0000000000978026

AUTHOR

Eva Tolosa

showing 2 related works from this author

Exploring the MHC-peptide matrix of central tolerance in the human thymus

2013

Ever since it was discovered that central tolerance to self is imposed on developing T cells in the thymus through their interaction with self-peptide major histocompatibility complexes on thymic antigen-presenting cells, immunologists have speculated about the nature of these peptides, particularly in humans. Here, to shed light on the so-far unknown human thymic peptide repertoire, we analyse peptides eluted from isolated thymic dendritic cells, dendritic cell-depleted antigen-presenting cells and whole thymus. Bioinformatic analysis of the 842 identified natural major histocompatibility complex I and II ligands reveals significant cross-talk between major histocompatibility complex-class…

MaleAdolescentT-LymphocytesEnolaseAntigen-Presenting CellsGeneral Physics and AstronomyAutoimmunity610 Medicine & healthPeptideVimentinThymus GlandMatrix (biology)LigandsMajor histocompatibility complexAutoantigensGeneral Biochemistry Genetics and Molecular BiologyMajor Histocompatibility ComplexEpitopesIn vivoHumansMyeloid Cells610 Medicine & healthchemistry.chemical_classificationAntigen PresentationMultidisciplinarybiologyRepertoireHistocompatibility Antigens Class IHistocompatibility Antigens Class IIInfantDendritic CellsGeneral ChemistryCD11c AntigenCell biologychemistryChild PreschoolCentral ToleranceImmunologybiology.proteinFemaleCentral tolerancePeptidesNature Communications
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Alternatively spliced transcripts of the thymus-specific protease PRSS16 are differentially expressed in human thymus.

2004

The putative serine protease PRSS16 is abundantly expressed in the thymic cortex and the gene is encoded within the HLA I complex. Although its function is not yet defined, the very restricted expression points to a role in T-cell development in the thymus. In this study, we show that the PRSS16 mRNA is alternatively spliced to generate at least five transcripts. Apart from the full-length sequence, we found two other isoforms with all putative active site residues of the serine protease, suggesting that those variants may also be functional. Semi-quantitative analysis of the splice variants in different tissue samples revealed a strong correlation between the specific formation of alternat…

Gene isoformAdultMaleThymomamedicine.medical_treatmentImmunologyMolecular Sequence DataMorphogenesisThymus GlandGene Expression Regulation EnzymologicMyasthenia GravisGeneticsmedicineMorphogenesisHumansGeneGenetics (clinical)Serine proteaseMessenger RNAProteasebiologyBase SequenceSerine EndopeptidasesMiddle Agedmedicine.diseaseMolecular biologyMyasthenia gravisIsoenzymesAlternative Splicingbiology.proteinFemaleGenes and immunity
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