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朱玲新

主任医师   博士生导师    硕士生导师

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  • 教师拼音名称: Zhu Lingxin
  • 电子邮箱:
  • 所在单位: 口腔医学院
  • 职务: 科研办公室主任
  • 学历: 博士研究生毕业
  • 办公地点: 武汉大学口腔医学院
  • 性别: 男
  • 在职信息: 在职
  • 主要任职: 中华口腔医学会口腔医学教育专委会常务委员、中国病理生理学会内分泌与代谢专委会委员、中国医院协会模拟医学专委会委员
  • 其他任职: 美国密西根大学客座副教授
  • 毕业院校: 武汉大学

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论文成果

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A Zeb1/mitochondrial creatine kinase metabolic axis controls osteoclast activation and skeletal remodeling.

发布时间:2024-10-26
点击次数:
DOI码:
10.15252/embj.2022111148
发表刊物:
EMBO J
摘要:
Osteoclasts are bone-resorbing polykaryons responsible for skeletal remodeling during health and disease. Coincident with their differentiation from myeloid precursors, osteoclasts undergo extensive transcriptional and metabolic reprogramming in order to acquire the cellular machinery necessary to demineralize bone and digest its interwoven extracellular matrix. While attempting to identify new regulatory molecules critical to bone resorption, we discovered that murine and human osteoclast differentiation is accompanied by the expression of Zeb1, a zinc-finger transcriptional repressor whose role in normal development is most frequently linked to the control of epithelial-mesenchymal programs. However, following targeting, we find that Zeb1 serves as an unexpected regulator of osteoclast energy metabolism. In vivo, Zeb1-null osteoclasts assume a hyperactivated state, markedly decreasing bone density due to excessive resorptive activity. Mechanistically, Zeb1 acts in a rheostat-like fashion to modulate murine and human osteoclast activity by transcriptionally repressing an ATP-buffering enzyme, mitochondrial creatine kinase 1 (MtCK1), thereby controlling the phosphocreatine energy shuttle and mitochondrial respiration. Together, these studies identify a novel Zeb1/MtCK1 axis that exerts metabolic control over bone resorption in vitro and in vivo.
合写作者:
Tang Y, Li XY, Kerk SA, Lyssiotis CA, Feng W, Sun X, Hespe GE, Wang Z, Stemmler MP, Brabletz S, Brabletz T, Keller ET, Ma J, Cho JS, Yang J
第一作者:
Zhu L
论文类型:
期刊论文
通讯作者:
Weiss SJ
页面范围:
e111148
是否译文:
发表时间:
2023-03-12
收录刊物:
SCI