miR-106b is a novel target to promote muscle regeneration and restore satellite stem cell function in injured Duchenne dystrophic muscle

Satellite cells (SCs), muscle stem cells, display functional heterogeneity, and dramatic changes linked to their regenerative capabilities are associated with muscle-wasting diseases. SC behavior is related to endogenous expression of the myogenic transcription factor MYF5 and the propensity to ente...

Full description

Saved in:
Bibliographic Details
Main Authors: Lara Rodriguez-Outeiriño (Author), Francisco Hernandez-Torres (Author), Felicitas Ramirez de Acuña (Author), Alberto Rastrojo (Author), Carlota Creus (Author), Alejandra Carvajal (Author), Luis Salmeron (Author), Marisol Montolio (Author), Patricia Soblechero-Martin (Author), Virginia Arechavala-Gomeza (Author), Diego Franco (Author), Amelia Eva Aranega (Author)
Format: Book
Published: Elsevier, 2022-09-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_e03b3b8ff3f848cdb79d4103a8b2c6f8
042 |a dc 
100 1 0 |a Lara Rodriguez-Outeiriño  |e author 
700 1 0 |a Francisco Hernandez-Torres  |e author 
700 1 0 |a Felicitas Ramirez de Acuña  |e author 
700 1 0 |a Alberto Rastrojo  |e author 
700 1 0 |a Carlota Creus  |e author 
700 1 0 |a Alejandra Carvajal  |e author 
700 1 0 |a Luis Salmeron  |e author 
700 1 0 |a Marisol Montolio  |e author 
700 1 0 |a Patricia Soblechero-Martin  |e author 
700 1 0 |a Virginia Arechavala-Gomeza  |e author 
700 1 0 |a Diego Franco  |e author 
700 1 0 |a Amelia Eva Aranega  |e author 
245 0 0 |a miR-106b is a novel target to promote muscle regeneration and restore satellite stem cell function in injured Duchenne dystrophic muscle 
260 |b Elsevier,   |c 2022-09-01T00:00:00Z. 
500 |a 2162-2531 
500 |a 10.1016/j.omtn.2022.08.025 
520 |a Satellite cells (SCs), muscle stem cells, display functional heterogeneity, and dramatic changes linked to their regenerative capabilities are associated with muscle-wasting diseases. SC behavior is related to endogenous expression of the myogenic transcription factor MYF5 and the propensity to enter into the cell cycle. Here, we report a role for miR-106b reinforcing MYF5 inhibition and blocking cell proliferation in a subset of highly quiescent SC population. miR-106b down-regulation occurs during SC activation and is required for proper muscle repair. In addition, miR-106b is increased in dystrophic mice, and intramuscular injection of antimiR in injured mdx mice enhances muscle regeneration promoting transcriptional changes involved in skeletal muscle differentiation. miR-106b inhibition promotes the engraftment of human muscle stem cells. Furthermore, miR-106b is also high in human dystrophic muscle stem cells and its inhibition improves intrinsic proliferative defects and increases their myogenic potential. This study demonstrates that miR-106b is an important modulator of SC quiescence, and that miR-106b may be a new target to develop therapeutic strategies to promote muscle regeneration improving the regenerative capabilities of injured dystrophic muscle. 
546 |a EN 
690 |a MT: Non-coding RNAs 
690 |a satellite cell 
690 |a miR-106b 
690 |a stemness 
690 |a muscle regeneration 
690 |a muscular dystrophy 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Molecular Therapy: Nucleic Acids, Vol 29, Iss , Pp 769-786 (2022) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S2162253122002244 
787 0 |n https://doaj.org/toc/2162-2531 
856 4 1 |u https://doaj.org/article/e03b3b8ff3f848cdb79d4103a8b2c6f8  |z Connect to this object online.