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Beyond comparison: Brillouin microscopy and AFM-based indentation reveal divergent insights into the mechanical profile of the murine retina

Möllmert, S.; Gutmann, M.; Müller, P.; Kim, K.; Bachir Salvador, J.; Aif, S.; Meinel, L.; Guck, J.

2024-01-29 biophysics
10.1101/2024.01.24.577013 bioRxiv
Show abstract

Mechanical tissue properties increasingly serve as pivotal phenotypic characteristics that are subject to change during development or pathological progression. The quantification of such material properties often relies on physical contact between a load-applying probe and an exposed sample surface. For most tissues, these requirements necessitate animal sacrifice, tissue dissection and sectioning. These invasive procedures bear the risk of yielding mechanical properties that do not portray the physiological mechanical state of a tissue within a functioning organism. Brillouin microscopy has emerged as a non-invasive, optical technique that allows to assess mechanical cell and tissue properties with high spatio-temporal resolution. In optically transparent specimens, this technique does not require animal sacrifice, tissue dissection or sectioning. However, the extent to which results obtained from Brillouin microscopy allow to infer conclusions about potential results obtained with a contact-based technique, and vice versa, is unclear. Potential sources for discrepancies include the varying characteristic temporal and spatial scales, the directionality of measurement, environmental factors, and mechanical moduli probed. In this work, we addressed those aspects by quantifying the mechanical properties of acutely dissected murine retinal tissues using Brillouin microscopy and atomic force microscopy (AFM)-based indentation measurements. Our results show a distinct mechanical profile of the retinal layers with respect to the Brillouin frequency shift, the Brillouin linewidth and the apparent Youngs modulus. Contrary to previous reports, our findings do not support a simple correlative relationship between Brillouin frequency shift and apparent Youngs modulus. Additionally, the divergent sensitivity of Brillouin microscopy and AFM-indentation measurements to cross-linking or changes post mortem underscores the dangers of assuming both methods can be generally used interchangeably. In conclusion, our study advocates for viewing Brillouin microscopy and AFM-based indentation measurements as complementary tools, discouraging direct comparisons a priori and suggesting their combined use for a more comprehensive understanding of tissue mechanical properties.

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