Yamaguchi Hiroyuki, Gutierrez Yolanda V, Faisal Maryam, Nakai Yuta, Tran Lauren T, Zhao Baohong, Mishina Yuji, Komatsu Yoshihiro
Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA; University of Texas Rio Grande Valley School of Medicine, Edinburg, TX, 78539, USA.
Biochem Biophys Res Commun. 2025 Sep 1;777:152260. doi: 10.1016/j.bbrc.2025.152260. Epub 2025 Jun 27.
Bone remodeling is a critical biological process required for bone homeostasis. Osteoclasts are essential skeletal cells for bone resorption, and pathological activation of osteoclastogenesis results in bone volume loss. A prior study suggests that bone morphogenetic protein (BMP) signaling via one of the BMP type I receptors, ALK2, positively regulates osteoclastogenesis in vitro. However, the mechanisms of how the activation of BMP signaling affects osteoclastogenesis in vivo remain elusive. To address this question, we utilized two osteoclast-specific Cre mice, Lysosome 2 (LysM)-Cre mice and Cathepsin K (Ctsk)-Cre, that enabled us to activate BMP signaling in osteoclast progenitors and/or mature osteoclasts, respectively. We then investigated the effect of osteoclast lineage-specific upregulation of BMP signaling via ALK2 by crossing constitutively active ALK2 (ca-Alk2) mice (hereafter ca-Alk2:LysM-Cre and ca-Alk2:Ctsk-Cre). Compared with controls, ca-Alk2:LysM-Cre and ca-Alk2:Ctsk-Cre mice displayed osteopenic phenotypes. While the number of RUNX2-positive osteoblasts was unchanged, we found the number of tartrate-resistant acid phosphatase (TRAP)- and CTSK-positive cells in the femur was significantly increased in both ca-Alk2:Ctsk-Cre and ca-Alk2:LysM-Cre mice. Our study suggests that enhanced BMP signaling in osteoclasts promotes osteoclastogenesis in an osteoclast-autonomous manner, leading to reduced bone volume in mice.
骨重塑是骨稳态所需的关键生物学过程。破骨细胞是骨吸收必不可少的骨骼细胞,破骨细胞生成的病理激活会导致骨量减少。先前的一项研究表明,骨形态发生蛋白(BMP)通过BMP I型受体之一ALK2发出的信号在体外对破骨细胞生成具有正向调节作用。然而,BMP信号激活在体内如何影响破骨细胞生成的机制仍不清楚。为了解决这个问题,我们利用了两种破骨细胞特异性Cre小鼠,即溶酶体2(LysM)-Cre小鼠和组织蛋白酶K(Ctsk)-Cre小鼠,它们分别使我们能够在破骨细胞祖细胞和/或成熟破骨细胞中激活BMP信号。然后,我们通过与组成型活性ALK2(ca-Alk2)小鼠(以下简称ca-Alk2:LysM-Cre和ca-Alk2:Ctsk-Cre)杂交,研究了通过ALK2对破骨细胞谱系特异性上调BMP信号的影响。与对照组相比,ca-Alk2:LysM-Cre和ca-Alk2:Ctsk-Cre小鼠表现出骨质减少的表型。虽然RUNX2阳性成骨细胞的数量没有变化,但我们发现,在ca-Alk2:Ctsk-Cre和ca-Alk2:LysM-Cre小鼠的股骨中,抗酒石酸酸性磷酸酶(TRAP)和CTSK阳性细胞的数量均显著增加。我们的研究表明,破骨细胞中增强的BMP信号以破骨细胞自主的方式促进破骨细胞生成,导致小鼠骨量减少。