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Top Voted Preprints
Q1 2024
ISSN 2817-8831
Candidate Preprints
Q1 2024
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A programmable arthritis-specific receptor for guided articular cartilage regenerative medicine

A programmable arthritis-specific receptor for guided articular cartilage regenerative medicine

Bonnie L. Walton, Rebecca Shattuck-Brandt, Catherine A. Hamann, Victoria W. Tung, Juan M. Colazo, David D. Brand, Karen A. Hasty, Craig L. Duvall, Jonathan M. Brunger

A synthetic receptor platform was developed to target cell therapies for osteoarthritis (OA) to damaged cartilage. Type II collagen-specific synNotch receptors enabled engineered mesenchymal stromal cells (MSCs) to activate only in response to cartilage degeneration, expressing therapeutic genes, reducing inflammation, and promoting cartilage repair, demonstrating targeted OA treatment potential.

Q1 2024
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Differential Responses of Dynamic and Entropic Aging Factors to Longevity Interventions

Differential Responses of Dynamic and Entropic Aging Factors to Longevity Interventions

Kristina Perevoshchikova, Peter O. Fedichev

Aging in species like mice and humans shows exponential mortality rate acceleration. By analyzing DNA methylation (DNAm) in aging mice, researchers identified an aging signature with exponential age dependency, reflecting the Gompertz law. This signature aligns with aging clocks and responds to interventions like caloric restriction. Additionally, a linear DNAm signature indicates global demethylation. Single-cell DNAm data reveal this signature captures the exponential expansion of the state space volume in aging organisms, indicating linearly increasing configuration entropy, likely an irreversible process unaffected by interventions.

Q1 2024
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Rejuvenation of aged oocyte through exposure to young follicular microenvironment

Rejuvenation of aged oocyte through exposure to young follicular microenvironment

HaiYang Wang, Zhongwei Huang, Yaelim Lee, XinJie Song, Xingyu Shen, Chang Shu, Lik Hang Wu, Leroy Sivappiragasam Pakkiri, Poh Leong Lim, Xi Zhang, Chester Lee Drum, Jin Zhu, Rong Li

Reproductive aging causes fertility decline due to decreased oocyte quality. Researchers created chimeric follicles by transplanting oocytes into different follicular environments. Young oocytes in aged follicles showed reduced maturation, while aged oocytes in young follicles improved significantly. The young environment enhanced oocyte interaction with somatic cells, improved mitochondrial function, and meiotic chromosome segregation, suggesting potential follicular somatic cell-based therapies for age-related infertility.

Q1 2024
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