Premium
Influence of retinoic acid and lithium on proliferation and dopaminergic potential of human NT2 cells
Author(s) -
Misiuta I.E.,
Saporta S.,
Sanberg P.R.,
Zigova T.,
Willing A.E.
Publication year - 2006
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.20718
Subject(s) - biology , retinoic acid , progenitor cell , neurogenesis , microbiology and biotechnology , gliogenesis , neural stem cell , neural development , cellular differentiation , cell culture , medicine , stem cell , biochemistry , gene , genetics
Our laboratory is working with the human NTera2/D1 (NT2) cell line, which has properties similar to those of progenitor cells in the central nervous system (CNS). These neural‐like precursor cells can differentiate into all three major lineages, neurons, astrocytes, and oligodendrocytes. The pure neuronal population, hNT neurons, possess characteristics of dopamine (DA) cells. First, we analyzed whether the retinoic acid (RA)‐treated hNT neurons and the NT2 precursor cells expressed two transcription factors required for development of the midbrain DA neurons. We report that NT2 cells endogenously expressed Engrailed‐1 and Ptx3, whereas RA‐treated hNT neurons did not express Engrailed‐1 or Ptx3. Next we examined the influence of lithium treatment on Engrailed‐1 and Ptx3 as well as another critical transcription factor, Nurr1. Previous research has shown that lithium can mimic the Wnt pathway, which is important for the induction of these transcription factors. Finally, we investigated the effect of lithium treatment on the viability and proliferation of NT2 cells, because lithium has been shown to stimulate neurogenesis in adult neural precursors. Lithium treatment increased the viability and proliferation of NT2 cells. The expression of transcription factors essential for the induction and maintenance of the DA phenotype was not increased in NT2 after lithium treatment. We conclude that the NT2 cell line is an excellent in vitro model system for studying the influence of pharmalogical agents on proliferation, differentiation, and apoptosis of a human neural progenitor cell line. © 2006 Wiley‐Liss, Inc.