| Autor: |
Heimel P; Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, Vienna, Austria.; Karl Donath Laboratory for Hard Tissue and Biomaterial Research, University Clinic of Dentistry, Medical University Vienna, Vienna, Austria.; Austrian Cluster for Tissue Regeneration, Vienna, Austria., Swiadek NV; Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, Vienna, Austria.; Austrian Cluster for Tissue Regeneration, Vienna, Austria., Slezak P; Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, Vienna, Austria.; Austrian Cluster for Tissue Regeneration, Vienna, Austria., Kerbl M; Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, Vienna, Austria.; Austrian Cluster for Tissue Regeneration, Vienna, Austria., Schneider C; Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, Vienna, Austria.; Austrian Cluster for Tissue Regeneration, Vienna, Austria., Nürnberger S; Austrian Cluster for Tissue Regeneration, Vienna, Austria.; Department of Trauma Surgery, Medical University Vienna, Vienna, Austria., Redl H; Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, Vienna, Austria.; Austrian Cluster for Tissue Regeneration, Vienna, Austria., Teuschl AH; Austrian Cluster for Tissue Regeneration, Vienna, Austria.; Department of Biochemical Engineering, UAS Technikum Wien, Vienna, Austria., Hercher D; Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, Vienna, Austria.; Austrian Cluster for Tissue Regeneration, Vienna, Austria. |
| Abstrakt: |
Microcomputed tomography ( μ CT) is widely used for the study of mineralized tissues, but a similar use for soft tissues is hindered by their low X-ray attenuation. This limitation can be overcome by the recent development of different staining techniques. Staining with Lugol's solution, a mixture of one part iodine and two parts potassium iodide in water, stands out among these techniques for its low complexity and cost. Currently, Lugol staining is mostly used for anatomical examination of tissues. In the present study, we seek to optimize the quality and reproducibility of the staining for ex vivo visualization of soft tissues in the context of a peripheral nerve regeneration model in the rat. We show that the staining result not only depends on the concentration of the staining solution but also on the amount of stain in relation to the tissue volume and composition, necessitating careful adaptation of the staining protocol to the respective specimen tissue. This optimization can be simplified by a stepwise staining which we show to yield a similar result compared to staining in a single step. Lugol staining solution results in concentration-dependent tissue shrinkage which can be minimized but not eliminated. We compared the shrinkage of tendon, nerve, skeletal muscle, heart, brain, and kidney with six iterations of Lugol staining. 60 ml of 0.3% Lugol's solution per cm 3 of tissue for 24 h yielded good results on the example of a peripheral nerve regeneration model, and we were able to show that the regenerating nerve inside a silk fibroin tube can be visualized in 3D using this staining technique. This information helps in deciding the region of interest for histological imaging and provides a 3D context to histological findings. Correlating both imaging modalities has the potential to improve the understanding of the regenerative process. |
