The Metalloprotease ADAM12 Regulates the Effector Function of Human Th17 Cells
Author(s) -
Angela X. Zhou,
Aimee El Hed,
Frances Mercer,
Lina Kozhaya,
Derya Unutmaz
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0081146
Subject(s) - microbiology and biotechnology , rar related orphan receptor gamma , gene silencing , c c chemokine receptor type 6 , interleukin 17 , cellular differentiation , immune system , gene knockdown , effector , biology , t cell , cell culture , immunology , foxp3 , chemokine , gene , genetics , chemokine receptor , biochemistry
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 TGFβ 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.
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