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Sema3A regulates bone-mass accrual through
LETTER
doi:10.1038/nature12115
Sema3A regulates bone-mass accrual through
sensory innervations
Toru Fukuda1*, Shu Takeda1*, Ren Xu2,3*, Hiroki Ochi1, Satoko Sunamura1, Tsuyoshi Sato4, Shinsuke Shibata5, Yutaka Yoshida6,
Zirong Gu6, Ayako Kimura2,7, Chengshan Ma2,3, Cheng Xu2,3, Waka Bando8, Koji Fujita2,3, Kenichi Shinomiya2, Takashi Hirai2,
Yoshinori Asou2, Mitsuhiro Enomoto2, Hideyuki Okano5, Atsushi Okawa2,3 Hiroshi Itoh8
Semaphorin 3A (Sema3A) is a diffusible axonal chemorepellent that
has an important role in axon guidance1–5. Previous studies have
demonstrated that Sema3a2/2 mice have multiple developmental
defects due to abnormal neuronal innervations6,7. 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, Sema3a2/2 mice had a low
bone mass due to decreased bone formation. However, osteoblast-
specific Sema3A-deficientmice (Sema3acol1
2/2 andSema3aosx
2/2mice)
had normal bone mass, even though the expression of Sema3A in
bone was substantially decreased. In contrast, mice lacking Sema3A
inneurons (Sema3asynapsin
2/2andSema3anestin
2/2mice)had lowbone
mass, similar to Sema3a2/2 mice, indicating that neuron-derived
Sema3A is responsible for the observed bone abnormalities inde-
pendent of the local effect of Sema3A inbone. Indeed, thenumberof
sensory innervations of trabecular bone was significantly decreased
in Sema3asynapsin
2/2 mice, whereas sympathetic innervations of
trabecular bonewereunchanged.Moreover, ablating sensorynerves
decreased bone mass in wild-type mice, whereas it did not reduce
the low bone mass in Sema3anestin
2/2 mice further, supporting the
essential role of the sensory nervous system in normal bone home-
ostasis. Finally, neuronal abnormalities in Sema3a2/2mice, such as
olfactory development, were identified in Sema3asynasin
2/2 mice,
demonstrating that neuron-derived Sema3A contributes to the
abnormalneur
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