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Microarray Profile of Gene Expression During Osteoclast Differentiation in Modelled Microgravity
Author(s) -
Sambandam Yuvaraj,
Blanchard Jeremy J.,
Daughtridge Giffin,
Kolb Robert J.,
Shanmugarajan Srinivasan,
Pandruvada Subramanya N. M.,
Bateman Ted A.,
Reddy Sakamuri V.
Publication year - 2010
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.22840
Subject(s) - microbiology and biotechnology , osteoclast , gene expression , runx2 , rankl , chemistry , microphthalmia associated transcription factor , progenitor cell , gene expression profiling , transcription factor , activator (genetics) , biology , gene , stem cell , in vitro , biochemistry
Microgravity (µXg) leads to a 10–15% loss of bone mass in astronauts during space flight. Osteoclast (OCL) is the multinucleated bone‐resorbing cell. In this study, we used the NASA developed ground‐based rotating wall vessel bioreactor (RWV), rotary cell culture system (RCCS) to simulate µXg conditions and demonstrated a significant increase (2‐fold) in osteoclastogenesis compared to normal gravity control (Xg). Gene expression profiling of RAW 264.7 OCL progenitor cells in modelled µXg by Agilent microarray analysis revealed significantly increased expression of critical molecules such as cytokines/growth factors, proteases and signalling proteins, which play an important role in enhanced OCL differentiation/function. Transcription factors such as c‐Jun, MITF and CREB implicated in OCL differentiation are upregulated; however no significant change in the levels of NFATc1 expression in preosteoclast cells subjected to modelled µXg. We also identified high‐level expression of calcium‐binding protein, S100A8 (calcium‐binding protein molecule A8/calgranulin A) in preosteoclast cells under µXg. Furthermore, modelled µXg stimulated RAW 264.7 cells showed elevated cytosolic calcium (Ca 2+ ) levels/oscillations compared to Xg cells. siRNA knock‐down of S100A8 expression in RAW 264.7 cells resulted in a significant decrease in modelled µXg stimulated OCL differentiation. We also identified elevated levels of phospho‐CREB in preosteoclast cells subjected to modelled µXg compared to Xg. Thus, modelled µXg regulated gene expression profiling in preosteoclast cells provide new insights into molecular mechanisms and therapeutic targets of enhanced OCL differentiation/activation to prevent bone loss and fracture risk in astronauts during space flight missions. J. Cell. Biochem. 111: 1179–1187, 2010. © 2010 Wiley‐Liss, Inc.