Activin E is a transforming growth factor β ligand that signals specifically through activin receptor-like kinase 7

被引:1
|
作者
Vestal, Kylie A. [1 ]
Kattamuri, Chandramohan [1 ]
Koyiloth, Muhasin [1 ]
Ongaro, Luisina [2 ]
Howard, James A. [3 ]
Deaton, Aimee M. [4 ]
Ticau, Simina [4 ]
Dubey, Aditi [4 ]
Bernard, Daniel J. [2 ]
Thompson, Thomas B. [1 ]
机构
[1] Univ Cincinnati, Dept Mol & Cellular Biosci, Cincinnati, OH 45267 USA
[2] McGill Univ, Ctr Res Reprod & Dev, Dept Pharmacol & Therapeut, Montreal, PQ, Canada
[3] Univ Cincinnati, Dept Pharmacol & Syst Physiol, Cincinnati, OH 45267 USA
[4] Alnylam Pharmaceut, Cambridge, MA USA
关键词
ADIPOSE-TISSUE; CDNA CLONING; EXPRESSION; FOLLISTATIN; ALK7; SUBUNITS; BINDING; DIFFERENTIATION; ADENOCARCINOMA; HETERODIMERS;
D O I
10.1042/BCJ20230404
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Activins are one of the three distinct subclasses within the greater Transforming growth factor 0 (TGF0) 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.
引用
收藏
页码:547 / 564
页数:18
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