Serinc5 Regulates Sequential Chondrocyte Differentiation by Inhibiting Sox9 Function in Pre-Hypertrophic Chondrocytes.

IF 4.5 2区 生物学 Q2 CELL BIOLOGY
Kenji Hata, Kanta Wakamori, Akane Hirakawa-Yamamura, Sachi Ichiyama-Kobayashi, Masaya Yamaguchi, Daisuke Okuzaki, Yoshifumi Takahata, Tomohiko Murakami, Narikazu Uzawa, Takashi Yamashiro, Riko Nishimura
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Abstract

The growth plate is the primary site of longitudinal bone growth with chondrocytes playing a pivotal role in endochondral bone development. Chondrocytes undergo a series of differentiation steps, resulting in the formation of a unique hierarchical columnar structure comprising round, proliferating, pre-hypertrophic, and hypertrophic chondrocytes. Pre-hypertrophic chondrocytes, which exist in the transitional stage between proliferating and hypertrophic stages, are a critical cell population in the growth plate. However, the molecular basis of pre-hypertrophic chondrocytes remains largely undefined. Here, we employed scRNA-seq analysis on fluorescently labeled growth plate chondrocytes for their molecular characterization. Serine incorporator 5 (Serinc5) was identified as a marker gene for pre-hypertrophic chondrocytes. Histological analysis revealed that Serinc5 is specifically expressed in pre-hypertrophic chondrocytes, overlapping with Indian hedgehog (Ihh). Serinc5 represses cell proliferation and Col2a1 and Acan expression by inhibiting the transcriptional activity of Sox9 in primary chondrocytes. Chromatin profiling using ChIP-seq and ATAC-seq revealed an active enhancer of Serinc5 located in intron 1, with its chromatin status progressively activated during chondrocyte differentiation. Collectively, our findings suggest that Serinc5 regulates sequential chondrocyte differentiation from proliferation to hypertrophy by inhibiting Sox9 function in pre-hypertrophic chondrocytes, providing novel insights into the mechanisms underlying chondrocyte differentiation in growth plates.

Serinc5 通过抑制肥大前期软骨细胞中 Sox9 的功能来调控软骨细胞的顺序分化
生长板是纵向骨生长的主要部位,软骨细胞在软骨内骨发育中起着关键作用。软骨细胞经过一系列分化步骤,形成了独特的分层柱状结构,包括圆形软骨细胞、增殖软骨细胞、前肥大软骨细胞和肥大软骨细胞。前肥大软骨细胞处于增殖期和肥大期之间的过渡阶段,是生长板中的一个关键细胞群。然而,肥大前软骨细胞的分子基础在很大程度上仍未确定。在此,我们对荧光标记的生长板软骨细胞进行了 scRNA-seq 分析,以确定其分子特征。丝氨酸整合因子 5(Serinc5)被鉴定为肥厚前软骨细胞的标记基因。组织学分析表明,Serinc5 在肥厚前软骨细胞中特异性表达,与印度刺猬(Ihh)重叠。Serinc5通过抑制原代软骨细胞中Sox9的转录活性来抑制细胞增殖以及Col2a1和Acan的表达。利用ChIP-seq和ATAC-seq进行的染色质谱分析发现,Serinc5的活性增强子位于内含子1,其染色质状态在软骨细胞分化过程中逐渐被激活。总之,我们的研究结果表明,Serinc5 通过抑制肥大前软骨细胞中 Sox9 的功能来调节软骨细胞从增殖到肥大的顺序分化,为了解生长板中软骨细胞分化的机制提供了新的视角。
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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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