Isolation and characterization of a population of immature dental pulp stem cells expressing OCT-4 and other embryonic stem cell markers

被引:329
作者
Kerkis, Irina
Kerkis, Alexandre
Dozortsev, Dmitri
Stukart-Parsons, Gaelle Chopin
Massironi, Silvia Maria Gomes
Pereira, Lygia V.
Caplan, Arnold I.
Cerruti, Humberto F.
机构
[1] Inst Butantan, Genet Lab, BR-05503900 Sao Paulo, SP, Brazil
[2] Clin CERA, Sao Paulo, Brazil
[3] Clin & Ctr Pesquisa Reprod Humana Roger Abdelmass, Sao Paulo, Brazil
[4] Univ Sao Paulo, Inst Biociencias, Dept Biol, Sao Paulo, Brazil
[5] Univ Sao Paulo, Inst Ciencias Biomed, Dept Imunol, BR-05508 Sao Paulo, Brazil
[6] Case Western Reserve Univ, Skeletal Res Ctr, Cleveland, OH 44106 USA
关键词
dental pulp stem cells; embryonic stem cell markers; engraftment; spontaneous differentiation; stem cell therapy;
D O I
10.1159/000099617
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
We report the isolation of a population of immature dental pulp stem cells (IDPSC), which express embryonic stem cell markers Oct-4, Nanog, SSEA-3, SSEA-4, TRA-1-60 and TRA-181 as well as several other mesenchymal stem cell markers during at least 25 passages while maintaining the normal karyotype and the rate of expansion characteristic of stem cells. The expression of these markers was maintained in subclones obtained from these cells. Moreover, in vitro these cells can be induced to undergo uniform differentiation into smooth and skeletal muscles, neurons, cartilage, and bone under chemically defined culture conditions. After in vivo transplantation of these cells into immunocompromised mice, they showed dense engraftment in various tissues. The relative ease of recovery and the expression profiles of various markers justify further exploration of IDPSC for clinical therapy. Copyright (c) 2007 S. Karger. AG, Basel
引用
收藏
页码:105 / 116
页数:12
相关论文
共 38 条
  • [1] Context, tissue plasticity, and cancer: Are tumor stem cells also regulated by the microenvironment?
    Bissell, MJ
    LaBarge, MA
    [J]. CANCER CELL, 2005, 7 (01) : 17 - 23
  • [2] MESENCHYMAL STEM-CELLS
    CAPLAN, AI
    [J]. JOURNAL OF ORTHOPAEDIC RESEARCH, 1991, 9 (05) : 641 - 650
  • [3] Mesenchymal stem cells: Cell-based reconstructive therapy in orthopedics
    Caplan, AI
    [J]. TISSUE ENGINEERING, 2005, 11 (7-8): : 1198 - 1211
  • [4] Design parameters for functional tissue engineering
    Caplan, AI
    [J]. FUNCTIONAL TISSUE ENGINEERING, 2003, : 129 - 138
  • [5] Mesenchymal stem cells: building blocks for molecular medicine in the 21st century
    Caplan, AI
    Bruder, SP
    [J]. TRENDS IN MOLECULAR MEDICINE, 2001, 7 (06) : 259 - 264
  • [6] Tissue engineering designs for the future: New logics, old molecules
    Caplan, AI
    [J]. TISSUE ENGINEERING, 2000, 6 (01): : 1 - 8
  • [7] Caplan AI, 2004, HDB STEM CELLS, V2, P299
  • [8] Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells
    Chambers, I
    Colby, D
    Robertson, M
    Nichols, J
    Lee, S
    Tweedie, S
    Smith, A
    [J]. CELL, 2003, 113 (05) : 643 - 655
  • [9] In vivo proliferation and cell cycle kinetics of long-term self-renewing hematopoietic stem cells
    Cheshier, SP
    Morrison, SJ
    Liao, XS
    Weissman, IL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) : 3120 - 3125
  • [10] Stemness, fusion and renewal of hematopoietic and embryonic stem cells
    Constantinescu, S
    [J]. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2003, 7 (02): : 103 - 112