Stress-recovery dynamics reveal a separatrix in transcriptomic landscapes across organs and aging
Abstract
Aging is often characterized statically as molecular profiles, but how these profiles may affect the capacity of systems to respond to the external environment remains elusive. We perturbed young and aged mice via transient sleep deprivation and profiled transcriptomes from six organs immediately after stress and following recovery. The same perturbation induced complex temporal dynamics for each gene in an organ- and age- dependent manner. A shape parameter distinguished genes that recovered toward control expression from those that continued to drift away during recovery. Transcriptomic vector fields were inferred from these transitions using neural ordinary differential equations, revealing distinct stability regimes across organ systems. Interestingly, that of testis from the young mice contained a separatrix bounding the region within which perturbed state can return toward control. These findings establish transient perturbation and recovery as a framework for probing age-dependent transcriptomic stability and identifying boundaries that determine whether a perturbed system can return.
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Research summary
The paper claims that transient stress and recovery dynamics reveal a separatrix in transcriptomic landscapes that defines the boundary between systems capable of returning to homeostasis and those that drift away, providing a dynamic framework for assessing age-dependent physiological resilience. This is relevant because it moves beyond static molecular aging markers to characterize the functional stability and recovery capacity of organ systems, offering a mechanistic basis for understanding how aging erodes the body's ability to maintain homeostasis.
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