| Literature DB >> 33709070 |
Adam Ponedal1, Shengshuang Zhu2, Anthony J Sprangers3, Xiao-Qi Wang4, David C Yeo5, Daniel C S Lio5, Mengjia Zheng5, Matthew Capek6, Suguna P Narayan6, Brian Meckes7, Amy S Paller4, Chenjie Xu8, Chad A Mirkin9.
Abstract
Abnormal scarring is a consequence of dysregulation in the wound healing process, with limited options for effective and noninvasive therapies. Given the ability of spherical nucleic acids (SNAs) to penetrate skin and regulate gene expression within, we investigated whether gold-core SNAs (AuSNAs) and liposome-core SNAs (LSNAs) bearing antisense oligonucleotides targeting transforming growth factor beta 1 (TGF-β1) can function as a topical therapy for scarring. Importantly, both SNA constructs appreciably downregulated TGF-β1 protein expression in primary hypertrophic and keloid scar fibroblasts in vitro. In vivo, topically applied AuSNAs and LSNAs downregulated TGF-β1 protein expression levels and improved scar histology as determined by the scar elevation index. These data underscore the potential of SNAs as a localized, self-manageable treatment for skin-related diseases and disorders that are driven by increased gene expression.Entities:
Keywords: TGF-beta; gene regulation; nanomedicine; scar; spherical nucleic acid; topical
Year: 2020 PMID: 33709070 PMCID: PMC7946158 DOI: 10.1021/acsabm.0c00990
Source DB: PubMed Journal: ACS Appl Bio Mater ISSN: 2576-6422