Linkhart T A, Linkhart S G, Kodama Y, Farley J R, Dimai H P, Wright K R, Wergedal J E, Sheng M, Beamer W G, Donahue L R, Rosen C J, Baylink D J
J.L. Pettis VA Medical Center, Loma Linda University, Loma Linda, California, USA; Department of Biochemistry, Loma Linda University, Loma Linda, California, USA; Department of Pediatrics, Loma Linda University, Loma Linda, California 92357, USA.
J Bone Miner Res. 1999 Jan;14(1):39-46. doi: 10.1359/jbmr.1999.14.1.39.
For the purpose of identifying genes that affect bone volume, we previously identified two inbred mouse strains (C57BL/6J and C3H/HeJ) with large differences in femoral bone density and medullary cavity volume. The lower density and larger medullary cavity volume in C57BL/6J mice could result from either decreased formation or increased resorption or both. We recently reported evidence suggesting that bone formation was increased in vivo and that osteoblast progenitor cells are more numerous in the bone marrow of C3H/HeJ compared with C57BL/6J mice. In the present study, we determined whether osteoclast numbers in vivo and osteoclast formation from bone marrow cells in vitro might also differ between the two mouse strains. We have found that the number of osteoclasts on bone surfaces of distal humerus secondary spongiosa was 2-fold higher in 5.5-week-old C57BL/6J mice than in C3H/HeJ mice of the same age (p < 0.001). Bone marrow cells of C57BL/6J mice cocultured with Swiss/Webster mouse osteoblasts consistently produced more osteoclasts than did C3H/HeJ bone marrow cells at all ages tested from 3.5-14 weeks of age (p < 0.001). Osteoclast formation was also greater from spleen cells of 3.5-week-old C57BL/6J mice than C3H/HeJ mice. The distribution of nuclei per osteoclast and the 1, 25-dihydroxyvitamin D3 dose dependence of osteoclast production from bone marrow cells were similar. Osteoclasts that developed from both C57BL/6J and C3H/HeJ marrow cells formed pits in dentin slices. Cultures from C57BL/6J marrow cells formed 2.5-fold more pits than cultures from C3H/HeJ marrow cells (p < 0.02). We compared the abilities of C57BL/6J and C3H/HeJ osteoblasts to support osteoclast formation. When bone marrow cells from either C57BL/6J or C3H/HeJ mice were cocultured with osteoblasts from either C57BL/6J or C3H/HeJ newborn calvaria, the strain from which osteoblasts were derived did not affect the number of osteoclasts formed from marrow cells of either strain. Together, these observations suggest that genes affecting the bone marrow osteoclast precursor population may contribute to the relative differences in bone density that occur between C3H/HeJ and C57BL/6J mouse strains.
为了鉴定影响骨体积的基因,我们之前鉴定出了两种近交系小鼠品系(C57BL/6J和C3H/HeJ),它们在股骨骨密度和髓腔体积上存在很大差异。C57BL/6J小鼠较低的骨密度和较大的髓腔体积可能是由于骨形成减少、骨吸收增加或两者兼而有之。我们最近报道的证据表明,C3H/HeJ小鼠与C57BL/6J小鼠相比,其体内骨形成增加,且骨髓中骨祖细胞数量更多。在本研究中,我们确定了这两种小鼠品系在体内破骨细胞数量以及体外骨髓细胞形成破骨细胞方面是否也存在差异。我们发现,5.5周龄的C57BL/6J小鼠肱骨远端次生海绵骨表面的破骨细胞数量比同年龄的C3H/HeJ小鼠高2倍(p < 0.001)。在3.5 - 14周龄的所有测试年龄段,与瑞士/韦伯斯特小鼠成骨细胞共培养的C57BL/6J小鼠骨髓细胞始终比C3H/HeJ小鼠骨髓细胞产生更多的破骨细胞(p < 0.001)。3.5周龄的C57BL/6J小鼠脾细胞形成破骨细胞的能力也比C3H/HeJ小鼠更强。每个破骨细胞核的分布以及骨髓细胞产生破骨细胞的1,25 - 二羟基维生素D3剂量依赖性是相似的。由C57BL/6J和C3H/HeJ骨髓细胞发育而来的破骨细胞在牙本质切片上都形成了凹陷。C57BL/6J骨髓细胞培养物形成的凹陷比C3H/HeJ骨髓细胞培养物多2.5倍(p < 0.02)。我们比较了C57BL/6J和C3H/HeJ成骨细胞支持破骨细胞形成的能力。当将C57BL/6J或C3H/HeJ小鼠的骨髓细胞与C57BL/6J或C3H/HeJ新生颅骨的成骨细胞共培养时,成骨细胞来源的品系并不影响两种品系骨髓细胞形成破骨细胞的数量。总之,这些观察结果表明,影响骨髓破骨细胞前体细胞群体的基因可能导致了C3H/HeJ和C57BL/6J小鼠品系之间骨密度的相对差异。