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Coogan, A. B.

Publications and source records attributed to Coogan, A. B..

2 recordsLinked to original sources

Designer DX-tile DNAns hydrogels

Pure deoxyribonucleic acid (DNA) hydrogels synthesized via the hybridization of multi-arm DNA tiles are uniquely programmable and functionalizable biomaterials suitable for applications ranging from biosensing to cell-free protein production and soft tissue engineering. However, the full potential of the design flexibility and functionalization offered by DNA molecules has not yet been leveraged for pure DNA hydrogels, thereby limiting their range of mechanical properties and reducing their versatility and broader use. In this study, we introduce multi-arm double-crossover (DX)-tile motifs, often used in DNA nanoparticle design, to enable greater control over the hydrogels mechanical properties and facilitate functionalization. Specifically, we demonstrate that modifying structural design parameters, such as the arm geometry, length, valency, and linker design, allows fine control of the elastic modulus and viscoelastic properties of the hydrogels. We also show that functionalization can be performed without compromising the hydrogels physical properties and exhibit enhanced mechanical strength and tunable properties, compared to simple duplex-based DNA hydrogels. Furthermore, these DNA hydrogels demonstrated printability and scalability, which pave the way towards the development of novel formulations and bioinks for the rational design of soft tissue engineering scaffolds and broaden the use of DNA hydrogels for other biomedical applications.

bioengineering↗

Damage signals preferentially activate killer CD8+/- regulatory T cells to protect injured tissue

Self-antigens that are obscure to immune cells under homeostasis, are exposed following tissue damage and can trigger autoimmunity. Our previous work showed that conventional type 1 dendritic cells (cDC1s) mediate immunoregulation after traumatic skeletal muscle injury. Here, we found that, immune responses to injury in cDC1-depleted mice (Batf3-/-) mirror those of autoimmune mice (Aire-/-). Mechanistically, we determined that cDC1s prime killer regulatory T cells (CD8+/-Ly49+Tregs) which express Ly49 inhibitory receptors and HELIOS. These killer-like Tregs are clonally diverse and carry T cell receptors associated with self-reactivity and response to hydrophobicity. cDC1 or CD8 deletion promoted CD62L+CCR7+ naive T cell retention and B cell recruitment to injured muscle. These naive T cells, which are implicated in autoimmunity, strongly correlate with B cell abundance in the muscle and are selectively pruned by CD8+/-Ly49+ Tregs. Furthermore, clinically used materials that promote wound healing enrich CD8+/-Ly49+ Treg function whereas those that are associated with pathology promote naive T cell and B cell accumulation. We hypothesize that CD8+/-Ly49+ Tregs maintain self-tolerance after tissue damage and avert autoimmunity by eliminating naive T cells and preventing pathogenic B cell activation.

immunology↗