Transcytosis of IL-11 and Apical Redirection of gp130 Is Mediated by IL-11α Receptor
Author(s) -
Niloufar Monhasery,
Jens M. Moll,
Carly Cuman,
Manuel Franke,
Larissa Lamertz,
Rebecca Nitz,
Boris Görg,
Dieter Häussinger,
Juliane Lokau,
Doreen M. Floß,
Roland P. Piekorz,
Evdokia Dimitriadis,
Christoph Garbers,
Jürgen Scheller
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2016.06.062
Subject(s) - transcytosis , microbiology and biotechnology , glycoprotein 130 , receptor , extracellular , signal transduction , cytokine , biology , chemistry , immunology , biochemistry , stat3 , endocytosis
Interleukin (IL)-11 signaling is involved in various processes, including epithelial intestinal cell regeneration and embryo implantation. IL-11 signaling is initiated upon binding of IL-11 to IL-11R1 or IL-11R2, two IL-11α-receptor splice variants, and gp130. Here, we show that IL-11 signaling via IL-11R1/2:gp130 complexes occurs on both the apical and basolateral sides of polarized cells, whereas IL-6 signaling via IL-6R:gp130 complexes is restricted to the basolateral side. We show that basolaterally supplied IL-11 is transported and released to the apical extracellular space via transcytosis in an IL-11R1-dependent manner. By contrast, IL-6R and IL-11R2 do not promote transcytosis. In addition, we show that transcytosis of IL-11 is dependent on the intracellular domain of IL-11R1 and that synthetic transfer of the intracellular domain of IL-11R1 to IL-6R promotes transcytosis of IL-6. Our data define IL-11R as a cytokine receptor with transcytotic activity by which IL-11 and IL-6:soluble IL-6R complexes are transported across cellular barriers.
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