“…These results provide an insight how altered gravity regulates the functions of neutrophils and the underlying mechanisms which mediate the innate immune responses for long-term, manned spaceflight. Grenon et al 2013; bFGF ↓ HDTBR, head-down-tilt bed rest; RWV, rotating wall vessel (i.e., RCCS used in the current work); RPM, random positioning machine IL, interleukin; G-CSF, granulocyte-macrophage colony-stimulating factor; MIP-1α, macrophage inflammatory protein-1α; MCP-1, monocyte chemotactic protein 1; TNF-α, tumour necrosis factor-α; IFN-γ , Interferon-γ ; TGF-β, transforming growth factor-β; bFGF, basic fibroblast growth factor LFA-1, lymphocyte function-associated antigen-1; Mac-1, macrophage-1 antigen; ICAM-1, VLA-4, very late antigen 4; PSGL-1, P-selectin glycoprotein ligand 1; ICAM-1, intercellular cell adhesion molecule-1; PECAM-1, platelet/endothelial cell adhesion molecule 1; VCAM-1, vascular cell adhesion molecule 1 NO, nitric oxide; eNOS, endothelial nitric oxide synthase H 2 O 2 , hydrogen peroxide; ROS, reactive oxygen species Legend: ↑, increased; ↓, decreased; -, unchanged The cytoskeletal proteins have been proposed as potential gravity sensor, and significant changes of cytoskeletal network have been observed under microgravity environment both during spaceflight and in ground-based simulation techniques (Vorselen et al 2014). Although we have not seen obvious disorganization of the F-actin under the effects of simulated microgravity, the cell shape changes of HL-60 cells (Fig.…”