Ceramide-1-phosphate regulates migration of multipotent stromal cells and endothelial progenitor cells - Implications for tissue regeneration

Chihwa Kim, Gabriela Schneider, Ahmed Abdel-Latif, Kasia Mierzejewska, Manjula Sunkara, Sylwia Borkowska, Janina Ratajczak, Andrew J. Morris, Magda Kucia, Mariusz Z. Ratajczak

Research output: Contribution to journalArticlepeer-review

76 Scopus citations

Abstract

Ceramide-1-phosphate (C1P) is a bioactive lipid that, in contrast to ceramide, is an antiapoptotic molecule released from cells that are damaged and "leaky." As reported recently, C1P promotes migration of hematopoietic cells. In this article, we tested the hypothesis that C1P released upon tissue damage may play an underappreciated role in chemoattraction of various types of stem cells and endothelial cells involved in tissue/organ regeneration. We show for the first time that C1P is upregulated in damaged tissues and chemoattracts bone marrow (BM)-derived multipotent stromal cells, endothelial progenitor cells, and very small embryonic- like stem cells. Furthermore, compared to other bioactive lipids, C1P more potently chemoattracted human umbilical vein endothelial cells and stimulated tube formation by these cells. C1P also promoted in vivo vascularization of Matrigel implants and stimulated secretion of stromal cell-derived factor-1 from BM-derived fibroblasts. Thus, our data demonstrate, for the first time, that C1P is a potent bioactive lipid released from damaged cells that potentially plays an important and novel role in recruitment of stem/progenitor cells to damaged organs and may promote their vascularization.

Original languageEnglish
Pages (from-to)500-510
Number of pages11
JournalStem Cells
Volume31
Issue number3
DOIs
StatePublished - Mar 2013

Funding

FundersFunder number
National Institute of General Medical SciencesP20GM103527

    Keywords

    • Angiogenesis
    • Ceramide-1-phosphate
    • Chemotaxis
    • Human umbilical vein endothelial cell
    • Multipotent stromal cell

    ASJC Scopus subject areas

    • Molecular Medicine
    • Developmental Biology
    • Cell Biology

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