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Overexpression of CXC chemokine receptors is required for the superior glioma-tracking property of umbilical cord blood-derived mesenchymal stem cells.

Abstract
Our observations indicate that umbilical cord blood-derived mesenchymal stem cells (UCB-MSCs) have a strong migration capacity toward the human glioma cell line, U-87 MG, LN18, U138, and U251, when compared to several other cancer cell lines. In order to identify soluble factors that function to attract UCB-MSCs, we used cytokine antibody arrays to screen changed cytokines in conditioned media from U-87 MG cells. Among these, interleukin-8 (IL-8) and growth-related oncogene (GRO-alpha) enhanced UCB-MSC migration. Furthermore, antibodies treatment against the IL-8 receptors reduced these migration events and overexpression of IL-8 in cells with lower level of IL-8 such as A549 could induce UCB-MSC migration. Since we found that the capacity of UCB-MSC migration is much higher than that of bone marrow-derived MSCs (BM-MSCs) toward either U-87 MG cells or recombinant IL-8, we compared the levels of the IL-8 receptor, CXC chemokine receptor 1 (CXCR1) and CXCR2 between two kinds of MSCs by RT-PCR and immunostaining. Expression levels of two receptors were much higher in UCB-MSCs than in BM-MSCs. These data suggest that higher levels of two IL-8 receptors could influence downstream signaling events affecting superior UCB-MSC migration toward the glioma cells.
AuthorsDal-Soo Kim, Ji Hyun Kim, Jae Kwon Lee, Soo Jin Choi, Jae-Sung Kim, Sin-Soo Jeun, Wonil Oh, Yoon Sun Yang, Jong Wook Chang
JournalStem cells and development (Stem Cells Dev) Vol. 18 Issue 3 Pg. 511-9 (Apr 2009) ISSN: 1557-8534 [Electronic] United States
PMID18624673 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Interleukin-8
  • Receptors, CXCR
  • Receptors, Interleukin-8
Topics
  • Cell Line, Tumor
  • Cell Movement (physiology)
  • Cells, Cultured
  • Fetal Blood (cytology)
  • Glioma (metabolism, pathology)
  • Humans
  • Interleukin-8 (metabolism)
  • Mesenchymal Stem Cells (cytology, physiology)
  • Receptors, CXCR (genetics, metabolism)
  • Receptors, Interleukin-8 (genetics, metabolism)

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