Česká Genetická Banka

JEM: 29. 7. 2013

JEM: CD28-inducible transcription factor DEC1 is required for efficient autoreactive CD4⁺ T cell response

"During the initial hours after activation, CD4⁺ T cells experience profound changes in gene expression. Co-stimulation via the CD28 receptor is required for efficient activation of naive T cells. However, the transcriptional consequences of CD28 co-stimulation are not completely understood. We performed expression microarray analysis to elucidate the effects of CD28 signals on the transcriptome of activated T cells. We show that the transcription factor DEC1 is highly induced in a CD28-dependent manner upon T cell activation, is involved in essential CD4⁺ effector T cell functions, and participates in the transcriptional regulation of several T cell activation pathways, including a large group of CD28-regulated genes. Antigen-specific, DEC1-deficient CD4⁺ T cells have cell-intrinsic defects in survival and proliferation. Furthermore, we found that DEC1 is required for the development of experimental autoimmune encephalomyelitis because of its critical role in the production of the proinflammatory cytokines GM-CSF, IFN-γ, and IL-2. Thus, we identify DEC1 as a critical transcriptional mediator in the activation of naive CD4⁺ T cells that is required for the development of a T cell–mediated autoimmune disease."

http://jem.rupress.org/content/210/8/1603.abstract

 

JEM: BRCA1 interacts with Nrf2 to regulate antioxidant signaling and cell survival

"Oxidative stress plays an important role in cancer development and treatment. Recent data implicate the tumor suppressor BRCA1 in regulating oxidative stress, but the molecular mechanism and the impact in BRCA1-associated tumorigenesis remain unclear. Here, we show that BRCA1 regulates Nrf2-dependent antioxidant signaling by physically interacting with Nrf2 and promoting its stability and activation. BRCA1-deficient mouse primary mammary epithelial cells show low expression of Nrf2-regulated antioxidant enzymes and accumulate reactive oxygen species (ROS) that impair survival in vivo. Increased Nrf2 activation rescues survival and ROS levels in BRCA1-null cells. Interestingly, 53BP1 inactivation, which has been shown to alleviate several defects associated with BRCA1 loss, rescues survival of BRCA1-null cells without restoring ROS levels. We demonstrate that estrogen treatment partially restores Nrf2 levels in the absence of BRCA1. Our data suggest that Nrf2-regulated antioxidant response plays a crucial role in controlling survival downstream of BRCA1 loss. The ability of estrogen to induce Nrf2 posits an involvement of an estrogen-Nrf2 connection in BRCA1 tumor suppression. Lastly, BRCA1-mutated tumors retain a defective antioxidant response that increases the sensitivity to oxidative stress. In conclusion, the role of BRCA1 in regulating Nrf2 activity suggests important implications for both the etiology and treatment of BRCA1-related cancers."

http://jem.rupress.org/content/210/8/1529.abstract

 

JEM: CD4+ T helper cells use CD154–CD40 interactions to counteract T reg cell– mediated suppression of CD8+ T cell responses to influenza

"CD4⁺ T cells promote CD8⁺ T cell priming by licensing dendritic cells (DCs) via CD40–CD154 interactions. However, the initial requirement for CD40 signaling may be replaced by the direct activation of DCs by pathogen-derived signals. Nevertheless, CD40–CD154 interactions are often required for optimal CD8⁺ T cell responses to pathogens for unknown reasons. Here we show that CD40 signaling is required to prevent the premature contraction of the influenza-specific CD8⁺ T cell response. CD40 is required on DCs but not on B cells or T cells, whereas CD154 is required on CD4⁺ T cells but not CD8⁺ T cells, NKT cells, or DCs. Paradoxically, even though CD154-expressing CD4⁺ T cells are required for robust CD8⁺ T cell responses, primary CD8⁺ T cell responses are apparently normal in the absence of CD4⁺ T cells. We resolved this paradox by showing that the interaction of CD40-bearing DCs with CD154-expressing CD4⁺ T cells precludes regulatory T cell (T reg cell)–mediated suppression and prevents premature contraction of the influenza-specific CD8⁺ T cell response. Thus, CD4⁺ T helper cells are not required for robust CD8⁺ T cell responses to influenza when T reg cells are absent."

http://jem.rupress.org/content/210/8/1591.abstract