Activin E is a transforming growth factor β ligand that signals specifically through activin receptor-like kinase 7
Open accessPublished version of a preprint
Abstract
Activins are one of the three distinct subclasses within the greater Transforming growth factor β (TGFβ) superfamily. First discovered for their critical roles in reproductive biology, activins have since been shown to alter cellular differentiation and proliferation. At present, members of the activin subclass include activin A (ActA), ActB, ActC, ActE, and the more distant members myostatin and GDF11. While the biological roles and signaling mechanisms of most activins class members have been well-studied, the signaling potential of ActE has remained largely unknown. Here, we characterized the signaling capacity of homodimeric ActE. Molecular modeling of the ligand:receptor complexes showed that ActC and ActE shared high similarity in both the type I and type II receptor binding epitopes. ActE signaled specifically through ALK7, utilized the canonical activin type II receptors, ActRIIA and ActRIIB, and was resistant to the extracellular antagonists follistatin and WFIKKN. In mature murine adipocytes, ActE invoked a SMAD2/3 response via ALK7, like ActC. Collectively, our results establish ActE as a specific signaling ligand which activates the type I receptor, ALK7.
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- Authors
- Vestal, K. A., Kattamuri, C., Koyiloth, M., Ongaro, L., Howard, J. A., Deaton, A. M., Ticau, S., Dubey, A., Bernard, D. J., & Thompson, T. B.
- Affiliations
- University of Cincinnati (US)
- McGill University (CA)
- 4Alnylam Pharmaceuticals, Cambridge, MA, U.S.A.
- Alnylam Pharmaceuticals (United States) (US)
- Corresponding author
- Thompson, Thomas B.
- ORCID
- Venue
- Biochemical Journal
- Publisher
- Portland Press Ltd.
- Published
- 2024-04-10
- Volume
- 481
- Issue
- 7
- Pages
- 547-564
- ISSN
- 0264-6021 (ISSN-L)
- 1470-8728
- PMC
- PMC11088876
- OpenAlex
- W4393225974
- Cited by
- 10
- References
- 7
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 4
- FWCI
- 1.36
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Biochemical Journal (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion, cc-by-nc-nd)
- Funders
- Foundation for the National Institutes of Health (R35GM134923-04)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Keywords
- ALK7, TGF-beta superfamily, activin signaling, ligand-receptor binding, Smad2/3 signaling, adipocytes, follistatin, type II receptor
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