Neuronal differentiation of human iPS-cells in a rat cortical primary culture

8Citations
Citations of this article
44Readers
Mendeley users who have this article in their library.

Abstract

We tested the neuronal differentiation of human iPS-cells under in vitro conditions. For this purpose we pre-differentiated human (h) iPS-cells into neural stem cells and co-cultivated them with a cortical primary culture from embryonic rats. After 2 days of co-cultivation a certain number of hiPS-cells exhibited a clear neuronal morphology combined with expression of betaIII-tubulin and doublecortin. In addition, we found hiPS-cells without neuronal differentiation and cells already expressing betaIII-tubulin but not having yet distinctive axonal and dendritic processes. Human neuronal progenitors, starting neuronal differentiation, were contacted by both neuronal processes from rat neurons and oligodendrocytes, indicating a possible instructive influence by the primary culture on human cells. After 7 days of co-cultivation, however, we observed a complete degeneration of human iPS-derived cells and phagocytosis by microglial cells. Immunocytochemical stainings surprisingly revealed that microglial cells of the cortical primary culture express both CD8 and T-cell receptors. © 2012 by Polish Neuroscience Society - PTBUN, Nencki Institute of Experimental Biology.

Cite

CITATION STYLE

APA

Braun, H., Günther-Kern, A., Reymann, K., & Onteniente, B. (2012). Neuronal differentiation of human iPS-cells in a rat cortical primary culture. Acta Neurobiologiae Experimentalis, 72(3), 219–229. https://doi.org/10.55782/ane-2012-1895

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free