Temporal AI model predicts drivers of cell state trajectories across human aging

Javier Gómez Ortega(Gladstone Institutes), Rangarajan D. Nadadur(Gladstone Institutes), Akira Kunitomi(Gladstone Institutes), Steven Kothen-Hill(Nvidia (United States)), Julian U G Wagner(Goethe University Frankfurt), Sarp Kurtoglu(Gladstone Institutes), Bumjoon Kim(Gladstone Institutes), Madigan M. Reid(Gladstone Institutes), Thomas X. Lu(Gladstone Institutes), Kaho Washizu(Gladstone Institutes), Lukas Zanders(Goethe University Frankfurt), Han Chen(Gladstone Institutes), Yujie Zhang(Gladstone Institutes), Sarah Ancheta(Gladstone Institutes), Sara Lichtarge(Gladstone Institutes), William A Johnson(Gladstone Institutes), Chris Thompson(Gladstone Institutes), Dereck M Phan(Gladstone Institutes), Alexis J. Combes(University of California, San Francisco), Andrew C Yang(Gladstone Institutes), Neha Tadimeti(Nvidia (United States)), Stefanie Dimmeler(Goethe University Frankfurt), Shinya Yamanaka(Gladstone Institutes), Michael Alexanian(Gladstone Institutes), Christina V. Theodoris(Gladstone Institutes)
bioRxiv (Cold Spring Harbor Laboratory)
April 1, 2026
Cited by 0Open Access
Full Text

Abstract

Foundational AI models have recently shown promise for predicting the impact of perturbations on cell states. However, current models typically consider only one cell state at a time, limiting their ability to learn how cellular responses unfold over time, particularly across long trajectories such as diseases of aging. Here, we develop a temporal AI model, MaxToki, trained on nearly 1 trillion gene tokens including cell state trajectories across the human lifespan to generate cell states across long timelapses of human aging. MaxToki generalized to unseen trajectories through in-context learning and predicted novel age-modulating targets that were experimentally verified to influence age-related gene programs and functional decline in vivo. MaxToki represents a promising strategy for temporal modeling to accelerate the discovery of interventions for programming therapeutic cellular trajectories.


Related Papers

No related papers found

Powered by citation graph analysis