Comparison of Immuno-Phenotypes of Stem Cells from Human Dental Pulp and Periodontal Ligament

Author:

Ponnaiyan D.1,Bhat K.M.2,Bhat G.S.3

Affiliation:

1. Department of Periodontics, S.R.M Dental College and Hospital, Chennai, Tamil Nadu

2. Department of Periodontics, Manipal College of Dental Sciences, Manipal, Karnataka

3. Department of Periodontics, Manipal College of Dental Sciences, Manipal, Karnataka, India

Abstract

It has been established that human dental pulp and periodontal ligament contain a population of mesenchymal stem cells (MSCs). However, the phenotypic analysis in terms of putative stem cell markers expressed by these stem cell populations is incomplete. It is relevant to understand whether stem cells derived from closely related tissues are programmed differently. The aim of the present study is to analyze whether these stem cells depict distinct characteristics by gaining insight into differences in their immunophenotype. Dental pulp and periodontal ligament tissue samples were obtained from extracted impacted wisdom teeth. Cell cultures were analyzed for surface and intracellular markers by indirect immunoflourescence. Detailed immunophenotype analysis was carried out by flow cytometry using relevant markers. The present study data shows dental pulp stem cells (DPSCs) and periodontal ligament stem cells (PDLSCs) expressed embryonic stem (ES) cell markers Oct-4, Nanog and mesodermal marker Vimentin by indirect immunoflourescence. PDLSCs, however, had a weak expression of Nanog. Immunophenotyping revealed strong expression of MSC markers (CD73, CD90) in DPSCs and PDLSCs. Differences were observed in expression of sternness-related markers. DPSCs displayed increased percentages of SSEA4, CD13 and CD166 and decreased CD9 expression compared to PDLSCs. Both stem cells express common MSC markers, different levels of expression suggests there might be more than one stem cell population existing within these tissues which differ in their embryonic status, and DPSCs are a more primitive stem cell population in comparison to PDLSCs.

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

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