TY - JOUR TI - Transferrin receptor 1-mediated iron uptake regulates bone mass in mice via osteoclast mitochondria and cytoskeleton AU - Das, Bhaba K AU - Wang, Lei AU - Fujiwara, Toshifumi AU - Zhou, Jian AU - Aykin-Burns, Nukhet AU - Krager, Kimberly J AU - Lan, Renny AU - Mackintosh, Samuel G AU - Edmondson, Ricky AU - Jennings, Michael L AU - Wang, Xiaofang AU - Feng, Jian Q AU - Barrientos, Tomasa AU - Gogoi, Jyoti AU - Kannan, Aarthi AU - Gao, Ling AU - Xing, Weirong AU - Mohan, Subburaman AU - Zhao, Haibo A2 - Ginzburg, Yelena A2 - Zaidi, Mone A2 - Pavlos, Nathan J VL - 11 PY - 2022 DA - 2022/06/27 SP - e73539 C1 - eLife 2022;11:e73539 DO - 10.7554/eLife.73539 UR - https://doi.org/10.7554/eLife.73539 AB - Increased intracellular iron spurs mitochondrial biogenesis and respiration to satisfy high-energy demand during osteoclast differentiation and bone-resorbing activities. Transferrin receptor 1 (Tfr1) mediates cellular iron uptake through endocytosis of iron-loaded transferrin, and its expression increases during osteoclast differentiation. Nonetheless, the precise functions of Tfr1 and Tfr1-mediated iron uptake in osteoclast biology and skeletal homeostasis remain incompletely understood. To investigate the role of Tfr1 in osteoclast lineage cells in vivo and in vitro, we crossed Tfrc (encoding Tfr1)-floxed mice with Lyz2 (LysM)-Cre and Cathepsin K (Ctsk)-Cre mice to generate Tfrc conditional knockout mice in myeloid osteoclast precursors (Tfr1ΔLysM) or differentiated osteoclasts (Tfr1ΔCtsk), respectively. Skeletal phenotyping by µCT and histology unveiled a significant increase in trabecular bone mass with normal osteoclast number in long bones of 10-week-old young and 6-month-old adult female but not male Tfr1ΔLysM mice. Although high trabecular bone volume in long bones was observed in both male and female Tfr1ΔCtsk mice, this phenotype was more pronounced in female knockout mice. Consistent with this gender-dependent phenomena, estrogen deficiency induced by ovariectomy decreased trabecular bone mass in Tfr1ΔLysM mice. Mechanistically, disruption of Tfr1 expression attenuated mitochondrial metabolism and cytoskeletal organization in mature osteoclasts in vitro by attenuating mitochondrial respiration and activation of the Src-Rac1-WAVE regulatory complex axis, respectively, leading to decreased bone resorption with little impact on osteoclast differentiation. These results indicate that Tfr1-mediated iron uptake is specifically required for osteoclast function and is indispensable for bone remodeling in a gender-dependent manner. KW - transferrin KW - transferrin receptor 1 KW - osteoclast KW - bone resorption KW - bone remodeling KW - mitochondria JF - eLife SN - 2050-084X PB - eLife Sciences Publications, Ltd ER -