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Three-dimensional observation of mouse tongue muscles using micro-computed tomography

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Abstract

The aim of this study is to obtain information about the mouse tongue muscle rendered using micro-computed tomography (μCT) at low, middle, and high magnifications. Three-dimensional (3D) μCT is used in various fields. Most μCT observations are restricted to hard tissue in biomaterial samples. Recently, with the use of osmium tetroxide, μCT has been effectively employed to observe soft tissue; it is now believed that μCT observation of soft tissue is feasible. On the other hand, the structure of the tongue muscle has been well studied, but cross-sectional imaging enhanced by 3D rendering is lacking. We chose the mouse tongue as a soft tissue case study for μCT and generated cross-sectional images of the tongue enhanced by 3-D image rendering with histological resolution. During this observation, we developed new methods of low-magnification observation to show the relation between the tongue muscles and surrounding tissues. We also applied high-resolution μCT in high-magnification observation of muscle fiber fascicles. Our methodological techniques give the following results: (1) For low-magnification observation (field of view: 12,000 μm), pretreatment with decalcification and freeze drying is suitable for observing the area between the muscle of the tongue and the bone around the tongue using μCT. (2) For middle-magnification observation (Field of view: 3,500 μm), the use of osmium tetroxide to observe the muscle arrangement of the tongue by μCT is suitable. (3) For high-magnification observation (Field of view: 450 μm), high-resolution μCT is suitable for observation of the transversus muscle fiber fascicles.

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References

  1. Feldkamp LA, Goldstein SA, Parfitt M, Jesion G, Kleereoper M. The direct examination of three-dimensional bone architecture in vitro by computed tomography. J Bone Miner Res. 1989;l4:3–11.

    Google Scholar 

  2. Peters OA, Peters CI, Scho K, Barbakow K. Pro taper rotary root canal preparation: effects of canal anatomy on final shape analysed by micro CT. Int Endod J. 2003;36:86–92.

    Article  PubMed  Google Scholar 

  3. Iwaka Y. Three-dimensional observation of the pulp cavity of mandibular first molars by micro-CT. J Oral Biosci. 2006;48:94–102.

    Article  Google Scholar 

  4. Parkinson CR, Sasov A. High-resolution non-destructive 3D interrogation of dentin using X-ray nanotomography. Dent Mater. 2008;24:773–7.

    Article  PubMed  Google Scholar 

  5. Cooper D, Turinsky A, Sensen C, Hallgrimsson B. Effect of voxel size on 3D micro-CT analysis of cortical bone porosity. Calcif Tissue Int. 2007;80:211–9.

    Article  PubMed  Google Scholar 

  6. Faraj KA, Cuijpers VMJI, Wismans RG, Walboomers XF, Jansen JA, van Kuppevelt TH, Daamen WF. Micro-computed tomographical imaging of soft biological materials using contrast techniques. Tissue engineerring: Part C. 2009;15(3):493–9.

    Google Scholar 

  7. Metscher BD. MicroCT for Developmental biology: a versatile tool for high-contrast 3D imaging at histological resolutions. Dev Dyn. 2009;238:632–40.

    Article  PubMed  Google Scholar 

  8. Metscher BD. MicroCT for comparative morphology: simple staining methods allow high-contrast 3D imaging of diverse non-mineralized animal tissues. BMC Physiol. 2009;9:11–24.

    Article  PubMed Central  PubMed  Google Scholar 

  9. Aoyagi H, Tsuchikawa K, Iwasaki S. Three-dimensional observation of the mouse embryo by micro-computed tomography: composition of the trigeminal ganglion. Odontology. 2010;98:26–30.

    Article  PubMed  Google Scholar 

  10. Aoyagi H, Tsuchikawa K, Iwasaki S. Three-dimensional observation of the mouse embryo by micro-computed tomography: Meckel’s cartilage, otocyst, and/or muscle of tongue. Odontology. 2012;100:134–43.

    Article  Google Scholar 

  11. Barnwell EM. Human Lingual Musculature: an Historical Review. Int J Oral Myol. 1976;2:31–41.

    PubMed  Google Scholar 

  12. Ogata S, Mine K, Tamatsu Y, Himada K. Morphological study of the human chondroglossus muscle in Japanese. Ann Anat. 2002;184:493–9.

    Article  PubMed  Google Scholar 

  13. Diogo R. The head and neck muscles of the Philippine colugo (Dermoptera: cynocephalus valans), with a comparison to tree-shrews, primates, and other mammals. J morph. 2009;270:14–51.

    Article  PubMed  Google Scholar 

  14. Smith JC, Goldberg SJ, Shall MS. Myosin heavy chain and fiber diameter of extrinsic tongue muscles in rhesus monkey. Arch Oral Biol. 2006;51:520–5.

    Article  PubMed  Google Scholar 

  15. Smith KK. Form and function of the tongue in Agamid lizards with comments on its phylogenic significance. J Morph. 1988;196:157–71.

    Article  PubMed  Google Scholar 

  16. Schwenk K. Why snakes have forked tongues. Science. 1994;263:1573–7.

    Article  PubMed  Google Scholar 

  17. Gans C, Gorniak GC. Functional morphology of lingual protrusion in Marine toads (bufo marinus). Am J Anat. 1982;163:195–222.

    Article  PubMed  Google Scholar 

  18. Herrel A, Meyers JJ, Nishikawa KC, Vree FD. Morphology and histochemistry of the hyolingual apparatus in chameleons. J morph. 2001;249:154–70.

    Article  PubMed  Google Scholar 

  19. Smith KK. Morphology and function of the tongue and hyoid apparatus in varanus (Varanidae, Lacertilia). J Morph. 1986;187:261–87.

    Article  PubMed  Google Scholar 

  20. Lombard RE, Wake D. Tongue evolution in the lungless salamanders, family Plethodontidae. II function and evolutionary diversity. J Morph. 1977;153:39–80.

    Article  PubMed  Google Scholar 

  21. Sosnovik DE, Wang R, Dai G, Wang T, Aikawa E, Novikov M, Rosenzweig A, Gilbert RJ, Wedeen VJ. Diffusion spectrum MRI tractography reveals the presence of a complex network of residual myofibers in infracted myocardium. Circ Cardiovasc Imaging. 2009;2:206–12.

    Article  PubMed Central  PubMed  Google Scholar 

  22. Kayalioglu M, Shcherbaty V, Seifi A, Liu ZJ. Roles of intrinsic and extrinsic tongue muscles in feeding: electromyographic study in pigs. Arch Oral Biol. 2007;52:786–96.

    Article  PubMed Central  PubMed  Google Scholar 

  23. Napadow VJ, Chen Q, Wedeen VJ, Gilbert RJ. Intramural mechanics of the human tongue in association with physiological deformations. J Biomech. 1999;32:1–12.

    Article  PubMed  Google Scholar 

  24. Mu L, Sanders I. Neuromuscular organization of the canine tongue. Anat Rec. 1999;256:412–24.

    Article  PubMed  Google Scholar 

  25. McClung JR, Goldberg SJ. Organization of the hypoglossal motoneurons that innervate the horizontal and oblique components of the genioglossus muscle in the rat. Brain Res. 2002;950:321–4.

    Article  PubMed  Google Scholar 

  26. Saito H, Itoh I. The three-dimensional architecture of the human styloglossus especially its posterior muscle bundles. Ann Anat. 2007;189:261–7.

    Article  PubMed  Google Scholar 

  27. Stutley J, Cooke J, Parsons C. Normal CT anatomy oh the tongue, floor of mouth and oropharynx. Clin Radiol. 1989;40:248–53.

    Article  PubMed  Google Scholar 

  28. Laine FJ, Smeker WRK. Oral cavity: anatomy and pathology. Semin Ultrasound CT MRI. 1995;16:527–45.

    Article  Google Scholar 

  29. Boom HPW, van Spronsen PH, van Ginkel FC, van Schijndel RA, Castelijns JA, Tuinzing DB. A comparison of human jaw muscle cross-sectional area and volume in long- and short-face subjects, using MRI. Arch Oral Biol. 2008;53(3):273–81.

    Article  PubMed  Google Scholar 

  30. Volk J, Kadivec M, Music MM, Ovsenik M. Three-dimensional ultrasound diagnostics of tongue posture in children with unilateral posterior crossbite. Am J Orthod Dentofacial Orthop. 2010;138:608–12.

    Article  PubMed  Google Scholar 

  31. Aoyagi H, Iwasaki S. 3D Observation of the Tongue by Using Micro-Computed tomography (Chapter XX), in Tongue: Anatomy, kinematics and Diseases. In: Hiroto Katō, Taiga Shimizu, 2012, Nova Publisher, New York, USA, pp 53–71.

  32. Jeffery NS, Stephenson RS, Gallagher JA, Jarvis JC, Cox PG. Micro-computed tomography with iodine staining resolves the arrangement of muscle fibres. J Biomech. 2011;44:189–92.

    Article  PubMed  Google Scholar 

  33. Shibata Y, Fujita S, Takahashi H, Yamaguchi A, Koji T. Assessment of decalcifying protocols for detection of specific RNA by non-radioactive in situ hybridization in calcified tissues. Histochem Cell Biol. 2000;113:153–9.

    Article  PubMed  Google Scholar 

  34. Takemoto H. Morphological analyses of the human tongue musculature for three-dimensional modeling. J Speech Lang Heat Res. 2001;44:1–13.

    Google Scholar 

  35. Nowinski WL, Johnson A, Chua BC, Nowinska NG. Three-dimensional interactive and stereotactic atlas of the cranial nerves and their nuclei correlated with surface neuroanatomy, vasculature and magnetic resonance imaging. J Neuro Meth. 2012;206:205–16.

    Article  Google Scholar 

  36. Schaffer J. Collective Review. Os Om Op: Clinical pathology of the tongue; 1951. p. 1287–316.

    Google Scholar 

  37. McClung JR, Goldberg SJ. Functional anatomy of the hypoglossal innervated muscles of the rat tongue: a model for elongation and protrusion of the mammalian tongue. Anat Rec. 2000;260:378–86.

    Article  PubMed  Google Scholar 

  38. O’Reilly PMR, Fitzgerald MJT. Fiber composition of the hypoglossal nerve in the rat. J Anat. 1990;172:227–43.

    PubMed Central  PubMed  Google Scholar 

  39. Im K, Lee JM, Jeon S, Kim JH, Seo SW, Na DL, Grant PE. Reliable identification of deep sulcal pits: The effects of scan session, scanner, and surface extraction tool. PLoS One. 2013;8:e53678 1– 10.

    Google Scholar 

  40. Saito S, Murase K. Detection and early phase assessment of radiation-induced lung injury in mice using micro-CT. PLoS One. 2012;7:e459601–6.

    Google Scholar 

  41. Fiebig T, Boll H, Figueiredo G, Kerl HU, Nittka S, Groden C, Kramer M, Brockmann MA. Three-dimensional in vivo imaging of the murine liver. PLoS One. 2012;7:e311791–9.

    Google Scholar 

  42. Mu L, Sanders I. Newly revealed cricothyropharyngeus muscle in the human laryngopharynx. Anat Rec. 2008;291:927–38.

    Article  Google Scholar 

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Acknowledgments

We are grateful to Prof. M. Tsuchimochi of the Department of Oral and Maxillofacial Radiology of the Nippon Dental University School of Life Dentistry at Niigata for his encouragement and constant support. We also wish to thank Prof. A. Ezura of General Dentistry at the Nippon Dental University School of Life Dentistry at Niigata for his help and suggestions. This research was supported by Research Promotion Grants (No. NDUF-12-07) from the Nippon Dental University.

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The authors declare that they have no conflict of interest.

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Correspondence to Hidekazu Aoyagi.

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Aoyagi, H., Iwasaki, Si. & Nakamura, K. Three-dimensional observation of mouse tongue muscles using micro-computed tomography. Odontology 103, 1–8 (2015). https://doi.org/10.1007/s10266-013-0131-4

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  • DOI: https://doi.org/10.1007/s10266-013-0131-4

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