Albano Giuseppe, Moor Matthias, Dolder Silvia, Siegrist Mark, Wagner Carsten A, Biber Jürg, Hernando Nati, Hofstetter Willy, Bonny Olivier, Fuster Daniel G
Division of Nephrology, Hypertension and Clinical Pharmacology, University Hospital of Bern, Bern, Switzerland; Institute of Biochemistry and Molecular Medicine, University of Bern, Bern, Switzerland; NCCR Transcure, University of Bern, Bern, Switzerland; NCCR Kidney.CH, University of Zürich, Zürich, Switzerland.
Department of Pharmacology and Toxicology, University of Lausanne, Lausanne, Switzerland; NCCR Kidney.CH, University of Zürich, Zürich, Switzerland.
PLoS One. 2015 Apr 24;10(4):e0125104. doi: 10.1371/journal.pone.0125104. eCollection 2015.
Osteoclasts are multinucleated bone degrading cells. Phosphate is an important constituent of mineralized bone and released in significant quantities during bone resorption. Molecular contributors to phosphate transport during the resorptive activity of osteoclasts have been controversially discussed. This study aimed at deciphering the role of sodium-dependent phosphate transporters during osteoclast differentiation and bone resorption. Our studies reveal RANKL-induced differential expression of sodium-dependent phosphate transport protein IIa (NaPi-IIa) transcript and protein during osteoclast development, but no expression of the closely related NaPi-IIb and NaPi-IIc SLC34 family isoforms. In vitro studies employing NaPi-IIa-deficient osteoclast precursors and mature osteoclasts reveal that NaPi-IIa is dispensable for bone resorption and osteoclast differentiation. These results are supported by the analysis of structural bone parameters by high-resolution microcomputed tomography that yielded no differences between adult NaPi-IIa WT and KO mice. By contrast, both type III sodium-dependent phosphate transporters Pit-1 and Pit-2 were abundantly expressed throughout osteoclast differentiation, indicating that they are the relevant sodium-dependent phosphate transporters in osteoclasts and osteoclast precursors. We conclude that phosphate transporters of the SLC34 family have no role in osteoclast differentiation and function and propose that Pit-dependent phosphate transport could be pivotal for bone resorption and should be addressed in further studies.
破骨细胞是多核的骨降解细胞。磷酸盐是矿化骨的重要组成部分,在骨吸收过程中大量释放。关于破骨细胞吸收活性过程中磷酸盐转运的分子机制一直存在争议。本研究旨在阐明钠依赖性磷酸盐转运体在破骨细胞分化和骨吸收过程中的作用。我们的研究揭示,在破骨细胞发育过程中,RANKL诱导钠依赖性磷酸盐转运蛋白IIa(NaPi-IIa)转录本和蛋白的差异表达,但密切相关的NaPi-IIb和NaPi-IIc SLC34家族异构体无表达。使用缺乏NaPi-IIa的破骨细胞前体和成熟破骨细胞进行的体外研究表明,NaPi-IIa对于骨吸收和破骨细胞分化并非必需。通过高分辨率微计算机断层扫描对骨结构参数的分析支持了这些结果,该分析显示成年NaPi-IIa野生型和敲除小鼠之间没有差异。相比之下,III型钠依赖性磷酸盐转运体Pit-1和Pit-2在整个破骨细胞分化过程中均大量表达,表明它们是破骨细胞和破骨细胞前体中相关的钠依赖性磷酸盐转运体。我们得出结论,SLC34家族的磷酸盐转运体在破骨细胞分化和功能中不起作用,并提出Pit依赖性磷酸盐转运可能对骨吸收至关重要,应在进一步研究中加以探讨。