Programmable chronogenetic gene circuits for self-regulated circadian delivery of biologic drugs
Year: 2025
Type: article
Abstract: Cells of the body rely on the circadian clock to orchestrate daily changes in physiology that impact both homeostatic and pathological conditions, such as the inflammatory autoimmune disease rheumatoid arthritis (RA). In RA, high levels of proinflammatory cytokines peak early in the morning hours, reflected by daily changes in joint stiffness. Chronotherapy (or circadian medicine) seeks to delivery drugs at optimal times to maximize their efficacy. However, chronotherapy remains a largely unexplored approach for disease modifying, antirheumatic treatment, particularly for cell-based therapies. In this study, we developed autonomous chronogenetic gene circuits that produce the biologic drug interleukin-1 receptor antagonist (IL-1Ra) with desired phase and amplitude. We compared expression of IL-1Ra from circuits that contained different circadian promoter elements (E'-boxes, D-boxes, or RREs) and their ability to respond to inflammatory challenges in murine pre-differentiated induced pluripotent stem cells (PDiPSC) or engineered cartilage pellets. We confirmed that each circuit reliably peaked at a distinct circadian time over multiple days. Engineered cells generated significant amounts of IL-1Ra on a circadian basis, which protected them from circadian dysregulation and inflammatory damage. These programmable chronogenetic circuits have the potential to align with an individual's circadian rhythm for optimized, self-regulated daily drug delivery.
Source: Journal of Controlled Release
Language: English
Subfield: Endocrine and Autonomic Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $4,440
Awards: The Role of Fat in Osteoarthritis, G2848147184, Obesity, Biomechanics, and Inflammation in Osteoarthritis, Synthetic Chronogenetic Gene Circuits for Circadian Cell Therapies, Deconstructing Cartilage Mechanotransduction by Piezo Channels, Viscoelastic Properties of Normal and OA Chondrons, G9000074605, G9000217772, G9000308115, Washington University Rheumatic Diseases Research Resource-based Center, The Role of Fat in Osteoarthritis, Genetically-engineered stem cells for self-regulating arthritis therapy, RESOURCE BASED CENTER FOR MUSCULOSKELETAL BIOLOGY AND MEDICINE
OpenAlex ID: W4411402756
