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10.1073/pnas.1612024114

http://scihub22266oqcxt.onion/10.1073/pnas.1612024114
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C5187732!5187732!27930306
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suck abstract from ncbi


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pmid27930306      Proc+Natl+Acad+Sci+U+S+A 2016 ; 113 (51): E8286-95
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  • miR-17?92 family clusters control iNKT cell ontogenesis via modulation of TGF-? signaling #MMPMID27930306
  • Fedeli M; Riba M; Garcia Manteiga JM; Tian L; Viganò V; Rossetti G; Pagani M; Xiao C; Liston A; Stupka E; Cittaro D; Abrignani S; Provero P; Dellabona P; Casorati G
  • Proc Natl Acad Sci U S A 2016[Dec]; 113 (51): E8286-95 PMID27930306show ga
  • CD1d-restricted invariant natural killer T (iNKT) cells are innate-like T lymphocytes that play fundamental roles in cancer, autoimmunity, and infections. iNKT cells acquire effector functions already in the thymus, because of a distinct developmentally regulated genetic program that is critically controlled by miRNAs. Our study unveils the unexpected requirement for miRNA-dependent fine-tuning of TGF-? signaling in the control of iNKT cell development and functional differentiation. The targeting of a lineage-specific cytokine signaling by miRNA represents a previously unknown level of developmental regulation in the thymus. Furthermore, our study provides a comprehensive atlas of miRNA-regulated molecular pathways involved in iNKT cell ontogenesis, and highlights molecular pathways targeted by defined miRNAs that are predicted to be involved in the development and maturation of CD1d-restricted iNKT cells.
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