Peritubular dentin, a highly mineralized, non-collagenous, component of dentin: Isolation and capture by laser microdissection

Jason R. Dorvee, Alix Deymier-Black, Lauren Gerkowicz, Arthur Veis*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

We demonstrate the capability and technique to perform microdissection and isolation of select regions of untreated, mineralized dentin using laser capture. Dentin is a complex, non-homogeneous tissue comprised of a mineralized collagenous matrix (intertubular dentin [ITD]), odontoblastic processes (ODPs), a void space (tubules) that forms within the ITD left behind by the retraction of ODPs during dentin maturation, and a highly mineralized non-collagenous component that exists at the interface between the tubules and ITD known as peritubular dentin (PTD). PTD forms as the dentin matures. The ODPs retract toward the direction of the pulp; leaving very little PTD at either the DEJ or near the pulp. Statistical analysis of thin cross-sections of coronal bovine dentin imaged by light microscopy reveal that the area occupied by PTD >50%. To examine the nature of PTD and its relation to both the tubules and ITD, we devised a series of steps to carefully prepare sections of coronal bovine dentin so that areas of the dentin tissue could be cut and isolated for further analysis. We demonstrate that it is possible to selectively isolate targeted regions of dentin for analysis and that high resolution analysis of such sections can be performed using electron microscopy. Results show that the mineralized PTD has a different texture than mineralized ITD and that there is a distinct boundary between the PTD and the ITD. Selective isolation of mineralized tissue components for further analytical study opens the door for the investigation of similar enigmatic mineralized structures.

Original languageEnglish (US)
Pages (from-to)9-14
Number of pages6
JournalConnective tissue research
Volume55
Issue numberSUPPL. 1
DOIs
StatePublished - 2014

Funding

Imaging work was performed at the Northwestern University Cell Imaging Facility: generously supported by CCSG P30 CA060553 awarded to the Robert H Lurie Comprehensive Cancer Center. Microdissection was performed on Zeiss PALM microdissection system purchased with the support of NCRR 1S10RR025624-01. FE-SEM and STEM work was performed at the Northwestern Electron Probe Instrument Center (EPIC), part of Northwestern University’s Atomic and Nanoscale Characterization Experimental Center (NUANCE). This work is funded by National Institute of Health, National Institute for Dental Research R01-DE001374-53.

Keywords

  • Bovine
  • ITD
  • Molar
  • Osteocytes
  • PTD
  • Texture

ASJC Scopus subject areas

  • Molecular Biology
  • Biochemistry
  • Rheumatology
  • Cell Biology
  • Orthopedics and Sports Medicine

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