Lipid rafts in neuronal signaling and function

2002 ◽  
Vol 25 (8) ◽  
pp. 412-417 ◽  
Author(s):  
Brian A Tsui-Pierchala ◽  
Mario Encinas ◽  
Jeffrey Milbrandt ◽  
Eugene M Johnson
2005 ◽  
Vol 72 ◽  
pp. 119-127 ◽  
Author(s):  
Tamara Golub ◽  
Caroni Pico

The interactions of cells with their environment involve regulated actin-based motility at defined positions along the cell surface. Sphingolipid- and cholesterol-dependent microdomains (rafts) order proteins at biological membranes, and have been implicated in most signalling processes at the cell surface. Many membrane-bound components that regulate actin cytoskeleton dynamics and cell-surface motility associate with PtdIns(4,5)P2-rich lipid rafts. Although raft integrity is not required for substrate-directed cell spreading, or to initiate signalling for motility, it is a prerequisite for sustained and organized motility. Plasmalemmal rafts redistribute rapidly in response to signals, triggering motility. This process involves the removal of rafts from sites that are not interacting with the substrate, apparently through endocytosis, and a local accumulation at sites of integrin-mediated substrate interactions. PtdIns(4,5)P2-rich lipid rafts can assemble into patches in a process depending on PtdIns(4,5)P2, Cdc42 (cell-division control 42), N-WASP (neural Wiskott-Aldrich syndrome protein) and actin cytoskeleton dynamics. The raft patches are sites of signal-induced actin assembly, and their accumulation locally promotes sustained motility. The patches capture microtubules, which promote patch clustering through PKA (protein kinase A), to steer motility. Raft accumulation at the cell surface, and its coupling to motility are influenced greatly by the expression of intrinsic raft-associated components that associate with the cytosolic leaflet of lipid rafts. Among them, GAP43 (growth-associated protein 43)-like proteins interact with PtdIns(4,5)P2 in a Ca2+/calmodulin and PKC (protein kinase C)-regulated manner, and function as intrinsic determinants of motility and anatomical plasticity. Plasmalemmal PtdIns(4,5)P2-rich raft assemblies thus provide powerful organizational principles for tight spatial and temporal control of signalling in motility.


2020 ◽  
Vol 13 ◽  
Author(s):  
Michihiro Igarashi ◽  
Atsuko Honda ◽  
Asami Kawasaki ◽  
Motohiro Nozumi

2003 ◽  
Vol 15 (3) ◽  
pp. 255-260 ◽  
Author(s):  
Paola Pizzo ◽  
Antonella Viola

Author(s):  
Jonathan D. Nickels ◽  
Jacob Hogg ◽  
Destini Cordner ◽  
John Katsaras

2005 ◽  
Vol 17 (6) ◽  
pp. 749-758 ◽  
Author(s):  
Shizue Tani-ichi ◽  
Koji Maruyama ◽  
Nami Kondo ◽  
Masakazu Nagafuku ◽  
Kazuya Kabayama ◽  
...  

2011 ◽  
Vol 7 ◽  
pp. 1744-8069-7-77 ◽  
Author(s):  
Aswini Gnanasekaran ◽  
Mayya Sundukova ◽  
Arn MJM van den Maagdenberg ◽  
Elsa Fabbretti ◽  
Andrea Nistri

Blood ◽  
2002 ◽  
Vol 99 (3) ◽  
pp. 978-984 ◽  
Author(s):  
Jaime Millán ◽  
Marı́a C. Montoya ◽  
David Sancho ◽  
Francisco Sánchez-Madrid ◽  
Miguel A. Alonso

Abstract Polarized migrating T cells possess 2 poles, the uropod protrusion at the rear and the leading edge at the front, with specific protein composition and function. The influenza virus hemagglutinin (HA) is a prototypical molecule that uses lipid rafts for biosynthetic transport to the apical surface in polarized epithelial Madin-Darby canine kidney (MDCK) cells. In this study, HA was used as a tool to investigate the role of lipid rafts in vectorial protein traffic in polarized T lymphocytes. Results show that newly synthesized HA becomes selectively targeted to the uropod subdomain in polarized T lymphoblasts. HA incorporates into rafts soon after biosynthesis, suggesting that delivery of HA to the uropod occurs through a pathway of transport reminiscent of that used for its specific targeting to the apical surface. HA and the adhesion molecules, intercellular adhesion molecule 3 (ICAM-3), CD44, and CD43, 3 endogenous uropod markers, were detected in surface rafts of T lymphoblasts. Cholesterol, a major component of lipid rafts, was predominantly located in the uropod. Disruption of lipid raft integrity by cholesterol sequestration produced unclustering of ICAM-3 and the loss of uropodia and severely impaired processes that require a polarized phenotype such as intercellular aggregation and cell migration. Collectively, these results indicate that lipid rafts constitute a route for selective targeting of proteins to the uropod and that the rafts are essential for the generation, maintenance, and functionality of T-cell anteroposterior polarity.


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