SIGNALING NETWORKS IN LIVING CELLS

Author(s):  
Michael A. White ◽  
Richard G.W. Anderson

Recent advances in cell signaling research suggest that multiple sets of signal transducing molecules are preorganized and sequestered in distinct compartments within the cell. These compartments are assembled and maintained by specific cellular machinery. The molecular ecology within a compartment creates an environment that favors the efficient and accurate integration of signaling information arriving from humoral, mechanical, and nutritional sources. The functional organization of these compartments suggests they are the location of signaling networks that naturally organize into hierarchical interconnected sets of molecules through their participation in different classes of interacting units. An important goal is to determine the contribution of the compartment to the function of these networks in living cells.

2007 ◽  
Vol 23 (3) ◽  
pp. 428-434 ◽  
Author(s):  
Irina Strizh ◽  
Alexei Joutchkov ◽  
Nikolay Tverdokhlebov ◽  
Sergey Golitsyn

2018 ◽  
Vol 25 (10) ◽  
pp. 2355-2372 ◽  
Author(s):  
Santiago G. Lago ◽  
Jakub Tomasik ◽  
Geertje F. van Rees ◽  
Jordan M. Ramsey ◽  
Frieder Haenisch ◽  
...  

Author(s):  
Ann E. Cowan ◽  
Ion I. Moraru ◽  
James C. Schaff ◽  
Boris M. Slepchenko ◽  
Leslie M. Loew

2021 ◽  
Vol 61 (1) ◽  
pp. 723-743
Author(s):  
Timothy R. Baffi ◽  
Ksenya Cohen-Katsenelson ◽  
Alexandra C. Newton

Whereas protein kinases have been successfully targeted for a variety of diseases, protein phosphatases remain an underutilized therapeutic target, in part because of incomplete characterization of their effects on signaling networks. The pleckstrin homology domain leucine-rich repeat protein phosphatase (PHLPP) is a relatively new player in the cell signaling field, and new roles in controlling the balance among cell survival, proliferation, and apoptosis are being increasingly identified. Originally characterized for its tumor-suppressive function in deactivating the prosurvival kinase Akt, PHLPP may have an opposing role in promoting survival, as recent evidence suggests. Additionally, identification of the transcription factor STAT1 as a substrate unveils a role for PHLPP as a critical mediator of transcriptional programs in cancer and the inflammatory response. This review summarizes the current knowledge of PHLPP as both a tumor suppressor and an oncogene and highlights emerging functions in regulating gene expression and the immune system. Understanding the context-dependent functions of PHLPP is essential for appropriate therapeutic intervention.


Physiology ◽  
2010 ◽  
Vol 25 (2) ◽  
pp. 72-84 ◽  
Author(s):  
Marie E. Burns ◽  
Edward N. Pugh

Phototransduction in retinal rods is one of the most extensively studied G-protein signaling systems. In recent years, our understanding of the biochemical steps that regulate the deactivation of the rod's response to light has greatly improved. Here, we summarize recent advances and highlight some of the remaining puzzles in this model signaling system.


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