Open AccessSpatiotemporal changes in Cx30 and Cx43 expression during neuronal differentiation of P19 EC and NT2/D1 cells
Author(s) -
Wan Carthur K.,
O'Carroll Simon J.,
Kim SueLing,
Green Colin R.,
Nicholson Louise F. B.
Publication year - 2013
Publication title -
cell biology international reports
Language(s) - English
Resource type - Journals
ISSN - 2041-5346
DOI - 10.1002/cbi3.10005
Subject(s) - doublecortin , immunocytochemistry , cellular differentiation , downregulation and upregulation , biology , microbiology and biotechnology , neurod , p19 cell , neuroscience , endocrinology , adult stem cell , central nervous system , gene , biochemistry , dentate gyrus
Abstract While connexins (Cxs) are thought to be involved in differentiation, their expression and role has yet to be fully elucidated. We investigated the temporal expression of Cx30, Cx36 and Cx43 in two in vitro models of neuronal differentiation: human NT2/D1 and murine P19 cells, and the spatial localisation of Cx30 and Cx43 in these models. A temporal Cx43 downregulation was confirmed in both cell lines during RA‐induced neuronal differentiation using RT‐PCR ( P < 0.05) preceding an increase in neuronal doublecortin protein. RT‐PCR showed Cx36 was upregulated twofold in NT2/D1 cells ( P < 0.05) and sixfold in P19 cells ( P < 0.001) during neuronal differentiation. Cx30 exhibited a transient peak in expression midway through the timecourse of differentiation increasing threefold in NT2/D1 cells ( P < 0.001) and eightfold in P19 cells ( P < 0.01). Qualitative immunocytochemistry was used to examine spatiotemporal patterns of Cx protein distribution alongside neuronal differentiation markers. The temporal immunolabelling pattern was similar to that seen using RT‐PCR. Cx43 was observed intracellularly and on cell surfaces, while Cx30 was seen as puncta. Spatially Cx43 was seen on doublecortin‐negative cells, which may indicate Cx43 downregulation is requisite for differentiation in these models. Conversely, Cx30 puncta were observed on doublecortin‐positive and ‐negative cells in NT2/D1 cells and examination of the Cx30 peak showed puncta also localized to nestin‐positive cells, with few puncta on MAP2‐positive cells. In P19 cells Cx30 was localized on clusters of cells surrounded by MAP2‐ and doublecortin‐positive processes. The expression pattern of Cx30 indicates a role in neuronal differentiation; the nature of that role warrants future investigation.