A direct interaction between TGFβ activated kinase 1 and the TGFβ type II receptor: implications for TGFβ signalling and cardiac hypertrophy

Watkins, Sarah J., Jonker, Leon ORCID: https://orcid.org/0000-0001-5867-4663 and Arthur, Helen M. (2006) A direct interaction between TGFβ activated kinase 1 and the TGFβ type II receptor: implications for TGFβ signalling and cardiac hypertrophy. Cardiovascular Research, 69 (2). pp. 432-439.

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Abstract

Objective: Transforming growth factor beta (TGFβ)-activated kinase 1 (TAK1) is a MAP kinase kinase kinase involved in numerous signalling pathways and is strongly implicated in cardiac hypertrophy and heart failure. TGFβ is also associated with hypertension and heart disease, and evidence suggests that TGFβ1 and TAK1 act together in a cardiac stress signalling pathway. Canonical TGFβ signalling is mediated through Smad transcription factors, but TGFβ can also rapidly activate TAK1. The activation of the Smad cascade is well characterised, but little is known about how TAK1 is activated in response to TGFβ, and no direct link between any MAPK kinase pathway and the TGFβ receptors has yet been established. Since TAK1 is activated by TGFβ within 1 min in cardiomyocytes, we hypothesised there might be a direct interaction between TAK1 and one of the TGFβ receptors.

Methods: We used a combination of in vitro binding assays and co-immunoprecipitation (IP) experiments to investigate whether TAK1 interacted with the type I (ALK1 or ALK5) or type II (TBRII) TGFβ receptors. Interactions between endogenous proteins were tested using mouse myoblast and rat cardiomyocyte cells.

Results: Immunoprecipitation and in vitro binding assays show that TAK1 binds directly to TBRII. Precipitation of endogenous TAK1 protein in rat cardiomyocytes shows that, in addition to a direct association with TBRII, it also interacts indirectly with ALK5.

Conclusions: We describe a novel and specific interaction between TAK1 and TBRII which, for the first time, directly links TAK1 to the TGFβ signalling cascade and potentially explains how TGFβ signalling in cardiomyocytes mediates a hypertrophic response.

Item Type:	Article
Journal / Publication Title:	Cardiovascular Research
Publisher:	Oxford University Press
ISSN:	1755-3245
Departments:	Institute of Health > Medical Sciences
Depositing User:	Insight Administrator
Date Deposited:	21 Jan 2022 09:15
Last Modified:	11 Jan 2024 19:15
URI:	https://insight.cumbria.ac.uk/id/eprint/6343

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