热情
生物
解剖
原基
细胞生物学
活体细胞成像
转基因
肌腱
细胞
基因
遗传学
生物化学
作者
Xinyi Yu,Ryosuke Kawakami,Shinsei Yambe,Yuki Yoshimoto,Takako Sasaki,Shinnosuke Higuchi,Hitomi Watanabe,Haruhiko Akiyama,Shigenori Miura,Ke Hu,Gen Kondoh,Ramu Sagasaki,Masafumi Inui,Taiji ADACHI,Denitsa Docheva,Takeshi Imamura,Chisa Shukunami
出处
期刊:Development
[The Company of Biologists]
日期:2025-03-15
卷期号:152 (6)
摘要
ABSTRACT Proper connections between cartilaginous and muscular primordia through tendinous/ligamentous primordia are essential for musculoskeletal integration. Herein, we report a novel double-reporter mouse model for investigating this process via fluorescently visualising scleraxis (Scx) and SRY-box containing gene 9 (Sox9) expression. We generated ScxTomato transgenic mice and crossed them with Sox9EGFP knock-in mice to obtain ScxTomato;Sox9EGFP mice. Deep imaging of optically cleared double-reporter embryos at E13.5 and E16.5 revealed previously unknown differences in the dynamic interactions between cartilaginous and tendinous/ligamentous primordia in control and Scx-deficient mice. Tendon/ligament maturation was evaluated through simultaneous detection of fluorescence and visualisation of collagen fibre formation using second harmonic generation imaging. Lack of deltoid tuberosity in Scx-deficient mice caused misdirected muscle attachment with morphological changes. Loss of Scx also dysregulated progenitor cell fate determination in the chondrotendinous junction, resulting in the formation of a rounded enthesis rather than the protruding enthesis observed in the control. Hence, our double-reporter mouse system, in combination with loss- or gain-of-function approaches, is a unique and powerful tool that could be used to gain a comprehensive understanding of musculoskeletal integration.
科研通智能强力驱动
Strongly Powered by AbleSci AI