11 research outputs found
Fluctuations in active membranes
Active contributions to fluctuations are a direct consequence of metabolic
energy consumption in living cells. Such metabolic processes continuously
create active forces, which deform the membrane to control motility,
proliferation as well as homeostasis. Membrane fluctuations contain therefore
valuable information on the nature of active forces, but classical analysis of
membrane fluctuations has been primarily centered on purely thermal driving.
This chapter provides an overview of relevant experimental and theoretical
approaches to measure, analyze and model active membrane fluctuations. In the
focus of the discussion remains the intrinsic problem that the sole fluctuation
analysis may not be sufficient to separate active from thermal contributions,
since the presence of activity may modify membrane mechanical properties
themselves. By combining independent measurements of spontaneous fluctuations
and mechanical response, it is possible to directly quantify time and
energy-scales of the active contributions, allowing for a refinement of current
theoretical descriptions of active membranes.Comment: 38 pages, 9 figures, book chapte
Contribuição dos fatores de risco psicossociais para o transtorno de déficit de atenção/hiperatividade
Knockdown of ezrin suppresses the migration and angiogenesis of human umbilical vein endothelial cells in vitro
Interaction of bride of sevenless membrane-bound ligand and the sevenless tyrosine-kinase receptor
Blood, Sphingosine-1-Phosphate and Lymphocyte Migration Dynamics in the Spleen
The spleen, the largest secondary lymphoid organ, has long been known to play important roles in immunity against blood-borne invaders. Yet how cells migrate within the spleen to ensure fast and effective responses is only now coming to light. Chemokines and oxysterols guide lymphocytes from sites of release at terminal arterioles into the lymphocyte-rich white pulp. Sphingosine-1-phosphate (S1P) and S1P-receptor-1 (S1PR1) promote lymphocyte egress from white to red pulp and back to circulation. Intravital two-photon microscopy has shown that marginal zone (MZ) B cells that are enriched between white and red pulps undergo continual oscillatory migration between the MZ and follicles, ferrying antigens. Cycles of G-protein-coupled receptor kinase-2 (GRK2) mediated S1PR1 desensitization and resensitization underlie this remarkable behavior. The findings discussed in this review have implications for understanding how splenic antibody and T-cell responses are mounted, how the immunosuppressant drug FTY720 (fingolimod) affects the spleen, and how cell shuttling behaviors contribute to immunity
Blood, sphingosine-1-phosphate and lymphocyte migration dynamics in the spleen.
The spleen, the largest secondary lymphoid organ, has long been known to play important roles in immunity against blood-borne invaders. Yet how cells migrate within the spleen to ensure fast and effective responses is only now coming to light. Chemokines and oxysterols guide lymphocytes from sites of release at terminal arterioles into the lymphocyte-rich white pulp. Sphingosine-1-phosphate (S1P) and S1P-receptor-1 (S1PR1) promote lymphocyte egress from white to red pulp and back to circulation. Intravital two-photon microscopy has shown that marginal zone (MZ) B cells that are enriched between white and red pulps undergo continual oscillatory migration between the MZ and follicles, ferrying antigens. Cycles of G-protein-coupled receptor kinase-2 (GRK2) mediated S1PR1 desensitization and resensitization underlie this remarkable behavior. The findings discussed in this review have implications for understanding how splenic antibody and T-cell responses are mounted, how the immunosuppressant drug FTY720 (fingolimod) affects the spleen, and how cell shuttling behaviors contribute to immunity