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A simple and reliable method for claustrum localization across age in mice.
Tarek Shaker1, Gwyneth J Dagpa1, Vanessa Cattaud1
1Department of Physiology, University of Alberta, 7-22 Medical Sciences Building, Edmonton, AB, T6G 2H7, Canada.
Molecular Brain
|February 17, 2024
Summary
A new immunolabelling method reliably identifies rodent claustrum cells using Nurr1/Nr2f2 and Tle4 markers. This technique aids in studying claustrum development and function, especially during neonatal stages.
Area of Science:
- Neuroscience
- Anatomy
- Molecular Biology
Background:
- The rodent claustrum's anatomical boundaries are poorly defined, hindering functional studies.
- Existing methods for claustrum identification often lack specificity or completeness, particularly during development.
Purpose of the Study:
- To develop a reliable immunolabelling method for identifying rodent claustrum projection neurons.
- To differentiate the claustrum from adjacent cortical structures using molecular markers.
Main Methods:
- Juxtaposing expression patterns of claustrum-enriched markers (Nurr1, Nr2f2) and a cortical marker (Tle4).
- Utilizing retrograde tracing to verify claustrum projection neuron characteristics.
- Assessing neuronal activation via c-Fos expression in response to environmental novelty.
Main Results:
- Claustrum cells expressing Nurr1/Nr2f2 were found to be Tle4-negative, enabling clear differentiation from cortical cells.
- This Nurr1-positive/Tle4-negative profile effectively identified claustrum projection neurons, including during neonatal development (7-21 days).
- Environmental novelty increased c-Fos expression in the claustrum, primarily in Nurr1-positive cells.
Conclusions:
- The proposed immunolabelling method provides a robust tool for studying the rodent claustrum.
- This technique enhances the ability to investigate claustrum anatomy and function across different developmental stages.
- The findings support the claustrum's role in processing environmental novelty.

