The metalloprotease ADAM12 regulates the effector function of human Th17 cells

11Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.

Abstract

A key modulator of immune homeostasis, TGFβ has an important role in the differentiation of regulatory T cells (Tregs) and IL-17-secreting T cells (Th17). How TGFβ regulates these functionally opposing T cell subsets is not well understood. We determined that an ADAM family metalloprotease called ADAM12 is specifically and highly expressed in both Tregs and CCR6+ Th17 cells. ADAM12 is induced in vitro upon differentiation of naïve T cells to Th17 cells or IL-17-secreting Tregs. Remarkably, silencing ADAM12 expression in CCR6+ memory T cells enhances the production of Th17 cytokines, similar to suppressing TGFâ signaling. Further, ADAM12 knockdown in naïve human T cells polarized towards Th17/Treg cells, or ectopically expressing RORC, greatly enhances IL-17-secreting cell differentiation, more potently then inhibiting TGFβ signals. Together, our findings reveal a novel regulatory role for ADAM12 in Th17 cell differentiation or function and may have implications in regulating their aberrant responses during immune pathologies. © 2013 Zhou et al.

Cite

CITATION STYLE

APA

Zhou, A. X., El Hed, A., Mercer, F., Kozhaya, L., & Unutmaz, D. (2013). The metalloprotease ADAM12 regulates the effector function of human Th17 cells. PLoS ONE, 8(11). https://doi.org/10.1371/journal.pone.0081146

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free