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| Status |
Public on Jul 13, 2021 |
| Title |
Engineering skeletal muscle tissues with advanced maturity improves synapse formation with human induced pluripotent stem cell-derived motor neurons |
| Organism |
Gallus gallus |
| Experiment type |
Expression profiling by high throughput sequencing
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| Summary |
To develop effective cures for neuromuscular diseases, human-relevant in vitro models of neuromuscular tissues are critically needed to probe disease mechanisms on the cellular and molecular level. However, previous attempts to co-culture motor neurons and skeletal muscle have resulted in relatively immature neuromuscular junctions (NMJs). In this study, NMJs formed by human induced pluripotent stem cell (hiPSC)-derived motor neurons were improved by optimizing the maturity of the co-cultured muscle tissue. First, muscle tissues were engineered from the C2C12 mouse myoblast cell line, cryopreserved primary human myoblasts, and freshly isolated primary chick myoblasts on micromolded gelatin hydrogels. After three weeks, only chick muscle tissues remained stably adhered to hydrogels and exhibited progressive increases in myogenic index and stress generation, approaching values generated by native muscle tissue. After three weeks of co-culture with hiPSC-derived motor neurons, engineered chick muscle tissues formed NMJs with increasing co-localization of pre- and post-synaptic markers as well as increased frequency and magnitude of synaptic activity, surpassing structural and functional maturity of previous in vitro models. Engineered chick muscle tissues also demonstrated increased expression of genes related to sarcomere maturation and innervation over time, revealing new insights into the molecular pathways that likely contribute to enhanced NMJ formation. These approaches for engineering human-relevant neuromuscular tissues with relatively mature NMJs and interrogating their structure and function have many applications in neuromuscular disease modeling and drug development.
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| Overall design |
mRNA profiles of primary Gallus gallus muscle tissue cultures on gelatin-transglutaminase hydrogels after one (5 replicates) or three (3 replicates) weeks of differentiation. Myogenic cells were derived from E10 chick embryo thighs.
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| Contributor(s) |
Santoso JW, McCain ML |
| Citation(s) |
34286174 |
| |
| Submission date |
Apr 21, 2021 |
| Last update date |
Jul 28, 2021 |
| Contact name |
Megan Laura McCain |
| Organization name |
University of Southern California
|
| Department |
Biomedical Engineering
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| Lab |
Laboratory for Living Systems Engineering
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| Street address |
1042 Downey Way
|
| City |
Los Angeles |
| State/province |
California |
| ZIP/Postal code |
90089 |
| Country |
USA |
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| Platforms (1) |
| GPL26853 |
Illumina NovaSeq 6000 (Gallus gallus) |
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| Samples (8)
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| Relations |
| BioProject |
PRJNA723607 |
| SRA |
SRP315777 |
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