Horowitz Mark C, Xi Yougen, Pflugh David L, Hesslein David G T, Schatz David G, Lorenzo Joseph A, Bothwell Alfred L M
Department of Orthopaedics and Rehabilitation, Yale University School of Medicine, New Haven, CT 06510, USA.
J Immunol. 2004 Dec 1;173(11):6583-91. doi: 10.4049/jimmunol.173.11.6583.
Pax5 encodes BSAP, a member of the paired box domain transcription factors, whose expression is restricted to B lymphocyte lineage cells. Pax5(-/-) mice have a developmental arrest of the B cell lineage at the pro-B cell stage. We show here that Pax5(-/-) mice are severely osteopenic, missing 60% of their bone mass. The osteopenia can be accounted for by a >100% increase in the number of osteoclasts in bone measured histomorphometrically. This is not due to a lack of B cells, because other strains of B cell-deficient mice do not exhibit this phenotype. There was no difference in the number of osteoclasts produced in vitro by wild-type and Pax5(-/-) bone marrow cells. In contrast, spleen cells from Pax5(-/-) mice produce as much as five times the number of osteoclasts as control spleen cells. Culture of Pax5(-/-) spleen cells yields a population of adherent cells that grow spontaneously in culture without added growth factors for >4 wk. These cells have a monocyte phenotype, produce large numbers of osteoclasts when induced in vitro, and therefore are highly enriched in osteoclast precursors. These data demonstrate a previously unsuspected connection between B cell and osteoclast development and a key role for Pax5 in the control of osteoclast development.
Pax5编码BSAP,它是配对盒结构域转录因子家族的成员之一,其表达仅限于B淋巴细胞系细胞。Pax5基因敲除(-/-)小鼠的B细胞系在pro-B细胞阶段出现发育停滞。我们在此表明,Pax5基因敲除(-/-)小鼠严重骨质减少,骨量缺失60%。通过组织形态计量学测量发现,骨质减少可归因于骨中破骨细胞数量增加超过100%。这并非由于缺乏B细胞,因为其他B细胞缺陷型小鼠品系未表现出这种表型。野生型和Pax5基因敲除(-/-)骨髓细胞在体外产生的破骨细胞数量没有差异。相反,Pax5基因敲除(-/-)小鼠的脾细胞产生的破骨细胞数量是对照脾细胞的五倍之多。培养Pax5基因敲除(-/-)脾细胞可产生一群贴壁细胞,这些细胞在无添加生长因子的情况下可在培养中自发生长超过4周。这些细胞具有单核细胞表型,在体外诱导时可产生大量破骨细胞,因此高度富集破骨细胞前体。这些数据证明了B细胞与破骨细胞发育之间此前未被怀疑的联系,以及Pax5在控制破骨细胞发育中的关键作用。