Berghuis H M, Dieudonné S C, Goei W, Veldhuijzen J P
Department of Orthodontics, Vrije Universiteit, Amsterdam, The Netherlands.
Eur J Orthod. 1994 Apr;16(2):130-7. doi: 10.1093/ejo/16.2.130.
To study the effects of transforming growth factor beta 2 (TGF-beta 2) on bone resorption, cultures of 17-day-old foetal mouse metatarsal long bones were used. The long bone rudiments were cultured for 5 days in medium supplemented with 10% rat serum. The effects of TGF-beta 2 were studied at concentrations of 1, 4, and 10 ng/ml. At all concentrations TGF-beta 2 caused a significant reduction in osteoclastic resorption measured as release of 45Ca from prelabelled bones. The same long bones were subsequently used for histological evaluations. Pre-osteoclasts and osteoclasts were identified as tartrate resistant acid phosphatase (TRAP) positive cells in the mineralized diaphysis, the periosteum around the diaphysis, and the perichondrium around the cartilaginous ends. The distribution of TRAP-positive cells over the three compartments showed that TGF-beta 2 inhibited the migration of TRAP-positive cells from the periosteum into the mineralized diaphysis in a dose dependent manner. In addition, TGF-beta 2 had a biphasic effect on TRAP cell differentiation, as 1 ng/ml increased, but 4 ng/ml and higher decreased TRAP cell numbers. We conclude that TGF-beta 2 is a potent regulator of osteoclastic bone resorption, by modulating both osteoclast migration and osteoclast differentiation.
为研究转化生长因子β2(TGF-β2)对骨吸收的影响,使用了17日龄胎鼠的跖骨长骨进行培养。将长骨原基在补充有10%大鼠血清的培养基中培养5天。研究了浓度为1、4和10 ng/ml的TGF-β2的作用。在所有浓度下,TGF-β2均导致破骨细胞吸收显著减少,这通过从预先标记的骨骼中释放45Ca来衡量。随后,对同一批长骨进行组织学评估。在矿化的骨干、骨干周围的骨膜以及软骨末端周围的软骨膜中,前破骨细胞和破骨细胞被鉴定为抗酒石酸酸性磷酸酶(TRAP)阳性细胞。TRAP阳性细胞在这三个区域的分布表明,TGF-β2以剂量依赖的方式抑制TRAP阳性细胞从骨膜向矿化骨干的迁移。此外,TGF-β2对TRAP细胞分化具有双相作用,因为1 ng/ml时TRAP细胞数量增加,但4 ng/ml及更高浓度时TRAP细胞数量减少。我们得出结论,TGF-β2通过调节破骨细胞迁移和破骨细胞分化,是破骨细胞性骨吸收的有效调节因子。