Daniel Vosoughi

ORCID: 0000-0003-4799-9715
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Transplantation: Methods and Outcomes
  • Renal Transplantation Outcomes and Treatments
  • Extracellular vesicles in disease
  • Mechanical Circulatory Support Devices
  • SARS-CoV-2 and COVID-19 Research
  • 3D Printing in Biomedical Research
  • Immune Cell Function and Interaction
  • Systemic Sclerosis and Related Diseases
  • RNA Interference and Gene Delivery
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • Congenital heart defects research
  • Advanced Biosensing Techniques and Applications
  • Autoimmune Bullous Skin Diseases
  • Respiratory viral infections research
  • MicroRNA in disease regulation
  • Tissue Engineering and Regenerative Medicine
  • Immunotherapy and Immune Responses
  • Cardiovascular Disease and Adiposity
  • Inhalation and Respiratory Drug Delivery
  • Receptor Mechanisms and Signaling
  • Systemic Lupus Erythematosus Research
  • Orthopedic Infections and Treatments

University Health Network
2021-2025

University of Toronto
2021-2025

Toronto General Hospital
2023-2025

Toronto General Hospital Research Institute
2024

Ionizable lipid nanoparticles (LNPs) pivotal to the success of COVID-19 mRNA (messenger RNA) vaccines hold substantial promise for expanding landscape mRNA-based therapies. Nevertheless, risk delivery off-target tissues highlights necessity LNPs with enhanced tissue selectivity. The intricate nature biological systems and inadequate knowledge structure–activity relationships emphasize significance high-throughput methods produce chemically diverse libraries screening. Here, we introduce a...

10.1073/pnas.2309472120 article EN cc-by-nc-nd Proceedings of the National Academy of Sciences 2023-12-07

Despite tremendous progress in the development of mature heart-on-a-chip models, human cell-based models myocardial inflammation are lacking. Here, we bioengineered a vascularized with circulating immune cells to model severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-induced myocarditis. We observed hallmarks disease (COVID-19)-induced inflammation, as presence augmented secretion proinflammatory cytokines, triggered progressive impairment contractile function, and altered...

10.1126/sciadv.adk0164 article EN cc-by-nc Science Advances 2024-03-27

Abstract The fabrication of complex and stable vasculature in engineered cardiac tissues represents a significant hurdle towards building physiologically relevant models the heart. Here, we implemented 3D model vasculogenesis, incorporating endothelial cells (EC), stromal cells, human induced pluripotent stem cell (iPSC)-derived cardiomyocytes (CM) fibrin hydrogel. presence CMs disrupted vessel formation tissues, resulting upregulation activation markers altered extracellular vesicle (EV)...

10.1088/1758-5090/ad76d9 article EN cc-by Biofabrication 2024-09-03

Survival after lung transplantation (LTx) is hampered by uncontrolled inflammation and alloimmunity. Regulatory T-cells (Tregs) are being studied as a cellular therapy in solid organ transplantation. Whether these systemically administered Tregs can function at the appropriate location time an important concern. We hypothesised that vitro-expanded recipient-derived be delivered to donor lungs prior LTx via ex vivo perfusion (EVLP), maintaining their immunomodulatory ability.In rat model,...

10.1183/13993003.00798-2021 article EN European Respiratory Journal 2021-09-02

Cardiovascular disease continues to take more human lives than all cancer combined, prompting the need for improved research models and treatment options. Despite a significant progress in development of mature heart-on-a-chip fibrosis cardiomyopathies starting from induced pluripotent stem cells (iPSCs), cell-based myocardial inflammation are lacking. Here, we bioengineered vascularized system with circulating immune model SARS-CoV-2-induced acute myocarditis. Briefly, observed hallmarks...

10.1101/2023.08.09.552495 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2023-08-09

Abstract Survival after lung transplantation (LTx) is hampered by uncontrolled inflammation and alloimmunity. Regulatory T cells (Tregs) are being studied for post-implantation cell therapy in solid organ transplantation. Whether these systemically administered Tregs can function at the appropriate location time an important concern. We hypothesized that vitro expanded, recipient-derived be delivered to donor lungs prior LTx via ex vivo perfusion (EVLP), maintaining their immunomodulatory...

10.1101/2021.02.07.430098 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2021-02-07
Coming Soon ...