Laser Lesion in the Mouse Visual Cortex Induces a Stem Cell Niche-Like Extracellular Matrix, Produced by Immature
Lars Roll1,2, Ulf T Eysel2,3, Andreas Faissner1,2
1Department of Cell Morphology and Molecular Neurobiology, Faculty of Biology and Biotechnology, Ruhr University Bochum, Bochum, Germany.
Frontiers in Cellular Neuroscience
|June 9, 2020
Summary
Mammalian central nervous system (CNS) injury triggers astrocyte proliferation and expression of progenitor markers. The extracellular matrix (ECM) in the injury vicinity contains components associated with neural stem cells, suggesting a shift towards immature cell fate.
Area of Science:
- Neuroscience
- Cell Biology
- Extracellular Matrix Research
Background:
- Mammalian central nervous system (CNS) exhibits limited regeneration compared to species like amphibians.
- The extracellular matrix (ECM) plays a crucial role in regulating cellular responses post-injury.
- Understanding the post-lesional ECM and cellular responses is vital for developing treatments for CNS damage.
Purpose of the Study:
- To analyze the extracellular matrix (ECM) and cellular changes in the vicinity of laser-induced lesions in the adult mouse visual cortex.
- To investigate the spatial distribution and expression of specific markers in astrocytes and ECM components after CNS injury.
Main Methods:
- Focal infrared laser lesions were induced in the adult mouse visual cortex.
- Cell type-specific markers (GFAP, vimentin, nestin, Ki-67) were used to identify different astroglial subtypes and proliferation.
- Extracellular matrix (ECM) molecules (tenascin-C, DSD-1 chondroitin sulfate epitope, WFA, aggrecan) were analyzed.
Main Results:
- Reactive astrocytes (GFAP) were broadly upregulated, while immature markers (vimentin, nestin) were expressed by a subset of cells.
- Proliferating astrocytes (Ki-67) were identified in the lesion penumbra.
- The ECM in the penumbra contained tenascin-C and DSD-1 chondroitin sulfate, typically associated with neural stem/progenitor cells.
Conclusions:
- Astrocyte subpopulations express progenitor markers and proliferate following CNS injury.
- The injured CNS environment contains ECM components linked to neural stem/progenitor cells.
- These findings suggest that the injury promotes an immature cell fate in astrocytes.


