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A miR-23~27~24 regulon that controls follicular helper T cell differentiation

ABSTRACT: Follicular helper T (Tfh) cells are essential for generating protective humoral immunity. To date, microRNAs (miRNAs) have emerged as important players in regulating Tfh cell biology. Here, we show that loss of miR-23~27~24 clusters in T cells resulted in elevated Tfh cell frequencies upon different immune challenges whereas overexpression of this miRNA family led to reduced Tfh cell responses. Mechanistically, miR-23~27~24 clusters coordinately control Tfh cells through targeting a network of genes that are crucial for Tfh cell biology. Among them, thymocyte selection-associated HMG-box protein (TOX) was identified as a central transcription regulator in Tfh cell development. TOX is highly up-regulated in both mouse and human Tfh cells in a BCL6-dependent manner. In turn, TOX promotes the expression of multiple molecules that play critical roles in Tfh cell differentiation and function. Collectively, our study on miR-23~27~24-mediated control of humoral immunity reveals a TOX-driven regulatory circuit in orchestrating Tfh cell responses.

ORGANISM(S): Mus musculus

PROVIDER: GSE118698 | GEO | 2019/08/21

REPOSITORIES: GEO

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miR-23~27~24 clusters control effector T cell differentiation and function

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2015-12-11 | GSE75909 | GEO

miR-23~27~24 clusters control effector T cell differentiation and function

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A miR-23~27~24 regulon that controls follicular helper T cell differentiation

Project description:A miR-23~27~24 regulon that controls follicular helper T cell differentiation

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MicroRNAs 24 and 27 suppress allergic inflammation and target a network of regulators of T helper-2 cell-associated cytokine production

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