Gap Junction-Mediated Intercellular Signaling in Health and Disease

1999 ◽  
Vol 22 (10) ◽  
pp. 479-480
Author(s):  
David C. Spray
2013 ◽  
Vol 14 (3) ◽  
pp. 5338-5366 ◽  
Author(s):  
Chiara Corrado ◽  
Stefania Raimondo ◽  
Antonio Chiesi ◽  
Francesco Ciccia ◽  
Giacomo De Leo ◽  
...  

2021 ◽  
Vol 22 (3) ◽  
pp. 1481
Author(s):  
Sara Casati ◽  
Chiara Giannasi ◽  
Stefania Niada ◽  
Roberta F. Bergamaschi ◽  
Marica Orioli ◽  
...  

Lipidomics is a lipid-targeted metabolomics approach that aims to the comprehensive analysis of lipids in biological systems in order to highlight the specific functions of lipid species in health and disease. Lipids play pivotal roles as they are major structural components of the cellular membranes and energy storage molecules but also, as most recently shown, they act as functional and regulatory components of intra- and intercellular signaling. Herein, emphasis is given to the recently highlighted roles of specific bioactive lipids species, as polyunsaturated fatty acids (PUFA)-derived mediators (generally known as eicosanoids), endocannabinoids (eCBs), and lysophospholipids (LPLs), and their involvement in the mesenchymal stem cells (MSCs)-related inflammatory scenario. Indeed, MSCs are a heterogenous population of multipotent cells that have attracted much attention for their potential in regulating inflammation, immunomodulatory capabilities, and reparative roles. The lipidomics of the inflammatory disease osteoarthritis (OA) and the influence of MSCs-derived lipids have also been addressed.


2015 ◽  
Vol 92 (5) ◽  
Author(s):  
P. A. Deymier ◽  
N. Swinteck ◽  
K. Runge ◽  
A. Deymier-Black ◽  
J. B. Hoying

Physiology ◽  
2009 ◽  
Vol 24 (4) ◽  
pp. 219-230 ◽  
Author(s):  
Jeremy E. Cook ◽  
David L. Becker

Gap-junction channels, the cytoplasmic proteins that associate with them, and the transcriptional networks that regulate them are increasingly being viewed as critical communications hubs for cell signaling in health and disease. As a result, the term “nexus,” which was the original structural name for these focal intercellular links, is coming back into use with new proteomic and transcriptomic meanings. The retina is better understood than any other part of the vertebrate central nervous system in respect of its developmental patterning, its diverse neuronal types and circuits, and the emergence of its definitive structure-function correlations. Thus, studies of the junctional and nonjunctional nexus roles of gap-junction proteins in coordinating retinal development should throw useful light on cell signaling in other developing nervous tissues.


2003 ◽  
Vol 83 (4) ◽  
pp. 1359-1400 ◽  
Author(s):  
JUAN C. SÁEZ ◽  
VIVIANA M. BERTHOUD ◽  
MARÍA C. BRAÑES ◽  
AGUSTÍN D. MARTÍNEZ ◽  
ERIC C. BEYER

Sáez, Juan C., Viviana M. Berthoud, María C. Brañes, Agustín D. Martínez, and Eric C. Beyer. Plasma Membrane Channels Formed by Connexins: Their Regulation and Functions. Physiol Rev 83: 1359-1400, 2003; 10.1152/physrev.00007.2003.—Members of the connexin gene family are integral membrane proteins that form hexamers called connexons. Most cells express two or more connexins. Open connexons found at the nonjunctional plasma membrane connect the cell interior with the extracellular milieu. They have been implicated in physiological functions including paracrine intercellular signaling and in induction of cell death under pathological conditions. Gap junction channels are formed by docking of two connexons and are found at cell-cell appositions. Gap junction channels are responsible for direct intercellular transfer of ions and small molecules including propagation of inositol trisphosphate-dependent calcium waves. They are involved in coordinating the electrical and metabolic responses of heterogeneous cells. New approaches have expanded our knowledge of channel structure and connexin biochemistry (e.g., protein trafficking/assembly, phosphorylation, and interactions with other connexins or other proteins). The physiological role of gap junctions in several tissues has been elucidated by the discovery of mutant connexins associated with genetic diseases and by the generation of mice with targeted ablation of specific connexin genes. The observed phenotypes range from specific tissue dysfunction to embryonic lethality.


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