Literature DB >> 23871383

Comparative characterization of STRO-1(neg)/CD146(pos) and STRO-1(pos)/CD146(pos) apical papilla stem cells enriched with flow cytometry.

A Bakopoulou1, G Leyhausen, J Volk, P Koidis, W Geurtsen.   

Abstract

OBJECTIVE: Stem Cells residing in the Apical Papilla (SCAP) of human permanent teeth represent a promising cell source for dental tissue regeneration. Therefore, the functional and molecular properties of specific subpopulations existing within heterogeneous cultures should be further investigated to give insight whether their selection could be beneficial for targeted therapeutic applications.
DESIGN: In this study we extensively characterized SCAP cultures established from 10 healthy subjects, as well as their STRO-1(pos/)CD146(pos) and STRO-1(neg/)CD146(pos) subpopulations isolated with fluorescence-activated cell sorting. SCAP were analyzed for embryonic (Nanog, Oct3/4, SSEA-3, TRA-1-60), mesenchymal (STRO-1, CD146/MUC18, CD105/endoglin, CD24, CD90/Thy-1, CD81-TAPA, CD34, CD49f/a6-integrin), neural (CD271/NGFR, nestin) and hematopoietic (CD117/c-kit, CD45) stem cell (SC) markers using flow cytometry. Multipotentiality was evaluated with culture specific staining (Alizarin-Red-S, Oil- Red-O) and RT-PCR analysis for osteo/odontogenic (DSPP, BSP, ALP, osteocalcin, osteonectin, BMP-2, Runx2), adipogenic (lipoprotein-lipase-LPL) and neurogenic (Neurofilament/NFL-L, nestin, β-tubulin-III, NCAM) markers.
RESULTS: Our results showed that the STRO-1(pos)/CD146(pos) subpopulation demonstrated higher CFU efficiency and much higher expression of several embryonic and mesenchymal SC markers compared to the non-sorted SCAP. They also showed enhanced odontogenic differentiation potential, as evidenced by higher mineralization capacity and expression of osteo/odontogenic markers. By contrast, absence of STRO-1 in the STRO-1(neg)/CD146(pos) subpopulation yielded the opposite results and was associated with significant downgrading of the above-mentioned properties.
CONCLUSIONS: These results suggest that STRO-1(pos)/CD146(pos) SCAP cells represent a very promising adult MSCs source with enhanced multipotent SC properties that could be easily isolated with simple flow cytometric methods to be used for tissue engineering applications.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Apical papilla stem cells (SCAP); CD146 perivascular antigen; Embryonic stem cell markers; Fluorescence-activated cell sorting; Multilineage differentiation potential; STRO-1 antigen

Mesh:

Substances:

Year:  2013        PMID: 23871383     DOI: 10.1016/j.archoralbio.2013.06.018

Source DB:  PubMed          Journal:  Arch Oral Biol        ISSN: 0003-9969            Impact factor:   2.633


  20 in total

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Review 4.  Stem Cells of Dental Origin: Current Research Trends and Key Milestones towards Clinical Application.

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5.  NOTCH3 is expressed in human apical papilla and in subpopulations of stem cells isolated from the tissue.

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6.  Osteo-/odontogenic differentiation of BMP2 and VEGF gene-co-transfected human stem cells from apical papilla.

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7.  Proliferation and odontogenic differentiation of BMP2 gene‑transfected stem cells from human tooth apical papilla: an in vitro study.

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8.  Mesenchymal Stem Cells Obtained from Synovial Fluid Mesenchymal Stem Cell-Derived Induced Pluripotent Stem Cells on a Matrigel Coating Exhibited Enhanced Proliferation and Differentiation Potential.

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9.  Single CD271 marker isolates mesenchymal stem cells from human dental pulp.

Authors:  Ruth Alvarez; Hye-Lim Lee; Christine Hong; Cun-Yu Wang
Journal:  Int J Oral Sci       Date:  2015-12-18       Impact factor: 6.344

10.  Characterization of the osteogenic potential of mesenchymal stem cells from human periodontal ligament based on cell surface markers.

Authors:  Ruth Alvarez; Hye-Lim Lee; Cun-Yu Wang; Christine Hong
Journal:  Int J Oral Sci       Date:  2015-12-18       Impact factor: 6.344

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