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Biology subjects

Qiao, G. G.

Publications and source records attributed to Qiao, G. G..

2 recordsLinked to original sources

Engineering in vitro models of skeletal muscle with neuromuscular junctions using hierarchical micro-nano biomaterials: Cooperative effect of adhesion ligand nanoclustering and surface anisotropy

Robust development of in vitro mature skeletal muscle with functional neuromuscular junctions is an unmet challenge that must be addressed for advances in skeletal muscle tissue engineering and for the development of skeletal muscle tissue models for disease modelling and drug discovery. Herein, we developed hierarchical, anisotropic biomaterials that induced early maturation of more mature myotubes and the development of neuromuscular junctions (NMJs) during co-culture with motor neurons. We accomplished this by creating micro-nano biomaterial interfaces that presented nanoclusters of integrin-binding ligands to promote mechanotransduction on the surface of aligned electrospun microfibers. Controlling surface topography and nanoscale ligand clustering led to 1.5 to 2.5-fold increases in myoblast proliferation, myotube formation, elongation, and alignment; resulting in spontaneous twitching; and enhanced myotube-neuron connections, including increasing acetylcholine receptor clustering, neurite branching, and myotube contraction compared to control surfaces. These findings highlight the importance of tailoring adhesive peptide distribution and presentation for the in vitro development of NMJs and synaptic organization. This approach offers a valuable platform for fundamental research on muscle development and neuromuscular diseases, paving the way for improved skeletal muscle tissue engineering and drug screening strategies.

bioengineering↗

Changing the Fate of Dystrophin-Deficient Myoblasts via Hetero ligand Nanoclusters on Biomaterial Surface: Effects of Integrin-Syndecan or Dystroglycan Crosstalk

Engineering skeletal muscle tissue regeneration, particularly in dystrophin-deficient muscles is dependent on facilitating myogenesis and recovery of myotube structure and function, which can be challenging due to compromised cell-extracellular matrix (ECM) interactions. The current study explored the potential impact of enhancing dystrophin-associated protein complex and focal adhesion formation and the interaction with associated target receptors to improve cellular response in both normal and Duchenne muscular dystrophy (Dmd) mutant myoblasts. This was achieved by multivalent dual ligands functionalization of RAFT-synthesized copolymer with fibronectin- and laminin-derived adhesion peptides (RGD, AG73, and A2G80) and their clustering at the biointerface. Our findings demonstrated the synergistic effect of integrin-syndecan/dystroglycan engagement and their clustering on enhancing myoblast adhesion, proliferation, and differentiation, partially overcoming the deficits caused by loss of dystrophin. Furthermore, enhanced focal adhesion formation and elevated receptor localization, particularly dystroglycan, at the sarcolemma were associated with improved structural organization, mechanical stability, and neuromuscular connectivity of myotubes. These results suggest a novel insight into harnessing next-generation molecularly engineered biomaterials with robust interaction with cells mechanosensors for advancing skeletal muscle tissue engineering, offering potential applications in the regeneration of dystrophic muscle and the development of neuromuscular disease models for drug testing. O_FIG O_LINKSMALLFIG WIDTH=174 HEIGHT=200 SRC="FIGDIR/small/717576v1_ufig1.gif" ALT="Figure 1"> View larger version (55K): org.highwire.dtl.DTLVardef@16c6b87org.highwire.dtl.DTLVardef@107a84borg.highwire.dtl.DTLVardef@1b9e4ddorg.highwire.dtl.DTLVardef@160a9a7_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOGraphical Abstract/ToCC_FLOATNO Current work developed molecularly engineered biomaterial surfaces with nanoscale clustering of integrin-, syndecan-, and/or dystroglycan-binding peptides for skeletal muscle tissue regeneration. By controlling peptide distribution and type at the biointerface, cell adhesion, proliferation, and differentiation were modulated in dystrophin-deficient myoblasts. Accordingly, the results demonstrated significant improvement in myotube structural organization, mechanical stiffness, and their innervation in response to heteronanoclusters. C_FIG

bioengineering↗