Description
ROCK inhibition affects morphology and MCP-1-induced migration in mouse BMSCs. Permeabilised serum-starved BMSCs immunofluorescently stained with F-actin (red) and α-tubulin (green) and DNA counter-stained with DAPI (blue). a Serum-starved BMSCs polarise in response to MCP-1; 10 μM Y27632 pre-treatment (24 h) results in a stellate morphology, with or without MCP-1 treatment. Scale bar = 10 μm. b Immunofluorescent images of representative fields of serum-starved (24 h) BMSCs pre-treated with 10 μM Y27632 and exposed to a gradient of MCP-1 in a 2D assay. Permeabilised serum-starved BMSC stained with F-actin (red) and α-tubulin (green) and DNA stained with DAPI (blue). Scale bar = 30 μm. 2D two-dimensional, BMSC bone marrow-derived stromal cell, DAPI 4′,6-diamidino-2-phenylindole, MCP-1 monocyte chemoattractant protein 1, ROCK Rho-associated, coiled-coil containing protein kinase. (PNG 1480 kb)
| Date made available | 2015 |
|---|---|
| Publisher | figshare |
Research output
- 1 Article
-
ROCK activity and the Gβγ complex mediate chemotactic migration of mouse bone marrow-derived stromal cells
Ryan, C. M., Brown, J. A. L., Bourke, E., Prendergast, Á. M., Kavanagh, C., Liu, Z., Owens, P., Shaw, G., Kolch, W., O'Brien, T. & Barry, F. P., Jul 24 2015, In: Stem Cell Research and Therapy. 6, 1, 136.Research output: Contribution to journal › Article › peer-review
Open Access15 Link opens in a new tab Scopus citations
Cite this
- DataSetCite