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MACF1 deficiency suppresses tooth mineralization through IGF1 mediated crosstalk between odontoblasts and ameloblasts

Rapid Communications

MACF1 deficiency suppresses tooth mineralization through IGF1 mediated crosstalk between odontoblasts and ameloblasts

Qiu Wuxia
Lin Xiao
Yang Shaoqing
Chen Zhihao
Zhang Kewen
Yang Chaofei
Li Yu
Miao Zhiping
Deng Xiaoni
Duan Xiaohong
Qian Airong
Genes & Diseases第11卷, 第5期纸质出版 2024-09-01在线发表 2023-09-14
3300

Tooth mineralization is a ubiquitous and tightly regulated process involving complicated interactions between dental epithelium and mesenchyme. Key molecules in tooth mineralization remain poorly identified. Microtubule actin cross-linking factor 1 (MACF1) is a spectraplakin protein that plays pivotal roles in the brain, muscle, lung, and bone developmental process.1, 2, 3 To study the specific functions of MACF1 in bone formation, we established Macf1 conditional knockout mice using the Cre-LoxP system driven by Osxterix promoter (Osx-Cre;Macf1f/f).2 Not surprisingly, Osx-Cre;Macf1f/f mice displayed the phenotypes of delayed ossification and decreased bone mass. Moreover, the Osx-Cre;Macf1f/f mice unexpectedly showed a white and opaque appearance of incisors, contrary to the normal yellow-brown and transparent incisors. Since Osxterix is expressed in dental mesenchyme during tooth development, the abnormal tooth appearance might imply a new function of MACF1 in odontoblasts, or even ameloblasts. Therefore, the present study aimed to investigate the role of MACF1 during tooth development.

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