Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/99841
Title: Neural cell adhesion molecule modulates mesenchymal stromal cell migration via activation of MAPK/ERK signaling
Authors: Shi, Yu
Xia, Yinyan
Wang, Lei
Liu, Rui
Khoo, King-Shung
Feng, Zhiwei
Keywords: DRNTU::Science::Biological sciences
Issue Date: 2012
Source: Shi, Y., Xia, Y., Wang, L., Liu, R., Khoo, K. S., & Feng, Z. (2012). Neural cell adhesion molecule modulates mesenchymal stromal cell migration via activation of MAPK/ERK signaling. Experimental cell research, 318(17), 2257-2267.
Series/Report no.: Experimental cell research
Abstract: Mesenchymal Stromal Cells (MSCs) represent promising tools for cellular therapy owing to their multipotentiality and ability to localize to injured, inflamed sites and tumor. Various approaches to manipulate expression of MSC surface markers, including adhesion molecules and chemokine receptors, have been explored to enhance homing of MSCs. Recently, Neural Cell Adhesion Molecule (NCAM) has been found to be expressed on MSCs yet its function remains largely elusive. Herein, we show that bone marrow-derived MSCs from NCAM deficient mice exhibit defective migratory ability and significantly impaired adipogenic and osteogenic differentiation potential. We further explore the mechanism governing NCAM mediated migration of MSCs by showing the interplay between NCAM and Fibroblast Growth Factor Receptor (FGFR) induces activation of MAPK/ERK signaling, thereby the migration of MSCs. In addition, re-expression of NCAM180, but not NCAM140, could restore the defective MAPK/ERK signaling thereby the migration of NCAM deficient MSCs. Finally, we demonstrate that NCAM180 expression level could be manipulated by pro-inflammatory cytokine Tumor Necrosis Factor (TNF)-α treatment. Overall, our data reveal the vital function of NCAM in MSCs migration and differentiation thus raising the possibility of manipulating NCAM expression to enhance homing and therapeutic potential of MSCs in cellular therapy.
URI: https://hdl.handle.net/10356/99841
http://hdl.handle.net/10220/16216
DOI: http://dx.doi.org/10.1016/j.yexcr.2012.05.029
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SBS Journal Articles

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