Gene expression related to the differentiation of osteoblastic cells is altered by microgravity

Bone. 1998 May;22(5 Suppl):139S-143S. doi: 10.1016/s8756-3282(98)00007-6.

Abstract

Bone loss is observed after exposure to weightlessness in both astronauts and inflight animals. Histological and biochemical studies on rats have shown a decrease in bone formation, probably as a result of altered osteoblast function. To investigate whether microgravity alters osteoblast differentiation in vitro, the human osteosarcoma cell line MG-63 was used as a model. MG-63 cells can be induced to differentiate by treating the cells with 1,25(OH)2D3 (10(-7) mol/L) and transforming growth factor-beta 2 (TGFbeta2) (10 ng/mL). The message level of differentiation-related genes was quantitated via competitive reverse transcription-polymerase chain reaction (RT-PCR), both in untreated and hormone-treated cells cultured under microgravity for 9 days aboard the unmanned Foton 10 spaceflight, and compared to ground and inflight unit-gravity cultures. At microgravity, gene expression for collagen Ialpha1 following treatment was reduced to 51% of unit-gravity levels (p < 0.05). The amount of alkaline phosphatase messenger ribonucleic acid (mRNA) following treatment at microgravity increased by only a factor of 5 compared to the tenfold increase at unit gravity (p < 0.02). The osteocalcin message level in treated cells cultured at microgravity was only 19% of the level found in cells grown at unit gravity (p < 0.02). In conclusion, microgravity reduces the differentiation of osteoblastic MG-63 cells in response to systemic hormones and growth factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / genetics
  • Alkaline Phosphatase / metabolism*
  • Calcitriol / pharmacology
  • Cell Differentiation
  • Cells, Cultured
  • Collagen / genetics
  • Collagen / metabolism*
  • Drug Combinations
  • Gene Expression*
  • Humans
  • Osteoblasts / cytology
  • Osteoblasts / drug effects
  • Osteoblasts / metabolism*
  • Osteocalcin / genetics
  • Osteocalcin / metabolism*
  • Polymerase Chain Reaction
  • RNA, Messenger / metabolism
  • Transforming Growth Factor beta / pharmacology
  • Weightlessness*

Substances

  • Drug Combinations
  • RNA, Messenger
  • Transforming Growth Factor beta
  • Osteocalcin
  • Collagen
  • Alkaline Phosphatase
  • Calcitriol