Association between integrin-dependent migration capacity of neural stem cells in vitro and anatomical repair following transplantation

Prestoz, Laetitia, Relvas, Jõao B., Hopkins, Katy, Patel, Sara, Sowinski, Peter, Price, Jack and Ffrench-Constant, Charles ORCID: https://orcid.org/0000-0002-5621-3377 (2001) Association between integrin-dependent migration capacity of neural stem cells in vitro and anatomical repair following transplantation. Molecular and Cellular Neuroscience, 18 (5). pp. 473-484. ISSN 1044-7431

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Abstract

In previous transplantation studies using neural stem cell lines immortalized by the temperature-sensitive SV40 large T-antigen, we have shown that animals with experimental hippocampal lesions resulting from four vessel occlusion recover spatial memory functions more effectively when grafted with the MHP36 cell line than with the MHP15 cell line [Gray et al. (1999). Philos. Trans. R. Soc. London Biol. Sci. 354: 1407-1421]. In the present study, we have investigated the cellular and molecular basis of these differences in repair capacity both in vivo and in vitro. Using the same model of hippocampal damage we have shown that following transplantation MHP36 cells migrate and align within the damaged CA1 of the ipsilateral hippocampus. MHP15 cells, in contrast, migrate in a more indiscriminate pattern that does not reflect the anatomy of the region. To analyze the migratory properties of these two cell lines in more detail, we performed migration assays at a nonpermissive temperature on the extracellular matrix substrates laminin, fibronectin, and vitronectin. These showed that MHP36 cells have a greater migration potential than the MHP15 cells. While the pattern of cell surface extracellular matrix receptors of the integrin family was identical in both cell lines, the different degrees of migration on vitronectin were both blocked by inhibitors of αV integrins. Differences in integrin signaling therefore contribute to the greater migration potential of the repairing MHP36 cell line.

Item Type: Article
Additional Information: Funding Information: These studies were supported by funding from the Medical Research Council, the European Commission, and the Biotechnology and Biological Science Research Council. J.B.R. was the recipient of a fellowship (BPD 11785) from the Programa Praxis XXI of the FCT, Portugal, and C. ff-C. holds a Research Leave Fellowship for Clinical Academics from the Wellcome Trust.
Uncontrolled Keywords: molecular biology,cellular and molecular neuroscience,cell biology ,/dk/atira/pure/subjectarea/asjc/1300/1312
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
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Depositing User: LivePure Connector
Date Deposited: 16 Jul 2022 13:30
Last Modified: 13 Aug 2022 02:22
URI: https://ueaeprints.uea.ac.uk/id/eprint/86359
DOI: 10.1006/mcne.2001.1037

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