1. Preservation of positional identity in fetus-derived neural stem (NS) cells from different mouse central nervous system compartments.
- Author
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Onorati M, Binetti M, Conti L, Camnasio S, Calabrese G, Albieri I, Di Febo F, Toselli M, Biella G, Martynoga B, Guillemot F, Consalez GG, and Cattaneo E
- Subjects
- Animals, Cell Differentiation, Cells, Cultured, Forkhead Transcription Factors genetics, Forkhead Transcription Factors metabolism, Homeodomain Proteins genetics, Homeodomain Proteins metabolism, Mice, Neocortex cytology, Neocortex embryology, Nerve Tissue Proteins genetics, Nerve Tissue Proteins metabolism, Otx Transcription Factors genetics, Otx Transcription Factors metabolism, Patch-Clamp Techniques, Spinal Cord cytology, Spinal Cord embryology, Transcription Factors genetics, Transcription Factors metabolism, Fetus cytology, Neural Stem Cells metabolism
- Abstract
Neural stem (NS) cells are a self-renewing population of symmetrically dividing multipotent radial glia-like stem cells, characterized by homogeneous expansion in monolayer. Here we report that fetal NS cells isolated from different regions of the developing mouse nervous system behave in a similar manner with respect to self-renewal and neuropotency, but exhibit distinct positional identities. For example, NS cells from the neocortex maintain the expression of anterior transcription factors, including Otx2 and Foxg1, while Hoxb4 and Hoxb9 are uniquely found in spinal cord-derived NS cells. This molecular signature was stable for over 20 passages and was strictly linked to the developmental stage of the donor, because only NS cells derived from E14.5 cortex, and not those derived from E12.5 cortex, carried a consistent transcription factor profile. We also showed that traits of this positional code are maintained during neuronal differentiation, leading to the generation of electrophysiologically active neurons, even if they do not acquire a complete neurochemical identity.
- Published
- 2011
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