Functional recovery of the human central nervous system after lesion is severely limited. In this context, the extracellular matrix plays an important role. It is secreted by the cells into the extracellular space and contains signals that regulate survival, differentiation, and migration of cells in the tissue as well as axon growth and the formation of synaptic contacts. After injury, a process called "reactive gliosis" is observed. Amonst others, astrocytes are activated and start to produce numerous molecules that regulate the cell fate of the adjacent cells. One such factor is Tenascin-C, which is also prominently expressed during development.
The project aims to unravel the role of extracellular molecules with regard to regeneration of brain lesions. The reciprocal influence of transplanted stem cells and extracellular matrix will be examined. This will improve the understanding of the molecular processes after injuries and may help to develop new strategies to promote the regenerative potential.
The following methods are applied in this project: First, focal laser lesions are induced in the mouse model (cooperation with Prof. U. T. Eysel). Afterwards, the extracellular matrix composition and the identity of the cells are analyzed by immunohistochemical stainings and fluorescence microscopy. Stem/progenitor cells are expanded in cell culture before transplantation and their influence on regeneration is elucidated by comparison with untreated control animals. In addition, PCR and Western blot are used to characterize the stem cells.
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