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Royall, L.

Publications and source records attributed to Royall, L..

2 recordsLinked to original sources

The Principal Component Life Trajectory (PCLT): Mapping Sex-Specific Physiological Change Across the Human Lifespan

Age- and sex-related variation in physiological biomarkers is well documented, yet how coordinated systemic physiology unfolds across life stages at the population level remains unclear. Here, we introduce the Principal Component Life Trajectory (PCLT), reconstructing physiological trajectories via multivariate analysis of 54 blood-based biomarkers from 11,124 participants in the National Health and Nutrition Examination Survey (NHANES). Quantifying year-on-year progression with Euclidean Trajectory Distance (ETD), we identify five distinct phases in an unbiased manner: Early adolescence, Sexual Divergence, Sexual Convergence, Late Adulthood, and Advanced Aging. Trajectories show early, pronounced sexual divergence validated in an ethnically distinct, independent cohort. Chronic disease is associated with PCLT displacement and increased ETD progression, whereas metabolic, behavioral, and psychosocial factors generate graded, phase-specific perturbations. Together, these findings establish PCLT as a reproducible framework for characterizing structured physiological change across the lifespan and for monitoring population-level health dynamics.

systems biology↗

Asymmetric inheritance of centrosomes maintains stem cell properties in human neural progenitor cells

During human forebrain development, neural progenitor cells (NPCs) in the ventricular zone (VZ) undergo asymmetric cell divisions to produce a self-renewed progenitor cell, maintaining the potential to go through additional rounds of cell divisions, and differentiating daughter cells, populating the developing cortex. Previous work in the embryonic rodent brain suggested that the preferential inheritance of the pre-existing (older) centrosome to the self-renewed progenitor cell is required to maintain stem cell properties, ensuring proper neurogenesis. If asymmetric segregation of centrosomes occurs in NPCs of the developing human brain, which depends on unique molecular regulators and species-specific cellular composition, remains unknown. Using a novel, recombination-induced tag exchange (RITE)-based genetic tool to birthdate and track the segregation of centrosomes over multiple cell divisions in human embryonic stem cell (hESC)-derived regionalized forebrain organoids, we show the preferential inheritance of the older mother centrosome towards self-renewed NPCs. Aberration of asymmetric segregation of centrosomes by genetic manipulation of the centrosomal, microtubule-associated protein Ninein alters fate decisions of NPCs and their maintenance in the VZ of human cortical organoids. Thus, the data described here use a novel genetic approach to birthdate centrosomes in human cells and identify asymmetric inheritance of centrosomes as a mechanism to maintain self-renewal properties and to ensure proper neurogenesis in human NPCs. Impact StatementGenetic birthdating in forebrain organoids shows asymmetric inheritance of centrosomes in human neural progenitor cells, required for proper human neurogenesis.

neuroscience↗