نتایج جستجو برای: cd95l

تعداد نتایج: 278  

Journal: :Journal of immunology 2009
Laura Strauss Christoph Bergmann Theresa L Whiteside

Mechanisms utilized by human regulatory T cells (Treg) for elimination of effector cells may vary. We investigated the possibility that the mechanism of Treg suppression depends on Fas/FasL-mediated apoptosis of responder cells (RC). CD4(+)CD25(high)Foxp3(+) Treg and autologous CD4(+)CD25(-) and CD8(+)CD25(-) subsets of RC were isolated from blood of 25 cancer patients and 15 normal controls an...

Journal: :Journal of immunology 2002
Loredana Frasca Cristiano Scottà Giovanna Lombardi Enza Piccolella

T cell suppression exerted by regulatory T cells represents a well-established phenomenon, but the mechanisms involved are still a matter of debate. Recent data suggest that anergic T cells can suppress responder T cell activation by inhibiting Ag presentation by dendritic cells (DC). In this study, we focused our attention on the mechanisms that regulate the susceptibility of DC to suppressive...

Journal: :Science signaling 2014
Stefan M Kallenberger Joël Beaudouin Juliane Claus Carmen Fischer Peter K Sorger Stefan Legewie Roland Eils

Apoptosis in response to the ligand CD95L (also known as Fas ligand) is initiated by caspase-8, which is activated by dimerization and self-cleavage at death-inducing signaling complexes (DISCs). Previous work indicated that the degree of substrate cleavage by caspase-8 determines whether a cell dies or survives in response to a death stimulus. To determine how a death ligand stimulus is effect...

Journal: :Neuro-oncology 2011
Günter Eisele Patrick Roth Kathy Hasenbach Steffen Aulwurm Fabian Wolpert Ghazaleh Tabatabai Wolfgang Wick Michael Weller

Death receptor targeting has emerged as one of the promising novel approaches of cancer therapy. The activation of one such prototypic death receptor, CD95 (Fas/APO-1), has remained controversial because CD95 agonistic molecules have exhibited either too strong toxicity or too little activity. The natural CD95 ligand (CD95L) is a cytokine, which needs to trimerize to mediate a cell death signal...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Nadine Khadra Laurence Bresson-Bepoldin Aubin Penna Benjamin Chaigne-Delalande Bruno Ségui Thierry Levade Anne-Marie Vacher Josy Reiffers Thomas Ducret Jean-François Moreau Michael D Cahalan Pierre Vacher Patrick Legembre

The death receptor CD95 plays a pivotal role in immune surveillance and immune tolerance. Binding of CD95L to CD95 leads to recruitment of the adaptor protein Fas-associated death domain protein (FADD), which in turn aggregates caspase-8 and caspase-10. Efficient formation of the CD95/FADD/caspase complex, known as the death-inducing signaling complex (DISC), culminates in the induction of apop...

2016
Anna Raimbault Cecile Pierre-Eugene Alexandra Rouquette Celine Deudon Lise Willems Nicolas Chapuis Stephanie Mathis Claudia Kunz Harald Fricke Olivier Kosmider Valerie Bardet Michaela Fontenay

CD95, a member of the death receptor family initiates a caspase-dependent apoptosis, when activated by its ligand CD95L, thought to negatively regulate erythrocyte production in the bone marrow. We have previously shown that CD95 is overexpressed in two thirds of patients with a lower risk myelodysplastic syndrome (MDS) and that resistance to erythropoiesis-stimulating agents (ESA) is linked to...

Journal: :Journal of autoimmunity 2000
C A White K B Nguyen M P Pender

The role and fate of B cells in the central nervous system (CNS) in experimental autoimmune encephalomyelitis (EAE) are unknown. Using enzyme-linked immunospot assays we now show that B cells reactive to myelin basic protein (MBP) accumulate in the CNS of Lewis rats with acute EAE induced by immunization with MBP and adjuvants. We also report that B cells are eliminated from the CNS by apoptosi...

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