间充质干细胞
生物
兰克尔
骨吸收
细胞生物学
平衡
癌症研究
骨髓
转录因子
STAT1
内分泌学
内科学
免疫学
信号转导
受体
激活剂(遗传学)
医学
遗传学
基因
作者
Takanori Yamada,Kazuya Fukasawa,Tetsuhiro Horie,Takuya Kadota,Jiajun Lyu,Kazuya Tokumura,Shinsuke Ochiai,Sayuki Iwahashi,Akane Suzuki,Gyujin Park,Rie Ueda,Megumi Yamamoto,Toshio Kitao,Hiroaki Shirahase,Hiroki Ochi,Shingo Sato,Takashi Iezaki,Eiichi Hinoi
标识
DOI:10.1016/j.stemcr.2022.06.001
摘要
Bone marrow mesenchymal stem cells (MSCs) are critical regulators of postnatal bone homeostasis. Osteoporosis is characterized by bone volume and strength deterioration, partly due to MSC dysfunction. Cyclin-dependent kinase 8 (CDK8) belongs to the transcription-related CDK family. Here, CDK8 in MSCs was identified as important for bone homeostasis. CDK8 level was increased in aged MSCs along with the association with aging-related signals. Mouse genetic studies revealed that CDK8 in MSCs plays a crucial role in bone resorption and homeostasis. Mechanistically, CDK8 in MSCs extrinsically controls osteoclastogenesis through the signal transducer and transcription 1 (STAT1)-receptor activator of the nuclear factor κ Β ligand (RANKL) axis. Moreover, aged MSCs have high osteoclastogenesis-supporting activity, partly through a CDK8-dependent manner. Finally, pharmacological inhibition of CDK8 effectively repressed MSC-dependent osteoclastogenesis and prevented ovariectomy-induced osteoclastic activation and bone loss. These findings highlight that the CDK8-STAT1-RANKL axis in MSCs could play a crucial role in bone resorption and homeostasis.
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