| Literature DB >> 25301940 |
Sara Pijuan-Galitó1, Christoffer Tamm1, Cecilia Annerén2.
Abstract
We have previously demonstrated that the Src family kinase Yes, the Yes-associated protein (YAP) and TEA domain TEAD2 transcription factor pathway are activated by leukemia inhibitory factor (LIF) and contribute to mouse embryonic stem (mES) cell maintenance of pluripotency and self-renewal. In addition, we have shown that fetal bovine serum (FBS) induces Yes auto-phosphorylation and activation. In the present study we confirm that serum also activates TEAD-dependent transcription in a time- and dose-dependent manner and we identify Inter-α-inhibitor (IαI) as a component in serum capable of activating the Yes/YAP/TEAD pathway by inducing Yes auto-phosphorylation, YAP nuclear localization and TEAD-dependent transcription. The cleaved heavy chain 2 (HC2) sub-component of IαI, is demonstrated to be responsible for this effect. Moreover, IαI is also shown to efficiently increase expression of TEAD-downstream target genes including well-known stem cell factors Nanog and Oct 3/4. IαI is not produced by the ES cells per se but is added to the cells via the cell culture medium containing serum or serum-derived components such as bovine serum albumin (BSA). In conclusion, we describe a novel function of IαI in activating key pluripotency pathways associated with ES cell maintenance and self-renewal.Entities:
Keywords: Cell Culture; Cell Signaling; Embryonic Stem Cell; Extracellular Matrix; Inter-α-inhibitor; TEAD; Transfection; YAP; Yes
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Year: 2014 PMID: 25301940 PMCID: PMC4246103 DOI: 10.1074/jbc.M114.580076
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157