Kumei Y, Shimokawa H, Katano H, Hara E, Akiyama H, Hirano M, Mukai C, Nagaoka S, Whitson P A, Sams C F
Faculty of Dentistry, Tokyo Medical and Dental University, Japan.
J Biotechnol. 1996 Jun 27;47(2-3):313-24. doi: 10.1016/0168-1656(96)01412-5.
It has been suggested that microgravity alters bone metabolism. Evidence for this phenomenon includes the negative calcium balance and decreased bone density in astronauts, as well as, inhibition of bone formation in rats flown for 2 to 3 weeks. However, the specific mechanisms that modulate these changes in microgravity are unknown. The purpose of this study was to clarify the mechanism of microgravity-induced bone demineralization using normal rat osteoblasts obtained from femur marrow cultures. The osteoblasts were cultured for 5 days during a Shuttle-Spacelab flight (STS-65). After collection of the culture medium, the cellular DNA and RNA were fixed on board. Enzyme-immunoassay of the culture medium for prostaglandin E2 (PGE2) indicated that microgravity induced a 4.5- to 136-fold increase in flight samples as compared to the ground control cultures. This increase of PGE2 production was consistent with a 3.3- to 9.5-fold elevation of inducible prostaglandin G/H synthase-2 (PGHS-2) mRNA, quantitated by reverse transcription-polymerase chain reaction (RT-PCR). The mRNA induction for the constitutive isozyme PGHS-1 was less than that for PGHS-2. The interleukin-6 (IL-6) mRNA was also increased (6.4- to 9.3-fold) in microgravity as compared to the ground controls. Since PGE2 and IL-6 are both known to play a role in osteoclast formation and bone resorption, these data provide molecular mechanisms that contribute to our understanding of microgravity-induced alterations in the bone resorption process.
有人提出微重力会改变骨代谢。这一现象的证据包括宇航员出现负钙平衡和骨密度降低,以及飞行2至3周的大鼠骨形成受到抑制。然而,调节微重力下这些变化的具体机制尚不清楚。本研究的目的是利用从股骨骨髓培养物中获得的正常大鼠成骨细胞,阐明微重力诱导骨脱矿的机制。成骨细胞在航天飞机-太空实验室飞行(STS-65)期间培养5天。收集培养基后,细胞DNA和RNA在飞船上固定。对培养基进行前列腺素E2(PGE2)的酶免疫分析表明,与地面对照培养物相比,微重力使飞行样本中的PGE2增加了4.5至136倍。PGE2产生的这种增加与通过逆转录-聚合酶链反应(RT-PCR)定量的诱导型前列腺素G/H合酶-2(PGHS-2)mRNA升高3.3至9.5倍一致。组成型同工酶PGHS-1的mRNA诱导低于PGHS-2。与地面对照相比,微重力下白细胞介素-6(IL-6)mRNA也增加了(6.4至9.3倍)。由于已知PGE2和IL-6在破骨细胞形成和骨吸收中都起作用,这些数据提供了有助于我们理解微重力诱导的骨吸收过程改变的分子机制。