BAMBI is a novel HIF1-dependent modulator of TGFβ-mediated disruption of cell polarity during hypoxia
Author(s) -
Irina Raykhel,
Fazeh Moafi,
Satu-Marja Myllymäki,
Patricia G. Greciano,
Karl S. Matlin,
José V. Moyano,
Aki Manninen,
Johanna Myllyharju
Publication year - 2018
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.210906
Subject(s) - biology , hypoxia (environmental) , polarity (international relations) , microbiology and biotechnology , cell , biophysics , biochemistry , oxygen , chemistry , organic chemistry
Hypoxia and loss of cell polarity are common features of malignant carcinomas. Hypoxia-inducible factor 1 (HIF1) is the major regulator of cellular hypoxia response through activation of ∼300 genes. Increased HIF1 signaling is known to be associated with epithelial-mesenchymal transformation. Here we report that hypoxia disrupts polarized epithelial morphogenesis of MDCK cells in HIF1α-dependent manner by modulating the transforming growth factor β (TGFβ) signaling pathway. Analysis of potential HIF1 targets in the TGFβ pathway identified the bone morphogenetic protein and activin membrane-bound inhibitor (BAMBI), a transmembrane glycoprotein related to the type I receptors of the TGFβ family, whose expression was essentially lost in HIF1-depleted cells. Similar to HIF1-deficient cells, BAMBI-depleted cells failed to efficiently activate TGFβ signaling and retained epithelial polarity in hypoxia. Taken together, we show that hypoxic conditions promote TGFβ signaling in HIF1-dependent manner and BAMBI is identified in this pathway as a novel HIF1 regulated gene that contributes to hypoxia-induced loss of epithelial polarity.
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