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Tatiana M. Moreno

First author of a healthy-aging cohort study showing that human autophagy flux is remodeled with age in a sex- and cell type-specific way, uncoupled from autophagy-gene transcription, and responsive to a mild exercise intervention

Graduate School of Biomedical Sciences, Sanford Burnham Prebys Medical Discovery Institute

Kumsta Lab, Sanford Burnham Prebys Medical Discovery Institute (La Jolla, California, USA) ↗

Tatiana M. Moreno is the first author of MOR2026, a study from Caroline Kumsta's group at Sanford Burnham Prebys that measured autophagy flux directly across subject-matched human cell types (skin fibroblasts, induced neurons and blood immune cells) from a healthy aging cohort. The study found that autophagy-gene transcription rises with age but autophagic flux itself does not move in lockstep with it: flux fell in male fibroblasts, held steady in female fibroblasts, rose in female induced neurons, and grew more variable in blood cells, becoming associated with reduced physical function only after age 70. A small pilot exercise intervention lowered blood-cell autophagy flux in older adults in parallel with improved physical function, suggesting the measurement is responsive to a real intervention, not just a fixed trait.

Milestones in the Atlas

A selection, not a full bibliography: only papers that meet the Atlas inclusion criteria.

YearEvidenceStudy
2026 H Autophagy Flux Is Remodeled Sex- and Cell Type-Specifically During Human Aging, and Is Linked to Reduced Physical Function in Older Adults MOR2026 First author of a healthy-aging cohort study showing human autophagy flux is sex- and cell type-specific, linked to physical function after age 70, and responsive to 12 weeks of mild exercise.

Co-authors in the Atlas

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