Lipoteichoic Acid Rescued Age-Related Bone Loss by Enhancing Neuroendocrine and Growth Hormone Secretion Through TLR2/COX2/PGE2 Signalling Pathway

被引:1
作者
Liu, Zixian [1 ,2 ,3 ,4 ]
Lin, Zexin [1 ,2 ]
Chen, Yingqi [1 ,2 ]
Lu, Mincheng [5 ]
Hong, Weisheng [1 ,2 ]
Yu, Bin [1 ,2 ]
Liu, Guanqiao [1 ,2 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Orthopaed, Guangzhou, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Guangdong Prov Key Lab Bone & Cartilage Regenerat, Guangzhou, Peoples R China
[3] Lanzhou Univ, Hosp 2, Lanzhou, Peoples R China
[4] Lanzhou Univ, Clin Med Sch, Lanzhou, Peoples R China
[5] Shenzhen Univ, Shenzhen Peoples Hosp 2, Affiliated Hosp 1, Dept Orthoped, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
bone loss; brain-bone; growth hormone; lipoteichoic acid; PGE2; OSTEOPOROSIS; MICROGLIA; E-2; CYCLOOXYGENASE-2; PROSTAGLANDIN-E2; TRANSCRIPTION; MACROPHAGES; RECEPTORS; FRACTURES; AXIS;
D O I
10.1111/jcmm.70247
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The phenomenon of brain-bone crosstalk pertains to the intricate interaction and communication pathways between the central nervous system and the skeletal system. Disruption in brain-bone crosstalk, particularly in disorders such as osteoporosis, can result in skeletal irregularities. Consequently, investigating and comprehending this communication network holds paramount importance in the realm of bone disease prevention and management. In this study, we found that Staphylococcus aureus lipoteichoic acid promoted the conversion of arachidonic acid to PGE2 by interacting with TLR2 receptors acting on the surface of microglial cells in the pituitary gland, leading to the upregulation of COX-2 expression. Subsequently, PGE2 bound to the EP4 receptor of growth hormone-secreting cells and activated the intracellular CREB signalling pathway, promoting GH secretion and ameliorating age-related bone loss.
引用
收藏
页数:18
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