Construction and Application Process of Aging Cell Identification Model
With the support of the National Natural Science Foundation of China's
"Digital Decoding of Immunity" major research project (approval number:
92374207), Professor Han Jingdong's team from the Center for Quantitative
Biology/Joint Center for Life Sciences at Peking University has made
breakthroughs in the study of cellular aging trajectories and regulatory
mechanisms. The research results, titled "Single cell aging identification
reveals aging heterogeneity, trajectories, and modulators," were published on
April 10, 2024 in the journal Cell Metabolism. The paper link is:
https://doi.org/10.1016/j.cmet.2024.03.009 .
Cellular aging plays a crucial role in many diseases, but current research
on cellular aging lacks universal aging cell markers and traditional
identification methods have limitations in detection. In response to the above
challenges, the research team has developed a machine learning based SenCID
(Senecent Cell Identification) algorithm to accurately identify aging cells and
evaluate the degree of aging from human single-cell transcriptome data. SenCID
divides cells into six types of "senescence IDs" (SIDs), and different SIDs
cells have significant differences in aging baseline, cell stemness, gene
function, and response to aging lysis; SenCID combined with trajectory
reconstruction algorithm reconstructed cell aging trajectories under different
physiological and pathological conditions such as normal individual aging,
chronic disease and COVID-19 infection on the basis of single cell data of human
tissues; SenCID has also been applied to transcriptome data of single-cell gene
perturbation technology to identify gene perturbation factors that can promote
or inhibit cellular aging; To lay the foundation for promoting research on the
mechanism of cellular aging and cellular aging intervention.