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测量单个成纤维细胞在自立纤维支架上产生的收缩力。

Measurement of contractile forces generated by individual fibroblasts on self-standing fiber scaffolds.

机构信息

Laser Thermal Laboratory, Department of Mechanical Engineering, University of California, Berkeley, CA 94720-1740, USA.

出版信息

Biomed Microdevices. 2011 Feb;13(1):107-15. doi: 10.1007/s10544-010-9475-5.

Abstract

Contractility of cells in wound site is important to understand pathological wound healing and develop therapeutic strategies. In particular, contractile force generated by cells is a basic element for designing artificial three-dimensional cell culture scaffolds. Direct assessment of deformation of three-dimensional structured materials has been used to calculate contractile forces by averaging total forces with respect to the cell population number. However, macroscopic methods have offered only lower bounds of contractility due to experimental assumptions and the large variance of the spatial and temporal cell response. In the present study, cell contractility was examined microscopically in order to measure contractile forces generated by individual cells on self-standing fiber scaffolds that were fabricated via femtosecond laser-induced two-photon polymerization. Experimental assumptions and calculation errors that arose in previous studies of macroscopic and microscopic contractile force measurements could be reduced by adopting a columnar buckling model on individual, standing fiber scaffolds. Via quantifying eccentric critical loads for the buckling of fibers with various diameters, contractile forces of single cells were calculated in the range between 30-116 nN. In the present study, a force magnitude of approximately 200 nN is suggested as upper bound of the contractile force exerted by single cells. In addition, contractile forces by multiple cells on a single fiber were calculated in the range between 241-709 nN.

摘要

细胞在创伤部位的收缩性对于理解病理性伤口愈合和开发治疗策略非常重要。特别是,细胞产生的收缩力是设计人工三维细胞培养支架的基本要素。通过将细胞群体数量的总力进行平均,可以直接评估三维结构材料的变形,从而计算出收缩力。然而,由于实验假设和细胞时空响应的巨大差异,宏观方法只能提供收缩力的下限。在本研究中,通过飞秒激光诱导的双光子聚合来制备独立纤维支架,在微观上检查了细胞的收缩性,以测量单个细胞在独立纤维支架上产生的收缩力。通过采用柱状屈曲模型,可以减少以前宏观和微观收缩力测量研究中出现的实验假设和计算误差。通过量化具有不同直径的纤维的偏心临界负载,计算出单个细胞的收缩力在 30-116 nN 之间。在本研究中,建议将大约 200 nN 的力幅度作为单个细胞施加的收缩力的上限。此外,还计算了单个纤维上多个细胞的收缩力在 241-709 nN 之间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/3028113/ac2677f211bd/10544_2010_9475_Fig1_HTML.jpg

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