| Literature DB >> 26850473 |
Nobuo Suzuki1, Taizo Hanmoto2, Sachiko Yano3, Yukihiro Furusawa4, Mika Ikegame5, Yoshiaki Tabuchi6, Takashi Kondo7, Kei-ichiro Kitamura8, Masato Endo9, Toshio Yamamoto5, Toshio Sekiguchi2, Makoto Urata10, Yuko Mikuni-Takagaki11, Atsuhiko Hattori12.
Abstract
Using fish scales in which osteoclasts and osteoblasts coexist on the calcified bone matrix, we examined the effects of low-intensity pulsed ultrasound (LIPUS) on both osteoclasts and osteoblasts. At 3h of incubation after LIPUS treatment, osteoclastic markers such as tartrate-resistant acid phosphatase (TRAP) and cathepsin K mRNA expressions decreased significantly while mRNA expressions of osteoblastic markers, osteocalcin, distal-less homeobox 5, runt-related transcription factor 2a, and runt-related transcription factor 2b, increased significantly. At 6 and 18h of incubation, however, both osteoclastic and osteoblastic marker mRNA expression did not change at least present conditions. Using GeneChip analysis of zebrafish scales treated with LIPUS, we found that cell death-related genes were upregulated with LIPUS treatment. Real-time PCR analysis indicated that the expression of apoptosis-related genes also increased significantly. To confirm the involvement of apoptosis in osteoclasts with LIPUS, osteoclasts were induced by autotransplanting scales in goldfish. Thereafter, the DNA fragmentation associated with apoptosis was detected in osteoclasts using the TUNEL (TdT-mediated dUTP nick end labeling) method. The multi-nuclei of TRAP-stained osteoclasts in the scales were labeled with TUNEL. TUNEL staining showed that the number of apoptotic osteoclasts in goldfish scales was significantly elevated by treatment with LIPUS at 3h of incubation. Thus, we are the first to demonstrate that LIPUS directly functions to osteoclasts and to conclude that LIPUS directly causes apoptosis in osteoclasts shortly after exposure.Entities:
Keywords: Apoptosis; Fish scales; GeneChip analysis; LIPUS; Osteoblasts; Osteoclasts
Mesh:
Year: 2016 PMID: 26850473 DOI: 10.1016/j.cbpa.2016.01.022
Source DB: PubMed Journal: Comp Biochem Physiol A Mol Integr Physiol ISSN: 1095-6433 Impact factor: 2.320