| Literature DB >> 28903040 |
Zeyu Chen1, Erietta Stelekati1, Makoto Kurachi1, Sixiang Yu2, Zhangying Cai3, Sasikanth Manne1, Omar Khan1, Xiaolu Yang2, E John Wherry4.
Abstract
MicroRNAs play an important role in T cell responses. However, how microRNAs regulate CD8 T cell memory remains poorly defined. Here, we found that miR-150 negatively regulates CD8 T cell memory in vivo. Genetic deletion of miR-150 disrupted the balance between memory precursor and terminal effector CD8 T cells following acute viral infection. Moreover, miR-150-deficient memory CD8 T cells were more protective upon rechallenge. A key circuit whereby miR-150 repressed memory CD8 T cell development through the transcription factor c-Myb was identified. Without miR-150, c-Myb was upregulated and anti-apoptotic targets of c-Myb, such as Bcl-2 and Bcl-xL, were also increased, suggesting a miR-150-c-Myb survival circuit during memory CD8 T cell development. Indeed, overexpression of non-repressible c-Myb rescued the memory CD8 T cell defects caused by overexpression of miR-150. Overall, these results identify a key role for miR-150 in memory CD8 T cells through a c-Myb-controlled enhanced survival circuit.Entities:
Keywords: Bcl-2; Bcl-xl; CD8 T cell; T cell differentiation; T cell memory; c-Myb; immune memory; miR-150; viral infection
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Year: 2017 PMID: 28903040 PMCID: PMC5611819 DOI: 10.1016/j.celrep.2017.08.060
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423