Microgravity Signal Ensnarls Cell Adhesion, Cytoskeleton, and Matrix Proteins of Rat Osteoblasts

Abstract:  Rat osteoblasts were cultured for 4 or 5 days aboard the Space Shuttle and solubilized during spaceflight. Post‐flight analyses by quantitative reverse transcriptase‐polymerase chain reaction (RT‐PCR) determined the relative mRNA levels of matrix proteins, adhesion molecules, and cytoskeletal proteins including osteopontin (OP), osteonectin (ON), CD44, α‐tubulin, actin, vimentin, fibronectin (FN), and β1‐integrin. The mRNA levels of OP and α‐tubulin in the flight cultures were decreased by 30% and 50% on day 4 and day 5 of flight, as compared to the ground controls. In contrast, the CD44 mRNA levels in the flight cultures increased by 280% and 570% of the ground controls on day 4 and day 5. The mRNA levels of ON and FN in the flight cultures were slightly increased as compared to ground controls. The mRNA levels of actin, vimentin, or β1‐integrin did not change in spaceflight conditions. The matrix proteins, adhesion molecules, and cytoskeletal proteins may form dynamic network complexity with signaling molecules as an adaptive response to perturbation of mechanical stress under microgravity.

[1]  C. Steele,et al.  Influence of increased mechanical loading by hypergravity on the microtubule cytoskeleton and prostaglandin E2 release in primary osteoblasts. , 2005, American journal of physiology. Cell physiology.

[2]  W. Fu,et al.  Prostaglandin E2 Stimulates Fibronectin Expression through EP1 Receptor, Phospholipase C, Protein Kinase Cα, and c-Src Pathway in Primary Cultured Rat Osteoblasts* , 2005, Journal of Biological Chemistry.

[3]  M. Noda,et al.  Osteopontin Expression in Osteoblasts and Osteocytes During Bone Formation Under Mechanical Stress in the Calvarial Suture In Vivo , 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[4]  Sadao Morita,et al.  Suppression of osteoblastic phenotypes and modulation of pro- and anti-apoptotic features in normal human osteoblastic cells under a vector-averaged gravity condition. , 2003, Journal of medical and dental sciences.

[5]  M. Noda,et al.  Resistance to Unloading‐Induced Three‐Dimensional Bone Loss in Osteopontin‐Deficient Mice , 2002, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[6]  M. Ringuette,et al.  Novel Functions of the Matricellular Proteins Osteopontin and Osteonectin/SPARC , 2002, Connective tissue research.

[7]  Xinjie Lin,et al.  Osteopontin Deficiency in Rat Vascular Smooth Muscle Cells is Associated with an Inability to Adhere to Collagen and Increased Apoptosis , 2000, Laboratory Investigation.

[8]  M. Amling,et al.  Osteopenia and decreased bone formation in osteonectin-deficient mice , 2000, The Journal of clinical investigation.

[9]  M. Gray,et al.  Osteoblast cytoskeletal modulation in response to mechanical strain in vitro , 1998, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[10]  H. Akiyama,et al.  Microgravity induces prostaglandin E2 and interleukin-6 production in normal rat osteoblasts: role in bone demineralization. , 1996, Journal of biotechnology.

[11]  A Guignandon,et al.  Shape changes of osteoblastic cells under gravitational variations during parabolic flight--relationship with PGE2 synthesis. , 1995, Cell structure and function.

[12]  D. Denhardt,et al.  Soluble osteopontin inhibits apoptosis of adherent endothelial cells deprived of growth factors * , 2002, Journal of cellular biochemistry.

[13]  J. Sleeman,et al.  CD44 variants but not CD44s cooperate with beta1-containing integrins to permit cells to bind to osteopontin independently of arginine-glycine-aspartic acid, thereby stimulating cell motility and chemotaxis. , 1999, Cancer research.