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Updated: Jan 7, 2026

Laser Capture Microdissection of Mouse Embryonic Cartilage and Bone for Gene Expression Analysis
Published on: December 18, 2019
CircTspan3 Promotes Cartilage Development Through ANNEXIN A2-Mediated Ferroptosis and Apoptosis Inhibition and
Yiming Pan1, Fengmei Zhang1, Jiayan Zhong1
1Department of Orthopedics, State Key Laboratory of Ultrasound in Medicine and Engineering, School of Basic Medical Sciences, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing, China.
Circular RNAs (circRNAs) regulate cartilage development. This study identifies circTspan3 as crucial for chondrocyte function and growth, offering potential for treating skeletal disorders.
Area of Science:
- Biochemistry
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) are stable, non-coding RNAs involved in various cellular functions.
- Cartilage development and homeostasis are critical for skeletal health.
- Dysregulation of cartilage development can lead to skeletal disorders.
Purpose of the Study:
- To identify novel circRNAs regulating cartilage development.
- To elucidate the role of circTspan3 in chondrogenesis and skeletal homeostasis.
- To explore the therapeutic potential of circTspan3 in cartilage repair.
Main Methods:
- Identification and characterization of circTspan3.
- Analysis of circTspan3 expression in X-box binding protein 1 (Xbp1) conditional knockout (cKO) mice.
- Investigating the regulatory mechanism of circTspan3 by XBP1 spliced (XBP1s).
- Assessing the function of circTspan3 in chondrocytes and in vivo cartilage repair models.
Main Results:
- circTspan3, derived from Tspan3 gene exons 2-6, is identified as a key regulator of cartilage development.
- circTspan3 expression is downregulated in chondrodysplasia models and correlates with anabolic markers.
- XBP1s transcriptionally upregulates circTspan3, promoting chondrocyte anabolism and suppressing apoptosis and ferroptosis.
- Phosphorylated ANNEXIN A2 (ANXA2) facilitates circTspan3 translocation and exosomal packaging for paracrine signaling.
- Exosomal circTspan3 promotes growth-plate expansion and repairs cartilage defects in vivo.
Conclusions:
- circTspan3 is a critical modulator of growth-plate homeostasis.
- circTspan3 plays a significant role in promoting chondrocyte anabolic activity and survival.
- circTspan3, delivered via exosomes, demonstrates therapeutic potential for cartilage repair and skeletal disorders.
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