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Published on: May 24, 2012
Nestin reporter transgene labels multiple central nervous system precursor cells
Avery S Walker1, Gwendolyn E Goings, Yongsoo Kim
1Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611-3008, USA.
Neural Plasticity
|April 30, 2011
Summary
A new transgenic mouse model expresses enhanced green fluorescent protein (eGFP) under the nestin promoter, enabling visualization of neural stem and progenitor cells. This tool aids research into neurogenesis and oligodendrocyte development.
Area of Science:
- Neuroscience
- Developmental Biology
- Stem Cell Biology
Background:
- Nestin is a key marker for neural stem and progenitor cells in both embryonic and adult brains.
- Understanding the lineage and dynamics of these cells is crucial for neurodevelopmental and regenerative studies.
Purpose of the Study:
- To characterize a novel transgenic mouse line using enhanced green fluorescent protein (eGFP) under the control of the nestin promoter.
- To evaluate the utility of this eGFP reporter line for studying neural stem and progenitor cell populations and their behavior in various physiological and pathological conditions.
Main Methods:
- Generation and characterization of a transgenic mouse line with eGFP expression driven by the nestin promoter's second intronic enhancer.
- Analysis of eGFP expression patterns in different brain regions during embryogenesis, postnatal development, and in adult neurogenic niches.
- Assessment of eGFP+ cell phenotypes using lineage markers and evaluation of their response to cortical injury.
- Examination of eGFP expression in non-neurogenic regions, specifically focusing on glial cells.
Main Results:
- The transgenic line exhibited distinct eGFP expression patterns, with numerous cells in the dorsal telencephalon during embryogenesis and enrichment in postnatal and adult neurogenic regions like the subventricular zone (SVZ).
- eGFP+ cells in the SVZ expressed markers consistent with neural progenitor cells and neuroblasts, indicating transgene expression throughout the neural lineage.
- Increased eGFP+ cell numbers were observed in the SVZ following cortical injury, suggesting suitability for studying post-injury neurogenesis.
- In non-neurogenic areas, eGFP was specifically detected in oligodendrocyte progenitors but not in astrocytes, even reactive ones.
Conclusions:
- The characterized nestin-eGFP transgenic mouse line serves as a valuable tool for tracking neural stem and progenitor cells.
- This model facilitates in-depth studies of both embryonic and adult neurogenesis, as well as the development and behavior of parenchymal oligodendrocytes.
- The reporter line's responsiveness to injury highlights its potential for investigating regenerative processes in the central nervous system.

