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Properties and regulation of gap junctional hemichannels in the plasma membranes of cultured cells.
Open accessAbstract
During the assembly of gap junctions, a hemichannel in the plasma membrane of one cell is thought to align and dock with another in an apposed membrane to form a cell-to-cell channel. We report here on the existence and properties of nonjunctional, plasma membrane connexin43 (Cx43) hemichannels. The opening of the hemichannels was demonstrated by the cellular uptake of 5(6)-carboxyfluorescein from the culture medium when extracellular calcium levels were reduced. Dye uptake exhibited properties similar to those of gap junction channels. For example, using different dyes, the levels of uptake were correlated with molecular size: 5(6)-carboxyfluorescein (approximately 32%), 7-hydroxycoumarin-3-carboxylic acid (approximately 24%), fura-2 (approximately 11%), and fluorescein-dextran (approximately 0.4%). Octanol and heptanol also reduced dye uptake by approximately 50%. Detailed analysis of one clone of Novikoff cells transfected with a Cx43 antisense expression vector revealed a reduction in dye uptake levels according to uptake assays and a corresponding decrease in intercellular dye transfer rates in microinjection experiments. In addition, a more limited decrease in membrane resistance upon reduction of extracellular calcium was detected in electrophysiological studies of antisense transfectants, in contrast to control cells. Studies of dye uptake in HeLa cells also demonstrated a large increase following transfection with Cx43. Together these observations indicate that Cx43 is responsible for the hemichannel function in these cultured cells. Similar dye uptake results were obtained with normal rat kidney (NRK) cells, which express Cx43. Dye uptake can be dramatically inhibited by 12-O-tetradeconylphorbol-13-acetate-activated protein kinase C in these cell systems and by a temperature-sensitive tyrosine protein kinase, pp60v-src in LA25-NRK cells. We conclude that Cx43 hemichannels are found in the plasma membrane, where they are regulated by multiple signaling pathways, and likely represent an important stage in gap junction assembly.
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Hamill, O. P., Marty, A., Neher, E., Sakmann, B., & Sigworth, F. J. (1981) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00656997 · Cited by 18,436
Cited by
Connexin43 phosphorylation: structural changes and biological effects
Solan, J. L., & Lampe, P. D. (2009) · Biochemical Journal · doi:10.1042/bj20082319 · Cited by 555
Self-citationPannexin 1 in erythrocytes: Function without a gap
Locovei, S., Bao, L., & Dahl, G. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601037103 · Cited by 508
Genetos, D. C., Kephart, C. J., Zhang, Y., Yellowley, C. E., & Donahue, H. J. (2007) · Journal of Cellular Physiology · doi:10.1002/jcp.21021 · Cited by 328
Contreras, J. E., Sánchez, H. A., Véliz, L. P., Bukauskas, F. F., Bennett, M. V. L., & Sáez, J. C. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.08.002 · Cited by 244
Connexins: Key Mediators of Endocrine Function
Bosco, D., Haefliger, J.-A., & Meda, P. (2011) · Physiological Reviews · doi:10.1152/physrev.00027.2010 · Cited by 169
Metadata
- Authors
- Li, H., Liu, T. F., Lazrak, A., Peracchia, C., Goldberg, G. S., Lampe, P. D., & Johnson, R. G.
- Venue
- The Journal of cell biology
- Publisher
- Rockefeller University Press
- Published
- 1996-08-15
- Volume
- 134
- Issue
- 4
- Pages
- 1019-1030
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W2146692959
- Cited by
- 328
- References
- 1
- FWCI
- 3.34
- Type
- journal article
- Language
- en
- Open access
- green
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- Li, H., Liu, T. F., Lazrak, A., Peracchia, C., Goldberg, G. S., Lampe, P. D., & Johnson, R. G. (1996). Properties and regulation of gap junctional hemichannels in the plasma membranes of cultured cells. The Journal of cell biology. https://doi.org/10.1083/jcb.134.4.1019
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