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1.
Aging (Albany NY) ; 16(17): 12168-12190, 2024 Sep 09.
Artículo en Inglés | MEDLINE | ID: mdl-39264584

RESUMEN

Current rejuvenation strategies, which range from calorie restriction to in vivo partial reprogramming, only improve a few specific cellular processes. In addition, the molecular mechanisms underlying these approaches are largely unknown, which hinders the design of more holistic cellular rejuvenation strategies. To address this issue, we developed SINGULAR (Single-cell RNA-seq Investigation of Rejuvenation Agents and Longevity), a cell rejuvenation atlas that provides a unified system biology analysis of diverse rejuvenation strategies across multiple organs at single-cell resolution. In particular, we leverage network biology approaches to characterize and compare the effects of each strategy at the level of intracellular signaling, cell-cell communication, and transcriptional regulation. As a result, we identified master regulators orchestrating the rejuvenation response and propose that targeting a combination of them leads to a more holistic improvement of age-dysregulated cellular processes. Thus, the interactive database accompanying SINGULAR is expected to facilitate the future design of synthetic rejuvenation interventions.


Asunto(s)
Rejuvenecimiento , Rejuvenecimiento/fisiología , Animales , Humanos , Redes Reguladoras de Genes , Análisis de la Célula Individual , Biología de Sistemas , Regulación de la Expresión Génica , Transducción de Señal , Longevidad/genética , Longevidad/fisiología , Comunicación Celular
2.
Aging Cell ; 22(5): e13799, 2023 05.
Artículo en Inglés | MEDLINE | ID: mdl-36929664

RESUMEN

The quantification of the biological age of cells yields great promises for accelerating the discovery of novel rejuvenation strategies. Here, we present MultiTIMER, the first multi-tissue aging clock that measures the biological, rather than chronological, age of cells from their transcriptional profiles by evaluating key cellular processes. We applied MultiTIMER to more than 70,000 transcriptional profiles and demonstrate that it accurately responds to cellular stressors and known interventions while informing about dysregulated cellular functions.


Asunto(s)
Envejecimiento , ARN , ARN/genética
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