitations to this technique?

Key limitations include the potential variability in cell yield and the requirement for specific tissue sources, which may not always be available.

What implications does this study have for neurobiology?

The findings enhance the understanding of epigenetic regulation in brain development and may inform future research on neurodevelopmental disorders.

What steps are involved in the ChIP process?

The ChIP process includes cell lysis, chromatin shearing, immunoprecipitation with specific antibodies, and subsequent analysis to assess histone modification levels.

Nous présentons une méthode efficace et reproductible pour isoler et de la culture des cellules progénitrices neurales de tissus du cerveau embryonnaire et postnatale pour l’immunoprécipitation de la chromatine (ChIP) de l’histone 3 lysine 79 MBD (H3K79me2) - une marque d’histone agrave la domaine globulaire de l’histone 3.

L’objectif général de cette procédure est d’analyser les modifications épigénétiques au cours du développement du cerveau, en particulier dans le cortex cérébral et le cervelet. Cette méthode peut être utilisée pour répondre à des questions clés dans le domaine de la neurobiologie, telles que la façon dont les modifications des histones comme la méthylation de H3K79 peuvent affecter le développement de la stratification corticale et cérébelleuse. Le principal avantage de cette technique est que nous pouvons étudier in vivo les modifications d’histones, spécifiques au locus ou à l’ensemble du génome, dans des régions cérébrales distinctes à des moments de développement spécifiques.

Commençons par des cerveaux de P5 à P7 et des souris IRM. Retirez toutes les méninges et les vaisseaux sanguins. Transférez ensuite trois à cinq cervelous par puce dans des tubes de 15 millilitres.

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