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Premature Neural Progenitor Cell Differentiation Into Astrocytes in Retinoic Acid-Induced Spina Bifida Rat Model.

Frontiers in molecular neuroscience (2022-07-06)
Marc Oria, Bedika Pathak, Zhen Li, Kenan Bakri, Kara Gouwens, Maria Florencia Varela, Kristin Lampe, Kendall P Murphy, Chia-Ying Lin, Jose L Peiro
RESUMEN

During embryonic spinal cord development, neural progenitor cells (NPCs) generate three major cell lines: neurons, oligodendrocytes, and astrocytes at precise times and locations within the spinal cord. Recent studies demonstrate early astrogenesis in animal models of spina bifida, which may play a role in neuronal dysfunction associated with this condition. However, to date, the pathophysiological mechanisms related to this early astrocytic response in spina bifida are poorly understood. This study aimed to characterize the development of early astrogliosis over time from Pax6+, Olig2+, or Nkx2.2+ NPCs using a retinoic acid-induced spina bifida rat model. At three gestational ages (E15, E17, and E20), spinal cords from fetuses with retinoic acid-induced spina bifida, their healthy sibling controls, or fetuses treated with the vehicle control were analyzed. Results indicated that premature astrogliosis and astrocytic activation were associated with an altered presence of Pax6+, Olig2+, and Nkx2.2+ NPCs in the lesion compared to the controls. Finally, this response correlated with an elevation in genes involved in the Notch-BMP signaling pathway. Taken together, changes in NPC patterning factor expression with Notch-BMP signaling upregulation may be responsible for the altered astrogenesis patterns observed in the spinal cord in a retinoic acid-induced spina bifida model.

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Sigma-Aldrich
Anticuerpo anti-Olig-2, Chemicon®, from rabbit
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Monoclonal Anti-Vimentin antibody produced in mouse, clone V9, ascites fluid
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Anti-Oligodendrocyte transcription factor 2 (OLIG2 Antibody), serum, from guinea pig
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Anti-S-100 (β-Subunit) antibody, Mouse monoclonal, clone SH-B1, purified from hybridoma cell culture