{"title":"A transition of dynamic rheological responses of single cells: from fluid-like to solid-like.","authors":"Lin-Ru Qiao,Zhuo Chang,Chen-He Li,Jiu-Tao Hang,Xian-Jun Wu,Yu-Hang Xiao,Guang-Kui Xu","doi":"10.1016/j.bpj.2025.09.010","DOIUrl":null,"url":null,"abstract":"The mechanical properties of cells are crucial for elucidating various physiological and pathological processes. Cells are found to exhibit a universal power-law rheological behavior at low frequencies. While they behave in a different manner at high frequency regimes, which leaves the transition region largely unexplored. Here, we investigate single-cell rheological behaviors across different cell types (primary hematopoietic stem cells, the hippocampal neuronal cell line and human dental pulp stem cells) by atomic force microscopy (AFM)-microrheology method, uncovering a universal two-stage power-law rheological behavior. Cells behave fluid-like at shorter time scales and solid-like at longer scales. To characterize the transition region between these stages, we introduce a time-scale parameter, termed \"transition time\". Notably, for all the cell types under study, we find that the transition time decreases with increasing elastic moduli and increases for larger power-law exponent. Furthermore, based on our previous self-similar hierarchical model, we propose a theoretical method to determine the upper and lower bounds of the transition time range. Our experimental results exhibit an excellent agreement, consistently falling within the predicted theoretical limits. Furthermore, we present six crucial mechanical indices that depict both the dynamic and static mechanical properties of single cells. These parameters can effectively differentiate cell types and provide a comprehensive perspective on the mechanical states of cells. Our study may offer new insights into the viscoelastic transformation of cells from fluid-like to solid-like behaviors, and highlights the mechanisms underlying various time scales during biomechanical processes.","PeriodicalId":8922,"journal":{"name":"Biophysical journal","volume":"33 1","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysical journal","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.bpj.2025.09.010","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
The mechanical properties of cells are crucial for elucidating various physiological and pathological processes. Cells are found to exhibit a universal power-law rheological behavior at low frequencies. While they behave in a different manner at high frequency regimes, which leaves the transition region largely unexplored. Here, we investigate single-cell rheological behaviors across different cell types (primary hematopoietic stem cells, the hippocampal neuronal cell line and human dental pulp stem cells) by atomic force microscopy (AFM)-microrheology method, uncovering a universal two-stage power-law rheological behavior. Cells behave fluid-like at shorter time scales and solid-like at longer scales. To characterize the transition region between these stages, we introduce a time-scale parameter, termed "transition time". Notably, for all the cell types under study, we find that the transition time decreases with increasing elastic moduli and increases for larger power-law exponent. Furthermore, based on our previous self-similar hierarchical model, we propose a theoretical method to determine the upper and lower bounds of the transition time range. Our experimental results exhibit an excellent agreement, consistently falling within the predicted theoretical limits. Furthermore, we present six crucial mechanical indices that depict both the dynamic and static mechanical properties of single cells. These parameters can effectively differentiate cell types and provide a comprehensive perspective on the mechanical states of cells. Our study may offer new insights into the viscoelastic transformation of cells from fluid-like to solid-like behaviors, and highlights the mechanisms underlying various time scales during biomechanical processes.
期刊介绍:
BJ publishes original articles, letters, and perspectives on important problems in modern biophysics. The papers should be written so as to be of interest to a broad community of biophysicists. BJ welcomes experimental studies that employ quantitative physical approaches for the study of biological systems, including or spanning scales from molecule to whole organism. Experimental studies of a purely descriptive or phenomenological nature, with no theoretical or mechanistic underpinning, are not appropriate for publication in BJ. Theoretical studies should offer new insights into the understanding ofexperimental results or suggest new experimentally testable hypotheses. Articles reporting significant methodological or technological advances, which have potential to open new areas of biophysical investigation, are also suitable for publication in BJ. Papers describing improvements in accuracy or speed of existing methods or extra detail within methods described previously are not suitable for BJ.