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研究细胞外基质分子结构的力学方法。

Mechanical Way To Study Molecular Structure of Pericellular Layer.

机构信息

Department of Mechanical Engineering, Tufts University, Medford, Massachusetts 02155, United States.

Department of Biophysical Microstructures, Institute of Nuclear Physics PAN, PL-31342 Kraków, Poland.

出版信息

ACS Appl Mater Interfaces. 2023 Aug 2;15(30):35962-35972. doi: 10.1021/acsami.3c06341. Epub 2023 Jul 25.

Abstract

Atomic force microscopy (AFM) has been used to study the mechanical properties of cells, in particular, malignant cells. Softening of various cancer cells compared to their nonmalignant counterparts has been reported for various cell types. However, in most AFM studies, the pericellular layer was ignored. As was shown, it could substantially change the measured cell rigidity and miss important information on the physical properties of the pericellular layer. Here we take into account the pericellular layer by using the brush model to do the AFM indentation study of bladder epithelial bladder nonmalignant (HCV29) and cancerous (TCCSUP) cells. It allows us to measure not only the quasistatic Young's modulus of the cell body but also the physical properties of the pericellular layer (the equilibrium length and grafting density). We found that the inner pericellular brush was longer for cancer cells, but its grafting density was similar to that found for nonmalignant cells. The outer brush was much shorter and less dense for cancer cells. Furthermore, we demonstrate a method to convert the obtained physical properties of the pericellular layer into biochemical language better known to the cell biology community. It is done by using heparinase I and neuraminidase enzymatic treatments that remove specific molecular parts of the pericellular layer. The presented here approach can also be used to decipher the molecular composition of not only pericellular but also other molecular layers.

摘要

原子力显微镜(AFM)已被用于研究细胞的机械性能,特别是恶性细胞。已经报道了各种癌细胞与非恶性细胞相比的软化现象,适用于各种细胞类型。然而,在大多数 AFM 研究中,细胞外基质层被忽略了。研究表明,它会显著改变测量的细胞硬度,并可能错过关于细胞外基质层物理性质的重要信息。在这里,我们通过使用刷子模型来考虑细胞外基质层,对膀胱上皮非恶性(HCV29)和恶性(TCCSUP)细胞进行 AFM 压痕研究。它不仅允许我们测量细胞体的准静态杨氏模量,还可以测量细胞外基质层的物理性质(平衡长度和接枝密度)。我们发现癌细胞的内细胞外基质刷子较长,但接枝密度与非恶性细胞相似。癌细胞的外刷子短得多,密度也小得多。此外,我们还展示了一种方法,可以将获得的细胞外基质层的物理性质转化为细胞生物学界更为熟悉的生化语言。这是通过使用肝素酶 I 和神经氨酸酶处理来完成的,这些处理可以去除细胞外基质层的特定分子部分。这里提出的方法也可以用于破译不仅是细胞外基质,还有其他分子层的分子组成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c50/10401571/5ed28a4b1ca7/am3c06341_0001.jpg

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