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HOXA10 promotes Gdf5 expression in articular chondrocytes
被引:0
|作者:
Murakami, Tomohiko
[1
]
Ruengsinpinya, Lerdluck
[2
]
Takahata, Yoshifumi
[1
]
Nakaminami, Yuri
[1
]
Hata, Kenji
[1
]
Nishimura, Riko
[1
]
机构:
[1] Osaka Univ, Dept Mol & Cellular Biochem, Grad Sch Dent, 1-8 Yamada Oka, Suita, Osaka 5650871, Japan
[2] Srinakharinwirot Univ, Fac Dent, Dept Oral Surg & Oral Med, Bangkok, Thailand
基金:
日本学术振兴会;
关键词:
CARTILAGE;
GENES;
JOINT;
MORPHOGENESIS;
MUTATIONS;
TISSUE;
D O I:
10.1038/s41598-023-50318-7
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Growth differentiation factor 5 (GDF5), a BMP family member, is highly expressed in the surface layer of articular cartilage. The GDF5 gene is a key risk locus for osteoarthritis and Gdf5-deficient mice show abnormal joint development, indicating that GDF5 is essential in joint development and homeostasis. In this study, we aimed to identify transcription factors involved in Gdf5 expression by performing two-step screening. We first performed microarray analyses to find transcription factors specifically and highly expressed in the superficial zone (SFZ) cells of articular cartilage, and isolated 11 transcription factors highly expressed in SFZ cells but not in costal chondrocytes. To further proceed with the identification, we generated Gdf5-HiBiT knock-in (Gdf5-HiBiT KI) mice, by which we can easily and reproducibly monitor Gdf5 expression, using CRISPR/Cas9 genome editing. Among the 11 transcription factors, Hoxa10 clearly upregulated HiBiT activity in the SFZ cells isolated from Gdf5-HiBiT KI mice. Hoxa10 overexpression increased Gdf5 expression while Hoxa10 knockdown decreased it in the SFZ cells. Moreover, ChIP and promoter assays proved the direct regulation of Gdf5 expression by HOXA10. Thus, our results indicate the important role played by HOXA10 in Gdf5 regulation and the usefulness of Gdf5-HiBiT KI mice for monitoring Gdf5 expression.
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页数:11
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