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Woellner-Santos, D.

Publications and source records attributed to Woellner-Santos, D..

2 recordsLinked to original sources

CD4+ T cell-intrinsic T-bet sustains protective CNS immunity and parasite control during Toxoplasma gondii infection

The transcription factor T-bet is widely regarded as the master regulator of type 1 immunity and is considered essential for host resistance to intracellular pathogens. Previous studies have demonstrated that global T-bet deficiency causes profound susceptibility to intracellular pathogens, including T. gondii. However, the specific cell-intrinsic requirement for T-bet within CD4+ T cells has remained unclear because T-bet regulates multiple innate and adaptive immune populations that contribute to protective immunity. Therefore, to define the cell-intrinsic role of T-bet in CD4+ T cells during infection, we utilized mice with conditional T-bet deletion in CD4+ T cells (CD4-Tbx21-/-) and found that CD4+ T cell-intrinsic T-bet was largely dispensable for acute parasite control and the generation of antigen-experienced IFN-{gamma}-producing CD4+ T cells. However, although CD4-Tbx21-/- mice controlled acute infection, our data reveal that as infection transitions to the chronic stage, CD4+ T cell-intrinsic T-bet becomes critical for sustaining cerebral immunity, promoting IFN-{gamma}-dependent antimicrobial responses, and maintaining parasite control within the brain. Collectively, our findings establish that CD4+ T cell-intrinsic T-bet is required for sustaining protective CD4+ T cell responses within the infected CNS and promotes IFN-{gamma}-dependent antiparasitic mechanisms that restrict tachyzoite persistence during the transition to chronic infection.

immunology↗

The human developing cerebral cortex is characterized by an increased de novo expression of lncRNAs in excitatory neurons

BackgroundOutstanding human cognitive abilities are computed in the cerebral cortex, a mammalian-specific brain region and the place of massive biological innovation. Long noncoding RNAs (lncRNAs) have emerged as gene regulatory elements with higher evolutionary turnover than mRNAs. The many lncRNAs identified in neural tissues make them candidates for molecular sources of cerebral cortex evolution and disease. Here, we characterized the genomic and cellular shifts that occurred during the evolution of the lncRNA repertoire expressed in the developing cerebral cortex of humans and explored their role in the evolution of this brain region. ResultsUsing systems biology approaches and comparative transcriptomics, we comprehensively annotated the cortical transcriptomes of humans, macaques, mice, and chickens and classified human cortical lncRNAs into evolutionary groups as a function of their predicted minimal ages. LncRNA evolutionary groups showed differences in expression levels, splicing efficiencies, transposable element contents, genomic distributions, and transcription factor binding to their promoters. Furthermore, older lncRNAs showed preferential expression in germinative zones, outer radial glial cells, and cortical inhibitory neurons. In comparison, younger lncRNAs showed preferential expression in cortical excitatory neurons, belonged to human-specific gene coexpression modules, and were dysregulated in autism spectrum disorder. ConclusionsThese results suggest a shift in the roles of cortical lncRNAs over evolution, highlighting the antique lncRNAs as a source of molecular evolution of conserved developmental programs; conversely, the de novo expression of primate and human-specific lncRNAs are sources of molecular evolution and dysfunction of cortical excitatory neurons.

evolutionary biology↗