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Establishing a technique for isolation and characterization of human periodontal ligament derived mesenchymal stem cells.
Banavar, Spoorthi Ravi; Rawal, Swati Yeshwant; Paterson, Ian Charles; Singh, Gurbind; Davamani, Fabian; Khoo, Suan Phaik; Tan, Eng Lai.
Affiliation
  • Banavar SR; Oral Diagnostic and Surgical Sciences, School of Dentistry, International Medical University, Kuala Lumpur, Malaysia.
  • Rawal SY; Department of Surgical Sciences, Marquette University, USA.
  • Paterson IC; Faculty of Dentistry, University of Malaya, Kuala Lumpur, Malaysia.
  • Singh G; School of Pharmacy, International Medical University, Kuala Lumpur, Malaysia.
  • Davamani F; School of Health Sciences, International Medical University, Kuala Lumpur, Malaysia.
  • Khoo SP; Oral Diagnostic and Surgical Sciences, School of Dentistry, International Medical University, Kuala Lumpur, Malaysia.
  • Tan EL; School of Pharmacy, International Medical University, Kuala Lumpur, Malaysia.
Saudi Dent J ; 33(7): 693-701, 2021 Nov.
Article in En | MEDLINE | ID: mdl-34803321
ABSTRACT
Mesenchymal stem cells (MSCs) are extensively used in tissue regenerative procedures. One source of MSCs is the periodontal ligament (PDL) of teeth. Isolation of MSCs from extracted teeth is reasonably simple, being less invasive and presenting fewer ethical concerns than does the harvesting of MSC's from other sites. The objectives of this study were to isolate and characterize the PDL stem cells (PDLSC) from healthy adults' extracted teeth and then to characterize them by comparing them with bone-marrow derived MSCs (BMMSC).

METHODS:

The PDL tissue was scraped from the roots of freshly extracted teeth to enzymatically digest using collagenase. The cells were sub-cultured. Flow-cytometric analysis for the MSC surface-markers CD105, CD73, CD166, CD90, CD34, CD45 and HLA-DR was performed. To confirm the phenotype, total RNA was extracted to synthesize cDNA and which was then subjected to RT-PCR. The gene-expression for Oct4A, Sox2, NANOG and GAPDH was determined by gel-electrophoresis. To assess their multilineage potential, cells were cultured with osteogenic, chondrogenic and adipogenic medium and then stained by Alizarin-red, Alcian-blue and Oil-Red-O respectively. MSCs from the bone-marrow were processed similarly to serve as controls.

RESULTS:

The cells isolated from extracted teeth expanded successfully. On flow-cytometric analysis, the cells were positive for CD73, CD90, CD105, CD166 and negative for CD34, CD45 and HLA-DR. The PDLSCs expressed Oct4A, Sox2, and NANOG mRNA with GAPDH expression. Cells cultured in the osteogenic, chondrogenic and adipogenic media stained positive for Alizarin-red, Alcian-blue and Oil- Red-O respectively. The surface marker expression and the trilineage differentiation characteristics were comparable to those of the BMMSCs.

CONCLUSIONS:

The periodontal ligament tissue of extracted teeth is a potential source of therapeutically useful MSCs. Harvesting them is not invasive and are a promising source of MSC as the PDLSCs showed characteristics similar to those of the highly regarded MSC's derived from bone-marrow.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Aspects: Ethics Language: En Journal: Saudi Dent J Year: 2021 Document type: Article Affiliation country: Malaysia

Full text: 1 Collection: 01-internacional Database: MEDLINE Aspects: Ethics Language: En Journal: Saudi Dent J Year: 2021 Document type: Article Affiliation country: Malaysia