Hobit and Blimp1 instruct a universal transcriptional program of tissue residency in lymphocytes
生物
医学教育
计算机科学
医学
作者
Laura K. Mackay,Martina Minnich,Natasja A. M. Kragten,Yang Liao,Benjamin Nota,Cyril Seillet,Ali Zaid,Kevin Man,Simon Preston,David Freestone,Asolina Braun,Erica Wynne-Jones,Felix M. Behr,Regina Stark,Daniel G. Pellicci,Dale I. Godfrey,Gabrielle T. Belz,Marc Pellegrini,Thomas Gebhardt,Meinrad Busslinger
出处
期刊:Science [American Association for the Advancement of Science (AAAS)] 日期:2016-04-21卷期号:352 (6284): 459-463被引量:924
Transcription factors define tissue T cells The immune system fights microbial invaders by maintaining multiple lines of defense. For instance, specialized memory T cells [resident memory T cells (T rms )] colonize portals of pathogen entry, such as the skin, lung, and gut, to quickly halt reinfections. Mackay et al. now report that in mice, T rms as well as other tissue-dwelling lymphocyte populations such as natural killer cells share a common transcriptional program driven by the related transcription factors Hobit and Blimp1. Tissue residency and retention of lymphocytes require expression of Hobit and Blimp1, which, among other functions, suppress genes that promote tissue exit. Science , this issue p. 459