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Isolation and characterization of multipotent human periodontal ligament stem cells.

Isolation and characterization of multipotent human periodontal ligament stem cells. Research Abstract Details 

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  • Isolation and characterization of multipotent human periodontal ligament stem cells. Abstract Text:

    i c gayI C Gay,s chenS Chen,m macdougallM MacDougall,

    BACKGROUND: Periodontal ligament (PDL) repair is thought to involve mesenchymal progenitor cells capable of forming fibroblasts, osteoblasts and cementoblasts. However, full characterization of PDL stem cell (SC) populations has not been achieved. OBJECTIVE: To isolate and characterize PDLSC and assess their capability to differentiate into bone, cartilage and adipose tissue. METHODS: Human PDL cells were stained for STRO-1, FACS sorted and expanded in culture. Human bone marrow SC (BMSC) served as a positive control. PDLSC and BMSC were cultured using standard conditions conducive for osteogenic, chondrogenic and adipogenic differentiation. Osteogenic induction was assayed using alizarine red S staining and expression of alkaline phosphatase (ALP) and bone sialoprotein (BSP). Adipogenic induction was assayed using Oil Red O staining and the expression of PPAR gamma 2 (early) and LPL (late) adipogenic markers. Chondrogenic induction was assayed by collagen type II expression and toluidine blue staining. RESULTS: Human PDL tissue contains about 27% STRO-1 positive cells with 3% strongly positive. In osteogenic cultures ALP was observed by day-7 in BMSC and day-14 in PDLSC. BSP expression was detectable by day-7; with more intense staining in PDLSC cultures. In adipogenic cultures both cell populations showed positive Oil Red O staining by day-25 with PPAR gamma 2 and LPL expression. By day-21, both BMSC and PDLSC chondrogenic induced cultures expressed collagen type II and glycosaminoglycans. CONCLUSIONS: The PDL contains SC that have the potential to differentiate into osteoblasts, chondrocytes and adipocytes, comparable with previously characterized BMSC. This adult PDLSC population can be utilized for potential therapeutic procedures related to PDL regeneration.

    Isolation and characterization of multipotent human periodontal ligament stem cells. Publishing Authors By Initials

    ic gayIC Gay,s chenS Chen,m macdougallM MacDougall,

    For similar sialoglycoproteins research abstracts see: sialoglycoproteins research

    PUBMED ID PMID:

    MEDLINE DATE:

    Isolation and characterization of multipotent human periodontal ligament stem cells. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Orthodontics & craniofacial research

    VOLUME: 10

    Page Numbers: 149-60

    Journal Abbreviation:

    ISSN: 1601-6335

    DAY: 3

    MONTH: Aug

    YEAR: 2007

    Isolation and characterization of multipotent human periodontal ligament stem cells. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101144387

    Isolation and characterization of multipotent human periodontal ligament stem cells. Keywords Mesh Terms:

    KEYWORDS: Sialoglycoproteins

    MESH TERMS: analysis

    Chemical & Substance for Abstract: Isolation and characterization of multipotent human periodontal ligament stem cells. Information

    Substance Name: Alkaline Phosphatase

    Registry Number: EC 3.1.3.1

    Grant and Affiliation Information for Isolation and characterization of multipotent human periodontal ligament stem cells.

    AFFILIATION: Institute of Oral Health Research, School of Dentistry, University of Alabama at Birmingham, Birmingham, AL 35294-0007, USA.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NCI

    GRANT: DE14318CO-STAR

    ACRONYM: CO

    MEDLINETA: Orthod Craniofac Res

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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