Department of Biochemistry, Dongguk University School of Medicine, Gyeongju, Korea.
Department of Molecular Medicine, Kyungpook National University School of Medicine, Daegu, Korea.
FEBS Lett. 2024 Apr;598(8):935-944. doi: 10.1002/1873-3468.14862. Epub 2024 Mar 29.
Chondrocyte differentiation is crucial for cartilage formation. However, the complex processes and mechanisms coordinating chondrocyte proliferation and differentiation remain incompletely understood. Here, we report a novel function of the adaptor protein Gulp1 in chondrocyte differentiation. Gulp1 expression is upregulated during chondrogenic differentiation. Gulp1 knockdown in chondrogenic ATDC5 cells reduces the expression of chondrogenic and hypertrophic marker genes during differentiation. Furthermore, Gulp1 knockdown impairs cell growth arrest during chondrocyte differentiation and reduces the expression of the cyclin-dependent kinase inhibitor p21. The activation of the TGF-β/SMAD2/3 pathway, which is associated with p21 expression in chondrocytes, is impaired in Gulp1 knockdown cells. Collectively, these results demonstrate that Gulp1 contributes to cell growth arrest and chondrocyte differentiation by modulating the TGF-β/SMAD2/3 pathway.
软骨细胞分化对于软骨形成至关重要。然而,协调软骨细胞增殖和分化的复杂过程和机制仍不完全清楚。在这里,我们报告了衔接蛋白 Gulp1 在软骨细胞分化中的一个新功能。Gulp1 在软骨形成过程中表达上调。在软骨形成的 ATDC5 细胞中敲低 Gulp1 会降低分化过程中软骨形成和肥大标记基因的表达。此外,Gulp1 敲低会损害软骨细胞分化过程中的细胞生长停滞,并降低细胞周期蛋白依赖性激酶抑制剂 p21 的表达。与软骨细胞中 p21 表达相关的 TGF-β/SMAD2/3 通路的激活在 Gulp1 敲低细胞中受到损害。总之,这些结果表明 Gulp1 通过调节 TGF-β/SMAD2/3 通路促进细胞生长停滞和软骨细胞分化。