Journal List > J Korean Acad Conserv Dent > v.33(4) > 1056310

Ahn, Kim, Kim, Kim, Kim, Lee, and Lee: Evaluation of the viability of periodontal ligament cell in rat teeth using slow cryopreservation method with magnetic field

Abstract

The purpose of this study was to evaluate the viability of periodontal ligament cell in rat teeth using slow cryopreservation method with magnetic field through MTT assay and TUNEL test. For each group, 12 teeth of 4 weeks old white female Sprague-Dawley rat were used for MTT assay, and 6 teeth in TUNEL test. The Maxillary left and right, first and second molars were extracted as atraumatically as possible under tiletamine anesthesia. The experimental groups were group1 (immediately extraction), group 2 (cold preservation at 4℃ for 1 week), group 3 (rapid cryopreservation in liquid nitrogen), group 4 (slow cryopreservation with magnetic field of 1 G), and group 5 (slow cryopreservation). F medium was used as preservation medium and 10% DMSO as cryoprotectant. After preservation and thawing, the MTT assay and TUNEL test were processed. One way ANOVA and Scheffe method were performed at the 95% level of confidence. The value of optical density obtained after MTT analysis was divided by the value of eosin staining for tissue volume standardization. In both MTT assay and TUNEL test, it had showed no significant difference among group 3, 4, and 5. And group 3 had showed higher viability of periodontal ligament cell than group 2.
From this study, slow cryopreservation method with magnetic field can be used as one of cryopreservation methods.

Figures and Tables

Figure 1
MTT/Eosin ratio.
1: immediately extraction
2: cold preservation at 4℃
3: rapid cryopresevation in liquid nitrogen
4: slow cryopreservation with magnetic field of 1G
5: slow cryopreservation
★: p < 0.05.
jkacd-33-332-g001
Figure 2
Average and standard deviation of percentage of positive cells by TUNEL test.
1: immediately extraction
2: cold preservation at 4℃
3: rapid cryopresevation in liquid nitrogen
4: slow cryopreservation with magnetic field of 1G
5: slow cryopreservation
★: p < 0.05.
jkacd-33-332-g002
Figure 3
Micrograph of experimental groups by TUNEL test. Arrow shows positive cell.
A. immediately extraction (× 400).
B. cold preservation (× 400).
C. rapid cryopreservation (× 400).
D. slow cryopreservation with magnetic field (× 400).
E. slow cryopreservation (× 400).
jkacd-33-332-g003

References

1. Kristerson L, Johansson LA, Kisch J, Stadler LE. Autotransplantation of third molars as treatment in advanced periodontal disease. J Clin Periodontol. 1991. 18:521–528.
crossref
2. Schwartz O. Cryopreservation as long-term storage of teeth for transplantation or replantation. Int J Oral Maxillofac Surg. 1986. 15:30–32.
crossref
3. Rubinsky B. Principles of low temperature cell preservation. Heart Fail Rev. 2003. 8:277–284.
4. Lovelock JE, Polge C. The immobilization of spermatozoa by freezing and thawing and the protective action of glycerol. Biochem J. 1954. 58:618–622.
crossref
5. Mazur P. Freezing of living cells: mechanisms and implications. Am J Physiol. 1984. 247:C125–C142.
crossref
6. Kawasaki N, Hamamoto Y, Nakajima T, Irie K, Ozawa H. Periodontal regeneration of transplanted rat molars after cryopreservation. Arch Oral Biol. 2004. 49:59–69.
crossref
7. Kawata T. Tooth transplantation by teeth bank-approach to human-Hiroshima. 2005. Department of Orthodontics, Hiroshima University School of Dentistry;Thesis.
8. Kim ES, Jeon IS, Kim JW, Kim J, Jung HS, Lee SJ. An MTT-based method for quantification of periodontal ligament cell viability. Oral Dis. 2007. 13:495–499.
crossref
9. Schwartz O, Andreasen JO, Greve T. Cryopreservation before replantation of mature teeth in monkeys(II). Effect of preincubation, different freezing and equilibration rates and endodontic treatment upon periodontal healing. Int J Oral Surg. 1985. 14:350–361.
10. Ashwood-Smith MJ. Low temperature preservation of cells, tissues and organs. 1980. Pitman Medical;19–45.
11. Stuart M. Wentworth. Fundamentals of electromagnetics with engineering application. 2004. 2nd ed. Chicago: Science & Technology;156–160.
12. Marsland TP, Evans S, Pegg DE. Dielectric measurements for the design of an electromagnetic rewarming system. Cryobiology. 1987. 24:311–323.
crossref
13. Wusteman M, Robinson M, Pegg D. Vitrification of large tissues with dielectric warming: biological problems and some approached to their solution. Cryobiology. 2004. 48:179–189.
crossref
14. Kaku M, Kamata H, Kawata T. Cryopreservation of PDL cells by use of program freezer with magnetic field for tooth banking. Dent Jpn (Tokyo). 2007. 43:82–86.
16. Jeon IS. Evaluation of periodontal ligament cell viability in rat teeth according to various extra-oral dry time using MTT assay and a histologic verification. 2004. Yonsei University, Graduate School;PhD Thesis.
17. Oh YH, Che ZM, Hong JC, Lee EJ, Lee SJ, Kim J. Cryopreservation of human teeth for future organization of a tooth bank-a preliminary study. Cryobiology. 2005. 51:322–329.
crossref
18. Ashkenazi M, Sarnat H, Keila S. In vitro viability, mitogenicity and clonogenic capacity of periodontal ligament cells after storage in six different media. Endod Dent Traumatol. 1999. 15:149–156.
crossref
19. Fischer S, Maclean AA, Liu M, Cardella JA, Slutsky AS, Suga M, Moreira JF, Keshavjee S. Dynamic changes in apoptotic and necrotic cell death correlate with severity of ischemia-reperfusion injury in lung transplantation. Am J Respir Crit Care Med. 2000. 162:1932–1939.
crossref
20. Kerr JF. History of the events leading to the formulation of the apoptosis concept. Toxicology. 2002. 181-182:471–474.
crossref
21. Park SY, Kim EY, Cui XS, Tae JC, Lee WD, Kim NH, Park SP, Lim JH. Increase in DNA fragmentation and apoptosis-related gene expression in frozen-thawed bovine blastocysts. Zygote. 2006. 14:125–131.
crossref
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