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前列腺素 E2 介导感觉神经对骨稳态的调节。

Prostaglandin E2 mediates sensory nerve regulation of bone homeostasis.

机构信息

Department of Orthopaedic Surgery, The Johns Hopkins University, Baltimore, MD, 21205, USA.

Department of Orthopaedic Surgery, First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, 215000, P. R. China.

出版信息

Nat Commun. 2019 Jan 14;10(1):181. doi: 10.1038/s41467-018-08097-7.

Abstract

Whether sensory nerve can sense bone density or metabolic activity to control bone homeostasis is unknown. Here we found prostaglandin E2 (PGE2) secreted by osteoblastic cells activates PGE2 receptor 4 (EP4) in sensory nerves to regulate bone formation by inhibiting sympathetic activity through the central nervous system. PGE2 secreted by osteoblasts increases when bone density decreases as demonstrated in osteoporotic animal models. Ablation of sensory nerves erodes the skeletal integrity. Specifically, knockout of the EP4 gene in the sensory nerves or cyclooxygenase-2 (COX2) in the osteoblastic cells significantly reduces bone volume in adult mice. Sympathetic tone is increased in sensory denervation models, and propranolol, a β2-adrenergic antagonist, rescues bone loss. Furthermore, injection of SW033291, a small molecule to increase PGE2 level locally, significantly boostes bone formation, whereas the effect is obstructed in EP4 knockout mice. Thus, we show that PGE2 mediates sensory nerve to control bone homeostasis and promote regeneration.

摘要

感觉神经是否能感知骨密度或代谢活动以控制骨稳态尚不清楚。在这里,我们发现成骨细胞分泌的前列腺素 E2(PGE2)激活感觉神经中的 PGE2 受体 4(EP4),通过中枢神经系统抑制交感神经活动来调节骨形成。在骨质疏松动物模型中,当骨密度降低时,骨细胞分泌的 PGE2 增加。感觉神经的缺失会破坏骨骼的完整性。具体来说,感觉神经中 EP4 基因或成骨细胞中环氧合酶-2(COX2)的缺失会显著减少成年小鼠的骨量。在感觉神经切断模型中,交感神经张力增加,β2-肾上腺素能拮抗剂普萘洛尔可挽救骨丢失。此外,局部注射增加 PGE2 水平的小分子 SW033291 可显著促进骨形成,而在 EP4 基因敲除小鼠中,该作用受阻。因此,我们表明 PGE2 介导感觉神经来控制骨稳态并促进再生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46c7/6331599/d92f2f626148/41467_2018_8097_Fig1_HTML.jpg

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