A multi-modal microscope for integrated mapping of cellular forces and Brillouin scattering with high resolution

被引:0
|
作者
Meek, Andrew T. [1 ]
Busse, Franziska [2 ]
Kronenberg, Nils M. [1 ,2 ]
Dinh, San Vinh [1 ]
Berghaus, Kim, V [3 ]
Booth, Jonathan H. [1 ]
Scarcelli, Giuliano [3 ]
Gather, Malte C. [1 ,2 ]
机构
[1] Univ St Andrews, Ctr Biophoton, Sch Phys & Astron, SUPA, St Andrews, Scotland
[2] Univ Cologne, Humboldt Ctr Nano & Biophoton, Dept Chem, Cologne, Germany
[3] Univ Maryland, Fischell Dept Bioengn, College Pk, MD USA
来源
JOURNAL OF PHYSICS-PHOTONICS | 2024年 / 6卷 / 02期
基金
欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
multi-modal; integrated microscope; cellular forces; mechanobiology; Brillouin microscopy; TRACTION FORCE; OPTICAL MICROSCOPY; CANCER-CELLS; MECHANICS; PRECISION; TOOL;
D O I
10.1088/2515-7647/ad3d1a
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Mechanical forces and stiffness play key roles in the health and development of cells and tissue, but despite the physical connection between these quantities, they cannot be monitored in parallel in most cases. Here, we introduce a fully integrated microscope that combines a method for high-resolution cell force imaging (elastic resonator interference stress microscopy, ERISM) with non-contact mapping of the elastic properties of cells (via Brillouin microscopy). In order to integrate both techniques, we had to account for the strong back reflection on the surface of the microcavity used for ERISM measurements as well as the local destruction of the cavity under illumination for Brillouin microscopy measurements. Therefore, we developed an elastic optical microcavity with minimal absorption that can perform ERISM measurements without sustaining laser damage during Brillouin microscopy. Furthermore, an unequal-arm Michelson interferometer was designed to suppress the back reflection of the laser on the ERISM microcavity surface using division by amplitude interference to reduce the reflected light and enhance the Brillouin signal. We show the utility of our integrated microscope by simultaneously mapping cellular forces and Brillouin shifts in cultures of fibroblast cells.
引用
收藏
页数:14
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