| Literature DB >> 35084170 |
Sayani Chattopadhyay1, Leandro B C Teixeira2, Laura L Kiessling1,3,4, Jonathan F McAnulty5, Ronald T Raines1,3,4.
Abstract
Transforming growth factor-β (TGF-β) plays important roles in wound healing. The activity of TGF-β is initiated upon the binding of the growth factor to the extracellular domains of its receptors. We sought to facilitate the activation by clustering these extracellular domains. To do so, we used a known peptide that binds to TGF-β receptors without diminishing their affinity for TGF-β. We conjugated this peptide to a collagen-mimetic peptide that can anneal to the damaged collagen in a wound bed. We find that the conjugate enhances collagen deposition and wound closure in mice in a manner consistent with the clustering of TGF-β receptors. This strategy provides a means to upregulate the TGF-β signaling pathway without adding exogenous TGF-β and could inspire means to treat severe wounds.Entities:
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Year: 2022 PMID: 35084170 PMCID: PMC8857044 DOI: 10.1021/acschembio.1c00745
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100