Rock activity and the gβγ complex mediate chemotactic migration of mouse bone marrow-derived stromal cells
Ryan, Caroline M.
Brown, James A. L.
Prendergast, Áine M.
Barry, Frank P.
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Ryan, Caroline M. Brown, James A. L.; Bourke, Emer; Prendergast, Áine M.; Kavanagh, Claire; Liu, Zhonglin; Owens, Peter; Shaw, Georgina; Kolch, Walter; O’Brien, Timothy; Barry, Frank P. (2015). Rock activity and the gβγ complex mediate chemotactic migration of mouse bone marrow-derived stromal cells. Stem Cell Research & Therapy 6 ,
Introduction: Bone marrow-derived stromal cells (BMSCs), also known as mesenchymal stem cells, are the focus of intensive efforts worldwide to elucidate their function and biology. Despite the importance of BMSC migration for their potential therapeutic uses, the mechanisms and signalling governing stem cell migration are still not fully elucidated. Methods: We investigated and detailed the effects of MCP-1 activation on BMSCs by using inhibitors of G protein-coupled receptor alpha beta (GPCR alpha beta), ROCK (Rho-associated, coiled-coil containing protein kinase), and PI3 kinase (PI3K). The effects of MCP-1 stimulation on intracellular signalling cascades were characterised by using immunoblotting and immunofluorescence. The effectors of MCP-1-mediated migration were investigated by using migration assays (both two-dimensional and three-dimensional) in combination with inhibitors. Results: We established the kinetics of the MCP-1-activated signalling cascade and show that this cascade correlates with cell surface re-localisation of chemokine (C motif) receptor 2 (CCR2) (the MCP-1 receptor) to the cell periphery following MCP-1 stimulation. We show that MCP-1-initiated signalling is dependent on the activation of beta gamma subunits from the GPCR alpha beta gamma complex. In addition, we characterise a novel role for PI3K gamma signalling for the activation of both PAK and ERK following MCP-1 stimulation. We present evidence that the G beta gamma complex is responsible for PI3K/Akt, PAK, and ERK signalling induced by MCP-1 in BMSCs. Importantly, we found that, in BMSCs, inhibition of ROCK significantly inhibits MCP-1-induced chemotactic migration, in contrast to previous reports in other systems. Conclusions: Our results indicate differential chemotactic signalling in mouse BMSCs, which has important implications for the translation of in vivo mouse model findings into human trials. We identified novel components and interactions activated by MCP-1-mediated signalling, which are important for stem cell migration. This work has identified additional potential therapeutic targets that could be manipulated to improve BMSC delivery and homing.