Robust formation and maintenance of continuous stratified cortical neuroepithelium by laminin-containing matrix in mouse ES cell culture

• Published in: PloS one 2012-12, Vol.7 (12), p.e53024-e53024
• Main Authors: Nasu, Makoto, Takata, Nozomu, Danjo, Teruko, Sakaguchi, Hideya, Kadoshima, Taisuke, Futaki, Sugiko, Sekiguchi, Kiyotoshi, Eiraku, Mototsugu, Sasai, Yoshiki
• Format: Article
• Language: English
• Subjects: Animals; Basement Membrane - metabolism; Biochemistry; Biology; Brain research; Cell culture; Cells, Cultured; Cerebral Cortex - cytology; Cerebral Cortex - metabolism; Cortex; Developmental biology; Embryonic Stem Cells - cytology; Embryonic Stem Cells - metabolism; Embryos; Extracellular matrix; Extracellular Matrix - metabolism; Fibroblasts; Floating structures; Growth factors; Integrins; Laboratories; Laminin; Laminin - metabolism; Low concentrations; Medicine; Mice; Neural stem cells; Neurogenesis; Neurons; Neurons - cytology; Neurons - metabolism; Neurosciences; Plates (structural members); Proteins; Rosette formation; Stem cells; Structural integrity; Telencephalon; Tissues; Ventricle
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0053024

In the mammalian cortex, the dorsal telencephalon exhibits a characteristic stratified structure. We previously reported that three-dimensional (3D) culture of mouse ES cells (mESCs) can efficiently generate cortical neuroepithelium (NE) and layer-specific cortical neurons. However, the cortical NE generated in this mESC culture was structurally unstable and broke into small neural rosettes by culture day 7, suggesting that some factors for reinforcing the structural integrity were missing. Here we report substantial supporting effects of the extracellular matrix (ECM) protein laminin on the continuous formation of properly polarized cortical NE in floating aggregate culture of mESCs. The addition of purified laminin and entactin (a laminin-associated protein), even at low concentrations, stabilized the formation of continuous cortical NE as well as the maintenance of basement membrane and prevented rosette formation. Treatment with the neutralizing ß1-integrin antibody impaired the continuous NE formation. The stabilized cortical NE exhibited typical interkinetic nuclear migration of cortical progenitors, as seen in the embryonic cortex. The laminin-treated cortical NE maintained a continuous structure even on culture days 12 and 15, and contained ventricular, basal-progenitor, cortical-plate and Cajal-Retzius cell layers. The cortical NE in this culture was flanked by cortical hem-like tissue. Furthermore, when Shh was added, ventral telencephalic structures such as lateral ganglionic eminence-like tissue formed in the region adjacent to the cortical NE. Thus, our results indicate that laminin-entactin ECM promotes the formation of structurally stable telencephalic tissues in 3D ESC culture, and supports the morphogenetic recapitulation of cortical development.