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Abstract

Preparation procedures after resection of animal tissues are commonly a series of chemical fixation, alcohol dehydration, paraffin or epoxy resin embedding, thick or thin sectioning, and dye or metal staining steps. During such preparation steps, various kinds of inevitable artifacts always modify their original morphology. Some problems are both molecular movement and structural changes of cells and tissues during the fixation time. Another problem is that dynamic morphological images in vivo are difficult to be captured by the conventional chemical fixation. Then, a strong effort of morphologists has been made to avoid such technical artifacts during the conventional preparation steps. The quick-freezing (QF) method was introduced for biological specimens at the middle of the twentieth century. For the final morphological purpose, various preparation procedures can be chosen after the quick-freezing. One of them is freeze-substitution (FS) fixation, in which the frozen specimens are usually incubated in cooled organic solvents containing chemical fixatives at about −80 °C. However, the freeze-substituted specimens are known to be affected to some extent by the organic solvents. Another deep-etching (DE) replication method has been developed, in which replica membranes of freeze-fractured and deeply etched tissues are obtained by rotary-shadowing with platinum metal at lower temperatures below −100 °C under high vacuum conditions. However, some pieces of tissues have to be always resected and taken out from living animal organs. Thus, the dynamically changing morphology of living animal organs is hardly investigated by the conventional QF method. To overcome these technical problems, it is necessary to avoid the tissue resection step of living animal organs and directly freeze them in vivo under normal blood circulation. The IVCT was an original technique to directly cryofix living animal organs without separating their tissues from blood circulation. The most significant point of IVCT is that normal blood circulation into living animal organs is strictly preserved at the exact moment of freezing.

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References

  1. Furukawa T, Ohno S, Oguchi H, Hora K, Tokunaga S, Furuta S (1991) Morphometric study of glomerular slit diaphragms fixed by rapid-freezing and freeze-substitution. Kidney Int 40:621–624

    Article  CAS  PubMed  Google Scholar 

  2. Yoshimura A, Ohno S, Nakano K, Oniki H, Inui K, Ideura T, Koshikawa S (1991) Three-dimensional ultrastructure of anionic sites of the glomerular basement membrane by a quick-freezing and deep-etching method using a cationic tracer. Histochemistry 96:107–113

    Article  CAS  PubMed  Google Scholar 

  3. Ohno S, Hora K, Furukawa T, Oguchi H (1992) Ultrastructural study of the glomerular slit diaphragm in fresh unfixed kidneys by a quick-freezing method. Virchows Arch B Cell Pathol 61:351–358

    Article  CAS  Google Scholar 

  4. Terada N, Ohno S (2004) Immunohistochemical application of cryotechniques to native morphology of cells and tissues. Acta Histochem Cytochem 37:339–345

    Article  Google Scholar 

  5. Zea-Aragon A, Terada N, Ohno N, Fujii Y, Baba T, Ohno S (2004) Effects of anoxia on serum immunoglobulin and albumin leakage through blood–brain barrier in mouse cerebellum as revealed by cryotechniques. J Neurosci Methods 138:89–95

    Article  CAS  PubMed  Google Scholar 

  6. Ohno N, Terada N, Murata S, Katoh R, Ohno S (2005) Application of cryotechniques with freeze-substitution for the immunohistochemical demonstration of intranuclear pCREB and chromosome territory. J Histochem Cytochem 53:55–62

    Article  CAS  PubMed  Google Scholar 

  7. van Harreveld A, Trubatch J (1975) Synaptic changes in frog brain after stimulation with potassium chloride. J Neurocytol 4:33–46

    Article  CAS  PubMed  Google Scholar 

  8. Jehl B, Bauer R, Dorge A, Rick R (1981) The use of propane/isopentane mixtures for rapid freezing of biological specimens. J Microsc 123:307–309

    Article  CAS  PubMed  Google Scholar 

  9. Cole R, Matuszek G, See C, Rieder CL (1990) A simple pneumatic device for plunge-freezing cells grown on electron microscopy grids. J Electron Microsc Tech 16:167–173

    Article  CAS  PubMed  Google Scholar 

  10. Yu Y, Leng CG, Kato Y, Ohno S (1997) Ultrastructural study of glomerular capillary loops at different perfusion pressures as revealed by quick-freezing, freeze-substitution and conventional fixation methods. Nephron 76:452–459

    Article  CAS  PubMed  Google Scholar 

  11. Yu Y, Leng CG, Kato Y, Terada N, Fujii Y, Ohno S (1998) Ultrastructural study of anionic sites in glomerular basement membranes at different perfusion pressures by quick-freezing and deep-etching method. Nephron 78:88–95

    Article  CAS  PubMed  Google Scholar 

  12. Ohno S, Terada N, Fujii Y, Ueda H, Takayama I (1996) Dynamic structure of glomerular capillary loop as revealed by an in vivo cryotechnique. Virchows Arch 427:519–527

    Article  CAS  PubMed  Google Scholar 

  13. Ohno N, Terada N, Fujii Y, Baba T, Ohno S (2004) “In vivo cryotechnique” for paradigm shift to “living morphology” of animal organs. Biomed Rev 15:1–19

    Article  Google Scholar 

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Correspondence to Shinichi Ohno .

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Ohno, S. (2016). Biomedical Significance and Development of “IVCT”. In: Ohno, S., Ohno, N., Terada, N. (eds) In Vivo Cryotechnique in Biomedical Research and Application for Bioimaging of Living Animal Organs. Springer, Tokyo. https://doi.org/10.1007/978-4-431-55723-4_2

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  • DOI: https://doi.org/10.1007/978-4-431-55723-4_2

  • Publisher Name: Springer, Tokyo

  • Print ISBN: 978-4-431-55722-7

  • Online ISBN: 978-4-431-55723-4

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