Overexpression of CXCR4 increases migration and proliferation of human adipose tissue stromal cells

被引:54
作者
Cho, Hyun Hwa
Kyoung, Kim Mi
Seo, Min Jeong
Kim, Yeon Jeong
Bae, Yong Chan
Jung, Jin Sup
机构
[1] Pusan Natl Univ, Coll Med, Dept Physiol, Pusan 602739, South Korea
[2] Pusan Natl Univ, Med Res Inst, Pusan 602739, South Korea
[3] Pusan Natl Univ, Coll Med, Dept Plast Surg, Pusan 602739, South Korea
[4] Pusan Natl Univ, Med Res Ctr Ischem Tissue Engn, Pusan 602739, South Korea
关键词
D O I
10.1089/scd.2006.15.853
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Stromal-derived factor-1 (SDF-1)-mediated CXCR4 signaling plays important roles in migration, engraftment, and proliferation of stem cells. We report here that CXCR4 overexpression on human adipose tissue stromal cells (hADSCs) using a lentiviral gene transfer technique helped navigate these cells to the injured tissues in response to SDF-1 signaling. Transduced hADSCs, expressing high levels of CXCR4, displayed an increased capacity for cellular growth and protection against etoposide-induced cell death. CXCR4-overexpressed cells showed higher ERK activity than that of vector-transduced cells. U0126, an ERK inhibitor, and AMD3100, a CXCR4 antagonist, inhibited the proliferation of CXCR4 overexpression-induced proliferation and ERK phosphorylation. CXCR4-overexpressing cells showed increased level of ss-catenin and luciferase activity driven by the Tcf promoter. Our results suggest CXCR4 overexpression for improved hADSC motility, retention, and proliferation could be beneficial for in vivo navigation and expansion of stem cells.
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页码:853 / 864
页数:12
相关论文
共 54 条
[1]   The chemokine SDF-1 is a chemoattractant for human CD34(+) hematopoietic progenitor cells and provides a new mechanism to explain the mobilization of CD34(+) progenitors to peripheral blood [J].
Aiuti, A ;
Webb, IJ ;
Bleul, C ;
Springer, T ;
GutierrezRamos, JC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (01) :111-120
[2]   Purification of primitive human hematopoietic cells capable of repopulating immune-deficient mice [J].
Bhatia, M ;
Wang, JCY ;
Kapp, U ;
Bonnet, D ;
Dick, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5320-5325
[3]   Stem cells in tissue engineering [J].
Bianco, P ;
Robey, PG .
NATURE, 2001, 414 (6859) :118-121
[4]   The lymphocyte chemoattractant SDF-1 is a ligand for LESTR/fusin and blocks HIV-1 entry [J].
Bleul, CC ;
Farzan, M ;
Choe, H ;
Parolin, C ;
ClarkLewis, I ;
Sodroski, J ;
Springer, TA .
NATURE, 1996, 382 (6594) :829-833
[5]   SDF-1 is both necessary and sufficient to promote proliferative retinopathy [J].
Butler, JM ;
Guthrie, SM ;
Koc, M ;
Afzal, A ;
Caballero, S ;
Brooks, HL ;
Mames, RN ;
Segal, MS ;
Grant, MB ;
Scott, EW .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (01) :86-93
[6]   Stromal-derived factor 1 inhibits the cycling of very primitive human hematopoietic cells in vitro and in NOD/SCID mice [J].
Cashman, J ;
Clark-Lewis, I ;
Eaves, A ;
Eaves, C .
BLOOD, 2002, 99 (03) :792-799
[7]   Endogenous Wnt signaling promotes proliferation and suppresses osteogenic differentiation in human adipose derived stromal cells [J].
Cho, HH ;
Kim, YJ ;
Kim, SJ ;
Kim, JH ;
Bae, YC ;
Ba, B ;
Jung, JS .
TISSUE ENGINEERING, 2006, 12 (01) :111-121
[8]   CXCR4 receptor expression on human retinal pigment epithelial cells from the blood-retina barrier leads to chemokine secretion and migration in response to stromal cell-derived factor 1α [J].
Crane, IJ ;
Wallace, CA ;
McKillop-Smith, S ;
Forrester, JV .
JOURNAL OF IMMUNOLOGY, 2000, 165 (08) :4372-4378
[9]   Myocardial expression of CC- and CXC-chemokines and their receptors in human end-stage heart failure [J].
Damås, JK ;
Eiken, HG ;
Oie, E ;
Bjerkeli, V ;
Yndestad, A ;
Ueland, T ;
Tonnessen, T ;
Geiran, OR ;
Aass, H ;
Simonsen, S ;
Christensen, G ;
Froland, SS ;
Attramadal, H ;
Gullestad, L ;
Aukrust, P .
CARDIOVASCULAR RESEARCH, 2000, 47 (04) :778-787
[10]   Cytokine expansion culture of cord blood CD34+ cells induces marked and sustained changes in adhesion receptor and CXCR4 expressions [J].
Denning-Kendall, P ;
Singha, S ;
Bradley, B ;
Hows, J .
STEM CELLS, 2003, 21 (01) :61-70