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FOXC1 和 FOXC2 调节胚胎鼠肢骨骼生长板软骨细胞向肥大成熟的方向分化。

FOXC1 and FOXC2 regulate growth plate chondrocyte maturation towards hypertrophy in the embryonic mouse limb skeleton.

机构信息

Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2E1, Canada.

Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute at Harvard Medical School, 240 Longwood Ave, Boston, MA 02115, USA.

出版信息

Development. 2024 Aug 15;151(16). doi: 10.1242/dev.202798. Epub 2024 Aug 22.

DOI:10.1242/dev.202798
PMID:39012257
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11361642/
Abstract

The Forkhead box transcription factors FOXC1 and FOXC2 are expressed in condensing mesenchyme cells at the onset of endochondral ossification. We used the Prx1-cre mouse to ablate Foxc1 and Foxc2 in limb skeletal progenitor cells. Prx1-cre;Foxc1Δ/Δ;Foxc2Δ/Δ limbs were shorter than controls, with worsening phenotypes in distal structures. Cartilage formation and mineralization was severely disrupted in the paws. The radius and tibia were malformed, whereas the fibula and ulna remained unmineralized. Chondrocyte maturation was delayed, with fewer Indian hedgehog-expressing, prehypertrophic chondrocytes forming and a smaller hypertrophic chondrocyte zone. Later, progression out of chondrocyte hypertrophy was slowed, leading to an accumulation of COLX-expressing hypertrophic chondrocytes and formation of a smaller primary ossification center with fewer osteoblast progenitor cells populating this region. Targeting Foxc1 and Foxc2 in hypertrophic chondrocytes with Col10a1-cre also resulted in an expanded hypertrophic chondrocyte zone and smaller primary ossification center. Our findings suggest that FOXC1 and FOXC2 direct chondrocyte maturation towards hypertrophic chondrocyte formation. At later stages, FOXC1 and FOXC2 regulate function in hypertrophic chondrocyte remodeling to allow primary ossification center formation and osteoblast recruitment.

摘要

叉头框转录因子 FOXC1 和 FOXC2 在软骨内骨化开始时表达于浓缩间充质细胞中。我们使用 Prx1-cre 小鼠在肢体骨骼祖细胞中缺失 Foxc1 和 Foxc2。Prx1-cre;Foxc1Δ/Δ;Foxc2Δ/Δ 肢体比对照组短,并且在远端结构中表现出更严重的表型。爪子中的软骨形成和矿化严重受损。桡骨和胫骨畸形,而腓骨和尺骨仍未矿化。软骨细胞成熟延迟,形成的 Indian hedgehog 表达较少的、预肥大的软骨细胞较少,肥大的软骨细胞区较小。后来,软骨细胞肥大的进展减缓,导致 COLX 表达的肥大软骨细胞的积累和较小的初级骨化中心的形成,该区域中较少的成骨前体细胞定植。用 Col10a1-cre 靶向肥大软骨细胞中的 Foxc1 和 Foxc2 也导致肥大软骨细胞区扩大和较小的初级骨化中心形成。我们的研究结果表明,FOXC1 和 FOXC2 指导软骨细胞成熟为肥大软骨细胞形成。在后期,FOXC1 和 FOXC2 调节肥大软骨细胞重塑的功能,以允许初级骨化中心形成和成骨细胞募集。

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