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Updated: Aug 11, 2026

In Utero Electroporation of Multiaddressable Genome-Integrating Color (MAGIC) Markers to Individualize Cortical Mouse Astrocytes
Published on: May 21, 2020
A transgenic marker mouse line labels Cajal-Retzius cells from the cortical hem and thalamocortical axons
Chunjie Zhao1, Wei Guan, Samuel J Pleasure
1Department of Neurology, Programs in Neuroscience and Developmental Biology, University of California, UCSF Mission Bay, Box 2722, Rock Hall, 1550 Fourth Street, Room RH-348D, San Francisco, CA 94143-2722, USA.
Abstract:
Cajal-Retzius (CR) cells are among the earliest born cortical neurons and are required for normal cortical development in rodents and humans; however, their embryonic origin has been controversial. Recent genetic lineage studies and direct visualization of migration of CR cells have demonstrated multiple germinative sources for CR cells on the edges of the developing pallium. We generated transgenic mice using 5' untranslated regions of the Frizzled10 gene in order to mark the cortical hem (the most caudomedial edge of the telencephalic neuroepithelium) and found that these mice faithfully reproduce the previously described expression pattern of Frizzled10 mRNA in the cortical hem, dorsal thalamus and dorsal neural tube. In the cortical hem, expression of LacZ mRNA was confined to the ventricular zone and perdurance of LacZ protein served as lineage marker for CR cells derived from the hem during embryonic life. When these marker mice were crossed with FoxG1 (BF1) mutants, they confirmed the previous finding that in these mice the cortical hem is expanded leading to increased production of CR cells from the medial wall of the cortex.

