دورية أكاديمية

DNA damage in dental pulp mesenchymal stem cells: An in vitro study.

التفاصيل البيبلوغرافية
العنوان: DNA damage in dental pulp mesenchymal stem cells: An in vitro study.
المؤلفون: Aramburú Junior JS; Graduate Program in Veterinary Medicine, Federal University of Santa Maria, Santa Maria, Brazil.; Biotecnos Research Center, Santa Maria, Rio Grande do Sul, Brazil; Catholic University of Uruguay, Montevideo, Uruguay., Eilers Treichel TL; Graduate Program in Veterinary Medicine, Federal University of Santa Maria, Santa Maria, Brazil., Lemos Pinto Filho ST; Graduate Program in Veterinary Medicine, Federal University of Santa Maria, Santa Maria, Brazil., Gehrke SA; Biotecnos Research Center, Santa Maria, Rio Grande do Sul, Brazil; Catholic University of Uruguay, Montevideo, Uruguay., Machado AK; Morphology Department, Federal University of Santa Maria, Santa Maria, Brazil., Cadoná FC; Morphology Department, Federal University of Santa Maria, Santa Maria, Brazil., Mânica da Cruz IB; Morphology Department, Federal University of Santa Maria, Santa Maria, Brazil., Pippi NL; Graduate Program in Veterinary Medicine, Federal University of Santa Maria, Santa Maria, Brazil.
المصدر: Veterinary research forum : an international quarterly journal [Vet Res Forum] 2018 Fall; Vol. 9 (4), pp. 293-299. Date of Electronic Publication: 2018 Dec 15.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Urmia University Press Country of Publication: Iran NLM ID: 101625812 Publication Model: Print-Electronic Cited Medium: Print ISSN: 2008-8140 (Print) Linking ISSN: 20088140 NLM ISO Abbreviation: Vet Res Forum Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Urmia : Urmia University Press
مستخلص: The aim of this study was to evaluate the potential use of a DNA comet assay, DNA fragmentation fluorimetric assay and reactive oxygen species levels as potential biomarkers of genome conditions of dental pulp stem cells (DPSCs) isolated from dog canine teeth. Mesenchymal stem cells were isolated from the dental pulp collected from dog teeth. The results obtained suggest the ideal moment for clinical application of cellular therapy for this type of cell. The cell culture was maintained with Dulbecco's modified Eagle's medium supplemented with 10.00% fetal bovine serum for eight passages. During each passage, cell proliferation, oxidative stress and level of DNA fragmentation were assessed by3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyltetrazolium (MTT) assay, testing 2,7 dichlorodihydro-fluorescein-diacetate and PicoGreen ® , respectively. There were important differences among the first three DPSC passages compared to passages 4-8 and a large number of nuclei with some levels of DNA damage (30.00 to 40.00% in initial DPSC passages and > 50.00% in late passages), indicating in vitro DPSC genomic fragility. Within the limitations of this study, the results suggest these relatively simple and inexpensive approaches - comet and DNA fragmentation assays - could help sort stem cells with less DNA damage for use in research or therapies.
Competing Interests: The authors declare that there is no conflicts of interest.
References: Anal Biochem. 1999 Jun 1;270(2):195-200. (PMID: 10334836)
Environ Mol Mutagen. 2000;35(3):206-21. (PMID: 10737956)
Proc Natl Acad Sci U S A. 2000 Dec 5;97(25):13625-30. (PMID: 11087820)
Mech Ageing Dev. 2001 May 31;122(7):713-34. (PMID: 11322994)
J Histochem Cytochem. 2001 Sep;49(9):1183-6. (PMID: 11511687)
Neoplasia. 2002 Jan-Feb;4(1):19-31. (PMID: 11922387)
Mutagenesis. 2003 Jan;18(1):45-51. (PMID: 12473734)
Nat Biotechnol. 2004 Apr;22(4):381-2; author reply 382. (PMID: 15060545)
Lancet. 2004 Jul 10-16;364(9429):149-55. (PMID: 15246727)
Methods Cell Biol. 2004;77:91-112. (PMID: 15602907)
Neurotoxicology. 2006 Jan;27(1):101-7. (PMID: 16168488)
Stem Cell Rev. 2005;1(2):139-44. (PMID: 17142848)
Cytotechnology. 2008 Sep;58(1):17-23. (PMID: 19002773)
Nat Protoc. 2009;4(2):125-31. (PMID: 19180084)
J Endod. 2009 Nov;35(11):1536-42. (PMID: 19840643)
Regen Med. 2009 Nov;4(6):899-909. (PMID: 19903007)
Adv Biochem Eng Biotechnol. 2010;123:219-63. (PMID: 20309674)
Tissue Eng Part C Methods. 2010 Dec;16(6):1575-83. (PMID: 20528665)
Cell Transplant. 2011;20(2):271-85. (PMID: 20719084)
Blood. 2011 Apr 28;117(17):4420-4. (PMID: 21304104)
PLoS One. 2011;6(5):e20514. (PMID: 21633706)
J Endod. 2011 Jul;37(7):973-9. (PMID: 21689554)
Stem Cells. 2011 Oct;29(10):1479-84. (PMID: 21898683)
J Mol Histol. 2012 Feb;43(1):89-94. (PMID: 22109772)
Tissue Eng Part C Methods. 2012 Jun;18(6):444-52. (PMID: 22195986)
Bull Exp Biol Med. 2011 Aug;151(4):550-2. (PMID: 22448389)
Nat Rev Genet. 2012 Oct;13(10):732-44. (PMID: 22965355)
Arch Oral Biol. 2012 Nov;57(11):1439-58. (PMID: 22981360)
Biochim Biophys Acta. 2013 Feb;1830(2):2345-53. (PMID: 22995214)
Mutat Res. 2013 Jan-Mar;752(1):25-35. (PMID: 23010441)
Ann Hematol. 2013 May;92(5):595-604. (PMID: 23307598)
Exp Cell Res. 1988 Mar;175(1):184-91. (PMID: 3345800)
فهرسة مساهمة: Keywords: DNA damage; Dental pulp; Genotoxicity; Mesenchymal stem cell; Oxidative stress
تواريخ الأحداث: Date Created: 20190205 Latest Revision: 20201001
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC6346493
DOI: 10.30466/vrf.2018.33083
PMID: 30713606
قاعدة البيانات: MEDLINE