Activin E is a TGFβ ligand that signals specifically through activin receptor-like kinase 7.


Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
25 Sep 2023
Historique:
pubmed: 9 10 2023
medline: 9 10 2023
entrez: 9 10 2023
Statut: epublish

Résumé

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, similar to ActC. Collectively, our results establish ActE as an ALK7 ligand, thereby providing a link between genetic and

Identifiants

pubmed: 37808681
doi: 10.1101/2023.09.25.559288
pmc: PMC10557571
pii:
doi:

Types de publication

Preprint

Langues

eng

Auteurs

Kylie A Vestal (KA)

Department of Molecular and Cellular Biosciences, University of Cincinnati, Cincinnati, OH 45267, USA.

Chandramohan Kattamuri (C)

Department of Molecular and Cellular Biosciences, University of Cincinnati, Cincinnati, OH 45267, USA.

Muhasin Koyiloth (M)

Department of Molecular and Cellular Biosciences, University of Cincinnati, Cincinnati, OH 45267, USA.

Luisina Ongaro (L)

Department of Pharmacology and Therapeutics, Centre for Research in Reproduction and Development, McGill University, Montreal, Quebec, Canada.

James A Howard (JA)

Department of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH 45267, USA.

Aimee Deaton (A)

Alnylam Pharmaceuticals, Cambridge, MA, USA.

Simina Ticau (S)

Alnylam Pharmaceuticals, Cambridge, MA, USA.

Aditi Dubey (A)

Alnylam Pharmaceuticals, Cambridge, MA, USA.

Daniel J Bernard (DJ)

Department of Pharmacology and Therapeutics, Centre for Research in Reproduction and Development, McGill University, Montreal, Quebec, Canada.

Thomas B Thompson (TB)

Department of Molecular and Cellular Biosciences, University of Cincinnati, Cincinnati, OH 45267, USA.

Classifications MeSH