Gap junctions and the propagation of cell survival and cell death signals
- 1 May 2005
- journal article
- review article
- Published by Springer Nature in Apoptosis
- Vol. 10 (3), 459-469
- https://doi.org/10.1007/s10495-005-1875-2
Abstract
Gap junctions are a unique type of intercellular channels that connect the cytoplasm of adjoining cells. Each gap junction channel is comprised of two hemichannels or connexons and each connexon is formed by the aggregation of six protein subunits known as connexins. Gap junction channels allow the intercellular passage of small (< 1.5 kDa) molecules and regulate essential processes during development and differentiation. However, their role in cell survival and cell death is poorly understood. We review experimental data that support the hypothesis that gap junction channels may propagate cell death and survival modulating signals. In addition, we explore the hypothesis that hemichannels (or unapposed connexons) might be used as a paracrine conduit to spread factors that modulate the fate of the surrounding cells. Finally, direct signal transduction activity of connexins in cell death and survival pathways is addressed.Keywords
This publication has 120 references indexed in Scilit:
- Cyclic AMP elevates tubulin expression without increasing intrinsic axon growth capacityExperimental Neurology, 2004
- Gap junctional communication is required to maintain mouse cortical neural progenitor cells in a proliferative stateDevelopmental Biology, 2004
- Beyond the gap: functions of unpaired connexon channelsNature Reviews Molecular Cell Biology, 2003
- Specificity of the Cyclic Adenosine 3′,5′-Monophosphate Signal in Granulosa Cell FunctionBiology of Reproduction, 2002
- Connexin 43–mediated bystander effect in two rat glioma cell modelsCancer Gene Therapy, 2002
- Purified herpes simplex virus thymidine kinase retroviral particles:Cancer Gene Therapy, 2002
- Connexin 43 (cx43) enhances chemotherapy-induced apoptosis in human glioblastoma cellsInternational Journal of Cancer, 2001
- Tentative Novel Mechanism of the Bystander Effect in Glioma Gene Therapy with HSV-TK/GCV SystemBiochemical and Biophysical Research Communications, 1999
- In vitro and in vivo effects of retrovirus-mediated transfer of the connexin 43 gene in malignant gliomas: consequences for HSVtk/GCV anticancer gene therapyGene Therapy, 1998
- Intercellular DiffusionScience, 1964