bioRxivBiophysicsPreprint
Mechanical mapping of spinal cord development and repair in living zebrafish larvae using Brillouin microscopy
Raimund SchlüßleriD, Stephanie MöllmertiD, Shada AbuhattumiD, Gheorghe Cojoc, Paul Müller, Kyoohyun KimiD, Conrad MöckeliD, Conrad Zimmermann, Jürgen Czarske, Jochen GuckiD
Abstract
The mechanical properties of biological tissues are increasingly recognized as important factors in developmental and pathological processes. Most existing mechanical measurement techniques either necessitate destruction of the tissue for access or provide insufficient spatial resolution. Here, we show for the first time a systematic application of confocal Brillouin microscopy to quantitatively map the mechanical properties of spinal cord tissues during biologically relevant processes in a contact-free and non-destructive manner. Living zebrafish larvae were mechanically imaged in all anatomical planes, during development and after spinal cord injury. These experiments revealed that Brillouin microscopy is capable of detecting the mechanical properties of distinct anatomical structures without interfering with the animals natural development. The Brillouin shift within the spinal cord increased during development and transiently decreased during the repair processes following spinal cord transection. By taking into account the refractive index distribution, we explicitly determined the apparent longitudinal modulus and viscosity of different larval zebrafish tissues. Importantly, mechanical properties differed between tissues in situ and in excised slices. The presented work constitutes the first step towards an in vivo assessment of spinal cord tissue mechanics during regeneration, provides a methodical basis to identify key determinants of mechanical tissue properties and allows to test their relative importance in combination with biochemical and genetic factors during developmental and regenerative processes.
- organism: zebrafish
- assay: imaging
- research focus: development & morphogenesis
- research focus: cell type annotation
- approach: microscopy & imaging analysis
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