Journal Article

Sema3A regulates bone-mass accrual through sensory innervations

Shibata, Shinsuke, Fujita, Koji, Takeda, Shu, Yoshida, Yutaka, Hirai, Takashi, Fukuda, Toru, Asou, Yoshinori, Enomoto, Mitsuhiro, Xu, Ren, Kimura, Ayako, Sato, Tsuyoshi, Bando, Waka, Itoh, Hiroshi, Xu, Cheng, Gu, Zirong, Sunamura, Satoko, Ma, Chengshan, Ochi, Hiroki, Shinomiya, Kenichi, Okawa, Atsushi, Okano, Hideyuki

2013

Overview

Sema3A, a member of the semaphorin family of proteins, is shown to regulate bone remodelling indirectly by modulating sensory nerve development in mice. A role for sensory nerves in bone remodelling The semaphorins are diffusible proteins involved in the development of the nervous system, organs and blood vessels, as well as in immunity. Osteoblasts and osteoclasts express semaphorin family members, and it has been shown recently that semaphorin 3A (Sema3A) can regulate bone remodelling by acting locally. Here Toru Fukuda et al . demonstrate that Sema3A regulates bone remodelling in vivo indirectly by modulating sensory nerve development. Semaphorin 3A (Sema3A) is a diffusible axonal chemorepellent that has an important role in axon guidance 1 , 2 , 3 , 4 , 5 . Previous studies have demonstrated that Sema3a −/− mice have multiple developmental defects due to abnormal neuronal innervations 6 , 7 . Here we show in mice that Sema3A is abundantly expressed in bone, and cell-based assays showed that Sema3A affected osteoblast differentiation in a cell-autonomous fashion. Accordingly, Sema3a −/− mice had a low bone mass due to decreased bone formation. However, osteoblast-specific Sema3A-deficient mice ( Sema3a col1 −/− and Sema3a osx −/− mice) had normal bone mass, even though the expression of Sema3A in bone was substantially decreased. In contrast, mice lacking Sema3A in neurons ( Sema3a synapsin −/− and Sema3a nestin −/− mice) had low bone mass, similar to Sema3a −/− mice, indicating that neuron-derived Sema3A is responsible for the observed bone abnormalities independent of the local effect of Sema3A in bone. Indeed, the number of sensory innervations of trabecular bone was significantly decreased in Sema3a synapsin −/− mice, whereas sympathetic innervations of trabecular bone were unchanged. Moreover, ablating sensory nerves decreased bone mass in wild-type mice, whereas it did not reduce the low bone mass in Sema3a nestin −/− mice further, supporting the essential role of the sensory nervous system in normal bone homeostasis. Finally, neuronal abnormalities in Sema3a −/− mice, such as olfactory development, were identified in Sema3a synasin −/− mice, demonstrating that neuron-derived Sema3A contributes to the abnormal neural development seen in Sema3a −/− mice, and indicating that Sema3A produced in neurons regulates neural development in an autocrine manner. This study demonstrates that Sema3A regulates bone remodelling indirectly by modulating sensory nerve development, but not directly by acting on osteoblasts.

• Publisher: Nature Publishing Group UK,Nature Publishing Group
• Subject: 631/136/815/817 / Animals / Biological control systems / Bone and Bones - anatomy & histology / Bone and Bones - innervation / Bone and Bones - metabolism / Bone density / Bone Remodeling / Bones / Cell adhesion & migration / Cell Differentiation / Cells, Cultured / Defects / Density / Female / Homeostasis / Humanities and Social Sciences / letter / Male / Membrane proteins / Mice / multidisciplinary / Musculoskeletal abnormalities / Neurons / Organ Size / Osteoblasts - cytology / Osteoblasts - metabolism / Osteoporosis / Physiological aspects / Proteins / Science / Semaphorin-3A - deficiency / Semaphorin-3A - genetics / Semaphorin-3A - metabolism / Semaphorins / Sensory Receptor Cells - cytology / Sensory Receptor Cells - metabolism / Sensory receptors