Regulatory T cell adaptation in the intestine and skin.

The intestine and skin are distinct microenvironments with unique physiological functions and are continually exposed to diverse environmental challenges. Host adaptation at these sites is an active process that involves interaction between immune cells and tissue cells. Regulatory T cells (Treg cells) play a pivotal role in enforcing homeostasis at barrier surfaces, illustrated by the development of intestinal and skin inflammation in diseases caused by primary deficiency in Treg cells. Treg cells at barrier sites are phenotypically distinct from their lymphoid-organ counterparts, and these 'tissue' signatures often reflect their tissue-adapted function. We discuss current understanding of Treg cell adaptation in the intestine and skin, including unique phenotypes, functions and metabolic demands, and how increased knowledge of Treg cells at barrier sites might guide precision medicine therapies.

Single-Cell Transcriptomics of Regulatory T Cells Reveals Trajectories of Tissue Adaptation.

Non-lymphoid tissues (NLTs) harbor a pool of adaptive immune cells with largely unexplored phenotype and development. We used single-cell RNA-seq to characterize 35,000 CD4+ regulatory (Treg) and memory (Tmem) T cells in mouse skin and colon, their respective draining lymph nodes (LNs) and spleen. In these tissues, we identified Treg cell subpopulations with distinct degrees of NLT phenotype. Subpopulation pseudotime ordering and gene kinetics were consistent in recruitment to skin and colon, yet the initial NLT-priming in LNs and the final stages of NLT functional adaptation reflected tissue-specific differences. Predicted kinetics were recapitulated using an in vivo melanoma-induction model, validating key regulators and receptors. Finally, we profiled human blood and NLT Treg and Tmem cells, and identified cross-mammalian conserved tissue signatures. In summary, we describe the relationship between Treg cell heterogeneity and recruitment to NLTs through the combined use of computational prediction and in vivo validation.

The impact of micropollutants on native algae and cyanobacteria communities in ecological filters during drinking water treatment.

An attractive alternative for drinking water production is ecological filtration. Previous studies have reported high removal levels of pharmaceutical and personal care products (PPCPs) by this technology. Algae and cyanobacteria play an important role in the biological activity of ecological filters. The aim of this study was to characterize and identify the community of algae and cyanobacteria in relation to its composition, density and biovolume from 22 ecological filters that received spikings of 2 µg L-1 PPCPs. For algae and cyanobacteria species, triplicate samples were collected before and 96 h after each spiking from the interface between the top sand layer of the ecological filters and the supernatant water. Results show that Chlorophyceae and Cyanobacteria were present in high numbers of taxa and abundance. The specie Lepocinclis cf. ovum (Euglenophyceae) had the highest percentage occurrence/abundance and frequency into the filters, indicating a possible tolerance by Lepocinclis cf. ovum to the concentration of selected PPCPs. Although the concentration of PPCPs did not affect the treated water quality, they did affect the algae and cyanobacteria community. No differences were detected between filters that received a single PPCP and filters that received a mixture of the six compounds. Also, changes in the composition of algae and cyanobacteria communities were observed before and 96 h after the spikings.

Foxp3+ T reg cells control psoriasiform inflammation by restraining an IFN-I-driven CD8+ T cell response.

Psoriasis is a complex inflammatory skin disease affecting ∼3% of the population worldwide. Although type I interferons (IFN-I) are thought to be involved in its pathogenesis, the details of this relationship remain elusive. Here we show that in a murine model of imiquimod-driven psoriatic skin inflammation, Foxp3+ regulatory T cells (T reg cells) control inflammation severity by restraining IFN-I. Depletion of T reg cells induces IFN-I and IFN-stimulated gene expression, and leads to accumulation of CD8+ T cells in lesional skin. Mononuclear phagocytes (MNPs) were the source of IFN-I, and their depletion reversed the effect of T reg cell depletion. Blockade of IFN-I signaling abolished CD8+ T cell infiltration and excess inflammation in the skin of T reg cell-depleted mice. Depletion of CD8+ T cells attenuated pathology, confirming their role as critical effector cells downstream of IFN-I. Our results describe an unexpected role for T reg cells in restraint of an MNP-IFN-I-driven CD8+ T cell response during psoriasiform skin inflammation. These findings highlight a pathway with potential relevance for the treatment of early-stage disease.

Macrophage function in tissue repair and remodeling requires IL-4 or IL-13 with apoptotic cells.

Tissue repair is a subset of a broad repertoire of interleukin-4 (IL-4)- and IL-13-dependent host responses during helminth infection. Here we show that IL-4 or IL-13 alone was not sufficient, but IL-4 or IL-13 together with apoptotic cells induced the tissue repair program in macrophages. Genetic ablation of sensors of apoptotic cells impaired the proliferation of tissue-resident macrophages and the induction of anti-inflammatory and tissue repair genes in the lungs after helminth infection or in the gut after induction of colitis. By contrast, the recognition of apoptotic cells was dispensable for cytokine-dependent induction of pattern recognition receptor, cell adhesion, or chemotaxis genes in macrophages. Detection of apoptotic cells can therefore spatially compartmentalize or prevent premature or ectopic activity of pleiotropic, soluble cytokines such as IL-4 or IL-13.

Checklist das Cryptophyceae do estado de São Paulo, Brasil / Checklist of Cryptophyceae from São Paulo State, Brazil

Usando como base de informações a monografia sobre o grupo publicada pelo projeto Flora Ficológica do Estado de São Paulo (Programa BIOTA), o acervo depositado no Herbário Científico do Estado de São Paulo "Maria Eneyda P. Kauffmann Fidalgo" (SP), a Lista de Espécies da Flora do Brasil e artigos científicos, dissertações e teses (com descrições e ilustrações) temos: nove gêneros e 39 espécies de criptoficeas, sendo 16 espécies exclusivas para o Estado de São Paulo, todas registradas em ambientes de água doce. A carência de especialistas no Estado de São Paulo e no Brasil, além de problemas de estratégia amostral, necessidade de uso da microscopia eletrônica e ausência de estudos de biologia molecular, são fatores que devem ter subestimado o conhecimento taxonômico de Cryptophyceae no Estado.

Based on the information provided by the monograph on the group published by the project Phycology Flora of São Paulo (BIOTA), the collection deposited in the Scientific Herbarium "Mary P. Eneyda Kauffmann Fidalgo " of the State of São Paulo, the List of Endangered Species of the Flora of Brazil and scientific papers, dissertations and theses (with descriptions and illustrations), there are nine genera and 39 species of cryptophytes, 16 of which are unique species to the State of São Paulo, all recorded in freshwater environments. The lack of specialists in the State of São Paulo and Brazil as well as problems in the sampling strategy, the necessary use of electronic microscopy and the absence of molecular biology studies are factors that must have underestimated the taxonomic knowledge of Cryptophyceae in the state.