Benayahu D, Peled A, Zipori D
Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
J Cell Biochem. 1994 Nov;56(3):374-84. doi: 10.1002/jcb.240560314.
Osteoclasts are derived from hemopoietic precursors in the marrow. Their differentiation pathway is still undefined, but an important role was observed for the marrow microenvironment in the regulation of osteoclastogenesis. Various marrow stromal cell subtypes were used to study their possible role in the formation of osteoclasts from myeloblast (M1) cells. Interactions between M1 cells and the 14F1.1 endothelial-adipocyte stromal cell line were demonstrated in a coculture model. M1 cells attached to the adherent layer of 14F1.1 cells and formed distinct foci reminiscente of "cobblestone areas." Following these interactions, M1 cells developed specific enzymatic activities and became multinucleated. Both mononuclear and multinuclear M1 cells became positive to tartrate-resistant acid phosphatase (TRaP) and ATPase, a feature characteristic of osteoclasts, and were also responsive to calcitonin. Furthermore, they attached to mineralized bone particles and their membrane changed into a ruffled border at the zone of interaction with the bone matrix. We thus demonstrated that marrow endothelial-adipocytes may play a role in regulating the differentiation of myeloblasts into osteoclasts.
破骨细胞起源于骨髓中的造血前体细胞。它们的分化途径仍不明确,但已观察到骨髓微环境在破骨细胞生成的调节中起重要作用。使用了各种骨髓基质细胞亚型来研究它们在成髓细胞(M1)细胞形成破骨细胞过程中可能发挥的作用。在共培养模型中证明了M1细胞与14F1.1内皮-脂肪基质细胞系之间的相互作用。M1细胞附着于14F1.1细胞的贴壁层,并形成类似于“鹅卵石区域”的独特病灶。在这些相互作用之后,M1细胞发展出特定的酶活性并变成多核细胞。单核和多核M1细胞对抗酒石酸酸性磷酸酶(TRaP)和ATP酶呈阳性,这是破骨细胞的特征,并且对降钙素也有反应。此外,它们附着于矿化的骨颗粒,并且其膜在与骨基质相互作用的区域变成褶皱边缘。因此,我们证明骨髓内皮-脂肪细胞可能在调节成髓细胞向破骨细胞的分化中起作用。