| Literature DB >> 27798620 |
Chen Xi Li1, Nilesh P Talele1, Stellar Boo1, Anne Koehler1, Ericka Knee-Walden1, Jenna L Balestrini2, Pam Speight3, Andras Kapus3, Boris Hinz1.
Abstract
Expansion on stiff culture substrates activates pro-fibrotic cell programs that are retained by mechanical memory. Here, we show that priming on physiologically soft silicone substrates suppresses fibrogenesis and desensitizes mesenchymal stem cells (MSCs) against subsequent mechanical activation in vitro and in vivo, and identify the microRNA miR-21 as a long-term memory keeper of the fibrogenic program in MSCs. During stiff priming, miR-21 levels were gradually increased by continued regulation through the acutely mechanosensitive myocardin-related transcription factor-A (MRTF-A/MLK-1) and remained high over 2 weeks after removal of the mechanical stimulus. Knocking down miR-21 once by the end of the stiff-priming period was sufficient to erase the mechanical memory and sensitize MSCs to subsequent exposure to soft substrates. Soft priming and erasing mechanical memory following cell culture expansion protects MSCs from fibrogenesis in the host wound environment and increases the chances for success of MSC therapy in tissue-repair applications.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27798620 DOI: 10.1038/nmat4780
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 43.841