Multipotent stromal cells derived from the infrapatellar fat pad of the knee

被引:312
作者
Wickham, MQ
Erickson, GR
Gimble, JM
Vail, TP
Guilak, F
机构
[1] Duke Univ, Med Ctr, Orthopaed Res Labs, Dept Surg, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Orthopaed Res Labs, Dept Biomed Engn, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Orthopaed Res Labs, Dept Mech Engn & Mat Sci, Durham, NC 27710 USA
[4] Artecel Sci Inc, Durham, NC USA
关键词
D O I
10.1097/01.blo.0000072467.53786.ca
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Tissue engineering approaches for promoting the repair of skeletal tissues have focused on cell-based therapies involving multipotent stromal cells. Recent studies have identified such cells in several tissues in the adult human, including skin, muscle, bone marrow, and subcutaneous fat. This study examined the hypothesis that the infrapatellar fat pad of the adult knee contains progenitor cells that have the ability to differentiate into chondrocytes, osteoblasts, or adipocytes under appropriate culture conditions. Cells isolated from the fat pad stroma had a profile of cell-surface molecules similar but not identical to that of bone marrow-derived mesenchymal stem cells. Using defined culture conditions, fat pad-derived stromal cells were induced to differentiate cells with phenotypic characteristics of: (1) chondrocytes, synthesizing cartilage matrix molecules; (2) adipocytes, producing lipid vacuoles and leptin; or (3) osteoblasts, forming mineralized tissue. The culture conditions also modulated the expression of characteristic gene markers for each lineage. This study supports the hypothesis that multipotent stromal cells are present in many connective tissues in the adult human. Given its location and accessibility, the fat pad may prove to be a potential source of progenitor cells for musculoskeletal tissue engineering.
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页码:196 / 212
页数:17
相关论文
共 76 条
  • [1] Engineering of osteochondral tissue with bone marrow mesenchymal progenitor: Cells in a derivatized hyaluronan-gelatin composite sponge
    Angele, P
    Kujat, R
    Nerlich, M
    Yoo, J
    Goldberg, V
    Johnstone, B
    [J]. TISSUE ENGINEERING, 1999, 5 (06): : 545 - 553
  • [2] [Anonymous], 1997, CLIN ORTHOP RELAT R, DOI DOI 10.1097/00003086-199709000-00033
  • [3] [Anonymous], CLIN ORTHOPAEDICS
  • [4] Chondrogenic differentiation of mesenchymal stem cells from bone marrow: Differentiation-dependent gene expression of matrix components
    Barry, F
    Boynton, RE
    Liu, BS
    Murphy, JM
    [J]. EXPERIMENTAL CELL RESEARCH, 2001, 268 (02) : 189 - 200
  • [5] The monoclonal antibody SH-2, raised against human mesenchymal stem cells, recognizes an epitope on endoglin (CD105)
    Barry, FP
    Boynton, RE
    Haynesworth, S
    Murphy, JM
    Zaia, J
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 265 (01) : 134 - 139
  • [6] Uno, nessuno e centomila:: Searching for the identity of mesodermal progenitors
    Bianco, P
    Cossu, G
    [J]. EXPERIMENTAL CELL RESEARCH, 1999, 251 (02) : 257 - 263
  • [7] Effect of cultured autologous chondrocytes on repair of chondral defects in a canine model
    Breinan, HA
    Minas, T
    Hsu, HP
    Nehrer, S
    Sledge, CB
    Spector, M
    [J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1997, 79A (10) : 1439 - 1451
  • [8] TREATMENT OF DEEP CARTILAGE DEFECTS IN THE KNEE WITH AUTOLOGOUS CHONDROCYTE TRANSPLANTATION
    BRITTBERG, M
    LINDAHL, A
    NILSSON, A
    OHLSSON, C
    ISAKSSON, O
    PETERSON, L
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (14) : 889 - 895
  • [9] BRITTBERG M, 1996, CLIN ORTHOP RELAT R, V326, P270
  • [10] Bone regeneration by implantation of purified, culture-expanded human mesenchymal stem cells
    Bruder, SP
    Kurth, AA
    Shea, M
    Hayes, WC
    Jaiswal, N
    Kadiyala, S
    [J]. JOURNAL OF ORTHOPAEDIC RESEARCH, 1998, 16 (02) : 155 - 162