Form follows function: Nuclear morphology as a quantifiable predictor of cellular senescence

被引:15
作者
Belhadj, Jakub [1 ,2 ]
Surina, Surina [1 ,2 ,3 ]
Hengstschlaeger, Markus [1 ]
Lomakin, Alexis J. [1 ,2 ]
机构
[1] Med Univ Vienna, Inst Med Genet, Ctr Pathobiochem & Genet, Vienna, Austria
[2] Med Univ Vienna, Inst Med Chem & Pathobiochem, Ctr Pathobiochem & Genet, Vienna, Austria
[3] Univ Campania Luigi Vanvitelli, Sch Med Sci, Naples, Italy
关键词
artificial intelligence; cell nucleus; cellular biophysics; cellular senescence; computer vision; machine learning; morphogenesis; quantitative microscopy; DNA-DAMAGE; MICROTUBULES;
D O I
10.1111/acel.14012
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Enlarged or irregularly shaped nuclei are frequently observed in tissue cells undergoing senescence. However, it remained unclear whether this peculiar morphology is a cause or a consequence of senescence and how informative it is in distinguishing between proliferative and senescent cells. Recent research reveals that nuclear morphology can act as a predictive biomarker of senescence, suggesting an active role for the nucleus in driving senescence phenotypes. By employing deep learning algorithms to analyze nuclear morphology, accurate classification of cells as proliferative or senescent is achievable across various cell types and species both in vitro and in vivo. This quantitative imaging-based approach can be employed to establish links between senescence burden and clinical data, aiding in the understanding of age-related diseases, as well as assisting in disease prognosis and treatment response.
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页数:7
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