Gap junction blockage interferes with neuronal and astroglial differentiation of mouse P19 embryonal carcinoma cells

✍ Scribed by Bani-Yaghoub, Mahmud ;Underhill, T. Michael ;Naus, Christian C.G.

• Publisher: John Wiley and Sons
• Year: 1999
• Tongue: English
• Weight: 657 KB
• Volume: 24
• Category: Article
• ISSN: 0192-253X
• DOI: 10.1002/(sici)1520-6408(1999)24:1/2<69::aid-dvg8>3.0.co;2-m

✦ Synopsis

During embryonic development, cells not only increase in number, they also undergo specialization and differentiate into diverse cell types that are organized into different tissues and organs. Nervous system development, for example, involves a complex series of events such as neuronal and astroglial differentiation that are coordinated among adjacent cells. The organization of growth and differentiation may be mediated, at least partly, by exchange of small ions and molecules via intercellular gap junction channels. These structures are made of connexons (hemichannels), which are hexameric assemblies of the gap junction proteins, connexins. We investigated the role of intercellular communication in neuronal and astroglial differentiation by using a gap junction blocking agent, carbenoxolone (CBX), in comparison to its inactive (control) analog, glycyrrhizic acid (GZA). We used the mouse P19 embryonal carcinoma cell line, which differentiates into neurons and astrocytes upon retinoic acid (RA) induction. Our results show that both GZA-and CBX-treated cells express ␣ 1 connexin (connexin43). The level of ␣ 1 connexin decreases upon RA induction. CBX treated cells show significant reduction in both neuronal (5-fold) and astrocytic (13-fold) differentiation compared with those of control. These results clearly indicate that the blockage of gap junction-mediated intercellular communication interferes with differentiation of P19 cells into neurons and astrocytes.