A synthetic chronogenetic gene circuit for programmed circadian drug delivery

Circadian medicine, the delivery of therapeutic interventions based on an individual's daily rhythms, has shown improved efficacy and reduced side-effects for various treatments. Rheumatoid arthritis and other inflammatory diseases are characterized by diurnal changes in cytokines, leading to inflammatory flares, with peak disease activity in the early morning. Using a combination of synthetic biology and tissue engineering, we developed circadian-based gene circuits, termed "chronogenetics", that express a prescribed transgene downstream of the core clock gene promoter, Period2 (Per2). Gene circuits were transduced into induced pluripotent stem cells that were tissue-engineered into cartilage constructs. Our anti-inflammatory chronogenetic constructs produced therapeutic concentrations of interleukin-1 receptor antagonist in vitro. Once implanted in vivo, the constructs expressed circadian rhythms and entrained to daily light cycles, producing daily increases in biologic drug at the peak of Per2 expression. This approach represents the development of a cell-based chronogenetic therapy for various applications in circadian medicine.

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Publication Details

Journal
Nature Communications
Published
2025-02-07
DOI
https://doi.org/10.1038/s41467-025-56584-5
Citations
11
Primary Topic
Circadian rhythm and melatonin
Type
article
Field-Weighted Citation Impact
10.06

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article

A synthetic chronogenetic gene circuit for programmed circadian drug delivery

Anna R. Damato, Erik D. Herzog, Daniel Palmer, Maria F. Gonzalez-Aponte et al.
11 citations
Nature Communications
Circadian rhythm and melatonin
10.06
article

A synthetic chronogenetic gene circuit for programmed circadian drug delivery

Anna R. Damato, Erik D. Herzog, Daniel Palmer, Maria F. Gonzalez-Aponte, Qing‐Jun Meng, Kristin L. Lenz, Lara Pferdehirt, Farshid Guilak
article en
11 citations

Abstract

Circadian medicine, the delivery of therapeutic interventions based on an individual's daily rhythms, has shown improved efficacy and reduced side-effects for various treatments. Rheumatoid arthritis and other inflammatory diseases are characterized by diurnal changes in cytokines, leading to inflammatory flares, with peak disease activity in the early morning. Using a combination of synthetic biology and tissue engineering, we developed circadian-based gene circuits, termed "chronogenetics", that express a prescribed transgene downstream of the core clock gene promoter, Period2 (Per2). Gene circuits were transduced into induced pluripotent stem cells that were tissue-engineered into cartilage constructs. Our anti-inflammatory chronogenetic constructs produced therapeutic concentrations of interleukin-1 receptor antagonist in vitro. Once implanted in vivo, the constructs expressed circadian rhythms and entrained to daily light cycles, producing daily increases in biologic drug at the peak of Per2 expression. This approach represents the development of a cell-based chronogenetic therapy for various applications in circadian medicine.

Nature CommunicationsVol. 16(1)
Washington University in St. Louis (US), Wellcome Centre for Cell-Matrix Research (GB), University of Manchester (GB), Shriners Hospitals for Children - St. Louis (US)
Shriners Hospitals for Children, Versus Arthritis, National Institutes of Health, Center of Regenerative Medicine, Washington University in St. Louis, Medical Research Council
Good health and well-being
Openalex Percentile: Top 2%
Circadian rhythm and melatonin
10.06
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