Bioprocessing technology of muscle stem cells: Implications for cultured meat

X Guan, J Zhou, G Du, J Chen - Trends in Biotechnology, 2022 - cell.com
Muscle stem cells (MuSCs) are essential for the growth, maintenance, and repair of skeletal
muscle. In the emerging area of cultured meat, meat products are manufactured with MuSCs …

The hallmarks of myotonic dystrophy type 1 muscle dysfunction

LL Ozimski, M Sabater‐Arcis, A Bargiela… - Biological …, 2021 - Wiley Online Library
ABSTRACT Myotonic dystrophy type 1 (DM1) is the most prevalent form of muscular
dystrophy in adults and yet there are currently no treatment options. Although this disease …

Immortalized bovine satellite cells for cultured meat applications

AJ Stout, MJ Arnett, K Chai, T Guo, L Liao… - ACS synthetic …, 2023 - ACS Publications
For cultured meat to succeed at scale, muscle cells from food-relevant species must be
expanded in vitro in a rapid and reliable manner to produce millions of metric tons of …

[HTML][HTML] Peptide-conjugated oligonucleotides evoke long-lasting myotonic dystrophy correction in patient-derived cells and mice

AF Klein, MA Varela, L Arandel… - The Journal of …, 2019 - Am Soc Clin Investig
Antisense oligonucleotides (ASOs) targeting pathologic RNAs have shown promising
therapeutic corrections for many genetic diseases including myotonic dystrophy (DM1) …

Precise small-molecule cleavage of an r (CUG) repeat expansion in a myotonic dystrophy mouse model

AJ Angelbello, SG Rzuczek… - Proceedings of the …, 2019 - National Acad Sciences
Myotonic dystrophy type 1 (DM1) is an incurable neuromuscular disorder caused by an
expanded CTG repeat that is transcribed into r (CUG) exp. The RNA repeat expansion …

Transcriptome-Wide Studies of RNA-Targeted Small Molecules Provide a Simple and Selective r(CUG)exp Degrader in Myotonic Dystrophy

QMR Gibaut, JA Bush, Y Tong, JT Baisden… - ACS Central …, 2023 - ACS Publications
Myotonic dystrophy type 1 (DM1) is caused by a highly structured RNA repeat expansion, r
(CUG) exp, harbored in the 3′ untranslated region (3′ UTR) of dystrophia myotonica …

Study of an RNA-focused DNA-encoded library informs design of a degrader of ar (CUG) repeat expansion

QMR Gibaut, Y Akahori, JA Bush… - Journal of the …, 2022 - ACS Publications
A solid-phase DNA-encoded library (DEL) was studied for binding the RNA repeat
expansion r (CUG) exp, the causative agent of the most common form of adult-onset …

[HTML][HTML] RNA-binding proteins in the post-transcriptional control of skeletal muscle development, regeneration and disease

DL Shi, R Grifone - Frontiers in Cell and Developmental Biology, 2021 - frontiersin.org
Embryonic myogenesis is a temporally and spatially regulated process that generates
skeletal muscle of the trunk and limbs. During this process, mononucleated myoblasts …

Reversal of RNA toxicity in myotonic dystrophy via a decoy RNA-binding protein with high affinity for expanded CUG repeats

L Arandel, M Matloka, AF Klein, F Rau… - Nature Biomedical …, 2022 - nature.com
Abstract Myotonic dystrophy type 1 (DM1) is an RNA-dominant disease whose pathogenesis
stems from the functional loss of muscleblind-like RNA-binding proteins (RBPs), which …

[HTML][HTML] Molecular therapies for myotonic dystrophy type 1: from small drugs to gene editing

M Izzo, J Battistini, C Provenzano, F Martelli… - International journal of …, 2022 - mdpi.com
Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy affecting many
different body tissues, predominantly skeletal and cardiac muscles and the central nervous …